







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 |
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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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | ||||
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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 |