1a30: Difference between revisions
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==About this Structure== | ==About this Structure== | ||
[[1a30]] is a 3 chain structure | [[1a30]] is a 3 chain structure 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=1A30 OCA]. | ||
==See Also== | ==See Also== | ||
Revision as of 19:02, 20 October 2012
HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR
Template:ABSTRACT PUBMED 9485357
About this Structure
1a30 is a 3 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
See Also
Reference
- Louis JM, Dyda F, Nashed NT, Kimmel AR, Davies DR. Hydrophilic peptides derived from the transframe region of Gag-Pol inhibit the HIV-1 protease. Biochemistry. 1998 Feb 24;37(8):2105-10. PMID:9485357 doi:10.1021/bi972059x
- Veit M. [New strategies for drug development]. Berl Munch Tierarztl Wochenschr. 2004 Jul-Aug;117(7-8):276-87. PMID:15298055
- Spyrakis F, Fornabaio M, Cozzini P, Mozzarelli A, Abraham DJ, Kellogg GE. Computational titration analysis of a multiprotic HIV-1 protease-ligand complex. J Am Chem Soc. 2004 Sep 29;126(38):11764-5. PMID:15382890 doi:10.1021/ja0465754
