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PDBsum entry 1bzc
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* Residue conservation analysis
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References listed in PDB file
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Key reference
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Title
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Structural basis for inhibition of the protein tyrosine phosphatase 1b by phosphotyrosine peptide mimetics.
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Authors
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M.R.Groves,
Z.J.Yao,
P.P.Roller,
T.R.Burke,
D.Barford.
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Ref.
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Biochemistry, 1998,
37,
17773-17783.
[DOI no: ]
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PubMed id
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Abstract
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Protein tyrosine phosphatases regulate diverse cellular processes and represent
important targets for therapeutic intervention in a number of diseases. The
crystal structures of protein tyrosine phosphatase 1B (PTP1B) in complex with
small molecule inhibitors based upon two classes of phosphotyrosine mimetics,
the (difluoronaphthylmethyl)phosphonic acids and the fluoromalonyl tyrosines,
have been determined to resolutions greater than 2.3 A. The fluoromalonyl
tyrosine residue was incorporated within a cyclic hexapeptide modeled on an
autophosphorylation site of the epidermal growth factor receptor. The structure
of this inhibitor bound to PTP1B represents the first crystal structure of a
non-phosphonate-containing inhibitor and reveals the mechanism of
phosphotyrosine mimicry by the fluoromalonyl tyrosine residue and the nature of
its interactions within the catalytic site of PTP1B. In contrast to complexes of
PTP1B with phosphotyrosine-containing peptides, binding of the fluoromalonyl
tyrosine residue to the catalytic site of PTP1B is not accompanied by closure of
the catalytic site WPD loop. Structures of PTP1B in complex with the
(difluoronaphthylmethyl)phosphonic acid derivatives reveal that substitutions of
the naphthalene ring modulate the mode of inhibitor binding to the catalytic
site and provide the potential for enhanced inhibitor affinity and the
generation of PTP-specific inhibitors. These results provide a framework for the
rational design of higher affinity and more specific phosphotyrosine mimetic
inhibitors of not only protein tyrosine phosphatases but also SH2 and PTB
domains.
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Secondary reference #1
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Title
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Crystal structure of human protein tyrosine phosphatase 1b.
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Authors
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D.Barford,
A.J.Flint,
N.K.Tonks.
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Ref.
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Science, 1994,
263,
1397-1404.
[DOI no: ]
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PubMed id
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