3sx4

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'''Unreleased structure'''
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[[Image:3sx4.png|left|200px]]
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The entry 3sx4 is ON HOLD until Paper Publication
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{{STRUCTURE_3sx4| PDB=3sx4 | SCENE= }}
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Authors: Klei, H.E.
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===Crystal structure of human dpp-iv in complex with sa-(+)-3-(aminomethyl)-4-(2,4-dichlorophenyl)-6-(2-methoxyphenyl)- 2-methyl-5h-pyrrolo[3,4-b]pyridin-7(6h)-one===
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Description: Crystal structure of human dpp-iv in complex with sa-(+)-3-(aminomethyl)-4-(2,4-dichlorophenyl)-6-(2-methoxyphenyl)-2-methyl-5h-pyrrolo[3,4-b]pyridin-7(6h)-one
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{{ABSTRACT_PUBMED_21996520}}
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==About this Structure==
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[[3sx4]] is a 2 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=3SX4 OCA].
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==Reference==
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<ref group="xtra">PMID:021996520</ref><references group="xtra"/>
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[[Category: Dipeptidyl-peptidase IV]]
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[[Category: Homo sapiens]]
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[[Category: Klei, H E.]]
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[[Category: Alpha/beta hydrolase fold]]
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[[Category: Aminopeptidase]]
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[[Category: Beta barrel]]
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[[Category: Beta propeller]]
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[[Category: Dimer]]
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[[Category: Dpp4]]
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[[Category: Exopeptidase]]
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[[Category: Glycoprotein]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
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[[Category: Membrane]]
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[[Category: Protease]]
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[[Category: Protein:inhibitor complex]]
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[[Category: Secreted]]
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[[Category: Serine protease]]
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[[Category: Signal- anchor]]
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[[Category: Transmembrane]]

Revision as of 09:17, 30 October 2011

Template:STRUCTURE 3sx4

Crystal structure of human dpp-iv in complex with sa-(+)-3-(aminomethyl)-4-(2,4-dichlorophenyl)-6-(2-methoxyphenyl)- 2-methyl-5h-pyrrolo[3,4-b]pyridin-7(6h)-one

Template:ABSTRACT PUBMED 21996520

About this Structure

3sx4 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Wang W, Devasthale P, Wang A, Harrity T, Egan D, Morgan N, Cap M, Fura A, Klei HE, Kish K, Weigelt C, Sun L, Levesque P, Li YX, Zahler R, Kirby MS, Hamann LG. 7-Oxopyrrolopyridine-derived DPP4 inhibitors-mitigation of CYP and hERG liabilities via introduction of polar functionalities in the active site. Bioorg Med Chem Lett. 2011 Nov 15;21(22):6646-51. Epub 2011 Sep 24. PMID:21996520 doi:10.1016/j.bmcl.2011.09.074

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