2bt4

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{{STRUCTURE_2bt4| PDB=2bt4 | SCENE= }}
{{STRUCTURE_2bt4| PDB=2bt4 | SCENE= }}
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'''TYPE II DEHYDROQUINASE INHIBITOR COMPLEX'''
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===TYPE II DEHYDROQUINASE INHIBITOR COMPLEX===
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==Overview==
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Selective inhibitors of type II dehydroquinase were rationally designed to explore a second binding-pocket in the active-site. The molecular modelling, synthesis, inhibition studies and crystal structure determination are described.
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(as it appears on PubMed at http://www.pubmed.gov), where 16106291 is the PubMed ID number.
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{{ABSTRACT_PUBMED_16106291}}
==About this Structure==
==About this Structure==
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[[Category: Lyase]]
[[Category: Lyase]]
[[Category: Shikimate pathway]]
[[Category: Shikimate pathway]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 20:45:43 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 14:15:54 2008''

Revision as of 11:15, 28 July 2008

Template:STRUCTURE 2bt4

TYPE II DEHYDROQUINASE INHIBITOR COMPLEX

Template:ABSTRACT PUBMED 16106291

About this Structure

2BT4 is a Single protein structure of sequence from Streptomyces coelicolor. Full crystallographic information is available from OCA.

Reference

Rational design of new bifunctional inhibitors of type II dehydroquinase., Toscano MD, Stewart KA, Coggins JR, Lapthorn AJ, Abell C, Org Biomol Chem. 2005 Sep 7;3(17):3102-4. Epub 2005 Aug 1. PMID:16106291

Page seeded by OCA on Mon Jul 28 14:15:54 2008

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