1mh1
From Proteopedia
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{{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | {{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | ||
- | + | ===SMALL G-PROTEIN=== | |
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==Disease== | ==Disease== | ||
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[[Category: Rho family]] | [[Category: Rho family]] | ||
[[Category: Small g-protein]] | [[Category: Small g-protein]] | ||
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Revision as of 20:56, 2 July 2008
Contents |
SMALL G-PROTEIN
Template:ABSTRACT PUBMED 9033596
Disease
Known disease associated with this structure: Night blindness, congenital stationery, rhodopsin-related OMIM:[180380], Retinitis pigmentosa, autosomal recessive OMIM:[180380], Retinitis pigmentosa-4, autosomal dominant OMIM:[180380]
About this Structure
1MH1 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
The crystal structure of human rac1, a member of the rho-family complexed with a GTP analogue., Hirshberg M, Stockley RW, Dodson G, Webb MR, Nat Struct Biol. 1997 Feb;4(2):147-52. PMID:9033596
Page seeded by OCA on Wed Jul 2 23:56:31 2008