1bht: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /> <applet load="1bht" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bht, resolution 2.0Å" /> '''NK1 FRAGMENT OF HUMA...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:1bht.gif|left|200px]]<br />
[[Image:1bht.gif|left|200px]]<br /><applet load="1bht" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1bht" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1bht, resolution 2.0&Aring;" />
caption="1bht, resolution 2.0&Aring;" />
'''NK1 FRAGMENT OF HUMAN HEPATOCYTE GROWTH FACTOR'''<br />
'''NK1 FRAGMENT OF HUMAN HEPATOCYTE GROWTH FACTOR'''<br />


==Overview==
==Overview==
BACKGROUND: Hepatocyte growth factor (HGF) is a mitogen for hepatocytes, and has also been implicated as an epithelial morphogen in tumor invasion., HGF activates its specific cellular receptor, c-met, through an, aggregation mechanism potentiated by heparan sulfate glycosaminoglycans., HGF consists of an N-terminal (N) domain, four kringle domains (the first, of which carries receptor-binding determinants), and an inactive, serine-protease-like domain. NK1, a naturally occurring fragment of HGF, acts as an antagonist of HGF in the absence of heparin. RESULTS: The N, domain of NK1 consists of a central five-stranded antiparallel beta sheet, flanked by an alpha helix and a two-stranded beta ribbon. The overall N, domain structure in the context of the NK1 fragment is similar to the, structure of the isolated domain; two lysines and an arginine residue, coordinate a bound sulfate ion. The NK1 kringle domain is homologous to, kringle 4 from plasminogen, except that the lysine-binding pocket is, altered by the insertion of a glycine residue. Here, a HEPES molecule is, bound in the pocket. The asymmetric unit of the crystal contains a, 'head-to-tail' NK1 dimer. We use this dimer to propose a model of the NK2, fragment of HGF. CONCLUSIONS: A cluster of exposed lysine and arginine, residues in or near the hairpin-loop region of the N domain might form, part of the NK1 heparin-binding site. In our NK2 model, both kringle, domains pack loosely against the N domain, and a long, positively charged, groove lines the interface. This groove might be involved in, glycosaminoglycan binding. The HGF receptor-binding determinants are, clustered near the binding pocket of the first kringle domain, opposite, the N domain.
BACKGROUND: Hepatocyte growth factor (HGF) is a mitogen for hepatocytes and has also been implicated as an epithelial morphogen in tumor invasion. HGF activates its specific cellular receptor, c-met, through an aggregation mechanism potentiated by heparan sulfate glycosaminoglycans. HGF consists of an N-terminal (N) domain, four kringle domains (the first of which carries receptor-binding determinants), and an inactive serine-protease-like domain. NK1, a naturally occurring fragment of HGF, acts as an antagonist of HGF in the absence of heparin. RESULTS: The N domain of NK1 consists of a central five-stranded antiparallel beta sheet flanked by an alpha helix and a two-stranded beta ribbon. The overall N domain structure in the context of the NK1 fragment is similar to the structure of the isolated domain; two lysines and an arginine residue coordinate a bound sulfate ion. The NK1 kringle domain is homologous to kringle 4 from plasminogen, except that the lysine-binding pocket is altered by the insertion of a glycine residue. Here, a HEPES molecule is bound in the pocket. The asymmetric unit of the crystal contains a 'head-to-tail' NK1 dimer. We use this dimer to propose a model of the NK2 fragment of HGF. CONCLUSIONS: A cluster of exposed lysine and arginine residues in or near the hairpin-loop region of the N domain might form part of the NK1 heparin-binding site. In our NK2 model, both kringle domains pack loosely against the N domain, and a long, positively charged groove lines the interface. This groove might be involved in glycosaminoglycan binding. The HGF receptor-binding determinants are clustered near the binding pocket of the first kringle domain, opposite the N domain.


==Disease==
==Disease==
Line 11: Line 10:


==About this Structure==
==About this Structure==
1BHT is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with SO4 and EPE as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BHT OCA].  
1BHT is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=EPE:'>EPE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BHT OCA].  


==Reference==
==Reference==
Line 17: Line 16:
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Godowski, P.J.]]
[[Category: Godowski, P J.]]
[[Category: Lokker, N.A.]]
[[Category: Lokker, N A.]]
[[Category: Ultsch, M.H.]]
[[Category: Ultsch, M H.]]
[[Category: Vos, A.M.De.]]
[[Category: Vos, A M.De.]]
[[Category: EPE]]
[[Category: EPE]]
[[Category: SO4]]
[[Category: SO4]]
Line 28: Line 27:
[[Category: kringle]]
[[Category: kringle]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:10:03 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:55:27 2008''