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ChemBioChem

Volumn 10, Issue 17, 2009, Pages 2772-2779

A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry

(5) Scott, Duncan E a Dawes, Gwen J a Ando, Michiyo a,b Abell, Chris a Ciulli, Alessio a

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

b Japan Patent Office (Japan)

Author keywords

Drug design; Dynamic chemistry; Enzymes; Inhibitors; Protein X ray crystallography

Indexed keywords

ADENOSINE; ADENOSINE TRIPHOSPHATASE; ADENYLATE KINASE; BACTERIAL ENZYME; BINDING PROTEIN; COENZYME A; DISULFIDE; PANTOTHENIC ACID SYNTHETASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; UNCLASSIFIED DRUG;

ARTICLE; BINDING SITE; COMBINATORIAL CHEMISTRY; COMBINATORIAL LIBRARY; COMPLEX FORMATION; CONTROLLED STUDY; CRYSTAL STRUCTURE; DRUG DESIGN; DRUG TARGETING; ENZYME ACTIVE SITE; ENZYME BINDING; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ISOTHERMAL TITRATION CALORIMETRY; LIGAND BINDING; MOLECULAR RECOGNITION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN MOTIF; PROTEIN STRUCTURE; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

ADENOSINE; COMBINATORIAL CHEMISTRY TECHNIQUES; CRYSTALLOGRAPHY, X-RAY; DISULFIDES; DRUG DESIGN; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; MYCOBACTERIUM TUBERCULOSIS; PEPTIDE SYNTHASES; PROTEIN CONFORMATION; THIONUCLEOSIDES;

MYCOBACTERIUM TUBERCULOSIS;

EID: 73149092359 PISSN: 14394227 EISSN: 14397633 Source Type: Journal
DOI: 10.1002/cbic.200900537 Document Type: Article

Times cited : (46)

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