1k4u
From Proteopedia
(Difference between revisions)
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{{STRUCTURE_1k4u| PDB=1k4u | SCENE= }} | {{STRUCTURE_1k4u| PDB=1k4u | SCENE= }} | ||
- | + | ===Solution structure of the C-terminal SH3 domain of p67phox complexed with the C-terminal tail region of p47phox=== | |
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- | The | + | The line below this paragraph, {{ABSTRACT_PUBMED_12169629}}, adds the Publication Abstract to the page |
+ | (as it appears on PubMed at http://www.pubmed.gov), where 12169629 is the PubMed ID number. | ||
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==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
- | 1K4U is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full | + | 1K4U is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1K4U OCA]. |
==Reference== | ==Reference== | ||
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[[Category: P67phox]] | [[Category: P67phox]] | ||
[[Category: Sh3-peptide complex]] | [[Category: Sh3-peptide complex]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 09:46:42 2008'' |
Revision as of 06:46, 2 July 2008
Contents |
Solution structure of the C-terminal SH3 domain of p67phox complexed with the C-terminal tail region of p47phox
Template:ABSTRACT PUBMED 12169629
Disease
Known disease associated with this structure: Chronic granulomatous disease due to deficiency of NCF-2 OMIM:[608515], Chronic granulomatous disease due to deficiency of NCF-1 OMIM:[608512]
About this Structure
1K4U is a Protein complex structure of sequences from Homo sapiens. Full experimental information is available from OCA.
Reference
Diverse recognition of non-PxxP peptide ligands by the SH3 domains from p67(phox), Grb2 and Pex13p., Kami K, Takeya R, Sumimoto H, Kohda D, EMBO J. 2002 Aug 15;21(16):4268-76. PMID:12169629
Page seeded by OCA on Wed Jul 2 09:46:42 2008