1mh1
From Proteopedia
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[[Image:1mh1.png|left|200px]] | [[Image:1mh1.png|left|200px]] | ||
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{{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | {{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | ||
===SMALL G-PROTEIN=== | ===SMALL G-PROTEIN=== | ||
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{{ABSTRACT_PUBMED_9033596}} | {{ABSTRACT_PUBMED_9033596}} | ||
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| - | ==Disease== | ||
| - | Known disease associated with this structure: Night blindness, congenital stationery, rhodopsin-related OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180380 180380]], Retinitis pigmentosa, autosomal recessive OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180380 180380]], Retinitis pigmentosa-4, autosomal dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180380 180380]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1mh1]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MH1 OCA]. | |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:009033596</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Dodson, G.]] | [[Category: Dodson, G.]] | ||
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[[Category: Rho family]] | [[Category: Rho family]] | ||
[[Category: Small g-protein]] | [[Category: Small g-protein]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 14:16:50 2009'' | ||
Revision as of 20:52, 5 December 2012
SMALL G-PROTEIN
Template:ABSTRACT PUBMED 9033596
About this Structure
1mh1 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Hirshberg M, Stockley RW, Dodson G, Webb MR. The crystal structure of human rac1, a member of the rho-family complexed with a GTP analogue. Nat Struct Biol. 1997 Feb;4(2):147-52. PMID:9033596
