| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YHR082C | KSP1 | SGDID:S000001124 | cgd3_2030 |
cgd3_2030 |
Cryptosporidium parvum | 3mes_a | Q5CUP2 | 98.80 | 9.70E-13 | 1.20E-16 | 131.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR082C | KSP1 | SGDID:S000001124 | CHKA CHK CKI |
Choline kinase alpha (CK) (EC 2.7.1.32) (CHETK-alpha) (Ethanolamine kinase) (EK) (EC 2.7.1.82) |
2.7.1.32,2.7.1.82, | Homo sapiens | Myopathy,Myocardial Infarction,Myositis,West Nile Encephalitis,Distal Muscular Dystrophy With Anterior Tibial Onset,Hemoglobin D Disease,Chanarin-Dorfman Syndrome,Colorectal Cancer,Muscular Dystrophy, Congenital, Megaconial Type,Hepatitis C Virus,Neuroleptic Malignant Syndrome,Prostate Cancer,Cecal Benign Neoplasm,Multiple Acyl-Coa Dehydrogenase Deficiency,Liver Rhabdomyosarcoma,Cecum Adenoma,Ceroid Lipofuscinosis, Neuronal, 2,Pycnodysostosis |
5ftg_a | P35790 | 98.80 | 6.10E-13 | 8.10E-17 | 130.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YHR082C | KSP1 | SGDID:S000001124 | 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 | 99.10 | 1.40E-14 | 1.50E-18 | 146.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR082C | KSP1 | SGDID:S000001124 | CHKB CHETK CHKL |
Choline/ethanolamine kinase (Choline kinase beta) (CK) (CKB) (EC 2.7.1.32) (Choline kinase-like protein) (Ethanolamine kinase) (EK) (EC 2.7.1.82) (Ethanolamine kinase beta) (EKB) (choline/ethanolamine kinase beta) (CKEKB) |
2.7.1.32,2.7.1.82, | Homo sapiens | 3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome,Narcolepsy,Myopathy,Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract,Neuromuscular Disease,Cataract 30,Muscular Dystrophy,Inflammatory Liposarcoma,Dilated Cardiomyopathy,Muscular Dystrophy, Congenital, Megaconial Type,Cataract 7,Hypersomnia,Lenz-Majewski Hyperostotic Dwarfism,Batten-Turner Congenital Myopathy,Sengers Syndrome,Proximal Myopathy With Focal Depletion Of Mitochondria |
3feg_a | Q9Y259 | 98.80 | 6.70E-13 | 8.70E-17 | 130.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YHR082C | KSP1 | SGDID:S000001124 | cka-2 C52B9.1 |
Choline kinase A2 (EC 2.7.1.32) (Ethanolamine kinase) (EC 2.7.1.82) |
2.7.1.32,2.7.1.82, | Caenorhabditis elegans | 1nw1_a | Q22942 | 98.80 | 8.20E-13 | 9.60E-17 | 137.20 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
| YHR082C | KSP1 | SGDID:S000001124 | PVX_091845 |
PVX_091845 |
Plasmodium vivax | 2qg7_e | A5K4Q6 | 99.00 | 7.10E-14 | 7.50E-18 | 149.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |