4pwy
From Proteopedia
Jump to navigationJump to search
Crystal structure of a Calmodulin-lysine N-methyltransferase fragment
| ||||||||||||
Structural highlights
DiseaseCMKMT_HUMAN Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome. FunctionCMKMT_HUMAN Catalyzes the trimethylation of 'Lys-116' in calmodulin.[1] References
| ||||||||||||||||||||
This page was last modified 17:24, 20 September 2023.