1sbg: Difference between revisions

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[[Image:1sbg.png|left|200px]]
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Revision as of 04:12, 5 January 2010

CAUTION: This structure might be fraudulent. See the official statement of the University of Alabama recommending retraction, and the wwPDB statement on Retraction of UAB PDB entries. Although not listed in the above statements, the reliability of 1bgx, 1ay1, 1hef, 1heg, 1sbg, 1hps, and 1hos have been called into question since they were co-authored by H. M. Krishna Murthy: see discussion of fraud. See also the list of recommended retractions.

File:1sbg.png

Template:STRUCTURE 1sbg

AN ORALLY-BIOAVAILABLE HIV-1 PROTEASE INHIBITOR CONTAINING AN IMIDAZOLE-DERIVED PEPTIDE BOND REPLACEMENT. CRYSTALLOGRAPHIC AND PHARMACOKINETIC ANALYSISAN ORALLY-BIOAVAILABLE HIV-1 PROTEASE INHIBITOR CONTAINING AN IMIDAZOLE-DERIVED PEPTIDE BOND REPLACEMENT. CRYSTALLOGRAPHIC AND PHARMACOKINETIC ANALYSIS

Template:ABSTRACT PUBMED 7918383

About this StructureAbout this Structure

1SBG is a 2 chains structure of sequences from Human immunodeficiency virus type 1 (isolate bh10). Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Abdel-Meguid SS, Metcalf BW, Carr TJ, Demarsh P, DesJarlais RL, Fisher S, Green DW, Ivanoff L, Lambert DM, Murthy KH, et al.. An orally bioavailable HIV-1 protease inhibitor containing an imidazole-derived peptide bond replacement: crystallographic and pharmacokinetic analysis. Biochemistry. 1994 Oct 4;33(39):11671-7. PMID:7918383

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OCA, Eric Martz