holocytochrome c synthase
| UniProt | Protein Name |
|---|---|
| P53701 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| animal organ morphogenesis | ||
| cytochrome c-heme linkage | ||
| respiratory electron transport chain |
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial inner membrane | ||
| cytosol |
| GO Term | Evidence Code | PMID |
|---|---|---|
| holocytochrome-c synthase activity | ||
| holocytochrome-c synthase activity | ||
| holocytochrome-c synthase activity | ||
| protein binding | ||
| heme binding |
| Gene Ontology |
|---|
| holocytochrome-c synthase activity |
| lyase activity |
| metal ion binding |
| InterPro |
|---|
| Holocytochrome c/c1 synthase |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0111808 | linear skin defects with multiple congenital anomalies 1 | |
| DOID:10629 | microphthalmia |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 8, 2025