2fav: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,331,613 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,331,613 edits
No edit summary
Line 1: Line 1:
[[Image:2fav.gif|left|200px]]
{{Seed}}
[[Image:2fav.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2fav|  PDB=2fav  |  SCENE=  }}  
{{STRUCTURE_2fav|  PDB=2fav  |  SCENE=  }}  


'''Crystal structure of SARS macro domain in complex with ADP-ribose at 1.8 A resolution'''
===Crystal structure of SARS macro domain in complex with ADP-ribose at 1.8 A resolution===




==Overview==
<!--
Macro domains constitute a protein module family found associated with specific histones and proteins involved in chromatin metabolism. In addition, a small number of animal RNA viruses, such as corona- and toroviruses, alphaviruses, and hepatitis E virus, encode macro domains for which, however, structural and functional information is extremely limited. Here, we characterized the macro domains from hepatitis E virus, Semliki Forest virus, and severe acute respiratory syndrome coronavirus (SARS-CoV). The crystal structure of the SARS-CoV macro domain was determined at 1.8-Angstroms resolution in complex with ADP-ribose. Information derived from structural, mutational, and sequence analyses suggests a close phylogenetic and, most probably, functional relationship between viral and cellular macro domain homologs. The data revealed that viral macro domains have relatively poor ADP-ribose 1"-phosphohydrolase activities (which were previously proposed to be their biologically relevant function) but bind efficiently free and poly(ADP-ribose) polymerase 1-bound poly(ADP-ribose) in vitro. Collectively, these results suggest to further evaluate the role of viral macro domains in host response to viral infection.
The line below this paragraph, {{ABSTRACT_PUBMED_16912299}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16912299 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_16912299}}


==About this Structure==
==About this Structure==
Line 30: Line 34:
[[Category: Structural genomic]]
[[Category: Structural genomic]]
[[Category: Structural proteomics in europe]]
[[Category: Structural proteomics in europe]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Apr 13 08:19:01 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 16:26:28 2008''

Revision as of 13:26, 29 July 2008

File:2fav.png

Template:STRUCTURE 2fav

Crystal structure of SARS macro domain in complex with ADP-ribose at 1.8 A resolution

Template:ABSTRACT PUBMED 16912299

About this Structure

2FAV is a Single protein structure of sequence from Human sars coronavirus. Full crystallographic information is available from OCA.

Reference

Structural and functional basis for ADP-ribose and poly(ADP-ribose) binding by viral macro domains., Egloff MP, Malet H, Putics A, Heinonen M, Dutartre H, Frangeul A, Gruez A, Campanacci V, Cambillau C, Ziebuhr J, Ahola T, Canard B, J Virol. 2006 Sep;80(17):8493-502. PMID:16912299

Page seeded by OCA on Tue Jul 29 16:26:28 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=2fav&oldid=748956"