5cp9

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m (Protected "5cp9" [edit=sysop:move=sysop])
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'''Unreleased structure'''
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==The structure of the NK1 fragment of HGF/SF complexed with MB605==
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<StructureSection load='5cp9' size='340' side='right' caption='[[5cp9]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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The entry 5cp9 is ON HOLD until Paper Publication
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5cp9]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5CP9 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5CP9 FirstGlance]. <br>
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Authors: Sigurdardottir, A.G., Winter, A., Sobkowicz, A., Fragai, M., Chirgadze, D.Y., Ascher, D.B., Blundell, T.L., Gherardi, E.
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=6O5:3-(FURAN-2-YL)PROPANOIC+ACID'>6O5</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></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=5cp9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5cp9 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=5cp9 RCSB], [http://www.ebi.ac.uk/pdbsum/5cp9 PDBsum]</span></td></tr>
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Description: The structure of the NK1 fragment of HGF/SF complexed with MB605
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</table>
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[[Category: Unreleased Structures]]
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== Disease ==
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[[Category: Gherardi, E]]
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[[http://www.uniprot.org/uniprot/HGF_HUMAN HGF_HUMAN]] Defects in HGF are the cause of deafness autosomal recessive type 39 (DFNB39) [MIM:[http://omim.org/entry/608265 608265]]. A form of profound prelingual sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.<ref>PMID:19576567</ref>
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[[Category: Chirgadze, D.Y]]
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== Function ==
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[[http://www.uniprot.org/uniprot/HGF_HUMAN HGF_HUMAN]] Potent mitogen for mature parenchymal hepatocyte cells, seems to be a hepatotrophic factor, and acts as a growth factor for a broad spectrum of tissues and cell types. Activating ligand for the receptor tyrosine kinase MET by binding to it and promoting its dimerization.<ref>PMID:15167892</ref> <ref>PMID:20624990</ref>
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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: Ascher, D B]]
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[[Category: Blundell, T L]]
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[[Category: Chirgadze, D Y]]
[[Category: Fragai, M]]
[[Category: Fragai, M]]
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[[Category: Sigurdardottir, A.G]]
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[[Category: Gherardi, E]]
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[[Category: Blundell, T.L]]
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[[Category: Sigurdardottir, A G]]
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[[Category: Ascher, D.B]]
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[[Category: Sobkowicz, A]]
[[Category: Sobkowicz, A]]
[[Category: Winter, A]]
[[Category: Winter, A]]
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[[Category: Cell cycle]]
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[[Category: Fragment based drug discovery]]
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[[Category: Growth factor]]
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[[Category: Hgf/sf]]
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[[Category: Hormone]]
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[[Category: New chemical entity]]
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[[Category: Nk1 fragment]]

Revision as of 14:55, 12 August 2015

The structure of the NK1 fragment of HGF/SF complexed with MB605

5cp9, resolution 1.90Å

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