1upj: Difference between revisions
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[[Image:1upj.png|left|200px]] | [[Image:1upj.png|left|200px]] | ||
{{STRUCTURE_1upj| PDB=1upj | SCENE= }} | {{STRUCTURE_1upj| PDB=1upj | SCENE= }} | ||
===HIV-1 PROTEASE COMPLEX WITH U095438 [3-[1-(4-BROMOPHENYL) ISOBUTYL]-4-HYDROXYCOUMARIN=== | ===HIV-1 PROTEASE COMPLEX WITH U095438 [3-[1-(4-BROMOPHENYL) ISOBUTYL]-4-HYDROXYCOUMARIN=== | ||
{{ABSTRACT_PUBMED_7658450}} | {{ABSTRACT_PUBMED_7658450}} | ||
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==See Also== | ==See Also== | ||
*[[Virus protease]] | *[[Virus protease|Virus protease]] | ||
==Reference== | ==Reference== | ||
Revision as of 13:48, 26 July 2012
HIV-1 PROTEASE COMPLEX WITH U095438 [3-[1-(4-BROMOPHENYL) ISOBUTYL]-4-HYDROXYCOUMARINHIV-1 PROTEASE COMPLEX WITH U095438 [3-[1-(4-BROMOPHENYL) ISOBUTYL]-4-HYDROXYCOUMARIN
Template:ABSTRACT PUBMED 7658450
About this StructureAbout this Structure
1upj is a 1 chain structure of Virus protease with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ 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