| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YGL062W | PYC1 | SGDID:S000003030 | oadA-2 ERS013165_02612 |
oadA-2 ERS013165_02612 |
2.1.3.1,4.1.1.3, | Vibrio cholerae | 2nx9_a | Q6A1F6 | 100.00 | 8.50E-50 | 7.40E-54 | 470.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YGL062W | PYC1 | SGDID:S000003030 | Mfla_1512 |
Mfla_1512 |
Methylobacillus flagellatus | 5ks8_c | Q1H157 | 100.00 | 3.70E-57 | 3.30E-61 | 551.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YGL062W | PYC1 | SGDID:S000003030 | pycA SAV1114 |
Pyruvate carboxylase (EC 6.4.1.1) |
6.4.1.1 | Staphylococcus aureus | 3hb9_a | A0A0H3JRU9 | 100.00 | 2.00E-129 | 1.00E-133 | 1264.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YGL062W | PYC1 | SGDID:S000003030 | 5S |
Methylmalonyl-CoA carboxyltransferase 5S subunit (EC 2.1.3.1) (Transcarboxylase 5S subunit) |
2.1.3.1 | Propionibacterium freudenreichii | 1rqb_a | Q70AC7 | 100.00 | 1.90E-52 | 1.70E-56 | 501.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YGL062W | PYC1 | SGDID:S000003030 | pyc RHE_CH04002 |
pyc RHE_CH04002 |
6.4.1.1 | Rhizobium etli | 2qf7_b | Q2K340 | 100.00 | 2.00E-123 | 2.00E-127 | 1208.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YGL062W | PYC1 | SGDID:S000003030 | PC |
Pyruvate carboxylase, mitochondrial (EC 6.4.1.1) (Pyruvic carboxylase) (PCB) |
6.4.1.1 | Homo sapiens | Urea Cycle Disorder,Multiple Carboxylase Deficiency,Malignant Astrocytoma,Acute Porphyria,Methylmalonic Acidemia,Fructose-1,6-Bisphosphatase Deficiency,Body Mass Index Quantitative Trait Locus 11,Glutaric Acidemia I,Glycogen Storage Disease Ia,Lactic Acidosis,Nystagmus 6, Congenital, X-Linked,Propionic Acidemia,Primary Cutaneous Amyloidosis,Hyperinsulinemic Hypoglycemia, Familial, 6,Biotin Deficiency,Mitochondrial Complex Ii Deficiency, Nuclear Type 1,Biotinidase Deficiency,Holocarboxylase Synthetase Deficiency,Pyruvate Dehydrogenase E1-Alpha Deficiency,Pyruvate Carboxylase Deficiency |
3bg3_a | P11498 | ENSG00000173599 | PC | 100.00 | 1.30E-85 | 1.10E-89 | 813.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |