3qbt: Difference between revisions
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[[Image:3qbt. | [[Image:3qbt.png|left|200px]] | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:021378754</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Phosphoinositide 5-phosphatase]] | [[Category: Phosphoinositide 5-phosphatase]] | ||
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[[Category: Itzen, A.]] | [[Category: Itzen, A.]] | ||
[[Category: Schoebel, S.]] | [[Category: Schoebel, S.]] | ||
[[Category: Appl1]] | |||
[[Category: Ash]] | |||
[[Category: Clathrin]] | |||
[[Category: Endocytosis]] | |||
[[Category: Gtpase]] | |||
[[Category: Immunoglobulin fold]] | |||
[[Category: Lowe syndrome]] | |||
[[Category: Ocrl1]] | |||
[[Category: Phosphoinositide]] | |||
[[Category: Protein transport]] | |||
[[Category: Protein transport-hydrolase complex]] | |||
[[Category: Rab8a]] | |||
[[Category: Rhogap]] | |||
[[Category: Vesicular trafficking]] | |||
Revision as of 07:31, 29 February 2012
Crystal structure of OCRL1 540-678 in complex with Rab8a:GppNHp
Template:ABSTRACT PUBMED 21378754
About this Structure
3qbt is a 8 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Hou X, Hagemann N, Schoebel S, Blankenfeldt W, Goody RS, Erdmann KS, Itzen A. A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1. EMBO J. 2011 Mar 4. PMID:21378754 doi:10.1038/emboj.2011.60
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Phosphoinositide 5-phosphatase
- Blankenfeldt, W.
- Erdmann, K S.
- Goody, R S.
- Hagemann, N.
- Hou, X.
- Itzen, A.
- Schoebel, S.
- Appl1
- Ash
- Clathrin
- Endocytosis
- Gtpase
- Immunoglobulin fold
- Lowe syndrome
- Ocrl1
- Phosphoinositide
- Protein transport
- Protein transport-hydrolase complex
- Rab8a
- Rhogap
- Vesicular trafficking