3mkp: Difference between revisions
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{{STRUCTURE_3mkp| PDB=3mkp | SCENE= }} | {{STRUCTURE_3mkp| PDB=3mkp | SCENE= }} | ||
===Crystal structure of 1K1 mutant of Hepatocyte Growth Factor/Scatter Factor fragment NK1 in complex with heparin=== | |||
{{ABSTRACT_PUBMED_20639469}} | |||
=== | ==Disease== | ||
[[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> | |||
==Function== | |||
[[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> | |||
==About this Structure== | ==About this Structure== | ||
[[3mkp]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3MKP OCA]. | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:020639469</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Blundell, T L.]] | [[Category: Blundell, T L.]] | ||
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[[Category: Nk1]] | [[Category: Nk1]] | ||
[[Category: Supramolecular assembly]] | [[Category: Supramolecular assembly]] | ||