Skip to main content Skip to navigation Skip to search
Open toolbar

Accessibility

Disclaimer
Accessibility arrangements
Home

Main menu

  • Home
  • Download
  • Information
  • Contact

Mobile Main Menu

  • Home
  • Download
  • Information
  • Contact
AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

Breadcrumb

  1. Home
YKL203C TOR2 / SGDID:S000001686
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
YKL203C TOR2 SGDID:S000001686
PRKDC HYRC HYRC1
DNA-dependent protein kinase catalytic subunit (DNA-PK catalytic subunit) (DNA-PKcs) (EC 2.7.11.1) (DNPK1) (p460)
2.7.11.1 Homo sapiens
Severe Combined Immunodeficiency,Melanoma,Immunodeficiency 26,Combined Immunodeficiency,Hemangioma Of Subcutaneous Tissue,Cerebellar Disease,Thymus Lymphoma,Dubowitz Syndrome,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Microcephaly,Werner Syndrome,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Omenn Syndrome,Hutchinson-Gilford Progeria Syndrome,Alpha-Thalassemia,Immunodeficiency 26 With Or Without Neurologic Abnormalities,Seckel Syndrome,Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked,Lig4 Syndrome,Autosomal Recessive Cerebellar Ataxia,Ataxia-Telangiectasia
5luq_b P78527 ENSG00000253729 PRKDC 100.00 1.30E-68 1.30E-72 755.40 1 1 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
MEC1 ESR1 SAD3 YBR136W YBR1012
Serine/threonine-protein kinase MEC1 (EC 2.7.11.1) (ATR homolog) (DNA-damage checkpoint kinase MEC1) (Mitosis entry checkpoint protein 1)
2.7.11.1 Saccharomyces cerevisiae
5x6o_c P38111 100.00 1.00E-86 1.00E-90 915.90 0 0 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
TOR2 DRR2 TSC14 YKL203C
Serine/threonine-protein kinase TOR2 (EC 2.7.1.67) (EC 2.7.11.1) (Dominant rapamycin resistance protein 2) (Phosphatidylinositol 4-kinase TOR2) (PI4-kinase TOR2) (PI4K TOR2) (PtdIns-4-kinase TOR2) (Target of rapamycin kinase 2) (Temperature-sensitive CSG2 suppressor protein 14)
2.7.1.67,2.7.11.1, Saccharomyces cerevisiae
6emk_c P32600 100.00 7.00E-217 9.00E-221 2181.20 0 0 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
ATM
Serine-protein kinase ATM (EC 2.7.11.1) (Ataxia telangiectasia mutated) (A-T mutated)
2.7.11.1 Homo sapiens
Skin Melanoma,Richter'S Syndrome,Retinitis Pigmentosa,Cll/Sll,Adenoid Cystic Carcinoma,Seizure Disorder,Cowden Syndrome,Plasma Cell Neoplasm,Rothmund-Thomson Syndrome, Type 2,Cervical Adenoma Malignum,Breast Juvenile Papillomatosis,Bilateral Breast Cancer,Synchronous Bilateral Breast Carcinoma,B-Cell Non-Hodgkin Lymphoma,Diffuse Gastric Cancer,B-Cell Lymphoma,Retinal Cancer,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Endocrine Exophthalmos,Leukemia,Maxillary Sinus Adenocarcinoma,Inherited Cancer-Predisposing Syndrome,Glioma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Telangiectasis,Hematologic Cancer,Combined Immunodeficiency,Oculomotor Apraxia,Dysplastic Nevus Syndrome,Dyskeratosis Congenita,Urethra Clear Cell Adenocarcinoma,Cerebellar Disease,Bile Duct Cystadenoma,Dystonia,T-Cell Prolymphocytic Leukemia,Prolymphocytic Leukemia,Ovarian Cancer,Burkitt Lymphoma,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Glioblastoma,Hereditary Breast Ovarian Cancer Syndrome,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Mediastinum Liposarcoma,Colorectal Cancer,Acute Anterolateral Myocardial Infarction,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Proctitis,Premature Menopause,Microcephaly,Rhabdomyosarcoma,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group A,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Skin Carcinoma,Hutchinson-Gilford Progeria Syndrome,Prostate Cancer,Disease Of Mental Health,Aceruloplasminemia,Lynch Syndrome,Chromosome 13q14 Deletion Syndrome,Lymphoma, Non-Hodgkin, Familial,Renal Cell Carcinoma, Papillary, 1,Esophageal Cancer,Seckel Syndrome,Asphyxiating Thoracic Dystrophy,Immune Deficiency Disease,Myelodysplastic Syndrome,Female Breast Cancer,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Autosomal Recessive Disease,Autosomal Genetic Disease,Mantle Cell Lymphoma,Lig4 Syndrome,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2,Cervical Dystonia,Colorectal Adenocarcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Lymphoma,Cataract 38,Apraxia,Nijmegen Breakage Syndrome,Leukemia, Chronic Lymphocytic,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Myeloma, Multiple,Medulloblastoma,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Melanoma, Cutaneous Malignant 1,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Lung Cancer,Ocular Motor Apraxia,Pancreatic Cancer
5np0_b Q13315 ENSG00000149311 ATM 100.00 2.40E-83 2.60E-87 899.80 1 1 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
TRA1 YHR099W
Transcription-associated protein 1 (p400 kDa component of SAGA)
Saccharomyces cerevisiae
5ojs_t P38811 100.00 7.20E-62 7.30E-66 685.30 0 0 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
TEL1 YBL088C YBL0706
Serine/threonine-protein kinase TEL1 (EC 2.7.11.1) (ATM homolog) (DNA-damage checkpoint kinase TEL1) (Telomere length regulation protein 1)
2.7.11.1 Saccharomyces cerevisiae
6jxc_a P38110 100.00 2.50E-69 2.70E-73 753.10 0 0 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
PAS_chr1-4_0571
PAS_chr1-4_0571
Komagataella phaffii
5oej_b C4QYV4 100.00 1.30E-59 1.30E-63 663.30 0 0 0 0 0 0 0 0
YKL203C TOR2 SGDID:S000001686
ATR FRP1
Serine/threonine-protein kinase ATR (EC 2.7.11.1) (Ataxia telangiectasia and Rad3-related protein) (FRAP-related protein 1)
2.7.11.1 Homo sapiens
Lattice Corneal Dystrophy,Chronic Active Epstein-Barr Virus Infection,Lung Large Cell Carcinoma,Cerebellar Disease,Fanconi Anemia, Complementation Group I,Blepharophimosis,Ovarian Cancer,Breast Cancer,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Autosomal Recessive Cerebellar Ataxia,Nijmegen Breakage Syndrome,Leukemia, Chronic Lymphocytic,Ceroid Lipofuscinosis, Neuronal, 2,Epithelial-Stromal Tgfbi Dystrophy,Ataxia-Telangiectasia,Seckel Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia
5yz0_b Q13535 ENSG00000175054 ATR 100.00 2.10E-96 2.00E-100 1022.90 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab