| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YER004W | FMP52 | SGDID:S000000806 | At5g28840 F7P1.20 |
GDP-mannose 3,5-epimerase (GDP-Man 3,5-epimerase) (EC 5.1.3.18) |
5.1.3.18 | Arabidopsis thaliana | 2c5a_a | Q93VR3 | 99.60 | 1.20E-19 | 6.50E-24 | 121.60 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YER004W | FMP52 | SGDID:S000000806 | YALI0_D24585g |
YALI0_D24585g |
Yarrowia lipolytica | 6gcs_e | Q6C7X4 | 99.60 | 2.20E-20 | 1.10E-24 | 125.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YER004W | FMP52 | SGDID:S000000806 | Monooxygenase |
Monooxygenase |
Micromonospora | 5f5n_b | A0A023GUL3 | 99.60 | 1.30E-20 | 6.70E-25 | 122.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YER004W | FMP52 | SGDID:S000000806 | Ndufb10 |
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10 (Complex I-PDSW) (CI-PDSW) (NADH-ubiquinone oxidoreductase PDSW subunit) |
Mus musculus | 6g2j_p | Q9DCS9 | 99.80 | 4.10E-25 | 2.20E-29 | 147.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YER004W | FMP52 | SGDID:S000000806 | rmd |
GDP-6-deoxy-D-mannose reductase (EC 1.1.1.281) |
1.1.1.281 | Aneurinibacillus thermoaerophilus | 2pk3_b | Q6T1X6 | 99.60 | 2.20E-19 | 1.10E-23 | 118.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YER004W | FMP52 | SGDID:S000000806 | NDUFA9 NDUFS2L |
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial (Complex I-39kD) (CI-39kD) (NADH-ubiquinone oxidoreductase 39 kDa subunit) |
Homo sapiens | Loeys-Dietz Syndrome 4,Listeria Meningitis,Listeriosis,Leigh Syndrome With Leukodystrophy,Optic Atrophy 1,Leukodystrophy,Mitochondrial Complex I Deficiency, Nuclear Type 26,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Complex I Deficiency, Nuclear Type 1,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii |
5xtb_j | Q16795 | ENSG00000139180 | NDUFA9 | 99.70 | 1.70E-22 | 8.80E-27 | 133.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER004W | FMP52 | SGDID:S000000806 | gmd yefA yefN b2053 JW2038 |
GDP-mannose 4,6-dehydratase (EC 4.2.1.47) (GDP-D-mannose dehydratase) |
4.2.1.47 | Escherichia coli | 1db3_a | P0AC88 | 99.80 | 4.00E-25 | 2.10E-29 | 147.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |