







Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YDR466W | PKH3 | SGDID:S000002874 | CRK2 PK5 |
Cell division control protein 2 homolog (EC 2.7.11.22) (EC 2.7.11.23) (PfPK5) |
2.7.11.22,2.7.11.23, | Plasmodium falciparum | 1v0b_a | Q07785 | 98.90 | 1.70E-13 | 2.10E-17 | 129.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | STK11 LKB1 PJS |
Serine/threonine-protein kinase STK11 (EC 2.7.11.1) (Liver kinase B1) (LKB1) (hLKB1) (Renal carcinoma antigen NY-REN-19) |
2.7.11.1 | Homo sapiens | Skin Melanoma,Squamous Cell Carcinoma,Lung Cancer Susceptibility 3,Cowden Syndrome,Melanoma,Rare Gynecological Tumor,Lung Non-Squamous Non-Small Cell Carcinoma,Cowden Syndrome 1,Cervical Adenoma Malignum,Pulmonary Large Cell Neuroendocrine Carcinoma,B-Lymphoblastic Leukemia/Lymphoma,Large Cell Carcinoma,Pancreatic Intraductal Papillary-Colloid Carcinoma,Inherited Cancer-Predisposing Syndrome,Gynecomastia,Vaginal Tubulovillous Adenoma,Hereditary Mixed Polyposis Syndrome,Hepatocellular Clear Cell Carcinoma,Carney Complex Variant,Intestinal Polyposis Syndrome,Dysplastic Nevus Syndrome,Skin Amelanotic Melanoma,Polyhydramnios,Small Intestine Cancer,Vaginal Adenoma,Testicular Germ Cell Tumor,Long Qt Syndrome,Lip And Oral Cavity Cancer,Ovarian Cancer,Adenocarcinoma,Tuberous Sclerosis 2,Tuberous Sclerosis,Testicular Cancer,Acinar Cell Carcinoma,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Acute Monoblastic Leukemia,Colorectal Cancer,Juvenile Polyposis Syndrome,Peutz-Jeghers Syndrome,Polyposis, Skin Pigmentation, Alopecia, And Fingernail Changes,Skin Carcinoma,Cervical Cancer,Lung Benign Neoplasm,Lynch Syndrome,Lung Squamous Cell Carcinoma,Pancreatic Serous Cystadenoma,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy,Diamond-Blackfan Anemia 20,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Tuberous Sclerosis 1,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Intussusception,Vaginal Benign Neoplasm,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Pancreatic Cancer |
2wtk_c | Q15831 | ENSG00000118046 | STK11 | 98.90 | 1.50E-13 | 1.90E-17 | 130.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CHEK1 CHK1 |
Serine/threonine-protein kinase Chk1 (EC 2.7.11.1) (CHK1 checkpoint homolog) (Cell cycle checkpoint kinase) (Checkpoint kinase-1) |
2.7.11.1 | Homo sapiens | Tongue Carcinoma,Neuroblastoma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cerebellar Disease,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Retinoblastoma,Esophageal Cancer,Seckel Syndrome,Mantle Cell Lymphoma,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Ovarian Clear Cell Carcinoma,Autosomal Recessive Cerebellar Ataxia,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer |
2e9v_b | O14757 | ENSG00000149554 | CHEK1 | 99.10 | 1.00E-14 | 1.30E-18 | 135.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | cgd5_820 |
cgd5_820 |
Cryptosporidium parvum | 3lij_a | Q5CS01 | 98.90 | 1.50E-13 | 1.80E-17 | 142.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | ERN1 IRE1 |
Serine/threonine-protein kinase/endoribonuclease IRE1 (Endoplasmic reticulum-to-nucleus signaling 1) (Inositol-requiring protein 1) (hIRE1p) (Ire1-alpha) (IRE1a) [Includes: Serine/threonine-protein kinase (EC 2.7.11.1); Endoribonuclease (EC 3.1.26.-)] |
2.7.11.1 | Homo sapiens | Retinitis Pigmentosa,Non-Alcoholic Fatty Liver Disease,Prion Disease,Alzheimer Disease,Ovarian Cancer,Wolfram Syndrome,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Huntington Disease |
6hx1_a | O75460 | ENSG00000178607 | ERN1 | 98.90 | 2.60E-13 | 3.00E-17 | 138.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | DYRK2 |
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1) |
2.7.12.1 | Homo sapiens | 4azf_a | Q92630 | ENSG00000127334 | DYRK2 | 99.10 | 9.00E-15 | 1.10E-18 | 150.50 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | SNF1 CAT1 CCR1 GLC2 PAS14 YDR477W D8035.20 |
Carbon catabolite-derepressing protein kinase (EC 2.7.11.1) (Sucrose nonfermentating protein 1) |
2.7.11.1 | Saccharomyces cerevisiae | 2fh9_a | P06782 | 98.90 | 8.10E-14 | 1.00E-17 | 131.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PLK3 CNK FNK PRK |
Serine/threonine-protein kinase PLK3 (EC 2.7.11.21) (Cytokine-inducible serine/threonine-protein kinase) (FGF-inducible kinase) (Polo-like kinase 3) (PLK-3) (Proliferation-related kinase) |
2.7.11.21 | Homo sapiens | Breast Cancer |
4b6l_a | Q9H4B4 | ENSG00000173846 | PLK3 | 99.10 | 1.30E-14 | 1.60E-18 | 137.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKACA |
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11) |
2.7.11.11 | Cricetulus griseus | 5n3j_a | P25321 | 99.20 | 1.50E-15 | 1.80E-19 | 151.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CDK9 CDC2L4 TAK |
Cyclin-dependent kinase 9 (EC 2.7.11.22) (EC 2.7.11.23) (C-2K) (Cell division cycle 2-like protein kinase 4) (Cell division protein kinase 9) (Serine/threonine-protein kinase PITALRE) (Tat-associated kinase complex catalytic subunit) |
2.7.11.22,2.7.11.23, | Homo sapiens | Leukemia, Acute Myeloid,Human Immunodeficiency Virus Type 1,Immune Deficiency Disease,Leukemia, Chronic Lymphocytic,Nut Midline Carcinoma |
3mi9_a | P50750 | ENSG00000136807 | CDK9 | 98.90 | 2.60E-13 | 3.10E-17 | 134.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | ROCK1 |
Rho-associated protein kinase 1 (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-35) (Rho-associated, coiled-coil-containing protein kinase 1) (Rho-associated, coiled-coil-containing protein kinase I) (ROCK-I) (p160 ROCK-1) (p160ROCK) |
2.7.11.1 | Homo sapiens | Coronary Artery Vasospasm,Ocular Hyperemia,Breast Cancer,Pediatric Osteosarcoma,Hutchinson-Gilford Progeria Syndrome,Tetralogy Of Fallot,Hypertension, Essential,Lung Cancer |
2v55_c | Q13464 | ENSG00000067900 | ROCK1 | 99.20 | 2.20E-15 | 2.50E-19 | 154.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | BN1205_040370 TGVEG_207820 |
BN1205_040370 TGVEG_207820 |
2.7.11.24 | Toxoplasma gondii | 3rp9_a | B6KP12 | 99.00 | 2.00E-14 | 2.50E-18 | 147.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | AAK1 KIAA1048 |
AP2-associated protein kinase 1 (EC 2.7.11.1) (Adaptor-associated kinase 1) |
2.7.11.1 | Homo sapiens | Parkinson Disease, Late-Onset,Cataract 8, Multiple Types,Hepatitis C Virus,Rabies |
5te0_a | Q2M2I8 | ENSG00000115977 | AAK1 | 98.90 | 1.80E-13 | 2.20E-17 | 134.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | mphB mph(B) DN703_20145 DN703_30815 ECTO6_04941 EHV81_22605 EHV81_28790 EHV90_14185 EHV90_28475 EHW09_19840 EHW09_29090 EXX87_25395 HVW76_22830 HVY77_26855 pO103_99 |
mphB mph(B) DN703_20145 DN703_30815 ECTO6_04941 EHV81_22605 EHV81_28790 EHV90_14185 EHV90_28475 EHW09_19840 EHW09_29090 EXX87_25395 HVW76_22830 HVY77_26855 pO103_99 |
Escherichia coli | 5iwu_a | O32553 | 99.00 | 6.10E-14 | 8.10E-18 | 130.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YDR466W | PKH3 | SGDID:S000002874 | PF3D7_0213400 |
PF3D7_0213400 |
2.7.11.1 | Plasmodium falciparum | 2pmn_x | Q7YTF7 | 98.90 | 1.10E-13 | 1.40E-17 | 137.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | MAP4K4 HGK KIAA0687 NIK |
Mitogen-activated protein kinase kinase kinase kinase 4 (EC 2.7.11.1) (HPK/GCK-like kinase HGK) (MAPK/ERK kinase kinase kinase 4) (MEK kinase kinase 4) (MEKKK 4) (Nck-interacting kinase) |
2.7.11.1 | Homo sapiens | Arteriovenous Malformations Of The Brain,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Theileriasis |
4u3y_a | O95819 | ENSG00000071054 | MAP4K4 | 99.00 | 2.20E-14 | 2.70E-18 | 140.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | NEK1 KIAA1901 |
Serine/threonine-protein kinase Nek1 (EC 2.7.11.1) (Never in mitosis A-related kinase 1) (NimA-related protein kinase 1) (Renal carcinoma antigen NY-REN-55) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease,Uterine Adnexa Cancer,Cor Triatriatum,Cor Triatriatum Dexter,Amyotrophic Lateral Sclerosis 1,Short-Rib Thoracic Dysplasia 12,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Lateral Sclerosis,Motor Neuron Disease,Nephronophthisis,Short-Rib Thoracic Dysplasia 3 With Or Without Polydactyly,Fundus Dystrophy,Kidney Disease,Ellis-Van Creveld Syndrome,Amyotrophic Lateral Sclerosis 24,Polydactyly,Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations,Cranioectodermal Dysplasia,Asphyxiating Thoracic Dystrophy,Weyers Acrofacial Dysostosis,Mohr Syndrome,Short-Rib Thoracic Dysplasia 1 With Or Without Polydactyly,Frontotemporal Dementia,Joubert Syndrome 1,Short-Rib Thoracic Dysplasia 6 With Or Without Polydactyly |
4apc_b | Q96PY6 | ENSG00000137601 | NEK1 | 98.90 | 1.40E-13 | 1.70E-17 | 136.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PHO85 SSG3 YPL031C P7102.18A |
Cyclin-dependent protein kinase PHO85 (EC 2.7.11.22) (Negative regulator of the PHO system) (Serine/threonine-protein kinase PHO85) |
2.7.11.22 | Saccharomyces cerevisiae | 4krd_a | P17157 | 98.80 | 3.80E-13 | 4.60E-17 | 130.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | EIF2AK3 PEK PERK |
Eukaryotic translation initiation factor 2-alpha kinase 3 (EC 2.7.11.1) (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK) |
2.7.11.1 | Homo sapiens | Skin Melanoma,Retinitis Pigmentosa,Neonatal Diabetes,Prion Disease,Diabetes Mellitus,Alzheimer Disease,Rasopathy,Retinal Degeneration,Subungual Glomus Tumor,Crisponi/Cold-Induced Sweating Syndrome 1,Osteoporosis,Wolfram Syndrome,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Disease Of Mental Health,Leukoencephalopathy With Vanishing White Matter,Odontochondrodysplasia,Trichothiodystrophy 5, Nonphotosensitive,Cardiomyopathy, Familial Hypertrophic, 25,Permanent Neonatal Diabetes Mellitus,Palmoplantar Keratoderma, Bothnian Type |
4g31_a | Q9NZJ5 | ENSG00000172071 | EIF2AK3 | 99.00 | 3.80E-14 | 4.90E-18 | 133.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | GRK5 GPRK5 |
G protein-coupled receptor kinase 5 (EC 2.7.11.16) (G protein-coupled receptor kinase GRK5) |
2.7.11.16 | Homo sapiens | Systolic Heart Failure,Palmoplantar Keratoderma And Congenital Alopecia 2,Asthma |
4tnd_a | P34947 | ENSG00000198873 | GRK5 | 99.10 | 1.60E-14 | 1.70E-18 | 159.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Gentamicin resistance protein |
Gentamicin resistance protein |
Enterococcus gallinarum | 6ctz_a | P96762 | 98.80 | 3.40E-13 | 4.70E-17 | 123.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | STK38 NDR1 |
Serine/threonine-protein kinase 38 (EC 2.7.11.1) (NDR1 protein kinase) (Nuclear Dbf2-related kinase 1) |
2.7.11.1 | Homo sapiens | Myeloproliferative Syndrome, Transient,Wilson-Turner X-Linked Mental Retardation Syndrome |
6bxi_a | Q15208 | ENSG00000112079 | STK38 | 99.10 | 1.40E-14 | 1.70E-18 | 142.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PLK4 SAK STK18 |
Serine/threonine-protein kinase PLK4 (EC 2.7.11.21) (Polo-like kinase 4) (PLK-4) (Serine/threonine-protein kinase 18) (Serine/threonine-protein kinase Sak) |
2.7.11.21 | Homo sapiens | Congenital Nervous System Abnormality,Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome,Colorectal Cancer,Microcephaly,Seckel Syndrome,Microcephaly And Chorioretinopathy, Autosomal Recessive, 2,Isolated Growth Hormone Deficiency,Primary Autosomal Recessive Microcephaly,Joubert Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia |
3cok_b | O00444 | ENSG00000142731 | PLK4 | 99.10 | 7.60E-15 | 9.60E-19 | 138.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PKH2 PKH1 CAALFM_C112410CA CaO19.12690 CaO19.5224 orf19.5224 |
Serine/threonine-protein kinase PKH2 (EC 2.7.11.1) (PKB-activating kinase homolog 2) |
2.7.11.1 | Candida albicans | 4c0t_a | Q5A3P6 | 99.20 | 7.30E-16 | 6.40E-20 | 181.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | ROCK2 KIAA0619 |
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho kinase 2) (Rho-associated, coiled-coil-containing protein kinase 2) (Rho-associated, coiled-coil-containing protein kinase II) (ROCK-II) (p164 ROCK-2) |
2.7.11.1 | Homo sapiens | Coronary Artery Vasospasm,Dextrocardia,Ureteral Obstruction,Breast Cancer,Tongue Squamous Cell Carcinoma,Hypertension, Essential |
4wot_b | O75116 | ENSG00000134318 | ROCK2 | 99.30 | 3.00E-16 | 3.50E-20 | 160.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | STK32A YANK1 |
Serine/threonine-protein kinase 32A (EC 2.7.11.1) (Yet another novel kinase 1) |
2.7.11.1 | Homo sapiens | 4fr4_a | Q8WU08 | ENSG00000169302 | STK32A | 99.10 | 6.80E-15 | 8.10E-19 | 149.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | INSR |
Insulin receptor (IR) (EC 2.7.10.1) (CD antigen CD220) [Cleaved into: Insulin receptor subunit alpha; Insulin receptor subunit beta] |
2.7.10.1 | Homo sapiens | Acanthosis Nigricans,Liver Disease,Heart Disease,Autosomal Dominant Polycystic Kidney Disease,Hyperglycemia,Hypertrichosis,Islet Cell Tumor,Myopathy,Polycystic Ovary Syndrome,Hyperandrogenism,Non-Alcoholic Fatty Liver Disease,Gestational Diabetes,Prediabetes Syndrome,Diabetes Mellitus,Fatty Liver Disease,Hyperinsulinism,Alzheimer Disease,Myotonic Disease,Myotonic Dystrophy 1,Fasting Hypoglycemia,Insulin-Like Growth Factor I,Fetal Macrosomia,Hypoglycemia,Liver Cirrhosis,Migraine With Aura,Insr-Related Severe Syndromic Insulin Resistance,Pigmentation Disease,Type 1 Diabetes Mellitus,Hyperinsulinemic Hypoglycemia,Ovarian Cancer,Adenocarcinoma,Glucose Intolerance,Breast Cancer,Colorectal Cancer,Lipid Metabolism Disorder,Ovarian Disease,Hyperinsulinemic Hypoglycemia, Familial, 5,Hyperinsulinemic Hypoglycemia, Familial, 4,Centronuclear Myopathy,Body Mass Index Quantitative Trait Locus 11,Diabetes Mellitus, Insulin-Resistant, With Acanthosis Nigricans,Type 2 Diabetes Mellitus,Abdominal Obesity-Metabolic Syndrome 1,Congenital Generalized Lipodystrophy,Maturity-Onset Diabetes Of The Young,Donohue Syndrome,Hypertension, Essential,Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities |
3bu3_a | P06213 | ENSG00000171105 | INSR | 98.90 | 2.70E-13 | 3.50E-17 | 128.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | aph(2')-Ib |
aph(2')-Ib |
Enterococcus faecium | 3ham_b | Q9EVD7 | 98.90 | 1.50E-13 | 2.00E-17 | 125.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | CDK2 CDKN2 |
Cyclin-dependent kinase 2 (EC 2.7.11.22) (Cell division protein kinase 2) (p33 protein kinase) |
2.7.11.22 | Homo sapiens | Pancreatic Adenocarcinoma,Endometrial Cancer,Smooth Muscle Tumor,Melanoma,Endometrial Hyperplasia,Leukemia, Chronic Myeloid,Leiomyosarcoma,Ocular Cancer,Retinal Cancer,Neuroblastoma,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Bladder Cancer,Lung Adenoma,Laryngeal Squamous Cell Carcinoma,Ovarian Cancer,Testicular Cancer,Eye Disease,Uterine Sarcoma,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Nervous System Cancer,Hepatocellular Carcinoma,Microcephaly,Pheochromocytoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Cecal Benign Neoplasm,Retinoblastoma,Sensory System Disease,Trichothiodystrophy 5, Nonphotosensitive,Mantle Cell Lymphoma,Gastrointestinal Stromal Tumor,Cecum Adenoma,Leukemia, Chronic Lymphocytic,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Pancreatic Cancer |
4i3z_c | P24941 | ENSG00000123374 | CDK2 | 99.00 | 3.40E-14 | 4.30E-18 | 134.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | GSK3B |
Glycogen synthase kinase-3 beta (GSK-3 beta) (EC 2.7.11.26) (Serine/threonine-protein kinase GSK3B) (EC 2.7.11.1) |
2.7.11.26 | Homo sapiens | Liver Disease,Endometrial Cancer,Epilepsy,Polycystic Kidney Disease,Diabetes Mellitus,Alzheimer Disease,Major Depressive Disorder,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Barbiturate Dependence,Alzheimer Disease 9,Dementia,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Parkinson Disease 1, Autosomal Dominant,Hepatocellular Carcinoma,Bipolar Disorder,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Type 2 Diabetes Mellitus,Schizophrenia,Ophthalmomyiasis,Familial Adenomatous Polyposis,Severe Congenital Neutropenia,Aneurysmal Bone Cysts,Attention Deficit-Hyperactivity Disorder,Medulloblastoma,Frontotemporal Dementia,Pancreatic Cancer |
1h8f_a | P49841 | ENSG00000082701 | GSK3B | 99.00 | 5.00E-14 | 6.10E-18 | 139.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | BTK AGMX1 ATK BPK |
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) |
2.7.10.2 | Homo sapiens | Pneumocystosis,X-Linked Recessive Disease,Lymphopenia,Conjunctivitis,Richter'S Syndrome,Macroglobulinemia,Pyoderma,Cll/Sll,Mast-Cell Leukemia,Polyarticular Juvenile Idiopathic Arthritis,Spherocytosis, Type 5,Ecthyma,B Cell Deficiency,Lung Large Cell Carcinoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Neutropenia,Agammaglobulinemia 1, Autosomal Recessive,Plasma Protein Metabolism Disease,Isolated Agammaglobulinemia,Poliomyelitis,Leukemia, Acute Myeloid,Growth Hormone Deficiency,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Bacterial Infectious Disease,Breast Cancer,Central Nervous System Hematologic Cancer,Congenital Hypogammaglobulinemia,Immunodeficiency 14,Panniculitis,Immunodeficiency 33,Lymphoma, Non-Hodgkin, Familial,Baylisascariasis,Agammaglobulinemia, X-Linked,Paralytic Poliomyelitis,Immune Deficiency Disease,Myelodysplastic Syndrome,Immunoglobulin A Deficiency 1,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Diffuse Large B-Cell Lymphoma,Mantle Cell Lymphoma,Lymphoplasmacytic Lymphoma,Marginal Zone B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Williams-Beuren Syndrome,Combined Oxidative Phosphorylation Deficiency 9,Mohr-Tranebjaerg Syndrome,Cd40 Ligand Deficiency,Isolated Growth Hormone Deficiency, Type Iii, With Agammaglobulinemia,Immunodeficiency 45,Immunodeficiency With Hyper-Igm, Type 1,Leukemia, Chronic Lymphocytic,Myeloma, Multiple,Isolated Growth Hormone Deficiency,Isolated Growth Hormone Deficiency Type Iii,Waldenstroem'S Macroglobulinemia |
5p9j_a | Q06187 | ENSG00000010671 | BTK | 98.90 | 3.00E-13 | 3.80E-17 | 126.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MAPK7 BMK1 ERK5 PRKM7 |
Mitogen-activated protein kinase 7 (MAP kinase 7) (MAPK 7) (EC 2.7.11.24) (Big MAP kinase 1) (BMK-1) (Extracellular signal-regulated kinase 5) (ERK-5) |
2.7.11.24 | Homo sapiens | Bone Cancer,Noma,Primary Bone Cancer,Dilated Cardiomyopathy,Breast Cancer,Prostate Cancer,Osteogenesis Imperfecta, Type Xviii,Scoliosis, Isolated 1,Scoliosis |
4zsg_a | Q13164 | ENSG00000166484 | MAPK7 | 99.00 | 7.70E-14 | 9.60E-18 | 137.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | pknB MRA_0016 |
pknB MRA_0016 |
2.7.11.1 | Mycobacterium tuberculosis | 3ork_a | A5TY84 | 98.90 | 2.60E-13 | 3.30E-17 | 130.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | ROP 2 |
ROP 2 |
Toxoplasma gondii | 2w1z_b | Q27007 | 99.00 | 4.90E-14 | 6.10E-18 | 139.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | ROP8 |
ROP8 |
Toxoplasma gondii | 3byv_a | O15693 | 99.10 | 1.30E-14 | 1.60E-18 | 145.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | Camk2d Kiaa4163 |
Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) |
2.7.11.17 | Mus musculus | 6bab_a | Q6PHZ2 | 99.00 | 3.30E-14 | 4.10E-18 | 137.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | STK10 LOK |
Serine/threonine-protein kinase 10 (EC 2.7.11.1) (Lymphocyte-oriented kinase) |
2.7.11.1 | Homo sapiens | Testicular Germ Cell Tumor |
4bc6_a | O94804 | ENSG00000072786 | STK10 | 99.10 | 1.00E-14 | 1.30E-18 | 138.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MASTL GW GWL THC2 |
Serine/threonine-protein kinase greatwall (GW) (GWL) (hGWL) (EC 2.7.11.1) (Microtubule-associated serine/threonine-protein kinase-like) (MAST-L) |
2.7.11.1 | Homo sapiens | Autosomal Thrombocytopenia With Normal Platelets,Sick Building Syndrome,Thrombocytopenia,Thrombocytopenia 2,Gray Platelet Syndrome,Ceroid Lipofuscinosis, Neuronal, 2 |
5loh_a | Q96GX5 | ENSG00000120539 | MASTL | 99.30 | 2.10E-16 | 2.50E-20 | 157.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PHKG2 |
Phosphorylase b kinase gamma catalytic chain, liver/testis isoform (PHK-gamma-LT) (PHK-gamma-T) (EC 2.7.11.19) (PSK-C3) (Phosphorylase kinase subunit gamma-2) |
2.7.11.19 | Homo sapiens | Glycogen Storage Disease Ixa,Glycogen Storage Disease Ixc,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency,Glycogen Storage Disease Ia,Glycogen Storage Disease, Type Ixd,Glycogen Storage Disease Ix,Glycogen Storage Disease Ixb |
2y7j_c | P15735 | ENSG00000156873 | PHKG2 | 99.10 | 4.20E-15 | 5.10E-19 | 148.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDK12 CRK7 CRKRS KIAA0904 |
Cyclin-dependent kinase 12 (EC 2.7.11.22) (EC 2.7.11.23) (Cdc2-related kinase, arginine/serine-rich) (CrkRS) (Cell division cycle 2-related protein kinase 7) (CDC2-related protein kinase 7) (Cell division protein kinase 12) (hCDK12) |
2.7.11.22,2.7.11.23, | Homo sapiens | Lung Cancer Susceptibility 3,Bartholin'S Gland Adenocarcinoma,Corneal Endothelial Dystrophy,Gastric Cancer,Lung Cancer |
4cxa_c | Q9NYV4 | ENSG00000167258 | CDK12 | 99.00 | 4.80E-14 | 5.90E-18 | 138.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | AKT1 PKB RAC |
RAC-alpha serine/threonine-protein kinase (EC 2.7.11.1) (Protein kinase B) (PKB) (Protein kinase B alpha) (PKB alpha) (Proto-oncogene c-Akt) (RAC-PK-alpha) |
2.7.11.1 | Homo sapiens | Adult Hepatocellular Carcinoma,Breast Papillomatosis,Esophageal Disease,Pancreatic Adenocarcinoma,Muscular Disease,Skin Melanoma,Liver Disease,Mitral Valve Disease,Heart Disease,Neurofibromatosis, Type Ii,Endometrial Cancer,Bile Duct Disease,Spinal Chordoma,Hepatopulmonary Syndrome,Squamous Cell Carcinoma,Pfeiffer Syndrome,Glucose Metabolism Disease,Childhood T-Cell Acute Lymphoblastic Leukemia,Hyperglycemia,Retinitis Pigmentosa,Thyroid Gland Cancer,Hair Disease,Macroglobulinemia,Lung Cancer Susceptibility 3,Kagami-Ogata Syndrome,Adenoid Cystic Carcinoma,Non-Alcoholic Fatty Liver Disease,Chordoma,Cowden Syndrome,Polycystic Kidney Disease,Microvascular Complications Of Diabetes 5,Suppression Of Tumorigenicity 12,Melanoma,Connective Tissue Disease,Ocular Hypertension,Leukemia, Chronic Myeloid,Overnutrition,Inherited Metabolic Disorder,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Adenoma,Spherocytosis, Type 5,Cowden Syndrome 1,Breast Juvenile Papillomatosis,Lipid Storage Disease,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Bone Sarcoma,Hypertrophic Cardiomyopathy,Placental Choriocarcinoma,Leukocyte Disease,Clear Cell Renal Cell Carcinoma,Hyperostosis,Alzheimer Disease,Hepatoblastoma,Rasopathy,Nasopharyngeal Disease,Myocardial Infarction,Major Depressive Disorder,Bile Duct Cancer,Intestinal Benign Neoplasm,Stroke, Ischemic,Teeth Hard Tissue Disease,Amyotrophic Lateral Sclerosis 1,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Amelogenesis Imperfecta,Retinal Cancer,Blood Platelet Disease,Biliary Tract Disease,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Infratentorial Cancer,Leptin Deficiency Or Dysfunction,Lymphatic System Disease,Neurofibromatosis, Type I,Insulin-Like Growth Factor I,Neuroblastoma,Colonic Benign Neoplasm,Subependymal Glioma,Blood Coagulation Disease,Benign Ependymoma,Pilocytic Astrocytoma,Diffuse Astrocytoma,Childhood Leukemia,Bile Duct Adenocarcinoma,Hemangioma Of Lung,Nevus, Epidermal,Distal Muscular Dystrophy With Anterior Tibial Onset,Retinal Vascular Disease,Psychotic Disorder,Leukemia, Acute Myeloid,Noonan Syndrome 1,Bone Marrow Cancer,Leber Plus Disease,Hemangioma,Leukemia, Acute Lymphoblastic,Cataract,Combined Immunodeficiency,Liver Cirrhosis,Pancreas Disease,Papilloma,Cardiovascular System Disease,Autonomic Nervous System Neoplasm,Kidney Cancer,Pleural Cancer,Basal Cell Nevus Syndrome,Cowden Syndrome 6,Bladder Cancer,Focal Segmental Glomerulosclerosis,Epithelial-Myoepithelial Carcinoma,Thymus Gland Disease,Brain Cancer,Colonic Disease,Lung Adenoma,Lung Oat Cell Carcinoma,Endometrial Adenocarcinoma,Oropharynx Cancer,Cervix Carcinoma,Ulcerative Colitis,Nervous System Disease,Osteoporosis,Anal Squamous Cell Carcinoma,Ovarian Cancer,Adenocarcinoma,Tuberous Sclerosis 2,In Situ Carcinoma,Tuberous Sclerosis,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Acute Megakaryocytic Leukemia,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Ovarian Serous Cystadenocarcinoma,Cystadenocarcinoma,Serous Cystadenocarcinoma,Gallbladder Cancer,Hepatocellular Carcinoma,Premature Menopause,Combined Hepatocellular Carcinoma And Cholangiocarcinoma,Skin Papilloma,Partial Third-Nerve Palsy,Neurilemmoma,Rhabdomyosarcoma,Ischemia,Tongue Disease,Chronic Granulomatous Disease,Thymoma,Thymus Cancer,Ovarian Disease,Noonan Syndrome With Multiple Lentigines,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Teratoma,Bipolar Disorder,Macular Degeneration, Age-Related, 1,Immunodeficiency 14,Sarcoma,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Proteus Syndrome,Cervical Cancer,Toxic Encephalopathy,Ovarian Cystadenocarcinoma,Body Mass Index Quantitative Trait Locus 11,Penile Disease,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Pulmonary Fibrosis, Idiopathic,Congenital Myasthenic Syndrome,Retinitis Pigmentosa 47,Respiratory System Disease,Integumentary System Disease,Skin Disease,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Cervical Squamous Cell Carcinoma,Lynch Syndrome,Hidradenoma,Lung Squamous Cell Carcinoma,Fragile X Syndrome,Thyroid Gland Follicular Carcinoma,Schizophrenia,Sensory System Disease,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Skeletal Muscle Cancer,Muscle Cancer,Small Cell Cancer Of The Lung,Immunodeficiency 36,Hypotrichosis 1,Exanthem,Esophageal Cancer,Severe Congenital Neutropenia,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Immune Deficiency Disease,Myelodysplastic Syndrome,Meningioma, Radiation-Induced,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Autosomal Genetic Disease,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Tuberous Sclerosis 1,Hashimoto Thyroiditis,Gastrointestinal Stromal Tumor,Diabetic Encephalopathy,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Huntington Disease,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Meningioma, Familial,Pre-Malignant Neoplasm,Lymphatic System Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Cell Type Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Uterine Benign Neoplasm,Acquired Metabolic Disease,Kaposi Sarcoma,Colitis,Klippel-Trenaunay-Weber Syndrome,Gallbladder Disease,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Systemic Lupus Erythematosus,Pelizaeus-Merzbacher Disease,Rett Syndrome,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lymphoproliferative Syndrome,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Oculoectodermal Syndrome,Osteogenic Sarcoma,Pancreatic Cancer |
4gv1_a | P31749 | ENSG00000142208 | AKT1 | 99.30 | 4.20E-16 | 5.10E-20 | 154.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CSNK2A1 CK2A1 |
Casein kinase II subunit alpha (CK II alpha) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Okur-Chung Neurodevelopmental Syndrome,Connective Tissue Disease,Alzheimer Disease,Prostate Stromal Sarcoma,Distal Muscular Dystrophy With Anterior Tibial Onset,Kidney Leiomyosarcoma,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Prostate Cancer,Disease Of Mental Health,Malaria |
3q04_a | P68400 | ENSG00000101266 | CSNK2A1 | 99.00 | 2.10E-14 | 2.70E-18 | 138.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CAMK1 |
Calcium/calmodulin-dependent protein kinase type 1 (EC 2.7.11.17) (CaM kinase I) (CaM-KI) (CaM kinase I alpha) (CaMKI-alpha) |
2.7.11.17 | Homo sapiens | Acrofacial Dysostosis 1, Nager Type |
4fg7_a | Q14012 | ENSG00000134072 | CAMK1 | 99.10 | 4.40E-15 | 5.40E-19 | 142.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | ROP5C |
ROP5C |
Toxoplasma gondii | 4lv8_a | I6ZQR7 | 98.80 | 3.50E-13 | 4.40E-17 | 133.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | mphA mph(A) mph2 A9R57_28020 AKG29_00750 AM465_27035 APT94_14590 AWB10_22655 AZ95_0038 B6V57_21760 B6V57_26915 B9N33_26275 B9T59_28660 BANRA_05393 BE963_00520 BEN53_26060 BFD68_26420 BJJ90_27660 BK248_28265 BK292_28790 BK296_27590 BK334_26695 BK373_25655 BK375_28440 BK383_16405 BON83_00200 BON86_00135 BON94_01620 BON96_04030 BON98_24665 BvCmsSIP044_05438 BVL39_07775 BVL39_26555 C5P01_27830 C5P44_28325 C6669_28275 C7235_26780 CI641_023240 CI641_027265 CQP61_00510 CR538_26720 CRT43_27540 CWS33_26285 D0X26_00065 D0X26_28390 D3O91_28150 D4U49_26725 D4U49_28850 D4V08_26930 D4V08_28620 D9K54_18860 DB359_27580 DJ503_27015 DL545_01115 DL545_26280 DM102_27005 DM129_26590 DM129_28130 DMZ50_26400 DMZ50_28240 DS732_30505 E2148_26085 E2855_05768 EA167_25450 EA191_26920 EA203_25400 EA433_24880 ECONIH1_26770 ECTO124_05299 EF082_27695 EF082_28360 EGT48_01480 EHH55_26515 EI021_26230 EI041_22580 EIA21_26660 EIZ93_26315 EJC75_00570 ELT17_24440 ELT17_26465 ELT31_24935 ELT31_26145 ELT33_25215 ELV00_24775 ELV08_25535 ELV15_24060 ELV22_23870 ELV22_25960 ELV24_24180 ELV24_25785 ELV28_26235 ELV28_27675 ELV28_29590 ELX56_25505 ELX56_25985 ELX61_23195 ELX68_23715 ELX68_25540 ELX76_26525 ELX76_27685 ELX79_23940 ELX79_27660 ELX83_25990 ELX83_26675 ELX96_23275 ELX96_27940 ELY23_24430 ELY23_26140 ELY32_25815 ELY32_27370 ELY41_23030 ELY41_28165 ELY50_24960 ELY50_26940 EQ823_24855 ERS085366_04054 ERS150873_04753 EST51_05890 ETN48_p0083 ExPECSC065_05095 EXX13_27015 EYD11_23960 F1E19_25850 F6T45_24105 F6T45_27355 F6T51_24705 F6T51_26410 FORC82_p033 FTV93_29750 G3565_27960 G5616_24605 GE087_26095 GE087_26865 GE096_24635 GP698_23880 GRC73_23725 GRC73_24610 HGR87_26435 HGR87_27495 HGS12_25940 HGS12_26860 HGS82_24915 HGS82_26380 HH456_005005 HH456_005213 HH814_005028 HH814_005237 HH830_004989 HH830_005256 HHA77_005061 HHA77_005227 HHJ44_24960 HHJ51_25125 HIA56_005086 HIA56_005275 HJI76_004975 HJI76_005383 HJT90_005211 HJT90_005339 HJU54_005032 HJU54_005224 HK427_004962 HK427_005083 HL186_24280 HL186_25120 HL465_24825 HL465_27485 HL601_25845 HL601_27150 HLI97_004826 HLI97_006009 HLT96_25635 HLT96_28645 HLU13_25260 HLU13_27740 HLY53_24310 HLY53_26530 HLZ85_23950 HLZ85_26045 HmCmsJML146_04797 HMP86_23800 HMP86_25195 HMPREF3040_01642 HMT01_26980 HMT01_28300 HMT08_29160 HNC38_25510 HNC38_27325 HNC59_25665 HNC59_29535 HNC80_25930 HNC80_27515 HNC94_26080 HNC94_27430 HNC99_25610 HNC99_29535 HND23_19740 HND23_28055 HNV94_25600 HNV94_28025 HNX16_25130 HNX16_27140 HNX34_24085 HNX34_26635 HPE39_25975 HVX17_27920 HWQ66_24190 MS6198_B122 MS8345_A00018 NCTC13846_04924 orf00017 pCTXM123_C0996_11 RCS105_pI0109 RCS28_PI0046 RCS42_P0046 RCS51_P0074 RCS55TR727_P0021 RCS57_p0100 RCS65_P0021 RCS78_P0037 RCS79_P0002 SAMEA4362930_00091 SAMEA4370330_00104 SAMEA4370365_00007 SAMEA4370473_00005 TUM18780_18910 TUM18780_46330 U14A_A00117 UN86_19875 WP5S18E08_P10220 WP7S18E09_P12070 YDC107_4986 |
mphA mph(A) mph2 A9R57_28020 AKG29_00750 AM465_27035 APT94_14590 AWB10_22655 AZ95_0038 B6V57_21760 B6V57_26915 B9N33_26275 B9T59_28660 BANRA_05393 BE963_00520 BEN53_26060 BFD68_26420 BJJ90_27660 BK248_28265 BK292_28790 BK296_27590 BK334_26695 BK373_25655 BK375_28440 BK383_16405 BON83_00200 BON86_00135 BON94_01620 BON96_04030 BON98_24665 BvCmsSIP044_05438 BVL39_07775 BVL39_26555 C5P01_27830 C5P44_28325 C6669_28275 C7235_26780 CI641_023240 CI641_027265 CQP61_00510 CR538_26720 CRT43_27540 CWS33_26285 D0X26_00065 D0X26_28390 D3O91_28150 D4U49_26725 D4U49_28850 D4V08_26930 D4V08_28620 D9K54_18860 DB359_27580 DJ503_27015 DL545_01115 DL545_26280 DM102_27005 DM129_26590 DM129_28130 DMZ50_26400 DMZ50_28240 DS732_30505 E2148_26085 E2855_05768 EA167_25450 EA191_26920 EA203_25400 EA433_24880 ECONIH1_26770 ECTO124_05299 EF082_27695 EF082_28360 EGT48_01480 EHH55_26515 EI021_26230 EI041_22580 EIA21_26660 EIZ93_26315 EJC75_00570 ELT17_24440 ELT17_26465 ELT31_24935 ELT31_26145 ELT33_25215 ELV00_24775 ELV08_25535 ELV15_24060 ELV22_23870 ELV22_25960 ELV24_24180 ELV24_25785 ELV28_26235 ELV28_27675 ELV28_29590 ELX56_25505 ELX56_25985 ELX61_23195 ELX68_23715 ELX68_25540 ELX76_26525 ELX76_27685 ELX79_23940 ELX79_27660 ELX83_25990 ELX83_26675 ELX96_23275 ELX96_27940 ELY23_24430 ELY23_26140 ELY32_25815 ELY32_27370 ELY41_23030 ELY41_28165 ELY50_24960 ELY50_26940 EQ823_24855 ERS085366_04054 ERS150873_04753 EST51_05890 ETN48_p0083 ExPECSC065_05095 EXX13_27015 EYD11_23960 F1E19_25850 F6T45_24105 F6T45_27355 F6T51_24705 F6T51_26410 FORC82_p033 FTV93_29750 G3565_27960 G5616_24605 GE087_26095 GE087_26865 GE096_24635 GP698_23880 GRC73_23725 GRC73_24610 HGR87_26435 HGR87_27495 HGS12_25940 HGS12_26860 HGS82_24915 HGS82_26380 HH456_005005 HH456_005213 HH814_005028 HH814_005237 HH830_004989 HH830_005256 HHA77_005061 HHA77_005227 HHJ44_24960 HHJ51_25125 HIA56_005086 HIA56_005275 HJI76_004975 HJI76_005383 HJT90_005211 HJT90_005339 HJU54_005032 HJU54_005224 HK427_004962 HK427_005083 HL186_24280 HL186_25120 HL465_24825 HL465_27485 HL601_25845 HL601_27150 HLI97_004826 HLI97_006009 HLT96_25635 HLT96_28645 HLU13_25260 HLU13_27740 HLY53_24310 HLY53_26530 HLZ85_23950 HLZ85_26045 HmCmsJML146_04797 HMP86_23800 HMP86_25195 HMPREF3040_01642 HMT01_26980 HMT01_28300 HMT08_29160 HNC38_25510 HNC38_27325 HNC59_25665 HNC59_29535 HNC80_25930 HNC80_27515 HNC94_26080 HNC94_27430 HNC99_25610 HNC99_29535 HND23_19740 HND23_28055 HNV94_25600 HNV94_28025 HNX16_25130 HNX16_27140 HNX34_24085 HNX34_26635 HPE39_25975 HVX17_27920 HWQ66_24190 MS6198_B122 MS8345_A00018 NCTC13846_04924 orf00017 pCTXM123_C0996_11 RCS105_pI0109 RCS28_PI0046 RCS42_P0046 RCS51_P0074 RCS55TR727_P0021 RCS57_p0100 RCS65_P0021 RCS78_P0037 RCS79_P0002 SAMEA4362930_00091 SAMEA4370330_00104 SAMEA4370365_00007 SAMEA4370473_00005 TUM18780_18910 TUM18780_46330 U14A_A00117 UN86_19875 WP5S18E08_P10220 WP7S18E09_P12070 YDC107_4986 |
Escherichia coli | 5igh_a | Q47396 | 99.10 | 4.50E-15 | 5.80E-19 | 139.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YDR466W | PKH3 | SGDID:S000002874 | aph(2'')-Id |
aph(2'')-Id |
Enterococcus casseliflavus | 3n4u_a | O68183 | 99.00 | 1.60E-14 | 2.30E-18 | 131.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | ULK2 KIAA0623 |
Serine/threonine-protein kinase ULK2 (EC 2.7.11.1) (Unc-51-like kinase 2) |
2.7.11.1 | Homo sapiens | 6qau_a | Q8IYT8 | ENSG00000083290 | ULK2 | 99.00 | 3.10E-14 | 4.00E-18 | 133.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | PHKG1 PHKG |
Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform (EC 2.7.11.19) (Phosphorylase kinase subunit gamma-1) (Serine/threonine-protein kinase PHKG1) (EC 2.7.11.1) (EC 2.7.11.26) |
2.7.11.1,2.7.11.19,2.7.11.26 | Oryctolagus cuniculus | 2phk_a | P00518 | 99.20 | 2.80E-15 | 3.70E-19 | 139.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CDPK1 |
CDPK1 |
Toxoplasma gondii | 3nyv_a | Q9BJF5 | 99.00 | 2.40E-14 | 3.00E-18 | 146.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | RPS6KB1 STK14A |
Ribosomal protein S6 kinase beta-1 (S6K-beta-1) (S6K1) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 1) (P70S6K1) (p70-S6K 1) (Ribosomal protein S6 kinase I) (Serine/threonine-protein kinase 14A) (p70 ribosomal S6 kinase alpha) (p70 S6 kinase alpha) (p70 S6K-alpha) (p70 S6KA) |
2.7.11.1 | Homo sapiens | Mitral Valve Disease,Retinitis Pigmentosa,Cowden Syndrome,Pyriform Sinus Cancer,Cowden Syndrome 1,Placental Choriocarcinoma,Uterus Perivascular Epithelioid Cell Tumor,Subependymal Glioma,Benign Ependymoma,Leukemia, Acute Myeloid,Nephronophthisis,Kidney Angiomyolipoma,Aortic Disease,Skin Amelanotic Melanoma,Ovarian Cancer,Tuberous Sclerosis 2,Tuberous Sclerosis,Breast Cancer,Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Rhabdomyosarcoma,Acute Laryngopharyngitis,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Diamond-Blackfan Anemia 20,Esophageal Cancer,Muscle Hypertrophy,Mantle Cell Lymphoma,Tuberous Sclerosis 1,Lymphangioleiomyomatosis,Leukodystrophy, Hypomyelinating, 12,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Pancreatic Cancer |
3wf7_a | P23443 | ENSG00000108443 | RPS6KB1 | 99.20 | 2.80E-15 | 3.50E-19 | 146.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Stk39 Spak |
STE20/SPS1-related proline-alanine-rich protein kinase (Ste-20-related kinase) (EC 2.7.11.1) (Serine/threonine-protein kinase 39) |
2.7.11.1 | Mus musculus | 5dbx_a | Q9Z1W9 | 99.00 | 1.90E-14 | 2.30E-18 | 140.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | MAPK8 JNK1 PRKM8 SAPK1 SAPK1C |
Mitogen-activated protein kinase 8 (MAP kinase 8) (MAPK 8) (EC 2.7.11.24) (JNK-46) (Stress-activated protein kinase 1c) (SAPK1c) (Stress-activated protein kinase JNK1) (c-Jun N-terminal kinase 1) |
2.7.11.24 | Homo sapiens | Liver Disease,Endometrial Cancer,Lung Cancer Susceptibility 3,Non-Alcoholic Fatty Liver Disease,Hepatitis C,Acantholytic Acanthoma,Leukemia, Chronic Myeloid,Diabetes Mellitus,Non-Alcoholic Steatohepatitis,Fatty Liver Disease,Alzheimer Disease,Epidermolysis Bullosa Simplex,Hepatitis,Colon Adenocarcinoma,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Hereditary Spastic Paraplegia,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Burkitt Lymphoma,Breast Cancer,Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Hepatocellular Carcinoma,Sarcoma,Fibrosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Type 2 Diabetes Mellitus,Renal Fibrosis,Acute Promyelocytic Leukemia,Huntington Disease,Nasopharyngeal Carcinoma,Cardiomyopathy, Familial Hypertrophic, 25,Neu-Laxova Syndrome 1,Lung Cancer,Pancreatic Cancer |
2xrw_a | P45983 | ENSG00000107643 | MAPK8 | 98.90 | 1.70E-13 | 2.10E-17 | 137.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MAP2K1 MEK1 PRKMK1 |
Dual specificity mitogen-activated protein kinase kinase 1 (MAP kinase kinase 1) (MAPKK 1) (MKK1) (EC 2.7.12.2) (ERK activator kinase 1) (MAPK/ERK kinase 1) (MEK 1) |
2.7.12.2 | Homo sapiens | Melorheostosis, Isolated,Skin Melanoma,Achondroplasia,Heart Disease,Ichthyosis,Squamous Cell Carcinoma,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Lung Cancer Susceptibility 3,Melorheostosis,Pulmonary Valve Stenosis,Suppression Of Tumorigenicity 12,Melanoma,Acneiform Dermatitis,Neurofibromatosis-Noonan Syndrome,Hypertrophic Cardiomyopathy,Osteopoikilosis,Alzheimer Disease,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Anthrax Disease,Extracranial Arteriovenous Malformation,Neurofibromatosis, Type I,Neuroblastoma,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Leukemia, Acute Myeloid,Noonan Syndrome 1,Senile Angioma,Hemangioma,Rosai-Dorfman Disease,Bladder Cancer,Mixed Cell Adenoma,Hairy Cell Leukemia,Prostate Squamous Cell Carcinoma,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Cardiofaciocutaneous Syndrome 3,Ovarian Cancer,Myeloid Leukemia,Adenocarcinoma,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Fibrosarcoma,Histiocytosis,Skin Carcinoma,Gastric Cancer,Arteriovenous Malformation,Prostate Cancer,Disease Of Mental Health,Gastric Adenocarcinoma,Langerhans Cell Histiocytosis,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Diamond-Blackfan Anemia 20,Acute Promyelocytic Leukemia,Ovarian Melanoma,Autism Spectrum Disorder,Kaposi Sarcoma,Cardiomyopathy, Familial Hypertrophic, 25,Medulloblastoma,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lung Cancer,Pancreatic Cancer |
3eqi_a | Q02750 | ENSG00000169032 | MAP2K1 | 98.80 | 3.40E-13 | 4.10E-17 | 134.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKAA1 AMPK1 |
5'-AMP-activated protein kinase catalytic subunit alpha-1 (AMPK subunit alpha-1) (EC 2.7.11.1) (Acetyl-CoA carboxylase kinase) (ACACA kinase) (EC 2.7.11.27) (Hydroxymethylglutaryl-CoA reductase kinase) (HMGCR kinase) (EC 2.7.11.31) (Tau-protein kinase PRKAA1) (EC 2.7.11.26) |
2.7.11.26,2.7.11.27,2.7.11.31 | Homo sapiens | Mixed Fibrolamellar Hepatocellular Carcinoma,Fatty Liver Disease,Breast Cancer,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Wolff-Parkinson-White Syndrome,Lung Cancer |
4red_a | Q13131 | ENSG00000132356 | PRKAA1 | 99.00 | 5.20E-14 | 6.20E-18 | 140.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | cgd3_920 |
cgd3_920 |
Cryptosporidium parvum | 2wei_a | A3FQ16 | 99.00 | 4.40E-14 | 5.50E-18 | 134.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | MAPK6 ERK3 PRKM6 |
Mitogen-activated protein kinase 6 (MAP kinase 6) (MAPK 6) (EC 2.7.11.24) (Extracellular signal-regulated kinase 3) (ERK-3) (MAP kinase isoform p97) (p97-MAPK) |
2.7.11.24 | Homo sapiens | Pulmonary Immaturity,Aromatase Excess Syndrome |
2i6l_a | Q16659 | ENSG00000069956 | MAPK6 | 98.90 | 2.10E-13 | 2.60E-17 | 130.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | DCLK1 DCAMKL1 DCDC3A KIAA0369 |
Serine/threonine-protein kinase DCLK1 (EC 2.7.11.1) (Doublecortin domain-containing protein 3A) (Doublecortin-like and CAM kinase-like 1) (Doublecortin-like kinase 1) |
2.7.11.1 | Homo sapiens | Zellweger Syndrome,Colorectal Cancer,Attention Deficit-Hyperactivity Disorder,Chemical Colitis,Band Heterotopia |
5jzj_b | O15075 | ENSG00000133083 | DCLK1 | 98.90 | 2.90E-13 | 3.60E-17 | 129.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | aurkb-a airk2-a |
Aurora kinase B-A (EC 2.7.11.1) (Aurora/IPL1-related kinase 2-A) (AIRK2-A) (XAIRK2-A) (Serine/threonine-protein kinase 12-A) (Serine/threonine-protein kinase aurora-B-A) (xAurora-B) |
2.7.11.1 | Xenopus laevis | 4c2v_b | Q6DE08 | 99.20 | 1.10E-15 | 1.40E-19 | 144.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CDKL5 STK9 |
Cyclin-dependent kinase-like 5 (EC 2.7.11.22) (Serine/threonine-protein kinase 9) |
2.7.11.22 | Homo sapiens | Cdkl5 Deficiency Disorder,Ohtahara Syndrome,Seizure Disorder,Childhood Absence Epilepsy,Epilepsy,Gait Apraxia,Gene Duplication Disease,Nicolaides-Baraitser Syndrome,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Focal Epilepsy,Developmental And Epileptic Encephalopathy 14,Epilepsy With Generalized Tonic-Clonic Seizures,Congenital Nervous System Abnormality,Developmental And Epileptic Encephalopathy,Fundus Dystrophy,Juvenile Retinoschisis,Bruxism,X-Linked Congenital Retinoschisis,Early Myoclonic Encephalopathy,Stxbp1 Encephalopathy,Microcephaly,Mental Retardation, Autosomal Dominant 20,Encephalopathy,Benign Neonatal Seizures,Alacrima, Achalasia, And Mental Retardation Syndrome,Benign Epilepsy With Centrotemporal Spikes,Developmental And Epileptic Encephalopathy 9,Methylmalonic Acidemia,Benign Familial Neonatal Epilepsy,West Syndrome,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Fragile X Syndrome,Pitt-Hopkins Syndrome,Mowat-Wilson Syndrome,Developmental And Epileptic Encephalopathy 2,Lennox-Gastaut Syndrome,Sturge-Weber Syndrome,Neonatal Period Electroclinical Syndrome,Infancy Electroclinical Syndrome,Childhood Electroclinical Syndrome,Early Infantile Epileptic Encephalopathy,Developmental And Epileptic Encephalopathy 4,Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Aicardi Syndrome,Specific Developmental Disorder,Pervasive Developmental Disorder,Dravet Syndrome,Developmental And Epileptic Encephalopathy 1,Benign Familial Infantile Epilepsy,Generalized Epilepsy With Febrile Seizures Plus,Pyruvate Dehydrogenase E1-Alpha Deficiency,Retinoschisis 1, X-Linked, Juvenile,Rett Syndrome,Epilepsy, Myoclonic Juvenile,Autism,Christianson Syndrome,Epilepsy, Idiopathic Generalized,Peho Syndrome |
4bgq_a | O76039 | ENSG00000008086 | CDKL5 | 99.10 | 7.70E-15 | 1.00E-18 | 138.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CIPK23 LKS1 PKS17 SnRK3.23 At1g30270 F12P21.6 |
CBL-interacting serine/threonine-protein kinase 23 (EC 2.7.11.1) (Protein LOW-K(+)-SENSITIVE 1) (SNF1-related kinase 3.23) (SOS2-like protein kinase PKS17) |
2.7.11.1 | Arabidopsis thaliana | 4czt_d | Q93VD3 | 99.00 | 5.70E-14 | 6.20E-18 | 149.70 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CDK4 |
Cyclin-dependent kinase 4 (EC 2.7.11.22) (Cell division protein kinase 4) (PSK-J3) |
2.7.11.22 | Homo sapiens | Melanoma In Congenital Melanocytic Nevus,Pancreatic Adenocarcinoma,Skin Melanoma,Endometrial Cancer,Malignant Inflammatory Fibrous Histiocytoma,Childhood Acute Lymphocytic Leukemia,Retinitis Pigmentosa,Pancreas Sarcoma,Lung Cancer Susceptibility 3,Chondrosarcoma,Myofibrillar Myopathy,Rhabdomyosarcoma 2,Malignant Fibrous Histiocytoma,Melanoma,Plasma Cell Neoplasm,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Myositis Ossificans,Leiomyosarcoma,Connective Tissue Cancer,Bone Sarcoma,Undifferentiated Embryonal Sarcoma Of The Liver,Infiltrating Lipoma,Large Cell Carcinoma,Ischemic Fasciitis,B-Cell Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Retinal Cancer,Familial Retinoblastoma,Embryonal Sarcoma,Retroperitoneal Sarcoma,Retroperitoneum Carcinoma,Neuroblastoma,Pilocytic Astrocytoma,Inherited Cancer-Predisposing Syndrome,Glioma,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Hereditary Melanoma,Ring Chromosome 7,Nodular Malignant Melanoma,Bladder Cancer,Spindle Cell Lipoma,Pleomorphic Lipoma,Lipoma Of Spermatic Cord,Paratesticular Lipoma,Melanoma, Cutaneous Malignant 3,Ring Chromosome,Lipoblastoma,Ovarian Cancer,Myeloid Leukemia,Burkitt Lymphoma,Adenocarcinoma,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Well-Differentiated Liposarcoma,Malignant Astrocytoma,Cellular Myxoid Liposarcoma,High Grade Glioma,Adult Liposarcoma,Pediatric Liposarcoma,Gliosarcoma,Gastric Liposarcoma,Breast Liposarcoma,Pleomorphic Liposarcoma,Mixed Liposarcoma,Spindle Cell Liposarcoma,Mediastinum Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Hepatocellular Carcinoma,Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Pheochromocytoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Myxoid Liposarcoma,Sarcoma,Extraosseous Osteosarcoma,Juxtacortical Osteosarcoma,Peripheral Osteosarcoma,Bone Osteosarcoma,Conventional Central Osteosarcoma,Liposarcoma Of Bone,Liposarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Infiltrating Angiolipoma,Thrombocytopenia,Retinoblastoma,Type 2 Diabetes Mellitus,Lung Squamous Cell Carcinoma,Diffuse Lipomatosis,Sensory System Disease,Muscle Cancer,Esophageal Cancer,Tumor Predisposition Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Acute Promyelocytic Leukemia,Inflammatory Myofibroblastic Tumor,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Nasopharyngeal Carcinoma,Lymphoma,Connective Tissue Benign Neoplasm,Kaposi Sarcoma,Leukemia, Chronic Lymphocytic,Li-Fraumeni Syndrome,Lipomatosis, Multiple,Dermatofibrosarcoma Protuberans,Parameningeal Embryonal Rhabdomyosarcoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Neu-Laxova Syndrome 1,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer |
2w99_b | P11802 | ENSG00000135446 | CDK4 | 99.10 | 1.00E-14 | 1.30E-18 | 139.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PAK6 PAK5 |
Serine/threonine-protein kinase PAK 6 (EC 2.7.11.1) (PAK-5) (p21-activated kinase 6) (PAK-6) |
2.7.11.1 | Homo sapiens | 4ks7_a | Q9NQU5 | ENSG00000137843 | BUB1B-PAK6 | 99.00 | 4.80E-14 | 6.10E-18 | 134.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | MAPK1 ERK2 PRKM1 PRKM2 |
Mitogen-activated protein kinase 1 (MAP kinase 1) (MAPK 1) (EC 2.7.11.24) (ERT1) (Extracellular signal-regulated kinase 2) (ERK-2) (MAP kinase isoform p42) (p42-MAPK) (Mitogen-activated protein kinase 2) (MAP kinase 2) (MAPK 2) |
2.7.11.24 | Homo sapiens | Pancreatic Adenocarcinoma,Heart Disease,Learning Disability,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Differentiating Neuroblastoma,Squamous Cell Carcinoma,Vascular Disease,Lung Cancer Susceptibility 3,Spinal Cord Injury,Polycystic Kidney Disease,Melanoma,Leukemia, Chronic Myeloid,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Noonan Syndrome 13,Alzheimer Disease,Rasopathy,Retrograde Amnesia,Bile Duct Cancer,Specific Learning Disability,Human Cytomegalovirus Infection,Hepatitis,Mesangial Proliferative Glomerulonephritis,Insulin-Like Growth Factor I,Neuroblastoma,Angioimmunoblastic T-Cell Lymphoma,Glioma,Noonan Syndrome 1,Dilated Cardiomyopathy,Bladder Cancer,Lung Adenoma,Pediculus Humanus Corporis Infestation,Cystic Kidney Disease,Ovarian Cancer,Myeloid Leukemia,Burkitt Lymphoma,Tuberous Sclerosis,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Microphthalmia,Colorectal Cancer,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Microcephaly,Opioid Addiction,Pheochromocytoma,Rhabdomyosarcoma,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Mood Disorder,Esophagus Sarcoma,Sarcoma,Anhidrosis,Pertussis,Fibrosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Cervical Cancer,Bladder Squamous Cell Carcinoma,Fragile X Syndrome,Bladder Urothelial Carcinoma,Esophageal Cancer,Muscle Hypertrophy,Fibrodysplasia Ossificans Progressiva,Chromosome 22q11.2 Deletion Syndrome, Distal,Ewing Sarcoma,Heart, Malformation Of,Acute Promyelocytic Leukemia,Kaposi Sarcoma,Cardiomyopathy, Familial Hypertrophic, 25,Lung Cancer,Gordon Holmes Syndrome,Pancreatic Cancer |
4zzn_a | P28482 | ENSG00000100030 | MAPK1 | 98.80 | 4.10E-13 | 5.10E-17 | 132.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | DAPK1 DAPK |
Death-associated protein kinase 1 (DAP kinase 1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Lung Cancer Susceptibility 3,Adenoid Cystic Carcinoma,Cholecystitis,Alzheimer Disease,B-Cell Lymphoma,Mixed Oligodendroglioma-Astrocytoma,Transitional Cell Carcinoma,Bladder Cancer,Tuberous Sclerosis 2,Parkinson Disease, Late-Onset,Colorectal Cancer,Pediatric Lymphoma,Oligodendroglioma,Central Neurocytoma,Ischemia,Gastric Cancer,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Cervical Cancer,Cervical Squamous Cell Carcinoma,Myelodysplastic Syndrome,Nasopharyngeal Carcinoma,Lung Cancer |
2w4k_a | P53355 | ENSG00000196730 | DAPK1 | 99.10 | 9.00E-15 | 1.10E-18 | 140.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKG1 PRKG1B PRKGR1A PRKGR1B |
cGMP-dependent protein kinase 1 (cGK 1) (cGK1) (EC 2.7.11.12) (cGMP-dependent protein kinase I) (cGKI) |
2.7.11.12 | Homo sapiens | Myopathy,Impotence,Connective Tissue Disease,Diabetes Mellitus,Aortic Dissection,Alzheimer Disease,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Cystic Fibrosis,Aortic Disease,Aortic Valve Disease 1,Heritable Thoracic Aortic Disease,Hemolytic Anemia,Non-Proliferative Fibrocystic Change Of The Breast,Aneurysm,Aortic Aneurysm, Familial Thoracic 8,Disease Of Mental Health,Pulmonary Hypertension,Body Mass Index Quantitative Trait Locus 11,Aortic Aneurysm,Loeys-Dietz Syndrome,Immune Deficiency Disease,Myelodysplastic Syndrome,Attention Deficit-Hyperactivity Disorder,Aortic Aneurysm, Familial Thoracic 1,Hypertension, Essential,Sexual Disorder |
6bg2_a | Q13976 | ENSG00000185532 | PRKG1 | 99.30 | 3.00E-16 | 3.60E-20 | 156.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PTSG_10090 |
PTSG_10090 |
2.7.11.17 | Salpingoeca rosetta | 5ig1_b | F2UPG5 | 99.10 | 1.60E-14 | 1.90E-18 | 143.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | Calmodulin-like domain protein kinase |
Calmodulin-like domain protein kinase |
Eimeria tenella | 4ysm_a | Q3HNM4 | 99.00 | 6.30E-14 | 7.70E-18 | 144.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | PBL2 APK2A KIN1 At1g14370 F14L17.14 |
Probable serine/threonine-protein kinase PBL2 (EC 2.7.11.1) (PBS1-like protein 2) (Protein kinase 2A) |
2.7.11.1 | Arabidopsis thaliana | 6j5t_d | O49839 | 98.90 | 1.70E-13 | 2.10E-17 | 140.10 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | MAP4K3 RAB8IPL1 |
Mitogen-activated protein kinase kinase kinase kinase 3 (EC 2.7.11.1) (Germinal center kinase-related protein kinase) (GLK) (MAPK/ERK kinase kinase kinase 3) (MEK kinase kinase 3) (MEKKK 3) |
2.7.11.1 | Homo sapiens | Adult-Onset Still'S Disease |
5j5t_a | Q8IVH8 | ENSG00000011566 | MAP4K3 | 99.20 | 1.90E-15 | 2.30E-19 | 151.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | pk7 |
pk7 |
Plasmodium falciparum | 2pml_x | O96214 | 98.90 | 1.40E-13 | 1.70E-17 | 136.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | MAP3K14 NIK |
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (HsNIK) (Serine/threonine-protein kinase NIK) |
2.7.11.25 | Homo sapiens | T-Cell Lymphoblastic Leukemia/Lymphoma,Nik Deficiency,Trichohepatoenteric Syndrome 1,Pancreatic Adenosquamous Carcinoma,Pancreatic Ductal Adenocarcinoma,Immunodeficiency 50 |
4idv_c | Q99558 | ENSG00000006062 | MAP3K14 | 98.90 | 2.60E-13 | 3.20E-17 | 134.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CSNK2A2 CK2A2 |
Casein kinase II subunit alpha' (CK II alpha') (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Connective Tissue Disease,Neonatal Leukemia,Distal Muscular Dystrophy With Anterior Tibial Onset,Spermatogenic Failure 50,Breast Adenocarcinoma,Theileriasis,Spermatogenic Failure 9 |
6hmq_a | P19784 | ENSG00000070770 | CSNK2A2 | 99.00 | 1.80E-14 | 2.10E-18 | 144.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Map3k14 Nik |
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (Serine/threonine-protein kinase NIK) |
2.7.11.25 | Mus musculus | 4g3f_a | Q9WUL6 | 98.90 | 1.60E-13 | 2.00E-17 | 134.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PRKCI DXS1179E |
Protein kinase C iota type (EC 2.7.11.13) (Atypical protein kinase C-lambda/iota) (PRKC-lambda/iota) (aPKC-lambda/iota) (nPKC-iota) |
2.7.11.13 | Homo sapiens | Glioblastoma,Lung Squamous Cell Carcinoma,Lung Cancer |
3a8x_a | P41743 | ENSG00000163558 | PRKCI | 99.10 | 5.30E-15 | 6.60E-19 | 145.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDK5 CDKN5 |
Cyclin-dependent-like kinase 5 (EC 2.7.11.1) (Cell division protein kinase 5) (Serine/threonine-protein kinase PSSALRE) (Tau protein kinase II catalytic subunit) (TPKII catalytic subunit) |
2.7.11.1 | Homo sapiens | Cerebellar Hypoplasia,Supranuclear Palsy, Progressive, 1,Polycystic Kidney Disease,Dyslexia,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Transient Cerebral Ischemia,Giant Axonal Neuropathy 2,Motor Neuron Disease,Neuroblastoma,Hereditary Spastic Paraplegia,Nephronophthisis,Alzheimer Disease 9,Scrapie,Parkinson Disease, Late-Onset,Lissencephaly With Cerebellar Hypoplasia,Pick Disease Of Brain,Ischemia,Developmental And Epileptic Encephalopathy 5,Disease Of Mental Health,Toxic Encephalopathy,Dementia, Lewy Body,Lissencephaly,Aneurysmal Bone Cysts,Lissencephaly 7 With Cerebellar Hypoplasia,Syndromic Intellectual Disability,Non-Syndromic Intellectual Disability,Multiple System Atrophy 1,Myasthenic Syndrome, Congenital, 19,Primary Autosomal Recessive Microcephaly,C Syndrome,Lung Cancer |
4au8_b | Q00535 | ENSG00000164885 | CDK5 | 99.00 | 4.70E-14 | 6.10E-18 | 132.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | DMPK DM1PK MDPK |
Myotonin-protein kinase (MT-PK) (EC 2.7.11.1) (DM-kinase) (DMK) (DM1 protein kinase) (DMPK) (Myotonic dystrophy protein kinase) |
2.7.11.1 | Homo sapiens | Muscular Disease,Fuchs' Endothelial Dystrophy,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Myotonic Disease,Myotonic Dystrophy 1,Muscular Dystrophy,Myotonic Dystrophy,Spinocerebellar Ataxia 8,Myotonic Cataract,Cataract,Oculopharyngeal Muscular Dystrophy,Hair Follicle Neoplasm,Myotonic Dystrophy 2,Myotonia,Immature Cataract,Lens Disease,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Fragile X Syndrome,Huntington Disease-Like 2,First-Degree Atrioventricular Block,Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Catecholaminergic Polymorphic Ventricular Tachycardia,Frontotemporal Dementia,3-Methylglutaconic Aciduria, Type Iii |
2vd5_a | Q09013 | ENSG00000104936 | DMPK | 99.30 | 2.60E-16 | 3.20E-20 | 160.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Camk1 |
Calcium/calmodulin-dependent protein kinase type 1 (EC 2.7.11.17) (CaM kinase I) (CaM-KI) (CaM kinase I alpha) (CaMKI-alpha) |
2.7.11.17 | Rattus norvegicus | 1a06_a | Q63450 | 99.70 | 1.90E-22 | 2.00E-26 | 207.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PKN1 PAK1 PKN PRK1 PRKCL1 |
Serine/threonine-protein kinase N1 (EC 2.7.11.13) (Protease-activated kinase 1) (PAK-1) (Protein kinase C-like 1) (Protein kinase C-like PKN) (Protein kinase PKN-alpha) (Protein-kinase C-related kinase 1) (Serine-threonine protein kinase N) |
2.7.11.13 | Homo sapiens | 4otd_a | Q16512 | ENSG00000123143 | PKN1 | 99.30 | 2.70E-16 | 3.30E-20 | 154.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | CASK LIN2 |
Peripheral plasma membrane protein CASK (hCASK) (EC 2.7.11.1) (Calcium/calmodulin-dependent serine protein kinase) (Protein lin-2 homolog) |
2.7.11.1 | Homo sapiens | Cask-Related Disorders,Cerebellar Hypoplasia,Constipation,Congenital Nystagmus,Pathologic Nystagmus,Neurofibromatosis, Type I,Fraser Syndrome 1,Cask Disorders,Cerebellar Disease,Dystonia,Glucosephosphate Dehydrogenase Deficiency,Lobular Neoplasia,X-Linked Intellectual Disability, Najm Type,Cask-Related Intellectual Disability,Microcephaly,Hypertonia,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Fg Syndrome 4,Helsmoortel-Van Der Aa Syndrome,Aland Island Eye Disease,Developmental And Epileptic Encephalopathy 8,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency,Coffin-Siris Syndrome 1,Early Infantile Epileptic Encephalopathy,Opitz-Kaveggia Syndrome,Pontocerebellar Hypoplasia,Autism,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay,Peho Syndrome |
3c0g_b | O14936 | ENSG00000147044 | CASK | 99.00 | 2.90E-14 | 3.40E-18 | 142.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | cgd7_1840 |
cgd7_1840 |
Cryptosporidium parvum | 3f3z_a | Q5CYL9 | 99.00 | 3.10E-14 | 3.90E-18 | 133.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | RPS6KA5 MSK1 |
Ribosomal protein S6 kinase alpha-5 (S6K-alpha-5) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 5) (Nuclear mitogen- and stress-activated protein kinase 1) (RSK-like protein kinase) (RSKL) |
2.7.11.1 | Homo sapiens | Septic Myocarditis,Coffin-Lowry Syndrome |
3kn5_b | O75582 | ENSG00000100784 | RPS6KA5 | 98.90 | 1.20E-13 | 1.50E-17 | 134.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDKL2 |
Cyclin-dependent kinase-like 2 (EC 2.7.11.22) (Protein kinase p56 KKIAMRE) (Serine/threonine-protein kinase KKIAMRE) |
2.7.11.22 | Homo sapiens | Papillary Serous Adenocarcinoma,Orofaciodigital Syndrome Vi |
4aaa_a | Q92772 | ENSG00000138769 | CDKL2 | 99.00 | 4.80E-14 | 5.80E-18 | 139.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | aacA-aphD R015 VRA0030 |
Bifunctional AAC/APH [Includes: 6'-aminoglycoside N-acetyltransferase (EC 2.3.1.-) (AAC(6')); Aminoglycoside 2''-phosphotransferase (2''-aminoglycoside phosphotransferase) (EC 2.7.1.190) (APH(2''))] |
2.7.1.190 | Staphylococcus aureus | 5iqf_d | P0A0C1 | 98.90 | 1.30E-13 | 1.70E-17 | 126.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | MKNK2 GPRK7 MNK2 |
MAP kinase-interacting serine/threonine-protein kinase 2 (EC 2.7.11.1) (MAP kinase signal-integrating kinase 2) (MAPK signal-integrating kinase 2) (Mnk2) |
2.7.11.1 | Homo sapiens | 2ac3_a | Q9HBH9 | ENSG00000099875 | MKNK2 | 98.80 | 3.40E-13 | 4.30E-17 | 129.20 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | MARK3 CTAK1 EMK2 |
MAP/microtubule affinity-regulating kinase 3 (EC 2.7.11.1) (C-TAK1) (cTAK1) (Cdc25C-associated protein kinase 1) (ELKL motif kinase 2) (EMK-2) (Protein kinase STK10) (Ser/Thr protein kinase PAR-1) (Par-1a) (Serine/threonine-protein kinase p78) |
2.7.11.1 | Homo sapiens | Focal Epithelial Hyperplasia,Osteoporosis,Peutz-Jeghers Syndrome,Gaucher Disease, Type Iii,Visual Impairment And Progressive Phthisis Bulbi |
2qnj_b | P27448 | ENSG00000075413 | MARK3 | 99.10 | 3.10E-15 | 3.80E-19 | 146.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | RPS6KA3 ISPK1 MAPKAPK1B RSK2 |
Ribosomal protein S6 kinase alpha-3 (S6K-alpha-3) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 3) (p90-RSK 3) (p90RSK3) (Insulin-stimulated protein kinase 1) (ISPK-1) (MAP kinase-activated protein kinase 1b) (MAPK-activated protein kinase 1b) (MAPKAP kinase 1b) (MAPKAPK-1b) (Ribosomal S6 kinase 2) (RSK-2) (pp90RSK2) |
2.7.11.1 | Homo sapiens | Ventricular Septal Defect,Learning Disability,Symptomatic Form Of Coffin-Lowry Syndrome In Female Carriers,Cohen Syndrome,Specific Learning Disability,Gastroesophageal Reflux,Breast Cancer,Cardiomyopathy, Familial Hypertrophic, 4,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Orthostatic Intolerance,Dyskeratosis Congenita, Autosomal Dominant 3,X-Linked Monogenic Disease,Non-Syndromic X-Linked Intellectual Disability,Coffin-Lowry Syndrome,Hypertelorism,Partington X-Linked Mental Retardation Syndrome,Scoliosis |
4d9u_a | P51812 | ENSG00000177189 | RPS6KA3 | 99.00 | 5.50E-14 | 6.60E-18 | 139.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CAMK2D CAMKD |
Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) |
2.7.11.17 | Homo sapiens | Dilated Cardiomyopathy,Cardiomyopathy, Dilated, 1dd |
2vn9_a | Q13557 | ENSG00000145349 | CAMK2D | 99.00 | 3.00E-14 | 3.70E-18 | 137.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | STT7 MICPUN_107392 |
STT7 MICPUN_107392 |
Micromonas commoda | 4ix3_b | C1EBN1 | 98.90 | 1.30E-13 | 1.70E-17 | 131.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | MPK6 At2g43790 F18O19.10 |
Mitogen-activated protein kinase 6 (AtMPK6) (MAP kinase 6) (EC 2.7.11.24) |
2.7.11.24 | Arabidopsis thaliana | 6dtl_a | Q39026 | 98.90 | 1.00E-13 | 1.20E-17 | 139.00 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | DAPK3 ZIPK |
Death-associated protein kinase 3 (DAP kinase 3) (EC 2.7.11.1) (DAP-like kinase) (Dlk) (MYPT1 kinase) (Zipper-interacting protein kinase) (ZIP-kinase) |
2.7.11.1 | Homo sapiens | Recessive Dystrophic Epidermolysis Bullosa |
1yrp_a | O43293 | ENSG00000167657 | DAPK3 | 99.00 | 1.90E-14 | 2.40E-18 | 135.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MYLK4 SGK085 |
Myosin light chain kinase family member 4 (EC 2.7.11.1) (Sugen kinase 85) (SgK085) |
2.7.11.1 | Homo sapiens | Cardiomyopathy, Familial Restrictive, 2,Deafness, Autosomal Recessive 17,Deafness, Autosomal Recessive 14,Cardiomyopathy, Familial Restrictive, 3 |
2x4f_a | Q86YV6 | ENSG00000145949 | MYLK4 | 99.20 | 1.20E-15 | 1.50E-19 | 153.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PAK4 KIAA1142 |
Serine/threonine-protein kinase PAK 4 (EC 2.7.11.1) (p21-activated kinase 4) (PAK-4) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
2j0i_a | O96013 | ENSG00000130669 | PAK4 | 99.00 | 3.00E-14 | 3.70E-18 | 138.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PASK KIAA0135 |
PAS domain-containing serine/threonine-protein kinase (PAS-kinase) (PASKIN) (hPASK) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Niemann-Pick Disease, Type C1 |
3dls_a | Q96RG2 | ENSG00000115687 | PASK | 98.90 | 9.70E-14 | 1.20E-17 | 137.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKACA PKACA |
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11) |
2.7.11.11 | Homo sapiens | Mixed Fibrolamellar Hepatocellular Carcinoma,Fibrolamellar Carcinoma,Cardioacrofacial Dysplasia 1,Dilated Cardiomyopathy,Acth-Independent Cushing Syndrome,Osteoporosis,Breast Cancer,Pigmented Nodular Adrenocortical Disease, Primary, 4,Primary Pigmented Nodular Adrenocortical Disease |
3ama_a | P17612 | ENSG00000072062 | PRKACA | 99.20 | 1.60E-15 | 1.90E-19 | 150.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MARK1 KIAA1477 MARK |
Serine/threonine-protein kinase MARK1 (EC 2.7.11.1) (EC 2.7.11.26) (MAP/microtubule affinity-regulating kinase 1) (PAR1 homolog c) (Par-1c) (Par1c) |
2.7.11.26 | Homo sapiens | Alzheimer Disease,Peutz-Jeghers Syndrome,Autism |
6c9d_a | Q9P0L2 | ENSG00000116141 | MARK1 | 98.90 | 1.30E-13 | 1.50E-17 | 145.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Btk Bpk |
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) (Kinase EMB) |
