4upj

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[[Image:4upj.png|left|200px]]
[[Image:4upj.png|left|200px]]
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{{STRUCTURE_4upj| PDB=4upj | SCENE= }}
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===HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 PROTEASE MUTANT WITH LYS 57 REPLACED BY LEU (K57L) COMPLEX WITH U097410 [4-HYDROXY-3-[1-[3-[[[[(TERT-BUTYLOXYCARBONYL) AMINOMETHYL]CARBONYL]AMINO]PHENYL]PROPYL]COUMARIN===
===HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 PROTEASE MUTANT WITH LYS 57 REPLACED BY LEU (K57L) COMPLEX WITH U097410 [4-HYDROXY-3-[1-[3-[[[[(TERT-BUTYLOXYCARBONYL) AMINOMETHYL]CARBONYL]AMINO]PHENYL]PROPYL]COUMARIN===
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{{ABSTRACT_PUBMED_7658450}}
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==See Also==
==See Also==
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*[[Virus protease]]
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*[[Virus protease|Virus protease]]
==Reference==
==Reference==

Revision as of 12:31, 26 July 2012

Template:STRUCTURE 4upj

Contents

HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 PROTEASE MUTANT WITH LYS 57 REPLACED BY LEU (K57L) COMPLEX WITH U097410 [4-HYDROXY-3-[1-[3-[[[[(TERT-BUTYLOXYCARBONYL) AMINOMETHYL]CARBONYL]AMINO]PHENYL]PROPYL]COUMARIN

Template:ABSTRACT PUBMED 7658450

About this Structure

4upj is a 2 chain structure of Virus protease with sequence from Human immunodeficiency virus 2. Full crystallographic information is available from OCA.

See Also

Reference

  • Thaisrivongs S, Watenpaugh KD, Howe WJ, Tomich PK, Dolak LA, Chong KT, Tomich CC, Tomasselli AG, Turner SR, Strohbach JW, et al.. Structure-based design of novel HIV protease inhibitors: carboxamide-containing 4-hydroxycoumarins and 4-hydroxy-2-pyrones as potent nonpeptidic inhibitors. J Med Chem. 1995 Sep 1;38(18):3624-37. PMID:7658450

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