Display title | Biology:Methylmalonyl-CoA mutase |
Default sort key | Methylmalonyl-CoA mutase |
Page length (in bytes) | 26,017 |
Namespace ID | 3026 |
Namespace | Biology |
Page ID | 320160 |
Page content language | en - English |
Page content model | wikitext |
Indexing by robots | Allowed |
Number of redirects to this page | 0 |
Counted as a content page | Yes |
Page image |  |
HandWiki item ID | None |
Edit | Allow all users (infinite) |
Move | Allow all users (infinite) |
Page creator | imported>Carolyn |
Date of page creation | 19:30, 10 February 2024 |
Latest editor | imported>Carolyn |
Date of latest edit | 19:30, 10 February 2024 |
Total number of edits | 1 |
Recent number of edits (within past 90 days) | 0 |
Recent number of distinct authors | 0 |
Description | Content |
Article description: (description ) This attribute controls the content of the description and og:description elements. | Methylmalonyl-CoA mutase (EC 5.4.99.2, MCM), mitochondrial, also known as methylmalonyl-CoA isomerase, is a protein that in humans is encoded by the MUT gene. This vitamin B12-dependent enzyme catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA in humans. Mutations in MUT gene may lead to... |