Why Is Phosphonodifluoromethyl Phenylalanine a More Potent Inhibitory Moiety Than Phosphonomethyl Phenylalanine Toward Protein-Tyrosine Phosphatases

Biochemical and Biophysical Research Communications

Volumn 216, Issue 3, 1995, Pages 976-984

  Chen, Li ^a   Wu, Li ^a,b   Otaka, Akira ^b   Smyth, Mark S ^b   Roller, Peter P ^b   Burke, Terrence R ^b   Den Hertog, Jeroen ^c   Zhang, Zhong Yin ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c HUBRECHT INSTITUTE   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME INHIBITOR; PHENYLALANINE DERIVATIVE; PROTEIN TYROSINE PHOSPHATASE;

ARTICLE; BINDING AFFINITY; DEPHOSPHORYLATION; ENZYME INHIBITOR INTERACTION; HYDROGEN BOND; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

AMINO ACID SEQUENCE; BINDING SITES; COMPARATIVE STUDY; ENZYME INHIBITORS; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; PEPTIDES; PHENYLALANINE; PROTEIN-TYROSINE-PHOSPHATASE; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028785789     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1006/bbrc.1995.2716     Document Type: Article

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