5a7j

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'''Unreleased structure'''
 
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The entry 5a7j is ON HOLD until Paper Publication
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==Crystal structure of INPP5B in complex with benzene 1,2,4,5- tetrakisphosphate==
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<StructureSection load='5a7j' size='340' side='right' caption='[[5a7j]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5a7j]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5A7J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5A7J FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=K2Y:BENZENE+1,2,4,5-TETRAYL+TETRAKIS[DIHYDROGEN+(PHOSPHATE)]'>K2Y</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5a7i|5a7i]]</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphoinositide_5-phosphatase Phosphoinositide 5-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.36 3.1.3.36] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5a7j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5a7j OCA], [http://pdbe.org/5a7j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5a7j RCSB], [http://www.ebi.ac.uk/pdbsum/5a7j PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/I5P2_HUMAN I5P2_HUMAN]] Hydrolyzes phosphatidylinositol 4,5-bisphosphate (PtIns(4,5)P2) and the signaling molecule phosphatidylinositol 1,4,5-trisphosphate (PtIns(1,4,5)P3), and thereby modulates cellular signaling events.<ref>PMID:7721860</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The inositol polyphosphate 5-phosphatase INPP5B hydrolyzes the 5-phosphate group from water- and lipid-soluble signaling messengers. Two synthetic benzene and biphenyl polyphosphates (BzP/BiPhPs), simplified surrogates of inositol phosphates and phospholipid headgroups, were identified by thermodynamic studies as potent INPP5B ligands. The X-ray structure of the complex between INPP5B and biphenyl 3,3',4,4',5,5'-hexakisphosphate [BiPh(3,3',4,4',5,5')P6, IC50 5.5 muM] was determined at 2.89 A resolution. One inhibitor pole locates in the phospholipid headgroup binding site and the second solvent-exposed ring binds to the His-Tag of another INPP5B molecule, while a molecule of inorganic phosphate is also present in the active site. Benzene 1,2,3-trisphosphate [Bz(1,2,3)P3] [one ring of BiPh(3,3',4,4',5,5')P6] inhibits INPP5B ca. 6-fold less potently. Co-crystallization with benzene 1,2,4,5-tetrakisphosphate [Bz(1,2,4,5)P4, IC50 = 6.3 muM] yielded a structure refined at 2.9 A resolution. Conserved residues among the 5-phosphatase family mediate interactions with Bz(1,2,4,5)P4 and BiPh(3,3',4,4',5,5')P6 similar to those with the polar groups present in positions 1, 4, 5, and 6 on the inositol ring of the substrate. 5-Phosphatase specificity most likely resides in the variable zone located close to the 2- and 3-positions of the inositol ring, offering insights to inhibitor design. We propose that the inorganic phosphate present in the INPP5B-BiPh(3,3',4,4',5,5')P6 complex mimics the postcleavage substrate 5-phosphate released by INPP5B in the catalytic site, allowing elucidation of two new key features in the catalytic mechanism proposed for the family of phosphoinositide 5-phosphatases: first, the involvement of the conserved Arg-451 in the interaction with the 5-phosphate and second, identification of the water molecule that initiates 5-phosphate hydrolysis. Our model also has implications for the proposed "moving metal" mechanism.
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Authors: Tresaugues, L., Mills, S.J., Silvander, C., Cozier, G., Potter, B.V.L., Nordlund, P.
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Crystal Structures of Type-II Inositol Polyphosphate 5-Phosphatase INPP5B with Synthetic Inositol Polyphosphate Surrogates Reveal New Mechanistic Insights for the Inositol 5-Phosphatase Family.,Mills SJ, Silvander C, Cozier G, Tresaugues L, Nordlund P, Potter BV Biochemistry. 2016 Mar 8;55(9):1384-97. doi: 10.1021/acs.biochem.5b00838. Epub, 2016 Feb 29. PMID:26854536<ref>PMID:26854536</ref>
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Description: Crystal structure of INPP5B in complex with benzene 1,2,4,5-tetrakisphosphate
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 5a7j" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Phosphoinositide 5-phosphatase]]
[[Category: Cozier, G]]
[[Category: Cozier, G]]
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[[Category: Mills, S J]]
[[Category: Nordlund, P]]
[[Category: Nordlund, P]]
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[[Category: Potter, B V.L]]
[[Category: Silvander, C]]
[[Category: Silvander, C]]
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[[Category: Mills, S.J]]
 
[[Category: Tresaugues, L]]
[[Category: Tresaugues, L]]
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[[Category: Potter, B.V.L]]
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[[Category: Hydrolase]]
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[[Category: Inhibitor]]
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[[Category: Magnesium binding]]
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[[Category: Phosphoinositides signalling]]
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[[Category: Protein-inhbitor complex]]
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[[Category: Sgc]]
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[[Category: Signalling]]
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[[Category: Structural genomic]]

Revision as of 11:22, 12 May 2016

Crystal structure of INPP5B in complex with benzene 1,2,4,5- tetrakisphosphate

5a7j, resolution 2.90Å

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