Entity Details
| Primary name |
MMAB_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q96EY8 |
| EntryName | MMAB_HUMAN |
| FullName | Corrinoid adenosyltransferase |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 250 |
| SequenceStatus | complete |
| DateCreated | 2003-11-07 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Mitochondrion |
Domains
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| Domain | Name | Category | Type |
| IPR016030 | Cobalamin adenosyltransferase-like | Domain | Domain |
| IPR029499 | ATP:cob(I)alamin adenosyltransferase, PduO-type | Family | Family |
| IPR036451 | Cobalamin adenosyltransferase-like superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 251110 | OMIM | Methylmalonic aciduria type cblB (MMAB) | A disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. The disease is caused by variants affecting the gene represented in this entry. |
Drugs
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| Drug | Name | Source | Type |
| DB00115 | Cyanocobalamin | Drugbank | small molecule |
Interactions
6 interactions