NMR observation of HIV-1 gp120 conformational flexibility resulting from V3 truncation

FEBS Journal

Volumn 281, Issue 13, 2014, Pages 3019-3031

  Moseri, Adi ^a   Schnur, Einat ^a   Noah, Eran ^a   Zherdev, Yuri ^a   Kessler, Naama ^a   Singhal Sinha, Eshu ^a   Abayev, Meital ^a   Naider, Fred ^b   Scherf, Tali ^a   Anglister, Jacob ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

^b CITY UNIVERSITY OF NEW YORK   (United States)

Author keywords

CD4M33; dynamics; gp120; NMR; V3

Indexed keywords

GLYCOPROTEIN GP 120;

ARTICLE; CHEMICAL LABELING; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; EQUILIBRIUM CONSTANT; HETERONUCLEAR SINGLE QUANTUM COHERENCE; HUMAN IMMUNODEFICIENCY VIRUS 1; MOLECULAR DYNAMICS; MUTATION; OLIGOMERIZATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN EXPRESSION; PROTEIN GLYCOSYLATION; PROTEIN LOCALIZATION; PROTEIN STABILITY; PROTON NUCLEAR MAGNETIC RESONANCE;

HUMAN IMMUNODEFICIENCY VIRUS 1; SIMIAN IMMUNODEFICIENCY VIRUS;

CD4M33; DYNAMICS; GP120; NMR; V3;

AMINO ACID SUBSTITUTION; ANTIGENS, CD4; HEK293 CELLS; HIV ENVELOPE PROTEIN GP120; HIV-1; HUMANS; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PEPTIDE FRAGMENTS; PROTEIN BINDING; PROTEIN STABILITY; PROTEIN STRUCTURE, QUATERNARY; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY;

EID: 84903817189     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/febs.12839     Document Type: Article

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