2.7.10.2 | Mus musculus | 4xi2_a | P35991 | 98.90 | 9.10E-14 | 1.10E-17 | 141.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | pknB Rv0014c MTCY10H4.14c |
Serine/threonine-protein kinase PknB (EC 2.7.11.1) |
2.7.11.1 | Mycobacterium tuberculosis | 6i2p_a | P9WI81 | 99.00 | 6.90E-14 | 9.00E-18 | 129.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | RPS6KA1 MAPKAPK1A RSK1 |
Ribosomal protein S6 kinase alpha-1 (S6K-alpha-1) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 1) (p90-RSK 1) (p90RSK1) (p90S6K) (MAP kinase-activated protein kinase 1a) (MAPK-activated protein kinase 1a) (MAPKAP kinase 1a) (MAPKAPK-1a) (Ribosomal S6 kinase 1) (RSK-1) |
2.7.11.1 | Homo sapiens | Tuberous Sclerosis 2,Tuberous Sclerosis,Cardiomyopathy, Familial Hypertrophic, 4,Disease Of Mental Health,Adrenal Cortical Adenocarcinoma,Dyskeratosis Congenita, Autosomal Dominant 3,Tuberous Sclerosis 1,Coffin-Lowry Syndrome,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
4nif_d | Q15418 | ENSG00000117676 | RPS6KA1 | 99.10 | 1.20E-14 | 1.40E-18 | 143.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | MAP2K7 JNKK2 MEK7 MKK7 PRKMK7 SKK4 |
Dual specificity mitogen-activated protein kinase kinase 7 (MAP kinase kinase 7) (MAPKK 7) (EC 2.7.12.2) (JNK-activating kinase 2) (MAPK/ERK kinase 7) (MEK 7) (Stress-activated protein kinase kinase 4) (SAPK kinase 4) (SAPKK-4) (SAPKK4) (c-Jun N-terminal kinase kinase 2) (JNK kinase 2) (JNKK 2) |
2.7.12.2 | Homo sapiens | Cardiomyopathy, Familial Hypertrophic, 25,Primary Autosomal Recessive Microcephaly |
5y90_a | O14733 | ENSG00000076984 | MAP2K7 | 98.80 | 3.50E-13 | 4.30E-17 | 131.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | cgd5_2510 |
cgd5_2510 |
Cryptosporidium parvum | 3niz_a | Q5CRJ8 | 99.00 | 6.10E-14 | 7.40E-18 | 136.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | ULK1 KIAA0722 |
Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) |
2.7.11.1 | Homo sapiens | Retinitis Pigmentosa,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Tuberous Sclerosis 2,Acute Laryngopharyngitis,Tuberous Sclerosis 1,Huntington Disease |
4wno_a | O75385 | ENSG00000177169 | ULK1 | 98.90 | 9.80E-14 | 1.20E-17 | 131.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | TTN |
Titin (EC 2.7.11.1) (Connectin) (Rhabdomyosarcoma antigen MU-RMS-40.14) |
2.7.11.1 | Homo sapiens | Muscular Disease,Heart Disease,Constrictive Pericarditis,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Amyloidosis,Cardiomyopathy, Dilated, 1e,Syncope,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Childhood-Onset Progressive Contractures-Limb-Girdle Weakness-Muscle Dystrophy Syndrome,Emery-Dreifuss Muscular Dystrophy,Cortical Thymoma,Muscle Tissue Disease,Morvan'S Fibrillary Chorea,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Lung Large Cell Carcinoma,Myopathy, Distal, 1,Myositis,Myotonic Dystrophy 1,Systolic Heart Failure,Myopathy, Myofibrillar, 1,Diastolic Heart Failure,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j,Muscular Atrophy,Tibial Muscular Dystrophy,Limb-Girdle Muscular Dystrophy,Arrhythmogenic Right Ventricular Dysplasia, Familial, 1,Epithelial Malignant Thymoma,Hyaline Body Myopathy,Isolated Elevated Serum Creatine Phosphokinase Levels,Noonan Syndrome 1,Newborn Respiratory Distress Syndrome,Thymus Clear Cell Carcinoma,Reducing Body Myopathy,Myocarditis,Atrial Standstill 1,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10,Hereditary Proximal Myopathy With Early Respiratory Failure,Dilated Cardiomyopathy,Alcoholic Cardiomyopathy,Lmna-Related Dilated Cardiomyopathy,Thymus Gland Disease,Long Qt Syndrome,Cardiomyopathy, Dilated, 1dd,Heart Conduction Disease,Udd Distal Myopathy - Tibial Muscular Dystrophy,Muscular Dystrophy, Congenital, Lmna-Related,Neuropathy,Perinephritis,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Myopathy, Myofibrillar, 3,Sick Sinus Syndrome,Multiminicore Disease,Cardiomyopathy, Familial Hypertrophic, 4,Cardiomyopathy, Dilated, 1a,Congestive Heart Failure,Myopathy, Myofibrillar, 4,Left Ventricular Noncompaction 2,Foot Drop,Myopathy, Myofibrillar, 5,Rhabdomyosarcoma,Rigid Spine Muscular Dystrophy 1,Epidermolysis Bullosa Simplex With Muscular Dystrophy,Thymoma,Thymus Cancer,Dendritic Cell Thymoma,Respiratory Failure,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Cardiomyopathy, Dilated, 1g,Congenital Myasthenic Syndrome,Cardiomyopathy, Familial Hypertrophic, 9,Cardiomyopathy, Dilated, 1h,Orthostatic Intolerance,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Lung Squamous Cell Carcinoma,Restrictive Cardiomyopathy,Extrinsic Cardiomyopathy,Lambert-Eaton Myasthenic Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Muscle Hypertrophy,Salih Myopathy,Nonaka Myopathy,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Familial Atrial Fibrillation,Hypermethioninemia Due To Adenosine Kinase Deficiency,Atrioventricular Block,Third-Degree Atrioventricular Block,Barth Syndrome,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Muscular Dystrophy-Dystroglycanopathy , Type C, 5,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scoliosis,Muscular Dystrophy, Duchenne Type,Myopathy, Centronuclear, X-Linked,Cardiac Arrest,Inguinal Hernia,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2,Myasthenia Gravis,Left Ventricular Noncompaction,Lethal Congenital Contracture Syndrome,Myopathy, Centronuclear, 2,Batten-Turner Congenital Myopathy,Miyoshi Muscular Dystrophy,Tibial Muscular Dystrophy, Tardive,Cardiomyopathy, Dilated, 1b |
1tki_b | Q8WZ42 | ENSG00000155657 | TTN | 99.20 | 1.40E-15 | 1.70E-19 | 149.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDK1 CDC2 CDC28A CDKN1 P34CDC2 |
Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase) |
2.7.11.22,2.7.11.23, | Homo sapiens | Bartholin'S Gland Adenocarcinoma,Bone Cancer,Polyploidy,Alzheimer Disease,Retinal Cancer,Neuroblastoma,Leukemia, Acute Myeloid,Hereditary Spastic Paraplegia,Leukemia, Acute Lymphoblastic,Bladder Cancer,Brain Cancer,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Western Equine Encephalitis,Rhabdomyosarcoma,Fanconi Anemia, Complementation Group A,Neuronal Ceroid Lipofuscinosis,Breast Adenocarcinoma,Prostate Cancer,Cervical Cancer,Retinoblastoma,Lymphoma, Non-Hodgkin, Familial,Esophageal Cancer,Seckel Syndrome,Trichothiodystrophy 5, Nonphotosensitive,Mantle Cell Lymphoma,Gastrointestinal Stromal Tumor,Acute Promyelocytic Leukemia,Leukemia, Chronic Lymphocytic,Ceroid Lipofuscinosis, Neuronal, 2,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Ceroid Lipofuscinosis, Neuronal, 1,Lung Cancer,Frontotemporal Dementia |
4yc3_a | P06493 | ENSG00000170312 | CDK1 | 99.00 | 3.80E-14 | 4.80E-18 | 135.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | TAOK3 DPK JIK KDS MAP3K18 |
Serine/threonine-protein kinase TAO3 (EC 2.7.11.1) (Cutaneous T-cell lymphoma-associated antigen HD-CL-09) (CTCL-associated antigen HD-CL-09) (Dendritic cell-derived protein kinase) (JNK/SAPK-inhibitory kinase) (Jun kinase-inhibitory kinase) (Kinase from chicken homolog A) (hKFC-A) (Thousand and one amino acid protein 3) |
2.7.11.1 | Homo sapiens | Cutaneous T Cell Lymphoma |
6bdn_a | Q9H2K8 | ENSG00000135090 | TAOK3 | 98.90 | 1.10E-13 | 1.40E-17 | 135.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | GRK2 ADRBK1 BARK BARK1 |
Beta-adrenergic receptor kinase 1 (Beta-ARK-1) (EC 2.7.11.15) (G-protein coupled receptor kinase 2) |
2.7.11.15 | Homo sapiens | Heart Disease,Alzheimer Disease,Myocardial Infarction,Exudative Vitreoretinopathy 5,Colorectal Cancer,Disease Of Mental Health,Hypertension, Essential |
3v5w_a | P25098 | ENSG00000173020 | GRK2 | 98.90 | 1.60E-13 | 1.60E-17 | 155.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDK7 CAK CAK1 CDKN7 MO15 STK1 |
Cyclin-dependent kinase 7 (EC 2.7.11.22) (EC 2.7.11.23) (39 kDa protein kinase) (p39 Mo15) (CDK-activating kinase 1) (Cell division protein kinase 7) (Serine/threonine-protein kinase 1) (TFIIH basal transcription factor complex kinase subunit) |
2.7.11.22,2.7.11.23, | Homo sapiens | Myofibrillar Myopathy,Cockayne Syndrome,Breast Cancer,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group B |
1ua2_b | P50613 | ENSG00000134058 | CDK7 | 99.10 | 1.50E-14 | 1.90E-18 | 142.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Rop2 |
Rop2 |
Toxoplasma gondii | 3dzo_a | Q06AK3 | 99.10 | 1.70E-14 | 2.00E-18 | 148.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | STK3 KRS1 MST2 |
Serine/threonine-protein kinase 3 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 2) (MST-2) (STE20-like kinase MST2) (Serine/threonine-protein kinase Krs-1) [Cleaved into: Serine/threonine-protein kinase 3 36kDa subunit (MST2/N); Serine/threonine-protein kinase 3 20kDa subunit (MST2/C)] |
2.7.11.1 | Homo sapiens | Non-Syndromic X-Linked Intellectual Disability |
4lg4_a | Q13188 | ENSG00000104375 | STK3 | 98.90 | 8.10E-14 | 1.00E-17 | 133.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | GL50803_008037 GL50803_8037 |
GL50803_008037 GL50803_8037 |
Giardia intestinalis | 3gbz_a | A8BZ95 | 99.10 | 1.60E-14 | 2.00E-18 | 141.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | ROCK2 |
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho-associated, coiled-coil-containing protein kinase 2) (Rho-associated, coiled-coil-containing protein kinase II) (ROCK-II) (p164 ROCK-2) |
2.7.11.1 | Bos taurus | 2f2u_b | Q28021 | 99.30 | 8.70E-17 | 1.00E-20 | 164.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CPK2 CDPK2 |
Calcium-dependent protein kinase 2 (EC 2.7.11.1) (PfCDPK2) |
2.7.11.1 | Plasmodium falciparum | 4mvf_a | O15865 | 99.10 | 5.30E-15 | 6.50E-19 | 153.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | STRADA LYK5 STRAD |
STE20-related kinase adapter protein alpha (STRAD alpha) (STE20-related adapter protein) (Serologically defined breast cancer antigen NY-BR-96) |
Homo sapiens | Epilepsy,Polyhydramnios,Endometrial Squamous Cell Carcinoma,Breast Cancer,Megalencephaly,Benign Epilepsy With Centrotemporal Spikes,Scheuermann Disease,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy |
2wtk_b | Q7RTN6 | ENSG00000266173 | STRADA | 99.00 | 5.40E-14 | 6.50E-18 | 140.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | OXSR1 KIAA1101 OSR1 |
Serine/threonine-protein kinase OSR1 (EC 2.7.11.1) (Oxidative stress-responsive 1 protein) |
2.7.11.1 | Homo sapiens | Bartter Disease,Arthrogryposis, Distal, Type 3,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypomagnesemia 3, Renal |
2vwi_c | O95747 | ENSG00000172939 | OXSR1 | 99.00 | 1.90E-14 | 2.40E-18 | 136.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CAMK1G CLICK3 VWS1 |
Calcium/calmodulin-dependent protein kinase type 1G (EC 2.7.11.17) (CaM kinase I gamma) (CaM kinase IG) (CaM-KI gamma) (CaMKI gamma) (CaMKIG) (CaMK-like CREB kinase III) (CLICK III) |
2.7.11.17 | Homo sapiens | 2jam_a | Q96NX5 | ENSG00000008118 | CAMK1G | 99.00 | 2.70E-14 | 3.30E-18 | 139.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | CKA1 YIL035C |
Casein kinase II subunit alpha (CK II subunit alpha) (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 4fi1_a | P15790 | 98.90 | 1.40E-13 | 1.70E-17 | 137.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PLK2 SNK |
Serine/threonine-protein kinase PLK2 (EC 2.7.11.21) (Polo-like kinase 2) (PLK-2) (hPlk2) (Serine/threonine-protein kinase SNK) (hSNK) (Serum-inducible kinase) |
2.7.11.21 | Homo sapiens | Epilepsy, Familial Temporal Lobe, 2 |
4i5p_a | Q9NYY3 | ENSG00000145632 | PLK2 | 99.00 | 1.80E-14 | 2.20E-18 | 140.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | TTK MPS1 MPS1L1 |
Dual specificity protein kinase TTK (EC 2.7.12.1) (Phosphotyrosine picked threonine-protein kinase) (PYT) |
2.7.12.1 | Homo sapiens | Polyposis Syndrome, Hereditary Mixed, 1,Hereditary Mixed Polyposis Syndrome,Osteogenesis Imperfecta, Type Xvii,Lung Cancer,Mosaic Variegated Aneuploidy Syndrome 1,Pancreatic Cancer |
4js8_a | P33981 | ENSG00000112742 | TTK | 98.80 | 3.30E-13 | 4.40E-17 | 124.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | Prkcb Pkcb Prkcb1 |
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13) |
2.7.11.13 | Rattus norvegicus | 3pfq_a | P68403 | 99.10 | 8.70E-15 | 1.00E-18 | 160.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | MELK KIAA0175 |
Maternal embryonic leucine zipper kinase (hMELK) (EC 2.7.11.1) (Protein kinase Eg3) (pEg3 kinase) (Protein kinase PK38) (hPK38) (Tyrosine-protein kinase MELK) (EC 2.7.10.2) |
2.7.10.2 | Homo sapiens | Colorectal Cancer |
5k00_a | Q14680 | ENSG00000165304 | MELK | 99.20 | 2.40E-15 | 2.90E-19 | 149.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | SGK1 SGK |
Serine/threonine-protein kinase Sgk1 (EC 2.7.11.1) (Serum/glucocorticoid-regulated kinase 1) |
2.7.11.1 | Homo sapiens | Plasma Cell Neoplasm,Pseudohypoaldosteronism,Cystic Fibrosis,Gastric Cancer,Disease Of Mental Health,Liddle Syndrome 1,Body Mass Index Quantitative Trait Locus 11,Pseudohypoaldosteronism, Type I, Autosomal Dominant,Tuberous Sclerosis 1,Hypertension, Essential,Rett Syndrome,Myeloma, Multiple |
2r5t_a | O00141 | ENSG00000118515 | SGK1 | 99.00 | 3.10E-14 | 3.80E-18 | 142.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | GSK3 LMJF_18_0270 |
GSK3 LMJF_18_0270 |
2.7.11.1 | Leishmania major | 3e3p_a | Q4QE15 | 98.90 | 1.90E-13 | 2.40E-17 | 135.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | ssp2 SPCC74.03c |
SNF1-like protein kinase ssp2 (EC 2.7.11.1) |
2.7.11.1 | Schizosaccharomyces pombe | 3h4j_b | O74536 | 99.10 | 1.20E-14 | 1.40E-18 | 143.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | CAMKK1 CAMKKA |
Calcium/calmodulin-dependent protein kinase kinase 1 (CaM-KK 1) (CaM-kinase kinase 1) (CaMKK 1) (EC 2.7.11.17) (CaM-kinase IV kinase) (Calcium/calmodulin-dependent protein kinase kinase alpha) (CaM-KK alpha) (CaM-kinase kinase alpha) (CaMKK alpha) |
2.7.11.17 | Homo sapiens | Tracheitis |
6ccf_b | Q8N5S9 | ENSG00000004660 | CAMKK1 | 98.90 | 1.50E-13 | 2.00E-17 | 128.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKCB PKCB PRKCB1 |
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13) |
2.7.11.13 | Homo sapiens | Severe Nonproliferative Diabetic Retinopathy,Hyperglycemia,Macroglobulinemia,Diabetic Macular Edema,Microvascular Complications Of Diabetes 5,Diabetes Mellitus,Macular Retinal Edema,B-Cell Lymphoma,Myotonic Dystrophy 1,Primary Biliary Cholangitis,Diabetic Neuropathy,Kidney Disease,Eye Disease,Glioblastoma,Hepatocellular Carcinoma,Type 2 Diabetes Mellitus,Leukemia, Chronic Lymphocytic,Autism,Lung Cancer |
2i0e_a | P05771 | ENSG00000166501 | PRKCB | 99.20 | 6.80E-16 | 8.40E-20 | 152.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | WNK3 KIAA1566 PRKWNK3 |
Serine/threonine-protein kinase WNK3 (EC 2.7.11.1) (Protein kinase lysine-deficient 3) (Protein kinase with no lysine 3) |
2.7.11.1 | Homo sapiens | Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Agenesis Of The Corpus Callosum With Peripheral Neuropathy,Arthrogryposis, Distal, Type 3,Liddle Syndrome 1,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypertension, Essential,Syndromic X-Linked Intellectual Disability Siderius Type,Gitelman Syndrome |
5o2c_a | Q9BYP7 | ENSG00000196632 | WNK3 | 99.00 | 3.70E-14 | 4.40E-18 | 143.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKCH PKCL PRKCL |
Protein kinase C eta type (EC 2.7.11.13) (PKC-L) (nPKC-eta) |
2.7.11.13 | Homo sapiens | Myofibrillar Myopathy,Amphetamine Abuse,Stroke, Ischemic,Glioblastoma |
3txo_a | P24723 | ENSG00000027075 | PRKCH | 99.30 | 9.30E-17 | 1.10E-20 | 159.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CLK1 CLK |
Dual specificity protein kinase CLK1 (EC 2.7.12.1) (CDC-like kinase 1) |
2.7.12.1 | Homo sapiens | Pick Disease Of Brain |
6ft8_a | P49759 | ENSG00000013441 | CLK1 | 99.00 | 6.30E-14 | 8.00E-18 | 135.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PRKCQ PRKCT |
Protein kinase C theta type (EC 2.7.11.13) (nPKC-theta) |
2.7.11.13 | Homo sapiens | Inflammatory Bowel Disease 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Crohn'S Disease,Breast Cancer,Gastrointestinal Stromal Tumor |
4ra5_a | Q04759 | ENSG00000065675 | PRKCQ | 99.20 | 6.00E-16 | 7.30E-20 | 152.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | PAK1 |
Serine/threonine-protein kinase PAK 1 (EC 2.7.11.1) (Alpha-PAK) (p21-activated kinase 1) (PAK-1) (p65-PAK) |
2.7.11.1 | Homo sapiens | Thymic Neuroendocrine Tumor,Prolapse Of Urethra,Gastroesophageal Junction Adenocarcinoma,Neurofibromatosis,Breast Cancer,Colorectal Cancer,Gastric Cancer,Intellectual Developmental Disorder With Macrocephaly, Seizures, And Speech Delay,Helicobacter Pylori Infection |
5kbq_a | Q13153 | ENSG00000149269 | PAK1 | 99.00 | 4.50E-14 | 5.70E-18 | 134.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | cgd4_240 |
cgd4_240 |
Cryptosporidium parvum | 3eb0_a | A3FQN0 | 99.10 | 5.60E-15 | 6.60E-19 | 149.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | unc-22 ZK617.1 |
Twitchin (EC 2.7.11.1) (Uncoordinated protein 22) |
2.7.11.1 | Caenorhabditis elegans | 3uto_a | Q23551 | 98.90 | 8.00E-14 | 9.80E-18 | 147.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PDPK1 PDK1 |
3-phosphoinositide-dependent protein kinase 1 (hPDK1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Endometrial Cancer,Noonan Syndrome 1,Esophageal Adenosquamous Carcinoma,Prostate Cancer,Tuberous Sclerosis 1,Lung Cancer |
1h1w_a | O15530 | ENSG00000140992 | PDPK1 | 99.30 | 2.30E-16 | 2.80E-20 | 150.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | ULK3 |
Serine/threonine-protein kinase ULK3 (EC 2.7.11.1) (Unc-51-like kinase 3) |
2.7.11.1 | Homo sapiens | 6fdy_u | Q6PHR2 | ENSG00000140474 | ULK3 | 99.10 | 1.00E-14 | 1.30E-18 | 137.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR466W | PKH3 | SGDID:S000002874 | STK17B DRAK2 |
Serine/threonine-protein kinase 17B (EC 2.7.11.1) (DAP kinase-related apoptosis-inducing protein kinase 2) |
2.7.11.1 | Homo sapiens | Colon Squamous Cell Carcinoma |
3lm5_a | O94768 | ENSG00000081320 | STK17B | 99.10 | 5.50E-15 | 6.60E-19 | 145.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | SRK2E OST1 SNRK2.6 At4g33950 F17I5.140 |
Serine/threonine-protein kinase SRK2E (EC 2.7.11.1) (Protein OPEN STOMATA 1) (SNF1-related kinase 2.6) (SnRK2.6) (Serine/threonine-protein kinase OST1) |
2.7.11.1 | Arabidopsis thaliana | 3udb_d | Q940H6 | 99.00 | 6.30E-14 | 7.60E-18 | 136.80 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | GCN2 AAS1 YDR283C |
eIF-2-alpha kinase GCN2 (EC 2.7.11.1) (General control non-derepressible protein 2) (Serine/threonine-protein kinase GCN2) |
2.7.11.1 | Saccharomyces cerevisiae | 1zxe_c | P15442 | 98.90 | 1.20E-13 | 1.50E-17 | 130.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | SNRK KIAA0096 SNFRK |
SNF-related serine/threonine-protein kinase (EC 2.7.11.1) (SNF1-related kinase) |
2.7.11.1 | Homo sapiens | Breast Angiosarcoma,Skin Angiosarcoma,Liver Angiosarcoma,Skin Sarcoma,Lymphangiosarcoma,Breast Sarcoma,Hydrolethalus Syndrome 1,Neuronopathy, Distal Hereditary Motor, Type Viii |
5yks_b | Q9NRH2 | ENSG00000163788 | SNRK | 99.00 | 3.20E-14 | 3.70E-18 | 144.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | ACK2 |
Casein kinase II subunit alpha (EC 2.7.11.1) (CK II) (CK2-alpha) |
2.7.11.1 | Zea mays | 4dgn_a | P28523 | 99.00 | 2.00E-14 | 2.50E-18 | 139.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR466W | PKH3 | SGDID:S000002874 | PRKAA2 AMPK AMPK2 |
5'-AMP-activated protein kinase catalytic subunit alpha-2 (AMPK subunit alpha-2) (EC 2.7.11.1) (Acetyl-CoA carboxylase kinase) (ACACA kinase) (EC 2.7.11.27) (Hydroxymethylglutaryl-CoA reductase kinase) (HMGCR kinase) (EC 2.7.11.31) |
2.7.11.27,2.7.11.31, | Homo sapiens | Hyperglycemia,Hypertrophic Cardiomyopathy,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Tuberous Sclerosis,Breast Cancer,Ischemia,Aromatase Deficiency,Peutz-Jeghers Syndrome,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Wolff-Parkinson-White Syndrome |
2h6d_a | P54646 | ENSG00000162409 | PRKAA2 | 99.10 | 1.60E-14 | 2.00E-18 | 135.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | CDK13 CDC2L CDC2L5 CHED KIAA1791 |
Cyclin-dependent kinase 13 (EC 2.7.11.22) (EC 2.7.11.23) (CDC2-related protein kinase 5) (Cell division cycle 2-like protein kinase 5) (Cell division protein kinase 13) (hCDK13) (Cholinesterase-related cell division controller) |
2.7.11.22,2.7.11.23, | Homo sapiens | Corneal Endothelial Dystrophy,Neuroblastoma,Congenital Heart Defects, Dysmorphic Facial Features, And Intellectual Developmental Disorder,Microcephaly,Corneal Dystrophy, Posterior Polymorphous, 1,Spinocerebellar Ataxia 14,Strabismus,White-Sutton Syndrome |
5efq_a | Q14004 | ENSG00000065883 | CDK13 | 98.90 | 1.50E-13 | 1.80E-17 | 135.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR466W | PKH3 | SGDID:S000002874 | ROP5B ROP5 TGRH88_057710 |
ROP5B ROP5 TGRH88_057710 |
Toxoplasma gondii | 4lv5_a | F2YGR7 | 98.90 | 1.70E-13 | 2.10E-17 | 136.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR466W | PKH3 | SGDID:S000002874 | TGRH88_017420 |
TGRH88_017420 |
Toxoplasma gondii | 3dxn_a | Q3HNM6 | 99.10 | 1.00E-14 | 1.30E-18 | 140.10 | 0 | 0 |