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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YOL045W PSK2 / SGDID:S000005405
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
YOL045W PSK2 SGDID:S000005405
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 98.40 3.50E-11 4.30E-15 120.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
cgd2_1960
cgd2_1960
2.7.11.24 Cryptosporidium parvum
3oz6_a A3FQ79 98.50 3.20E-11 3.90E-15 123.10 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 7.10E-12 8.70E-16 125.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 3.00E-11 3.80E-15 117.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Taok2 Tao2
Serine/threonine-protein kinase TAO2 (EC 2.7.11.1) (Thousand and one amino acid protein 2)
2.7.11.1 Rattus norvegicus
1u5r_b Q9JLS3 98.50 2.80E-11 3.30E-15 123.30 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.30E-11 3.00E-15 115.30 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 1.10E-11 1.40E-15 123.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 4.80E-12 6.20E-16 121.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.80E-11 2.20E-15 119.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 5.80E-11 7.40E-15 113.50 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
LDBPK_331470
LDBPK_331470
Leishmania donovani
4qny_a E9BQ78 98.40 3.50E-11 4.30E-15 121.30 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 5.20E-11 6.30E-15 120.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PAK3 OPHN3
Serine/threonine-protein kinase PAK 3 (EC 2.7.11.1) (Beta-PAK) (Oligophrenin-3) (p21-activated kinase 3) (PAK-3)
2.7.11.1 Homo sapiens
Non-Syndromic X-Linked Intellectual Disability 30,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Non-Syndromic X-Linked Intellectual Disability,Arts Syndrome,Syndromic X-Linked Intellectual Disability
6fd3_a O75914 ENSG00000077264 PAK3 98.50 1.90E-11 2.40E-15 119.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CDC42BPB KIAA1124
Serine/threonine-protein kinase MRCK beta (EC 2.7.11.1) (CDC42-binding protein kinase beta) (CDC42BP-beta) (DMPK-like beta) (Myotonic dystrophy kinase-related CDC42-binding kinase beta) (MRCK beta) (Myotonic dystrophy protein kinase-like beta)
2.7.11.1 Homo sapiens
Myotonic Dystrophy,Epidermolysis Bullosa Simplex, Dowling-Meara Type
5ote_a Q9Y5S2 ENSG00000198752 CDC42BPB 98.40 3.80E-11 4.50E-15 125.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 3.90E-11 4.80E-15 122.40 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.50E-11 1.70E-15 126.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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
3eqc_a Q02750 ENSG00000169032 MAP2K1 98.40 4.10E-11 5.00E-15 121.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.70E-11 2.00E-15 123.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
ROP 2
ROP 2
Toxoplasma gondii
2w1z_b Q27007 98.50 1.60E-11 2.00E-15 123.80 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 99.40 8.20E-18 8.60E-22 176.50 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 8.10E-11 1.00E-14 112.30 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
AURKA AIK AIRK1 ARK1 AURA AYK1 BTAK IAK1 STK15 STK6
Aurora kinase A (EC 2.7.11.1) (Aurora 2) (Aurora/IPL1-related kinase 1) (ARK-1) (Aurora-related kinase 1) (hARK1) (Breast tumor-amplified kinase) (Serine/threonine-protein kinase 15) (Serine/threonine-protein kinase 6) (Serine/threonine-protein kinase aurora-A)
2.7.11.1 Homo sapiens
Endometrial Cancer,Melanoma,Plasma Cell Neoplasm,Uterine Corpus Cancer,Atypical Teratoid Rhabdoid Tumor,Neuroblastoma,Childhood Malignant Schwannoma,Adult Malignant Schwannoma,Bladder Cancer,Laryngeal Squamous Cell Carcinoma,Tetraploidy,Ovarian Cancer,Prostate Neuroendocrine Neoplasm,Breast Cancer,Colorectal Cancer,Endometrial Serous Adenocarcinoma,Hepatocellular Carcinoma,Rhabdomyosarcoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Lynch Syndrome,Esophageal Cancer,Donohue Syndrome,Colorectal Adenocarcinoma,Myeloma, Multiple,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer
3h10_a O14965 ENSG00000087586 AURKA 98.70 2.20E-12 2.80E-16 123.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.60E-11 2.00E-15 118.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CHEK2 CDS1 CHK2 RAD53
Serine/threonine-protein kinase Chk2 (EC 2.7.11.1) (CHK2 checkpoint homolog) (Cds1 homolog) (Hucds1) (hCds1) (Checkpoint kinase 2)
2.7.11.1 Homo sapiens
Squamous Cell Carcinoma,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Adenoid Cystic Carcinoma,Cowden Syndrome,Cervical Adenoma Malignum,Leiomyosarcoma,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Diffuse Midline Glioma, H3 K27m-Mutant,Essential Thrombocythemia,Congenital Heart Defects, Multiple Types, 3,Familial Colorectal Cancer,Leukemia,Inherited Cancer-Predisposing Syndrome,Wilms Tumor 5,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Li-Fraumeni Syndrome 1,Telangiectasis,Basal Cell Carcinoma,Lung Leiomyosarcoma,Prostate Leiomyosarcoma,Cerebellar Disease,Bile Duct Cystadenoma,T-Cell Prolymphocytic Leukemia,Nk-Cell Enteropathy,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Li-Fraumeni Syndrome 2,Premature Menopause,Rhabdomyosarcoma,Xeroderma Pigmentosum, Variant Type,Sarcoma,Fanconi Anemia, Complementation Group A,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Thrombocytopenia,Lynch Syndrome,Esophageal Cancer,Seckel Syndrome,Myelodysplastic Syndrome,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Wilms Tumor 1,Autosomal Recessive Cerebellar Ataxia,Lymphoma,Nijmegen Breakage Syndrome,Colitis,Li-Fraumeni Syndrome,Premature Ovarian Failure 1,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Osteogenic Sarcoma
3i6u_a O96017 ENSG00000183765 CHEK2 98.60 8.00E-12 9.30E-16 131.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 3.30E-11 4.00E-15 121.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PLK1 PLK
Serine/threonine-protein kinase PLK1 (EC 2.7.11.21) (Polo-like kinase 1) (PLK-1) (Serine/threonine-protein kinase 13) (STPK13)
2.7.11.21 Homo sapiens
Breast Papillomatosis,Squamous Cell Carcinoma,Cornelia De Lange Syndrome,Leukemia, Chronic Myeloid,Gonococcal Keratitis,Leukemia, Acute Myeloid,Trichothiodystrophy 1, Photosensitive,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Microcephaly,Rhabdomyosarcoma,Gastric Cancer,Prostate Cancer,Lung Squamous Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Dyskeratosis Congenita, Autosomal Dominant 3,Esophageal Cancer,Brain Glioma,Ataxia-Telangiectasia,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer
2rku_a P53350 ENSG00000166851 PLK1 98.40 7.00E-11 8.70E-15 115.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 4.40E-12 5.50E-16 123.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Brsk2 Kiaa4256 Sada
Serine/threonine-protein kinase BRSK2 (EC 2.7.11.1) (EC 2.7.11.26) (Brain-specific serine/threonine-protein kinase 2) (BR serine/threonine-protein kinase 2) (Serine/threonine-protein kinase SAD-A)
2.7.11.26 Mus musculus
4ynz_b Q69Z98 98.40 4.40E-11 5.40E-15 120.60 0 0 1 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
nahK lnpB BLLJ_1622
N-acetylhexosamine 1-kinase (EC 2.7.1.162) (N-acetylgalactosamine/N-acetylglucosamine 1-kinase)
2.7.1.162 Bifidobacterium longum
