3nwv
From Proteopedia
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{{STRUCTURE_3nwv| PDB=3nwv | SCENE= }} | {{STRUCTURE_3nwv| PDB=3nwv | SCENE= }} | ||
===Human cytochrome c G41S=== | ===Human cytochrome c G41S=== | ||
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{{ABSTRACT_PUBMED_21192676}} | {{ABSTRACT_PUBMED_21192676}} | ||
==About this Structure== | ==About this Structure== | ||
| - | [[3nwv]] is a 4 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=3NWV OCA]. | + | [[3nwv]] is a 4 chain structure of [[Cytochrome c]] 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=3NWV OCA]. |
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| + | ==See Also== | ||
| + | *[[Cytochrome c|Cytochrome c]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:021192676</ref><ref group="xtra">PMID:018345000</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Fagerlund, R D.]] | [[Category: Fagerlund, R D.]] | ||
[[Category: Wilbanks, S M.]] | [[Category: Wilbanks, S M.]] | ||
| + | [[Category: Apaf-1]] | ||
| + | [[Category: Apoptosis]] | ||
| + | [[Category: Cytochrome]] | ||
| + | [[Category: Electron transport]] | ||
| + | [[Category: Heme]] | ||
| + | [[Category: Mitochondia]] | ||
Revision as of 21:13, 26 July 2012
Contents |
Human cytochrome c G41S
Template:ABSTRACT PUBMED 21192676
About this Structure
3nwv is a 4 chain structure of Cytochrome c with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Liptak MD, Fagerlund RD, Ledgerwood EC, Wilbanks SM, Bren KL. The proapoptotic G41S mutation to human cytochrome c alters the heme electronic structure and increases the electron self-exchange rate. J Am Chem Soc. 2011 Feb 9;133(5):1153-5. Epub 2010 Dec 30. PMID:21192676 doi:10.1021/ja106328k
- Morison IM, Cramer Borde EM, Cheesman EJ, Cheong PL, Holyoake AJ, Fichelson S, Weeks RJ, Lo A, Davies SM, Wilbanks SM, Fagerlund RD, Ludgate MW, da Silva Tatley FM, Coker MS, Bockett NA, Hughes G, Pippig DA, Smith MP, Capron C, Ledgerwood EC. A mutation of human cytochrome c enhances the intrinsic apoptotic pathway but causes only thrombocytopenia. Nat Genet. 2008 Apr;40(4):387-9. Epub 2008 Mar 16. PMID:18345000 doi:ng.103
