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Volumn 12, Issue 15, 2011, Pages 2311-2315

Crystal structures of novel allosteric peptide inhibitors of HIV integrase identify new interactions at the LEDGF binding site

(10) Rhodes, David I a,d Peat, Thomas S b Vandegraaff, Nick a Jeevarajah, Dharshini a Newman, Janet b Martyn, John a Coates, Jonathan A V a Ede, Nicholas J c Rea, Philip c Deadman, John J a,d

a Avexa Ltd (Australia)

b CSIRO (Australia)

c Mimotopes Pty Ltd (Australia)

d JDJ Bioservices Ltd (Australia)

Author keywords

Co crystal structures; Cyclic peptides; HIV 1 integrase; Inhibitors; LEDGF

Indexed keywords

HYDROGEN; INTEGRASE; INTEGRASE INHIBITOR; LENS EPITHELIUM DERIVED GROWTH FACTOR;

ARTICLE; BINDING SITE; CRYSTAL STRUCTURE; CRYSTALLOGRAPHY; CYCLIZATION; ENZYME ACTIVE SITE; HUMAN IMMUNODEFICIENCY VIRUS; HYDROGEN BOND; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN INTERACTION; PROTEIN STRUCTURE;

AMINO ACID SEQUENCE; BINDING SITES; CRYSTALLOGRAPHY, X-RAY; HIV INFECTIONS; HIV INTEGRASE; HIV INTEGRASE INHIBITORS; HIV-1; HUMANS; HYDROGEN BONDING; MOLECULAR DOCKING SIMULATION; PEPTIDES, CYCLIC;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 80053644039 PISSN: 14394227 EISSN: 14397633 Source Type: Journal
DOI: 10.1002/cbic.201100350 Document Type: Article

Times cited : (32)

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