4wh3_a E8MF12 98.80 7.90E-13 1.00E-16 130.00 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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_b Q96GX5 ENSG00000120539 MASTL 98.40 8.80E-11 1.00E-14 118.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 3.10E-12 3.70E-16 133.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 4.50E-11 5.10E-15 128.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 1.40E-12 1.80E-16 126.00 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.10E-11 2.80E-15 114.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.30E-11 1.70E-15 118.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 3.60E-11 4.50E-15 117.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.50E-11 3.20E-15 118.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 3.00E-12 3.60E-16 131.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.80 1.10E-12 1.40E-16 124.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CDPK1
CDPK1
Toxoplasma gondii
5t6i_a Q9BJF5 98.40 7.90E-11 9.60E-15 125.50 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.00E-11 2.50E-15 121.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
RAD53 MEC2 SAD1 SPK1 YPL153C P2588
Serine/threonine-protein kinase RAD53 (EC 2.7.12.1) (CHEK2 homolog) (Serine-protein kinase 1)
2.7.12.1 Saccharomyces cerevisiae
4pdp_a P22216 98.50 1.90E-11 2.40E-15 123.20 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
NEK2 NEK2A NLK1
Serine/threonine-protein kinase Nek2 (EC 2.7.11.1) (HSPK 21) (Never in mitosis A-related kinase 2) (NimA-related protein kinase 2) (NimA-like protein kinase 1)
2.7.11.1 Homo sapiens
Retinitis Pigmentosa,Plexiform Neurofibroma,Malignant Peripheral Nerve Sheath Tumor,Fanconi Anemia, Complementation Group A,Retinitis Pigmentosa 67
2w5a_a P51955 ENSG00000117650 NEK2 98.30 8.50E-11 1.10E-14 112.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
STK4 KRS2 MST1
Serine/threonine-protein kinase 4 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 1) (MST-1) (STE20-like kinase MST1) (Serine/threonine-protein kinase Krs-2) [Cleaved into: Serine/threonine-protein kinase 4 37kDa subunit (MST1/N); Serine/threonine-protein kinase 4 18kDa subunit (MST1/C)]
2.7.11.1 Homo sapiens
T-Cell Immunodeficiency, Recurrent Infections, And Autoimmunity With Or Without Cardiac Malformations,Myeloproliferative Syndrome, Transient,Lymphoproliferative Syndrome 2,Epidermodysplasia Verruciformis 1,Immunodeficiency 13,Prostate Cancer,Coronin-1a Deficiency,Wilson-Turner X-Linked Mental Retardation Syndrome,Lung Cancer
3com_a Q13043 ENSG00000101109 STK4 98.50 1.80E-11 2.20E-15 121.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
TGRH88_017420
TGRH88_017420
Toxoplasma gondii
3dxn_a Q3HNM6 98.40 5.90E-11 7.30E-15 116.10 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
BN1205_040370 TGVEG_207820
BN1205_040370 TGVEG_207820
2.7.11.24 Toxoplasma gondii
3rp9_a B6KP12 98.60 1.20E-11 1.40E-15 129.80 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
MAP4K1 HPK1
Mitogen-activated protein kinase kinase kinase kinase 1 (EC 2.7.11.1) (Hematopoietic progenitor kinase) (MAPK/ERK kinase kinase kinase 1) (MEK kinase kinase 1) (MEKKK 1)
2.7.11.1 Homo sapiens
6cqd_b Q92918 ENSG00000104814 MAP4K1 98.60 1.10E-11 1.40E-15 120.70 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
unc-43 K11E8.1
Calcium/calmodulin-dependent protein kinase type II (CaM kinase II) (EC 2.7.11.17) (Uncoordinated protein 43)
2.7.11.17 Caenorhabditis elegans
2bdw_b O62305 98.50 1.70E-11 2.00E-15 125.30 0 0 0 0 0 1 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 4.20E-11 5.10E-15 119.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
WEE2 WEE1B
Wee1-like protein kinase 2 (EC 2.7.10.2) (Wee1-like protein kinase 1B) (Wee1B kinase)
2.7.10.2 Homo sapiens
Female Infertility Due To Oocyte Meiotic Arrest,Infertility,Oocyte Maturation Defect 5
5vdk_a P0C1S8 ENSG00000214102 WEE2 98.30 8.50E-11 1.10E-14 113.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
WEE1
Wee1-like protein kinase (WEE1hu) (EC 2.7.10.2) (Wee1A kinase)
2.7.10.2 Homo sapiens
Tongue Carcinoma,Vulva Squamous Cell Carcinoma,Gum Cancer,Breast Cancer,Western Equine Encephalitis,Beckwith-Wiedemann Syndrome,Medulloblastoma
1x8b_a P30291 ENSG00000166483 WEE1 98.50 2.50E-11 3.30E-15 116.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
pknB Rv0014c MTCY10H4.14c
Serine/threonine-protein kinase PknB (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
6i2p_a P9WI81 98.40 3.70E-11 4.80E-15 113.60 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 4.90E-11 5.90E-15 120.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
MAPK14 CSBP CSBP1 CSBP2 CSPB1 MXI2 SAPK2A
Mitogen-activated protein kinase 14 (MAP kinase 14) (MAPK 14) (EC 2.7.11.24) (Cytokine suppressive anti-inflammatory drug-binding protein) (CSAID-binding protein) (CSBP) (MAP kinase MXI2) (MAX-interacting protein 2) (Mitogen-activated protein kinase p38 alpha) (MAP kinase p38 alpha) (Stress-activated protein kinase 2a) (SAPK2a)
2.7.11.24 Homo sapiens
Psoriasis,Heart Disease,Bladder Lateral Wall Cancer,Leukemia, Chronic Myeloid,Gaucher'S Disease,Alzheimer Disease,Myocardial Infarction,Doxorubicin Induced Cardiomyopathy,Human Cytomegalovirus Infection,Vitreous Abscess,Anthrax Disease,Colon Adenocarcinoma,Autoimmune Disease,Dilated Cardiomyopathy,Ureteral Obstruction,Ovarian Cancer,Tuberous Sclerosis 2,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Hepatocellular Carcinoma,Septic Myocarditis,Pheochromocytoma,Ischemia,Skin Carcinoma,Chlamydia,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Skin Disease,Retinoblastoma,Rheumatoid Arthritis,Inflammatory Bowel Disease,Trichothiodystrophy 5, Nonphotosensitive,Fibrodysplasia Ossificans Progressiva,Acute Promyelocytic Leukemia,Pulmonary Disease, Chronic Obstructive,Lipoprotein Quantitative Trait Locus,Cardiomyopathy, Familial Hypertrophic, 25,Alexander Disease,Lung Cancer,Osteogenic Sarcoma,Asthma
2fst_x Q16539 ENSG00000112062 MAPK14 98.40 8.90E-11 1.00E-14 120.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 3.40E-12 4.10E-16 131.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CDC7 CDC7L1
Cell division cycle 7-related protein kinase (CDC7-related kinase) (HsCdc7) (huCdc7) (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Open-Angle Glaucoma,Glaucoma, Primary Open Angle,Masa Syndrome
4f9c_a O00311 ENSG00000097046 CDC7 98.40 5.10E-11 6.20E-15 120.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PKMYT1 MYT1
Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase (EC 2.7.11.1) (Myt1 kinase)
2.7.11.1 Homo sapiens
5vcy_a Q99640 ENSG00000127564 PKMYT1 98.60 4.20E-12 5.20E-16 124.90 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.20E-11 2.80E-15 117.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Rps6ka3 Mapkapk1b Rps6ka-rs1 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) (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 Mus musculus
5o1s_a P18654 98.40 5.40E-11 6.40E-15 122.40 0 0 1 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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
4or5_f P50750 ENSG00000136807 CDK9 98.40 4.20E-11 5.30E-15 117.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 8.20E-11 1.00E-14 113.50 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 3.60E-11 4.30E-15 122.90 0 0 0 0 0 0 1 0
YOL045W PSK2 SGDID:S000005405
cgd4_240
cgd4_240
Cryptosporidium parvum
3eb0_a A3FQN0 98.50 2.20E-11 2.60E-15 125.70 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
DYRK2
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1)
2.7.12.1 Homo sapiens
4azf_a Q92630 ENSG00000127334 DYRK2 98.60 4.90E-12 5.70E-16 132.80 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
ROP8
ROP8
Toxoplasma gondii
3byv_a O15693 98.60 5.00E-12 6.00E-16 129.70 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.50E-11 1.90E-15 119.40 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.90E-11 3.70E-15 117.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.20E-11 1.50E-15 124.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Mapk1 Erk2 Mapk Prkm1
