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PDBsum entry 1g1g
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Hydrolase, signaling protein
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PDB id
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1g1g
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Contents |
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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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Molecular basis for the dephosphorylation of the activation segment of the insulin receptor by protein tyrosine phosphatase 1b.
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Authors
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A.Salmeen,
J.N.Andersen,
M.P.Myers,
N.K.Tonks,
D.Barford.
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Ref.
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Mol Cell, 2000,
6,
1401-1412.
[DOI no: ]
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PubMed id
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Abstract
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The protein tyrosine phosphatase PTP1B is responsible for negatively regulating
insulin signaling by dephosphorylating the phosphotyrosine residues of the
insulin receptor kinase (IRK) activation segment. Here, by integrating
crystallographic, kinetic, and PTP1B peptide binding studies, we define the
molecular specificity of this reaction. Extensive interactions are formed
between PTP1B and the IRK sequence encompassing the tandem pTyr residues at 1162
and 1163 such that pTyr-1162 is selected at the catalytic site and pTyr-1163 is
located within an adjacent pTyr recognition site. This selectivity is attributed
to the 70-fold greater affinity for tandem pTyr-containing peptides relative to
mono-pTyr peptides and predicts a hierarchical dephosphorylation process. Many
elements of the PTP1B-IRK interaction are unique to PTP1B, indicating that it
may be feasible to generate specific, small molecule inhibitors of this
interaction to treat diabetes and obesity.
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Figure 2.
Figure 2. Structure of the PTP1B Bisphosphorylated IR
Peptide Complex(A) Overview. The PTP loop (residues 215–222)
of PTP1B is shown in yellow, the WPD loop (residues 179-185) in
maroon, the pTyr loop (residues 45–49) in purple, and the Q
loop (residues 258–262) in pink.(B) Stereo view showing
details of the interactions between the bisphosphorylated IRK
peptide and PTP1B.(C) 2F[o]-F[c] electron density omit map,
contoured at the 1 σ level, for the IRK peptide; only pTyr-1162
was included in the refinement and phase calculation of the map.
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Figure 5.
Figure 5. Schematic Representation of the PTP1B
Bisphosphorylated IR Peptide Interactions
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The above figures are
reprinted
by permission from Cell Press:
Mol Cell
(2000,
6,
1401-1412)
copyright 2000.
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