NADH:ubiquinone oxidoreductase core subunit S2
| UniProt | Protein Name |
|---|---|
| A0A7I2V4G5 |
|
| O75306 |
|
| B7Z792 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial electron transport, NADH to ubiquinone | ||
| mitochondrial electron transport, NADH to ubiquinone | ||
| mitochondrial electron transport, NADH to ubiquinone | ||
| aerobic respiration | ||
| neurogenesis |
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm |
|
|
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial inner membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| NADH dehydrogenase activity | ||
| protein binding | ||
| NADH dehydrogenase (ubiquinone) activity | ||
| NADH dehydrogenase (ubiquinone) activity | ||
| electron transfer activity |
| Gene Ontology |
|---|
| mitochondrial electron transport, NADH to ubiquinone |
| oxidoreductase activity, acting on NAD(P)H |
| quinone binding |
| InterPro |
|---|
| NAD(P)H-quinone oxidoreductase subunit D/H |
| NADH-quinone oxidoreductase, subunit D |
| NADH |
| [NiFe]-hydrogenase, large subunit |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112066 | nuclear type mitochondrial complex I deficiency 6 | |
| DOID:11984 | hypertrophic cardiomyopathy | |
| DOID:2377 | multiple sclerosis | |
| DOID:3652 | Leigh disease | |
| DOID:655 | inherited metabolic disorder |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026