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 Rattus norvegicus
4xne_a P63086 98.30 9.10E-11 1.10E-14 118.40 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.80E-11 2.10E-15 127.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.30E-11 7.80E-15 116.40 0 0 1 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PTSG_10090
PTSG_10090
2.7.11.17 Salpingoeca rosetta
5ig1_b F2UPG5 98.50 2.00E-11 2.40E-15 123.80 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 7.00E-12 8.40E-16 126.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 1.00E-11 1.30E-15 119.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
STK24 MST3 STK3
Serine/threonine-protein kinase 24 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 3) (MST-3) (STE20-like kinase MST3) [Cleaved into: Serine/threonine-protein kinase 24 36 kDa subunit (Mammalian STE20-like protein kinase 3 N-terminal) (MST3/N); Serine/threonine-protein kinase 24 12 kDa subunit (Mammalian STE20-like protein kinase 3 C-terminal) (MST3/C)]
2.7.11.1 Homo sapiens
Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Myeloproliferative Syndrome, Transient,Arthrogryposis, Distal, Type 3,Cerebral Cavernous Malformations,Cerebrocostomandibular Syndrome,Cerebral Cavernous Malformations 3,Distal Arthrogryposis,Inflammatory Bowel Disease 14,Hypertension, Essential,Gitelman Syndrome
3a7i_a Q9Y6E0 ENSG00000102572 STK24 98.40 3.90E-11 4.80E-15 118.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 8.50E-11 1.00E-14 116.60 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.80E-11 8.30E-15 119.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 4.60E-11 5.60E-15 119.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.20E-11 1.50E-15 120.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 3.50E-12 4.10E-16 133.00 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
SAPK10
SAPK10
Saccharum officinarum
5wax_a A0A238LNS4 98.40 7.20E-11 8.80E-15 117.00 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.80 9.20E-13 1.20E-16 125.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 3.70E-11 4.50E-15 117.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Wnk1 Hsn2 Prkwnk1
Serine/threonine-protein kinase WNK1 (EC 2.7.11.1) (Protein kinase lysine-deficient 1) (Protein kinase with no lysine 1)
2.7.11.1 Rattus norvegicus
5drb_a Q9JIH7 98.50 2.80E-11 3.50E-15 117.00 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
pk7
pk7
Plasmodium falciparum
2pml_x O96214 98.40 8.80E-11 1.10E-14 118.90 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 9.00E-12 1.20E-15 120.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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
2x0g_a P53355 ENSG00000196730 DAPK1 98.50 1.90E-11 2.30E-15 122.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 5.30E-12 6.60E-16 126.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 7.10E-12 9.10E-16 120.90 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
LDBPK_100540
LDBPK_100540
2.7.11.24 Leishmania donovani
4o2z_a E9BA99 98.40 8.40E-11 9.80E-15 121.60 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.40E-11 2.90E-15 120.60 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.60E-11 8.00E-15 117.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PIM2
Serine/threonine-protein kinase pim-2 (EC 2.7.11.1) (Pim-2h)
2.7.11.1 Homo sapiens
Croup,Hepatocellular Carcinoma,Osteogenesis Imperfecta, Type Xii,Mantle Cell Lymphoma,Colorectal Adenocarcinoma,Lymphoma
2iwi_b Q9P1W9 ENSG00000102096 PIM2 98.50 3.10E-11 3.90E-15 118.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 1.30E-12 1.60E-16 133.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
MAP3K8 COT ESTF
Mitogen-activated protein kinase kinase kinase 8 (EC 2.7.11.25) (Cancer Osaka thyroid oncogene) (Proto-oncogene c-Cot) (Serine/threonine-protein kinase cot) (Tumor progression locus 2) (TPL-2)
2.7.11.25 Homo sapiens
Indolent Plasma Cell Myeloma,Paronychia,Skin Lipoma,Rheumatoid Arthritis,Lung Cancer
4y85_b P41279 ENSG00000107968 MAP3K8 98.40 4.80E-11 5.90E-15 119.20 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CDK16 PCTAIRE1 PCTK1
Cyclin-dependent kinase 16 (EC 2.7.11.22) (Cell division protein kinase 16) (PCTAIRE-motif protein kinase 1) (Serine/threonine-protein kinase PCTAIRE-1)
2.7.11.22 Homo sapiens
5g6v_a Q00536 ENSG00000102225 CDK16 98.50 3.10E-11 3.80E-15 121.10 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 7.70E-12 9.20E-16 126.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
unc-22 ZK617.1
Twitchin (EC 2.7.11.1) (Uncoordinated protein 22)
2.7.11.1 Caenorhabditis elegans
3uto_a Q23551 98.40 5.00E-11 6.10E-15 128.20 0 0 0 0 0 1 0 0
YOL045W PSK2 SGDID:S000005405
CDKL3 NKIAMRE
Cyclin-dependent kinase-like 3 (EC 2.7.11.22) (Serine/threonine-protein kinase NKIAMRE)
2.7.11.22 Homo sapiens
Orofaciodigital Syndrome Vi
3zdu_a Q8IVW4 ENSG00000006837 CDKL3 98.50 1.60E-11 1.90E-15 122.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 7.40E-12 8.80E-16 127.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 9.40E-12 1.10E-15 128.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.00E-11 2.40E-15 120.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 5.10E-11 6.30E-15 118.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
MAP2K6 MEK6 MKK6 PRKMK6 SKK3
Dual specificity mitogen-activated protein kinase kinase 6 (MAP kinase kinase 6) (MAPKK 6) (EC 2.7.12.2) (MAPK/ERK kinase 6) (MEK 6) (Stress-activated protein kinase kinase 3) (SAPK kinase 3) (SAPKK-3) (SAPKK3)
2.7.12.2 Homo sapiens
Human Cytomegalovirus Infection,Anthrax Disease,Cardiomyopathy, Familial Hypertrophic, 25
3fme_a P52564 ENSG00000108984 MAP2K6 98.60 1.10E-11 1.40E-15 118.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 4.50E-11 5.30E-15 121.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
cgd7_1840
cgd7_1840
Cryptosporidium parvum
3f3z_a Q5CYL9 98.40 5.60E-11 7.20E-15 113.30 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Blon_2173
Blon_2173
Bifidobacterium longum
4ocv_a B7GN78 98.50 2.50E-11 3.20E-15 121.40 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.30 1.00E-10 1.10E-14 127.00 0 0 0 0 0 0 1 0
YOL045W PSK2 SGDID:S000005405
ssp2 SPCC74.03c
SNF1-like protein kinase ssp2 (EC 2.7.11.1)
2.7.11.1 Schizosaccharomyces pombe
3h4j_b O74536 98.60 6.00E-12 7.20E-16 126.80 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 6.30E-12 8.10E-16 121.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
PIM1
Serine/threonine-protein kinase pim-1 (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Retinitis Pigmentosa,Polyploidy,Plasma Protein Metabolism Disease,Primary Central Nervous System Lymphoma,Diamond-Blackfan Anemia,Myeloid Leukemia,Prostate Cancer,Mantle Cell Lymphoma
1xr1_a P11309 ENSG00000137193 PIM1 98.50 1.30E-11 1.60E-15 120.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.70E-11 2.00E-15 123.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CDKL1
Cyclin-dependent kinase-like 1 (EC 2.7.11.22) (Protein kinase p42 KKIALRE) (Serine/threonine-protein kinase KKIALRE)
2.7.11.22 Homo sapiens
Fraser Syndrome 1
4agu_b Q00532 ENSG00000100490 CDKL1 98.50 3.10E-11 3.80E-15 118.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.10E-11 7.50E-15 119.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CAMK4 CAMK CAMK-GR CAMKIV
Calcium/calmodulin-dependent protein kinase type IV (CaMK IV) (EC 2.7.11.17) (CaM kinase-GR)
2.7.11.17 Homo sapiens
Lung Large Cell Carcinoma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Crouzon Syndrome With Acanthosis Nigricans,Systemic Lupus Erythematosus,Gingival Fibromatosis
2w4o_a Q16566 ENSG00000152495 CAMK4 98.50 2.10E-11 2.50E-15 124.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CPK4 CDPK4 PF07_0072
