1w7g: Difference between revisions
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[[Image:1w7g.png|left|200px]] | [[Image:1w7g.png|left|200px]] | ||
{{STRUCTURE_1w7g| PDB=1w7g | SCENE= }} | {{STRUCTURE_1w7g| PDB=1w7g | SCENE= }} | ||
===ALPHA-THROMBIN COMPLEX WITH SULFATED HIRUDIN (RESIDUES 54-65) AND L-ARGININE TEMPLATE INHIBITOR CS107=== | ===ALPHA-THROMBIN COMPLEX WITH SULFATED HIRUDIN (RESIDUES 54-65) AND L-ARGININE TEMPLATE INHIBITOR CS107=== | ||
{{ABSTRACT_PUBMED_16294249}} | {{ABSTRACT_PUBMED_16294249}} | ||
==About this Structure== | ==About this Structure== | ||
[[1w7g]] is a 3 chain structure of [[Hirudin]] 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=1W7G OCA]. | [[1w7g]] is a 3 chain structure of [[Hirudin]] and [[Thrombin]] 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=1W7G OCA]. | ||
==See Also== | ==See Also== | ||
*[[Hirudin]] | *[[Hirudin|Hirudin]] | ||
*[[Thrombin|Thrombin]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:016294249</ref><ref group="xtra">PMID:001939071</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Thrombin]] | [[Category: Thrombin]] | ||
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[[Category: Sauvage, E.]] | [[Category: Sauvage, E.]] | ||
[[Category: Argatroban]] | [[Category: Argatroban]] | ||
[[Category: Blood coagulation-inhibitor]] | |||
[[Category: Coagulation]] | [[Category: Coagulation]] | ||
[[Category: Hydrolase | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
[[Category: Serine protease]] | [[Category: Serine protease]] | ||
[[Category: Thrombin]] | [[Category: Thrombin]] | ||
Revision as of 17:15, 26 July 2012
ALPHA-THROMBIN COMPLEX WITH SULFATED HIRUDIN (RESIDUES 54-65) AND L-ARGININE TEMPLATE INHIBITOR CS107
Template:ABSTRACT PUBMED 16294249
About this Structure
1w7g is a 3 chain structure of Hirudin and Thrombin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Salvagnini C, Michaux C, Remiche J, Wouters J, Charlier P, Marchand-Brynaert J. Design, synthesis and evaluation of graftable thrombin inhibitors for the preparation of blood-compatible polymer materials. Org Biomol Chem. 2005 Dec 7;3(23):4209-20. Epub 2005 Oct 19. PMID:16294249 doi:10.1039/b510239a
- Banner DW, Hadvary P. Crystallographic analysis at 3.0-A resolution of the binding to human thrombin of four active site-directed inhibitors. J Biol Chem. 1991 Oct 25;266(30):20085-93. PMID:1939071