2i4e: Difference between revisions
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|PDB= 2i4e |SIZE=350|CAPTION= <scene name='initialview01'>2i4e</scene>, resolution 1.750Å | |PDB= 2i4e |SIZE=350|CAPTION= <scene name='initialview01'>2i4e</scene>, resolution 1.750Å | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=VO4:VANADATE ION'>VO4</scene> | |LIGAND= <scene name='pdbligand=VO4:VANADATE+ION'>VO4</scene> | ||
|ACTIVITY= [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] | |ACTIVITY= <span class='plainlinks'>[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] </span> | ||
|GENE= PTPRB, PTPB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= PTPRB, PTPB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
|DOMAIN= | |||
|RELATEDENTRY=[[2i3u|2I3U]], [[2i3r|2I3R]], [[2hc1|2HC1]], [[2hc2|2HC2]], [[2i4g|2I4G]], [[2i4h|2I4H]] | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2i4e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2i4e OCA], [http://www.ebi.ac.uk/pdbsum/2i4e PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2i4e RCSB]</span> | |||
}} | }} | ||
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[[Category: Pokross, M E.]] | [[Category: Pokross, M E.]] | ||
[[Category: Walter, R L.]] | [[Category: Walter, R L.]] | ||
[[Category: drug design]] | [[Category: drug design]] | ||
[[Category: inhibitor]] | [[Category: inhibitor]] | ||
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[[Category: wpd-loop]] | [[Category: wpd-loop]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:39:29 2008'' |
Revision as of 03:39, 31 March 2008
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, resolution 1.750Å | |||||||
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Ligands: | |||||||
Gene: | PTPRB, PTPB (Homo sapiens) | ||||||
Activity: | Protein-tyrosine-phosphatase, with EC number 3.1.3.48 | ||||||
Related: | 2I3U, 2I3R, 2HC1, 2HC2, 2I4G, 2I4H
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Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Structural studies of protein tyrosine phosphatase beta catalytic domain in complex with inhibitors
OverviewOverview
Protein tyrosine phosphatases (PTPs) play roles in many biological processes and are considered to be important targets for drug discovery. As inhibitor development has proven challenging, crystal structure-based design will be very helpful to advance inhibitor potency and selectivity. Successful application of protein crystallography to drug discovery heavily relies on high-quality crystal structures of the protein of interest complexed with pharmaceutically interesting ligands. It is very important to be able to produce protein-ligand crystals rapidly and reproducibly for as many ligands as necessary. This study details our efforts to engineer the catalytic domain of human protein tyrosine phosphatase beta (HPTPbeta-CD) with properties suitable for rapid-turnaround crystallography. Structures of apo HPTPbeta-CD and its complexes with several novel small-molecule inhibitors are presented here for the first time.
About this StructureAbout this Structure
2I4E is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
Engineering the catalytic domain of human protein tyrosine phosphatase beta for structure-based drug discovery., Evdokimov AG, Pokross M, Walter R, Mekel M, Cox B, Li C, Bechard R, Genbauffe F, Andrews R, Diven C, Howard B, Rastogi V, Gray J, Maier M, Peters KG, Acta Crystallogr D Biol Crystallogr. 2006 Dec;62(Pt 12):1435-45. Epub 2006, Nov 23. PMID:17139078
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