This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
1mh1
From Proteopedia
| Line 1: | Line 1: | ||
| - | [[Image:1mh1. | + | {{Seed}} |
| + | [[Image:1mh1.png|left|200px]] | ||
<!-- | <!-- | ||
| Line 9: | Line 10: | ||
{{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | {{STRUCTURE_1mh1| PDB=1mh1 | SCENE= }} | ||
| - | + | ===SMALL G-PROTEIN=== | |
| - | + | <!-- | |
| - | The | + | The line below this paragraph, {{ABSTRACT_PUBMED_9033596}}, adds the Publication Abstract to the page |
| + | (as it appears on PubMed at http://www.pubmed.gov), where 9033596 is the PubMed ID number. | ||
| + | --> | ||
| + | {{ABSTRACT_PUBMED_9033596}} | ||
==Disease== | ==Disease== | ||
| Line 34: | Line 38: | ||
[[Category: Rho family]] | [[Category: Rho family]] | ||
[[Category: Small g-protein]] | [[Category: Small g-protein]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 23:56:31 2008'' | ||
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
