3nwv

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
+
[[Image:3nwv.jpg|left|200px]]
-
The entry 3nwv is ON HOLD until Paper Publication
+
<!--
 +
The line below this paragraph, containing "STRUCTURE_3nwv", 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_3nwv| PDB=3nwv | SCENE= }}
-
Authors: Fagerlund, R.D., Wilbanks, S.M.
+
===Human cytochrome c G41S===
-
Description: Human cytochrome c G41S
 
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 1 09:34:38 2010''
+
<!--
 +
The line below this paragraph, {{ABSTRACT_PUBMED_21192676}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 21192676 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_21192676}}
 +
 
 +
==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].
 +
 
 +
==Reference==
 +
<ref group="xtra">PMID:21192676</ref><ref group="xtra">PMID:18345000</ref><references group="xtra"/>
 +
[[Category: Homo sapiens]]
 +
[[Category: Fagerlund, R D.]]
 +
[[Category: Wilbanks, S M.]]

Revision as of 06:23, 9 March 2011

Template:STRUCTURE 3nwv

Human cytochrome c G41S

Template:ABSTRACT PUBMED 21192676

About this Structure

3nwv is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

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

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools