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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YOL113W | SKM1 | SGDID:S000005473 | 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 |
2wel_a | Q13557 | ENSG00000145349 | CAMK2D | 98.50 | 3.50E-11 | 2.70E-15 | 121.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 3.20E-11 | 2.40E-15 | 125.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.60 | 6.50E-12 | 4.90E-16 | 129.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 4.50E-11 | 3.40E-15 | 121.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 2.70E-11 | 2.00E-15 | 121.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.60 | 1.40E-11 | 1.10E-15 | 121.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 6.10E-12 | 4.60E-16 | 130.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 2.30E-11 | 1.70E-15 | 125.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 4.80E-11 | 3.70E-15 | 117.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 4.50E-15 | 3.50E-19 | 152.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 3.60E-11 | 2.70E-15 | 125.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.60 | 1.90E-11 | 1.40E-15 | 122.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 5.00E-11 | 3.80E-15 | 122.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 99.50 | 3.00E-18 | 2.20E-22 | 173.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 4.50E-11 | 3.40E-15 | 121.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 2.10E-11 | 1.60E-15 | 121.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 4.60E-11 | 3.50E-15 | 120.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 1.30E-11 | 1.00E-15 | 122.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 3.20E-11 | 2.40E-15 | 122.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 1.90E-11 | 1.50E-15 | 128.70 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | pck spr1147 |
pck spr1147 |
Streptococcus pneumoniae | 4r78_a | Q8DPI4 | 98.50 | 2.60E-11 | 2.00E-15 | 121.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 2.90E-11 | 2.20E-15 | 124.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 4.50E-11 | 3.40E-15 | 118.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL113W | SKM1 | SGDID:S000005473 | PTSG_10090 |
PTSG_10090 |
2.7.11.17 | Salpingoeca rosetta | 5ig1_b | F2UPG5 | 98.50 | 4.40E-11 | 3.30E-15 | 122.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | TNNI3K CARK |
Serine/threonine-protein kinase TNNI3K (EC 2.7.11.1) (Cardiac ankyrin repeat kinase) (Cardiac troponin I-interacting kinase) (TNNI3-interacting kinase) |
2.7.11.1 | Homo sapiens | Dilated Cardiomyopathy,Restrictive Cardiomyopathy,Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy,Familial Atrial Fibrillation |
4yfi_a | Q59H18 | ENSG00000259030 | FPGT-TNNI3K | 98.50 | 3.10E-11 | 2.40E-15 | 121.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | hph |
Hygromycin-B 4-O-kinase (EC 2.7.1.163) (APH(4)) (Hygromycin B phosphotransferase) (Hygromycin-B kinase) |
2.7.1.163 | Escherichia coli | 3w0o_a | P00557 | 98.50 | 3.30E-11 | 2.60E-15 | 121.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 3.00E-11 | 2.30E-15 | 117.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | Blon_2173 |
Blon_2173 |
Bifidobacterium longum | 4ocv_a | B7GN78 | 99.30 | 2.00E-16 | 1.60E-20 | 164.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOL113W | SKM1 | SGDID:S000005473 | unc-22 ZK617.1 |
Twitchin (EC 2.7.11.1) (Uncoordinated protein 22) |
2.7.11.1 | Caenorhabditis elegans | 3uto_a | Q23551 | 98.50 | 2.20E-11 | 1.70E-15 | 133.30 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.60 | 1.10E-11 | 8.30E-16 | 122.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL113W | SKM1 | SGDID:S000005473 | 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 | 98.50 | 2.90E-11 | 2.20E-15 | 120.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |