1a30 | pdb_00001a30

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Template:STRUCTURE 1a30

File:1a30.png

HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR

Template:ABSTRACT PUBMED 9485357

About this Structure

1a30 is a 3 chain structure of Hemoglobin and Virus protease with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  1. 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
  2. Veit M. [New strategies for drug development]. Berl Munch Tierarztl Wochenschr. 2004 Jul-Aug;117(7-8):276-87. PMID:15298055
  3. 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

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