Calcium-dependent protein kinase 4 (EC 2.7.11.1)
2.7.11.1 Plasmodium falciparum
4rgj_a Q8IBS5 98.50 2.40E-11 3.10E-15 127.70 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 3.60E-12 4.50E-16 123.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
MAP3K5 ASK1 MAPKKK5 MEKK5
Mitogen-activated protein kinase kinase kinase 5 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 1) (ASK-1) (MAPK/ERK kinase kinase 5) (MEK kinase 5) (MEKK 5)
2.7.11.25 Homo sapiens
Liver Disease,Non-Alcoholic Fatty Liver Disease,Pyriform Sinus Cancer,Fatty Liver Disease,Alzheimer Disease,Glottis Squamous Cell Carcinoma,Partial Third-Nerve Palsy,Neural Tube Defects,Huntington Disease
5uox_a Q99683 ENSG00000197442 MAP3K5 98.70 2.50E-12 3.20E-16 122.10 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.00E-11 2.60E-15 117.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.70 2.00E-12 2.40E-16 132.40 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.80E-11 3.40E-15 122.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 2.20E-11 2.70E-15 125.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
SRK2I 41K OSKL2 SNRK2.3 At5g66880 MUD21.14
Serine/threonine-protein kinase SRK2I (EC 2.7.11.1) (OST1-kinase-like 2) (Protein ATHPROKIN B) (SNF1-related kinase 2.3) (SnRK2.3)
2.7.11.1 Arabidopsis thaliana
3uc3_a Q39193 98.60 7.40E-12 9.10E-16 127.00 0 0 0 0 0 0 1 0
YOL045W PSK2 SGDID:S000005405
GL50803_008037 GL50803_8037
GL50803_008037 GL50803_8037
Giardia intestinalis
3gbz_a A8BZ95 98.40 4.20E-11 5.10E-15 119.50 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 1.50E-11 1.80E-15 124.30 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.10E-11 7.70E-15 113.50 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.50 3.40E-11 3.90E-15 124.90 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 8.80E-12 1.10E-15 119.60 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
ACK2
Casein kinase II subunit alpha (EC 2.7.11.1) (CK II) (CK2-alpha)
2.7.11.1 Zea mays
4dgn_a P28523 98.60 6.40E-12 7.90E-16 124.70 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 6.40E-12 8.10E-16 124.00 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 5.40E-11 6.70E-15 116.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 6.20E-12 7.70E-16 125.90 0 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
TLK2
Serine/threonine-protein kinase tousled-like 2 (EC 2.7.11.1) (HsHPK) (PKU-alpha) (Tousled-like kinase 2)
2.7.11.1 Homo sapiens
Pica Disease,Mental Retardation, Autosomal Dominant 57
5o0y_a Q86UE8 ENSG00000146872 TLK2 98.40 9.00E-11 9.20E-15 132.70 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
ROP5B ROP5 TGRH88_057710
ROP5B ROP5 TGRH88_057710
Toxoplasma gondii
4lv5_a F2YGR7 98.60 8.70E-12 1.10E-15 127.30 0 0 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
CAMKK2 CAMKKB KIAA0787
Calcium/calmodulin-dependent protein kinase kinase 2 (CaM-KK 2) (CaM-kinase kinase 2) (CaMKK 2) (EC 2.7.11.17) (Calcium/calmodulin-dependent protein kinase kinase beta) (CaM-KK beta) (CaM-kinase kinase beta) (CaMKK beta)
2.7.11.17 Homo sapiens
Parkinson Disease, Late-Onset
5uy6_a Q96RR4 ENSG00000110931 CAMKK2 98.70 1.90E-12 2.50E-16 124.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 5.20E-11 6.20E-15 119.60 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.40 6.70E-11 8.30E-15 117.20 0 0 1 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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
4wb8_a P17612 ENSG00000072062 PRKACA 98.40 5.90E-11 7.20E-15 118.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
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 98.60 9.40E-12 1.20E-15 124.80 1 1 0 0 0 0 0 0
YOL045W PSK2 SGDID:S000005405
Rop2
Rop2
Toxoplasma gondii
3dzo_a Q06AK3 98.50 1.30E-11 1.60E-15 129.20 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab