3qbt: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''
[[Image:3qbt.jpg|left|200px]]


The entry 3qbt is ON HOLD until Paper Publication
<!--
The line below this paragraph, containing "STRUCTURE_3qbt", creates the "Structure Box" on the page.
You may change the PDB parameter (which sets the PDB file loaded into the applet)
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
or leave the SCENE parameter empty for the default display.
-->
{{STRUCTURE_3qbt|  PDB=3qbt  |  SCENE=  }}


Authors: Hou, X., Hagemann, N., Schoebel, S., Blankenfeldt, W., Goody, R.S., Erdmann, K.S., Itzen, A.
===Crystal structure of OCRL1 540-678 in complex with Rab8a:GppNHp===


Description: Crystal structure of OCRL1 540-678 in complex with Rab8a:GppNHp
 
<!--
The line below this paragraph, {{ABSTRACT_PUBMED_21378754}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 21378754 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_21378754}}
 
==About this Structure==
[[3qbt]] is a 8 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=3QBT OCA].
 
==Reference==
<ref group="xtra">PMID:21378754</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Phosphoinositide 5-phosphatase]]
[[Category: Blankenfeldt, W.]]
[[Category: Erdmann, K S.]]
[[Category: Goody, R S.]]
[[Category: Hagemann, N.]]
[[Category: Hou, X.]]
[[Category: Itzen, A.]]
[[Category: Schoebel, S.]]

Revision as of 07:06, 23 March 2011

File:3qbt.jpg

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

  1. 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?)

OCA