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
YPL058C PDR12 / SGDID:S000005979
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
YPL058C PDR12 SGDID:S000005979
ecfA2 cbiO2 Ldb0425
Energy-coupling factor transporter ATP-binding protein EcfA2 (ECF transporter A component EcfA2) (EC 3.6.3.-)
3.6.3.- Lactobacillus delbrueckii
5jsz_f Q1GBI9 98.80 5.00E-13 6.00E-17 137.00 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
TM_1403
TM_1403
Thermotoga maritima
4yer_a Q9X1C3 98.50 1.50E-11 1.70E-15 131.20 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
TM_0421
TM_0421
Thermotoga maritima
2yyz_a Q9WYQ2 98.80 6.50E-13 7.60E-17 142.20 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCG2 ABCP BCRP BCRP1 MXR
Broad substrate specificity ATP-binding cassette transporter ABCG2 (EC 7.6.2.2) (ATP-binding cassette sub-family G member 2) (Breast cancer resistance protein) (CDw338) (Mitoxantrone resistance-associated protein) (Placenta-specific ATP-binding cassette transporter) (Urate exporter) (CD antigen CD338)
7.6.2.2 Homo sapiens
Stomach Carcinoma In Situ,Epilepsy,Hyperuricemia,Placental Choriocarcinoma,Gestational Choriocarcinoma,Ocular Cancer,Core Binding Factor Acute Myeloid Leukemia,Nail Disorder, Nonsyndromic Congenital, 1,Sitosterolemia,Erythroplakia,Acute Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Persistent Fetal Circulation Syndrome,Bilirubin Metabolic Disorder,Gout,Brain Cancer,Diarrhea,Ovarian Cancer,Adult Acute Lymphocytic Leukemia,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Polyneuropathy Due To Drug,Rhabdomyosarcoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Choriocarcinoma,Toxic Encephalopathy,Thrombocytopenia,Multiple Sclerosis,Esophageal Cancer,Uric Acid Concentration, Serum, Quantitative Trait Locus 1,Blood Group, Junior System,Renal Cell Carcinoma, Nonpapillary,Ischiocoxopodopatellar Syndrome With Or Without Pulmonary Arterial Hypertension,Medulloblastoma,Hyperekplexia,Childhood Acute Myeloid Leukemia,Lung Cancer,Pancreatic Cancer
6hbu_a Q9UNQ0 ENSG00000118777 ABCG2 99.80 5.30E-26 6.40E-30 263.10 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
algS
algS
Sphingomonas sp.
4tqu_s Q9KWT9 98.40 8.10E-11 9.30E-15 126.60 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
PA4461
PA4461
Pseudomonas aeruginosa
5x5y_a Q9HVV6 98.40 8.20E-11 9.90E-15 117.80 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCG5
ATP-binding cassette sub-family G member 5 (EC 7.6.2.-) (Sterolin-1)
7.6.2.- Homo sapiens
Lysosomal And Lipase Deficiency,Short-Rib Thoracic Dysplasia 15 With Polydactyly,Homozygous Familial Hypercholesterolemia,Biliary Tract Disease,Sitosterolemia,Arcus Corneae,Leber Plus Disease,Atherosclerosis Susceptibility,Cholestasis, Progressive Familial Intrahepatic, 2,Cholelithiasis,Aortic Atherosclerosis,Cholestasis, Progressive Familial Intrahepatic, 3,Familial Hypercholesterolemia,Hypolipoproteinemia,Thrombocytopenia,Type 2 Diabetes Mellitus,Cholestasis, Benign Recurrent Intrahepatic, 2,Gallbladder Disease 4,Cholestasis, Benign Recurrent Intrahepatic, 1,Sitosterolemia 2,Hyperlipoproteinemia, Type Iv,Gallbladder Disease,Tangier Disease,Short-Rib Thoracic Dysplasia 1 With Or Without Polydactyly,Sitosterolemia 1,Progressive Familial Intrahepatic Cholestasis,Cholestasis, Progressive Familial Intrahepatic, 1,Niemann-Pick Disease, Type C1
5do7_a Q9H222 ENSG00000138075 ABCG5 99.90 5.60E-29 6.70E-33 289.60 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCG8
ATP-binding cassette sub-family G member 8 (EC 7.6.2.-) (Sterolin-2)
7.6.2.- Homo sapiens
Homozygous Familial Hypercholesterolemia,Sea-Blue Histiocyte Disease,Sitosterolemia,Arcus Corneae,Leber Plus Disease,Cholestasis, Progressive Familial Intrahepatic, 2,Cholelithiasis,Aortic Atherosclerosis,Cholestasis, Progressive Familial Intrahepatic, 3,Familial Hypercholesterolemia,Hypolipoproteinemia,Hemolytic Anemia,Thrombocytopenia,Type 2 Diabetes Mellitus,Gallbladder Disease 4,Cholestasis, Benign Recurrent Intrahepatic, 1,Sitosterolemia 2,Gallbladder Disease,Tangier Disease,Sitosterolemia 1,Progressive Familial Intrahepatic Cholestasis,Cholestasis, Progressive Familial Intrahepatic, 1
5do7_b Q9H221 ENSG00000143921 ABCG8 99.80 1.60E-26 1.90E-30 269.70 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
dppD TTE0057
Dipeptide transport ATP-binding protein DppD (EC 7.4.2.9)
7.4.2.9 Caldanaerobacter subterraneus
4fwi_b Q8RDH4 98.30 1.00E-10 1.20E-14 124.20 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ecfA2 cbiO2 TTE2260
Energy-coupling factor transporter ATP-binding protein EcfA2 (ECF transporter A component EcfA2) (EC 3.6.3.-)
3.6.3.- Caldanaerobacter subterraneus
4mki_a Q8R7Y5 98.60 8.40E-12 1.00E-15 129.00 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCC1 MRP1
Multidrug resistance-associated protein 1 (EC 7.6.2.2) (ATP-binding cassette sub-family C member 1) (Glutathione-S-conjugate-translocating ATPase ABCC1) (EC 7.6.2.3) (Leukotriene C(4) transporter) (LTC4 transporter)
7.6.2.2,7.6.2.3, Bos taurus
5uja_a Q8HXQ5 98.80 7.70E-13 8.60E-17 168.90 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
fbpC NGO0215
Fe(3+) ions import ATP-binding protein FbpC (EC 7.2.2.7)
7.2.2.7 Neisseria gonorrhoeae
3fvq_b Q5FA19 98.60 1.00E-11 1.20E-15 134.00 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
molC HI_1470
Molybdate import ATP-binding protein MolC (EC 7.3.2.5)
7.3.2.5 Haemophilus influenzae
2nq2_c Q57399 98.50 2.10E-11 2.50E-15 122.60 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
hmuV YPO0279 y0539 YP_0434
Hemin import ATP-binding protein HmuV (EC 7.6.2.-)
7.6.2.- Yersinia pestis
4g1u_c Q56993 98.40 5.50E-11 6.70E-15 120.40 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
hisP STM2351
Histidine transport ATP-binding protein HisP
Salmonella typhimurium
1b0u_a P02915 99.30 7.30E-17 6.70E-21 175.50 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCC8 SUR
ATP-binding cassette sub-family C member 8 (Sulfonylurea receptor 1)
Cricetus cricetus
5twv_b Q09427 98.50 2.10E-11 2.30E-15 157.10 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ecfA2 cbiO2 LVIS_1661
Energy-coupling factor transporter ATP-binding protein EcfA2 (ECF transporter A component EcfA2) (EC 3.6.3.-)
3.6.3.- Lactobacillus brevis
4huq_a Q03PY6 98.90 2.30E-13 2.80E-17 140.10 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ecfA1 cbiO1 LVIS_1662
Energy-coupling factor transporter ATP-binding protein EcfA1 (ECF transporter A component EcfA1) (EC 7.-.-.-)
Lactobacillus brevis
4huq_b Q03PY5 98.90 1.70E-13 2.00E-17 140.80 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
TAP1 ABCB2 PSF1 RING4 Y3
Antigen peptide transporter 1 (APT1) (EC 7.4.2.-) (ATP-binding cassette sub-family B member 2) (Peptide supply factor 1) (Peptide transporter PSF1) (PSF-1) (Peptide transporter TAP1) (Peptide transporter involved in antigen processing 1) (Really interesting new gene 4 protein) (RING4)
7.4.2.- Homo sapiens
Diabetes Mellitus,Posterior Uveal Melanoma,Spondylitis,Alveolar Echinococcosis,Spondyloarthropathy 1,Cystic Fibrosis,Recurrent Respiratory Papillomatosis,Autoimmune Disease,Idiopathic Bronchiectasis,Type 1 Diabetes Mellitus,Herpes Simplex,Immunodeficiency By Defective Expression Of Mhc Class I,Bare Lymphocyte Syndrome, Type I,Dyschromatosis Universalis Hereditaria,Lung Cancer
5u1d_a Q03518 ENSG00000168394 TAP1 98.40 5.10E-11 5.50E-15 142.60 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
malK b4035 JW3995
Maltose/maltodextrin import ATP-binding protein MalK (EC 7.5.2.1)
7.5.2.1 Escherichia coli
2awo_b P68187 98.40 6.70E-11 7.40E-15 129.70 0 0 0 0 0 0 0 1
YPL058C PDR12 SGDID:S000005979
ATM1 MDY YMR301C YM9952.03C
Iron-sulfur clusters transporter ATM1, mitochondrial (EC 7.-.-.-)
Saccharomyces cerevisiae
4myc_c P40416 98.50 1.90E-11 2.30E-15 138.20 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
pgp-1 K08E7.9
Multidrug resistance protein pgp-1 (EC 7.6.2.2) (P-glycoprotein A) (P-glycoprotein-related protein 1)
7.6.2.2 Caenorhabditis elegans
4f4c_a P34712 98.60 5.10E-12 6.10E-16 157.10 0 0 0 0 0 1 0 0
YPL058C PDR12 SGDID:S000005979
metN abc b0199 JW0195
Methionine import ATP-binding protein MetN (EC 7.4.2.11)
7.4.2.11 Escherichia coli
3dhw_d P30750 98.40 6.00E-11 7.10E-15 125.50 0 0 0 0 0 0 0 1
YPL058C PDR12 SGDID:S000005979
CFTR ABCC7
Cystic fibrosis transmembrane conductance regulator (CFTR) (ATP-binding cassette sub-family C member 7) (Channel conductance-controlling ATPase) (EC 5.6.1.6) (cAMP-dependent chloride channel)
5.6.1.6 Homo sapiens
Megacolon,Pulmonary Edema,Bronchitis,Biliary Dyskinesia,Autosomal Dominant Polycystic Kidney Disease,Intestinal Pseudo-Obstruction,Retinitis Pigmentosa,Acrokeratoderma, Hereditary Papulotranslucent,Polycystic Kidney Disease,Urea Cycle Disorder,Bronchial Disease,Diabetes Mellitus,Protein-Energy Malnutrition,Cholangitis,Spermatocele,Bartter Disease,Mycobacterium Abscessus,Pseudohypoaldosteronism,Primary Ciliary Dyskinesia,Male Infertility With Azoospermia Or Oligozoospermia Due To Single Gene Mutation,Bronchiectasis,Nontuberculous Mycobacterial Lung Disease,Ciliary Dyskinesia, Primary, 19,Primary Biliary Cholangitis,Male Infertility,Muscular Dystrophy,Plasma Protein Metabolism Disease,Cryptorchidism, Unilateral Or Bilateral,Mite Infestation,Cystic Fibrosis,Alcoholic Pancreatitis,Pancreatitis,Intestinal Obstruction,Ileus,Cystic Fibrosis And Congenital Absence Of The Vas Deferens,Idiopathic Bronchiectasis,Infertility,Bilirubin Metabolic Disorder,Lung Disease,Allergic Bronchopulmonary Aspergillosis,Tay-Sachs Disease,Prss1-Related Hereditary Pancreatitis,Diarrhea,Typhoid Fever,Exocrine Pancreatic Insufficiency,Acute Pancreatitis,Osteoporosis,Pneumonia,Bacterial Infectious Disease,Common Cold,Cystic Kidney Disease,Kidney Disease,Duodenal Atresia,Paranasal Sinus Disease,Pancreatitis, Hereditary,Miliaria,Portal Hypertension,Aquagenic Syringeal Acrokeratoderma,Vas Deferens, Congenital Bilateral Aplasia Of,Azoospermia,Oligospermia,Sclerosing Cholangitis,Alpha-1-Antitrypsin Deficiency,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Miliaria Rubra,Respiratory Failure,Mammary Paget'S Disease,Cholera,Pelvic Organ Prolapse,Disease Of Mental Health,Liddle Syndrome 1,Cholangitis, Primary Sclerosing,Diabetes Insipidus, Nephrogenic, Autosomal,Type 2 Diabetes Mellitus,Autoimmune Pancreatitis,Hemochromatosis, Type 1,Disease By Infectious Agent,Secretory Diarrhea,Kartagener Syndrome,Aspergillosis,Vas Deferens, Congenital Bilateral Aplasia Of, X-Linked,Cholestasis, Benign Recurrent Intrahepatic, 1,X-Linked Monogenic Disease,Autosomal Recessive Disease,Autosomal Genetic Disease,Polycystic Liver Disease,Renal Hypodysplasia/Aplasia 1,Chylomicron Retention Disease,Pulmonary Disease, Chronic Obstructive,Meconium Ileus,Intussusception,Specific Language Impairment,Gallbladder Disease,Diarrhea 8, Secretory Sodium, Congenital,Progressive Familial Intrahepatic Cholestasis,Bronchiectasis With Or Without Elevated Sweat Chloride 1,Asthma,Pancreatic Cancer,Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease,Pseudoxanthoma Elasticum
1xmi_c P13569 ENSG00000001626 CFTR 98.50 2.90E-11 3.30E-15 127.10 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
ABCA1 ABC1 CERP
Phospholipid-transporting ATPase ABCA1 (EC 7.6.2.1) (ATP-binding cassette sub-family A member 1) (ATP-binding cassette transporter 1) (ABC-1) (ATP-binding cassette 1) (Cholesterol efflux regulatory protein)
7.6.2.1 Homo sapiens
Heart Disease,Chediak-Higashi Syndrome,Vascular Disease,Familial Hyperlipidemia,Inherited Metabolic Disorder,Diabetes Mellitus,Myopia,Ichthyosis, Congenital, Autosomal Recessive 4a,Cerebrovascular Disease,Homozygous Familial Hypercholesterolemia,Alzheimer Disease,Myocardial Infarction,Pulmonary Alveolar Proteinosis,Stroke, Ischemic,Primary Biliary Cholangitis,Sitosterolemia,Smith-Lemli-Opitz Syndrome,Hypoalphalipoproteinemia,Atherosclerosis Susceptibility,Cardiovascular System Disease,Coronary Heart Disease 5,Splenomegaly,Aortic Atherosclerosis,Xanthomatosis,Colorectal Cancer,Open-Angle Glaucoma,Familial Hypercholesterolemia,Hypolipoproteinemia,Lipid Metabolism Disorder,Stargardt Disease,Lysosomal Acid Lipase Deficiency,Macular Degeneration, Age-Related, 1,Huntington Disease-Like 1,Niemann-Pick Disease,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Hypoalphalipoproteinemia, Primary, 1,Type 2 Diabetes Mellitus,Malaria,Fetal Akinesia Deformation Sequence 4,Ichthyosis, Congenital, Autosomal Recessive 4b,Hypoalphalipoproteinemia, Primary, 2,Glaucoma, Primary Open Angle,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Tangier Disease,Autosomal Recessive Congenital Ichthyosis,C Syndrome,Niemann-Pick Disease, Type C1,Scott Syndrome
5xjy_a O95477 ENSG00000165029 ABCA1 99.80 8.70E-26 8.20E-30 301.90 1 1 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
cbiO cbiO2 RCAP_rcc02034
Cobalt import ATP-binding protein CbiO (EC 7.2.2.-) (Energy-coupling factor transporter ATP-binding protein CbiO) (ECF transporter A component CbiO)
7.2.2.- Rhodobacter capsulatus
5x3x_a O68106 98.60 6.40E-12 7.60E-16 129.40 0 0 0 0 0 0 0 0
YPL058C PDR12 SGDID:S000005979
PH0022
PH0022
Pyrococcus horikoshii
1v43_a O57758 98.40 4.40E-11 5.10E-15 129.40 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab