2j0f: Difference between revisions

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[[Image:2j0f.png|left|200px]]
[[Image:2j0f.png|left|200px]]


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===STRUCTURAL BASIS FOR NON-COMPETITIVE PRODUCT INHIBITION IN HUMAN THYMIDINE PHOSPHORYLASE: IMPLICATION FOR DRUG DESIGN===
===STRUCTURAL BASIS FOR NON-COMPETITIVE PRODUCT INHIBITION IN HUMAN THYMIDINE PHOSPHORYLASE: IMPLICATION FOR DRUG DESIGN===


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{{ABSTRACT_PUBMED_16803458}}
{{ABSTRACT_PUBMED_16803458}}


==About this Structure==
==About this Structure==
2J0F is a 4 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=2J0F OCA].  
[[2j0f]] 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=2J0F OCA].  


==Reference==
==Reference==
<ref group="xtra">PMID:16803458</ref><references group="xtra"/>
<ref group="xtra">PMID:016803458</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Thymidine phosphorylase]]
[[Category: Thymidine phosphorylase]]
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[[Category: Htp]]
[[Category: Htp]]
[[Category: Human thymidine phosphorylase]]
[[Category: Human thymidine phosphorylase]]
[[Category: Polymorphism]]
[[Category: Transferase]]
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 22 11:18:53 2009''

Revision as of 10:36, 7 January 2013

File:2j0f.png

Template:STRUCTURE 2j0f

STRUCTURAL BASIS FOR NON-COMPETITIVE PRODUCT INHIBITION IN HUMAN THYMIDINE PHOSPHORYLASE: IMPLICATION FOR DRUG DESIGN

Template:ABSTRACT PUBMED 16803458

About this Structure

2j0f is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. El Omari K, Bronckaers A, Liekens S, Perez-Perez MJ, Balzarini J, Stammers DK. Structural basis for non-competitive product inhibition in human thymidine phosphorylase: implications for drug design. Biochem J. 2006 Oct 15;399(2):199-204. PMID:16803458 doi:10.1042/BJ20060513

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