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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YNL259C | ATX1 | SGDID:S000005203 | ATX1 YNL259C N0840 |
Metal homeostasis factor ATX1 |
Saccharomyces cerevisiae | 2ggp_a | P38636 | 98.90 | 1.90E-13 | 1.30E-17 | 61.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | ATOX1 HAH1 |
Copper transport protein ATOX1 (Metal transport protein ATX1) |
Homo sapiens | Metal Metabolism Disorder,Dopamine Beta-Hydroxylase Deficiency,Wilson Disease,Deficiency Anemia,Aceruloplasminemia,Spinal Muscular Atrophy, Distal, X-Linked 3,Occipital Horn Syndrome,Menkes Disease |
1fe0_a | O00244 | 99.70 | 1.50E-21 | 1.00E-25 | 89.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | ATOX1 HAH1 |
Copper transport protein ATOX1 (Metal transport protein ATX1) |
Homo sapiens | Metal Metabolism Disorder,Dopamine Beta-Hydroxylase Deficiency,Wilson Disease,Deficiency Anemia,Aceruloplasminemia,Spinal Muscular Atrophy, Distal, X-Linked 3,Occipital Horn Syndrome,Menkes Disease |
3iwl_a | O00244 | ENSG00000177556 | ATOX1 | 98.60 | 8.10E-12 | 5.50E-16 | 54.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL259C | ATX1 | SGDID:S000005203 | SAOUHSC_02321 |
SAOUHSC_02321 |
Staphylococcus aureus | 6ff1_a | Q2FWH0 | 98.20 | 8.30E-10 | 5.60E-14 | 47.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | ATP7B PWD WC1 WND |
Copper-transporting ATPase 2 (EC 7.2.2.8) (Copper pump 2) (Wilson disease-associated protein) [Cleaved into: WND/140 kDa] |
7.2.2.8 | Homo sapiens | Liver Disease,Metal Metabolism Disorder,Inherited Metabolic Disorder,Complement Component 2 Deficiency,Movement Disease,Liver Cirrhosis,Dystonia,Ovarian Cancer,Cholestasis, Progressive Familial Intrahepatic, 3,Disorder Of Copper Metabolism,Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma,Hemolytic Anemia,Wilson Disease,Deficiency Anemia,Methylmalonic Acidemia,Aceruloplasminemia,Spinal Muscular Atrophy, Distal, X-Linked 3,Hemochromatosis, Type 1,Occipital Horn Syndrome,Menkes Disease |
2ew9_a | P35670 | ENSG00000123191 | ATP7B | 98.20 | 4.90E-10 | 3.30E-14 | 56.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL259C | ATX1 | SGDID:S000005203 | TM_0320 |
TM_0320 |
Thermotoga maritima | 2kyz_a | Q9WYF6 | 98.30 | 1.80E-10 | 1.20E-14 | 50.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | czcP Rmet_5970 |
czcP Rmet_5970 |
Cupriavidus metallidurans | 4u9r_a | Q1LAJ7 | 97.80 | 1.70E-08 | 1.10E-12 | 53.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | Pikp-1 |
Pikp-1 |
Oryza sativa | 5a6p_b | E9KPB5 | 99.00 | 8.30E-14 | 5.60E-18 | 63.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | HMA4 At2g19110 T20K24.12 |
Putative cadmium/zinc-transporting ATPase HMA4 (EC 7.2.2.12) (EC 7.2.2.21) (Protein HEAVY METAL ATPASE 4) (Putative cadmium/zinc-transporting ATPase 2) |
7.2.2.12,7.2.2.21, | Arabidopsis thaliana | 2kkh_a | O64474 | 97.40 | 1.70E-07 | 1.20E-11 | 43.10 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | cadA |
Probable cadmium-transporting ATPase (EC 7.2.2.21) (Cadmium-efflux ATPase) |
7.2.2.21 | Listeria monocytogenes | 2aj1_a | Q60048 | 98.00 | 2.50E-09 | 1.70E-13 | 46.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | pacS sll1920 |
Probable copper-transporting ATPase PacS (EC 7.2.2.8) |
7.2.2.8 | Synechocystis sp. | 4a4j_a | P73241 | 98.30 | 3.40E-10 | 2.30E-14 | 49.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | Atu1203 |
Atu1203 |
Agrobacterium fabrum | 2n4c_a | A9CJD6 | 98.50 | 2.50E-11 | 1.70E-15 | 56.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | copA yvgX BSU33500 |
Copper-exporting P-type ATPase (Protein CopA) (EC 7.2.2.8) (Copper-exporting P-type ATPase A) (Cu(+)-exporting ATPase) |
7.2.2.8 | Bacillus subtilis | 1jww_a | O32220 | 97.90 | 8.40E-09 | 5.70E-13 | 46.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | ziaA slr0798 |
Zinc-transporting ATPase (EC 7.2.2.12) (Zn(2+)-translocating P-type ATPase) |
7.2.2.12 | Synechocystis sp. | 2ofg_x | Q59998 | 98.30 | 2.60E-10 | 1.70E-14 | 55.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | CCC2 YDR270W D9954.6 |
Copper-transporting ATPase (EC 7.2.2.8) (Cu(2+)-ATPase) |
7.2.2.8 | Saccharomyces cerevisiae | 1fvs_a | P38995 | 98.40 | 1.10E-10 | 7.40E-15 | 51.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | STMDT2_03511 |
STMDT2_03511 |
Salmonella typhimurium | 4y2i_a | A0A140UHB4 | 98.10 | 9.40E-10 | 6.40E-14 | 46.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | CCS |
Copper chaperone for superoxide dismutase (Superoxide dismutase copper chaperone) |
Homo sapiens | Amyotrophic Lateral Sclerosis 1,Wilson Disease,Menkes Disease |
2crl_a | O14618 | ENSG00000173992 | CCS | 98.40 | 8.00E-11 | 5.30E-15 | 56.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL259C | ATX1 | SGDID:S000005203 | zntA SSON_3707 |
Zinc/cadmium/lead-transporting P-type ATPase (EC 7.2.2.-) (EC 7.2.2.12) (EC 7.2.2.21) (Zn(2+)/Cd(2+)/Pb(2+) export ATPase) |
7.2.2.12,7.2.2.21, | Shigella sonnei | 4umw_a | Q3YW59 | 98.30 | 2.40E-10 | 1.60E-14 | 69.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | zntA yhhO b3469 JW3434 |
Zinc/cadmium/lead-transporting P-type ATPase (EC 7.2.2.-) (EC 7.2.2.12) (EC 7.2.2.21) (Pb(II)/Cd(II)/Zn(II)-translocating ATPase) (Zn(2+)/Cd(2+)/Pb(2+) export ATPase) |
7.2.2.12,7.2.2.21, | Escherichia coli | 1mwy_a | P37617 | 98.70 | 4.40E-12 | 3.00E-16 | 56.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YNL259C | ATX1 | SGDID:S000005203 | copZ SAOUHSC_02874 |
Copper chaperone CopZ |
Staphylococcus aureus | 6ff2_a | Q2FV63 | 98.40 | 7.50E-11 | 5.10E-15 | 51.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | RGA5 |
Disease resistance protein RGA5 (Os11gRGA5) (SasRGA5) |
Oryza sativa | 5zne_a | F7J0N2 | 99.10 | 6.40E-15 | 4.30E-19 | 75.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | merA |
Mercuric reductase (EC 1.16.1.1) (Hg(II) reductase) |
1.16.1.1 | Pseudomonas aeruginosa | 2kt2_a | P00392 | 98.30 | 1.80E-10 | 1.20E-14 | 50.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | RAN1 HMA7 At5g44790 K23L20.14 T19K24.18 |
Copper-transporting ATPase RAN1 (EC 7.2.2.8) (Protein HEAVY METAL ATPASE 7) (Protein RESPONSIVE TO ANTAGONIST 1) |
7.2.2.8 | Arabidopsis thaliana | 3dxs_x | Q9S7J8 | 98.20 | 4.30E-10 | 2.90E-14 | 49.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | ATP7A MC1 MNK |
Copper-transporting ATPase 1 (EC 7.2.2.8) (Copper pump 1) (Menkes disease-associated protein) |
7.2.2.8 | Homo sapiens | Metal Metabolism Disorder,Mast-Cell Leukemia,Connective Tissue Disease,Inherited Metabolic Disorder,X-Linked Distal Hereditary Motor Neuropathy,Indolent Systemic Mastocytosis,Sialuria,Dopamine Beta-Hydroxylase Deficiency,Spinal Muscular Atrophy,Aggressive Systemic Mastocytosis,Muscular Atrophy,Neuroblastoma,Capillary Malformations, Congenital,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Noonan Syndrome 1,Atp7a-Related Copper Transport Disorders,Copper Deficiency Myelopathy,Bladder Diverticulum,Ovarian Cancer,Charcot-Marie-Tooth Disease,Disorder Of Copper Metabolism,Cutis Laxa,Mansonelliasis,Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma,Tooth Disease,Pick Disease Of Brain,Wilson Disease,Deficiency Anemia,Disease Of Mental Health,Mast Cell Neoplasm,Aceruloplasminemia,Hermansky-Pudlak Syndrome,Spinal Muscular Atrophy, Distal, X-Linked 3,Nonaka Myopathy,Occipital Horn Syndrome,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3,Menkes Disease,Spinal Muscular Atrophy, Type Iii,Mastocytosis, Cutaneous,Autosomal Recessive Cutis Laxa Type Ii Classic Type |
1s6u_a | Q04656 | ENSG00000165240 | ATP7A | 98.10 | 1.00E-09 | 7.10E-14 | 48.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL259C | ATX1 | SGDID:S000005203 | PIKM1-TS PI-KM1 |
Disease resistance protein Pikm1-TS |
Oryza sativa | 6fu9_c | B5UBC1 | 99.20 | 1.10E-15 | 7.30E-20 | 71.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | copZ yvgY BSU33510 |
Copper chaperone CopZ (Copper-ion-binding protein) |
Bacillus subtilis | 2qif_a | O32221 | 98.30 | 1.70E-10 | 1.10E-14 | 50.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | TTHA1718 |
TTHA1718 |
Thermus thermophilus | 2rog_a | Q5SHL2 | 98.50 | 4.10E-11 | 2.80E-15 | 52.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | ssr2857 |
ssr2857 |
Synechocystis | 2xmj_b | P73213 | 98.60 | 1.90E-11 | 1.30E-15 | 52.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | GBAA_3860 |
GBAA_3860 |
Bacillus anthracis | 2l3m_a | A0A348A7Y6 | 98.20 | 4.90E-10 | 3.30E-14 | 48.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL259C | ATX1 | SGDID:S000005203 | copA pacS AF_0473 |
Probable copper-exporting P-type ATPase (EC 7.2.2.8) (Copper-exporting P-type ATPase A) (Cu(+)-exporting ATPase) |
7.2.2.8 | Archaeoglobus fulgidus | 3fry_a | O29777 | 97.70 | 3.00E-08 | 2.00E-12 | 43.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL259C | ATX1 | SGDID:S000005203 | copP HP_1073 |
COP-associated protein (Copper ion-binding protein) |
Helicobacter pylori | 1yg0_a | Q48271 | 97.80 | 9.80E-09 | 6.60E-13 | 43.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |