3hr0

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[[Image:3hr0.png|left|200px]]
[[Image:3hr0.png|left|200px]]
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{{STRUCTURE_3hr0| PDB=3hr0 | SCENE= }}
{{STRUCTURE_3hr0| PDB=3hr0 | SCENE= }}
===Crystal structure of Homo sapiens Conserved Oligomeric Golgi subunit 4===
===Crystal structure of Homo sapiens Conserved Oligomeric Golgi subunit 4===
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{{ABSTRACT_PUBMED_19651599}}
{{ABSTRACT_PUBMED_19651599}}
==About this Structure==
==About this Structure==
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3HR0 is a 2 chains structure of sequences 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=3HR0 OCA].
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[[3hr0]] is a 2 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=3HR0 OCA].
==Reference==
==Reference==
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<ref group="xtra">PMID:19651599</ref><references group="xtra"/>
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<ref group="xtra">PMID:019651599</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Hughson, F M.]]
[[Category: Hughson, F M.]]
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[[Category: Richardson, B C.]]
[[Category: Richardson, B C.]]
[[Category: Ungar, D.]]
[[Category: Ungar, D.]]
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[[Category: Alternative splicing]]
 
[[Category: Conserved oligomeric golgi complex]]
[[Category: Conserved oligomeric golgi complex]]
[[Category: Exocyst]]
[[Category: Exocyst]]
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[[Category: Transport protein]]
[[Category: Transport protein]]
[[Category: Vesicle tethering]]
[[Category: Vesicle tethering]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 19 13:15:24 2009''
 

Revision as of 14:51, 6 March 2013

Image:3hr0.png

Template:STRUCTURE 3hr0

Crystal structure of Homo sapiens Conserved Oligomeric Golgi subunit 4

Template:ABSTRACT PUBMED 19651599

About this Structure

3hr0 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Richardson BC, Smith RD, Ungar D, Nakamura A, Jeffrey PD, Lupashin VV, Hughson FM. Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene. Proc Natl Acad Sci U S A. 2009 Jul 27. PMID:19651599

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