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3qbt

From Proteopedia

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[[Image:3qbt.jpg|left|200px]]
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==Reference==
==Reference==
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<ref group="xtra">PMID:21378754</ref><references group="xtra"/>
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<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.]]
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[[Category: Appl1]]
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[[Category: Ash]]
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[[Category: Clathrin]]
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[[Category: Endocytosis]]
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[[Category: Gtpase]]
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[[Category: Immunoglobulin fold]]
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[[Category: Lowe syndrome]]
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[[Category: Ocrl1]]
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[[Category: Phosphoinositide]]
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[[Category: Protein transport]]
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[[Category: Protein transport-hydrolase complex]]
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[[Category: Rab8a]]
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[[Category: Rhogap]]
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[[Category: Vesicular trafficking]]

Revision as of 07:31, 29 February 2012

Template:STRUCTURE 3qbt

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

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