1pxh: Difference between revisions
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caption="1pxh, resolution 2.15Å" /> | caption="1pxh, resolution 2.15Å" /> | ||
'''Crystal structure of protein tyrosine phosphatase 1B with potent and selective bidentate inhibitor compound 2'''<br /> | '''Crystal structure of protein tyrosine phosphatase 1B with potent and selective bidentate inhibitor compound 2'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
1PXH is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MG, SNA and ACY as [http://en.wikipedia.org/wiki/ligands ligands]. This structure superseeds the now removed PDB entry 1N6W. Active as [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48] Full crystallographic information is available from [http:// | 1PXH is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=MG:'>MG</scene>, <scene name='pdbligand=SNA:'>SNA</scene> and <scene name='pdbligand=ACY:'>ACY</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. This structure superseeds the now removed PDB entry 1N6W. Active as [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PXH OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: x-ray diffraction]] | [[Category: x-ray diffraction]] | ||
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Revision as of 17:42, 15 February 2008
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Crystal structure of protein tyrosine phosphatase 1B with potent and selective bidentate inhibitor compound 2
OverviewOverview
Protein-tyrosine phosphatase 1B (PTP1B) has been implicated as an, important regulator in several signaling pathways including those, initiated by insulin and leptin. Potent and specific PTP1B inhibitors, could serve as useful tools in elucidating the physiological functions of, PTP1B and may constitute valuable therapeutics in the treatment of several, human diseases. We have determined the crystal structure of PTP1B in, complex with compound 2, the most potent and selective PTP1B inhibitor, reported to date. The structure at 2.15-A resolution reveals that compound, 2 simultaneously binds to the active site and a unique proximal, noncatalytic site formed by Lys-41, Arg-47, and Asp-48. The structural, data are further corroborated by results from kinetic analyses of the, interactions of PTP1B and its site-directed mutants with compound 2 and, several of its variants. Although many of the residues important for, interactions between PTP1B and compound 2 are not unique to PTP1B, the, combinations of all contact residues differ between PTP isozymes, which, provide a structural basis for potent and selective PTP1B inhibition. Our, data further suggest that potent, yet highly selective, PTP1B inhibitory, agents can be acquired by targeting the area defined by residues Lys-41, Arg-47, and Asp-48, in addition to the previously identified second aryl, phosphate-binding pocket.
DiseaseDisease
Known diseases associated with this structure: Abdominal body fat distribution, modifier of OMIM:[176885], Insulin resistance, susceptibility to OMIM:[176885]
About this StructureAbout this Structure
1PXH is a Single protein structure of sequence from Homo sapiens with , and as ligands. This structure superseeds the now removed PDB entry 1N6W. Active as Protein-tyrosine-phosphatase, with EC number 3.1.3.48 Full crystallographic information is available from OCA.
ReferenceReference
Crystal structure of PTP1B complexed with a potent and selective bidentate inhibitor., Sun JP, Fedorov AA, Lee SY, Guo XL, Shen K, Lawrence DS, Almo SC, Zhang ZY, J Biol Chem. 2003 Apr 4;278(14):12406-14. Epub 2003 Jan 23. PMID:12547827
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