| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 1.50E-17 | 1.50E-21 | 178.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR096W | KIN2 | SGDID:S000004086 | Blon_2173 |
Blon_2173 |
Bifidobacterium longum | 4ocv_a | B7GN78 | 99.30 | 2.20E-16 | 2.60E-20 | 164.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 99.20 | 1.10E-15 | 1.30E-19 | 156.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 2.60E-12 | 3.10E-16 | 128.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 98.80 | 1.00E-12 | 1.20E-16 | 138.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 98.80 | 1.20E-12 | 1.40E-16 | 134.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR096W | KIN2 | SGDID:S000004086 | 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 |
3aqv_a | P54646 | ENSG00000162409 | PRKAA2 | 98.70 | 1.40E-12 | 1.60E-16 | 130.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 98.80 | 1.20E-12 | 1.30E-16 | 137.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR096W | KIN2 | SGDID:S000004086 | cgd3_2030 |
cgd3_2030 |
Cryptosporidium parvum | 3mes_a | Q5CUP2 | 98.90 | 1.00E-13 | 1.20E-17 | 149.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR096W | KIN2 | SGDID:S000004086 | 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 | 98.80 | 9.70E-13 | 1.10E-16 | 137.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
| YLR096W | KIN2 | SGDID:S000004086 | 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 |
3ose_a | Q9P0L2 | ENSG00000116141 | MARK1 | 98.70 | 1.50E-12 | 1.50E-16 | 121.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |