1qbs

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
{{Seed}}
 
[[Image:1qbs.png|left|200px]]
[[Image:1qbs.png|left|200px]]
Line 20: Line 19:
==About this Structure==
==About this Structure==
-
1QBS is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QBS OCA].
+
[[1qbs]] is a 2 chain structure of [[Virus protease]] with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QBS OCA].
 +
 
 +
==See Also==
 +
*[[Virus protease]]
==Reference==
==Reference==
-
<ref group="xtra">PMID:8784449</ref><references group="xtra"/>
+
<ref group="xtra">PMID:008784449</ref><ref group="xtra">PMID:011152609</ref><references group="xtra"/>
[[Category: HIV-1 retropepsin]]
[[Category: HIV-1 retropepsin]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
Line 29: Line 31:
[[Category: Chang, C H.]]
[[Category: Chang, C H.]]
[[Category: Aspartyl protease]]
[[Category: Aspartyl protease]]
- 
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 06:00:53 2009''
 

Revision as of 06:47, 22 February 2012

Template:STRUCTURE 1qbs

Contents

HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY

Template:ABSTRACT PUBMED 8784449

About this Structure

1qbs is a 2 chain structure of Virus protease with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Lam PY, Ru Y, Jadhav PK, Aldrich PE, DeLucca GV, Eyermann CJ, Chang CH, Emmett G, Holler ER, Daneker WF, Li L, Confalone PN, McHugh RJ, Han Q, Li R, Markwalder JA, Seitz SP, Sharpe TR, Bacheler LT, Rayner MM, Klabe RM, Shum L, Winslow DL, Kornhauser DM, Hodge CN, et al.. Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas. J Med Chem. 1996 Aug 30;39(18):3514-25. PMID:8784449 doi:10.1021/jm9602571
  • Ishima R, Louis JM, Torchia DA. Characterization of two hydrophobic methyl clusters in HIV-1 protease by NMR spin relaxation in solution. J Mol Biol. 2001 Jan 19;305(3):515-21. PMID:11152609 doi:10.1006/jmbi.2000.4321

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools