4hl4 | pdb_00004hl4
From Proteopedia
Crystal structure of the human TBC1D20 RabGAP domain
| ||||||||||||
Structural highlights
DiseaseTBC20_HUMAN Micro syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionTBC20_HUMAN GTPase-activating protein specific for Rab1 and Rab2 small GTPase families for which it can accelerate the intrinsic GTP hydrolysis rate by more than five orders of magnitude. Contents | ||||||||||||||||||||
This page was last modified 08:51, 20 March 2024.