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Bioorganic and Medicinal Chemistry Letters

Volumn 22, Issue 12, 2012, Pages 3900-3904

The co-crystal structure of ubiquitin carboxy-terminal hydrolase L1 (UCHL1) with a tripeptide fluoromethyl ketone (Z-VAE(OMe)-FMK)

(7) Davies, Christopher W a Chaney, Joseph a Korbel, Gregory b Ringe, Dagmar c Petsko, Gregory A c Ploegh, Hidde b Das, Chittaranjan a

a PURDUE UNIVERSITY (United States)

b WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (United States)

c BRANDEIS UNIVERSITY (United States)

Author keywords

Deubiquitinating enzymes; Enzyme inhibitors; Fluoromethyl ketone; Ubiquitin hydrolase

Indexed keywords

CYSTEINE; ENZYME INHIBITOR; FLUOROMETHYL KETONE INHIBITOR; HISTIDINE; HYDROLASE; KETONE DERIVATIVE; TRIPEPTIDE DERIVATIVE; UBIQUITIN; UBIQUITIN CARBOXY TERMINAL HYDROLASE L1; UNCLASSIFIED DRUG;

ARTICLE; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CATALYSIS; CONTROLLED STUDY; CRYSTAL STRUCTURE; CRYSTALLIZATION; DRUG POTENCY; DRUG SELECTIVITY; ENZYME ACTIVE SITE; ENZYME BINDING; ENZYME MODIFICATION; OPTICAL RESOLUTION; PROTEIN STRUCTURE; UBIQUITINATION;

AMINO ACID CHLOROMETHYL KETONES; ANIMALS; CATALYTIC DOMAIN; CRYSTALLIZATION; CRYSTALLOGRAPHY, X-RAY; HUMANS; MODELS, MOLECULAR; OLIGOPEPTIDES; PROTEIN BINDING; PROTEIN CONFORMATION; SUBSTRATE SPECIFICITY; UBIQUITIN; UBIQUITIN THIOLESTERASE;

EID: 84861574737 PISSN: 0960894X EISSN: 14643405 Source Type: Journal
DOI: 10.1016/j.bmcl.2012.04.124 Document Type: Article

Times cited : (32)

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