5csq: Difference between revisions
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==The structure of the NK1 fragment of HGF/SF complexed with MOPS== | ==The structure of the NK1 fragment of HGF/SF complexed with MOPS== | ||
<StructureSection load='5csq' size='340' side='right' caption='[[5csq]], [[Resolution|resolution]] 1.95Å' scene=''> | <StructureSection load='5csq' size='340' side='right'caption='[[5csq]], [[Resolution|resolution]] 1.95Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[5csq]] is a 2 chain structure with sequence from [ | <table><tr><td colspan='2'>[[5csq]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5CSQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5CSQ FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.95Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MPO:3[N-MORPHOLINO]PROPANE+SULFONIC+ACID'>MPO</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5csq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5csq OCA], [https://pdbe.org/5csq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5csq RCSB], [https://www.ebi.ac.uk/pdbsum/5csq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5csq ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/HGF_HUMAN HGF_HUMAN] Defects in HGF are the cause of deafness autosomal recessive type 39 (DFNB39) [MIM:[https://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> | ||
== Function == | == Function == | ||
[ | [https://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> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Ascher | [[Category: Large Structures]] | ||
[[Category: Blundell | [[Category: Ascher DB]] | ||
[[Category: Chirgadze | [[Category: Blundell TL]] | ||
[[Category: Fragai | [[Category: Chirgadze DY]] | ||
[[Category: Gherardi | [[Category: Fragai M]] | ||
[[Category: Sigurdardottir | [[Category: Gherardi E]] | ||
[[Category: Sobkowicz | [[Category: Sigurdardottir AG]] | ||
[[Category: Winter | [[Category: Sobkowicz A]] | ||
[[Category: Winter A]] | |||