3v7t
From Proteopedia
(Difference between revisions)
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- | + | [[Image:3v7t.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3v7t", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3v7t| PDB=3v7t | SCENE= }} | ||
- | + | ===Crystal Structure of Human Beta-Tryptase Complexed with a Synthetic Inhibitor with a Tropanylamide Scaffold=== | |
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+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_22264487}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 22264487 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_22264487}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3v7t]] 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=3V7T OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:022264487</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Colonna, C.]] | ||
+ | [[Category: Michot, N.]] | ||
+ | [[Category: Zhang, Y.]] | ||
+ | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
+ | [[Category: Protein-ligand complex]] | ||
+ | [[Category: Serine protease]] | ||
+ | [[Category: Tetramer]] | ||
+ | [[Category: Tryptase]] |
Revision as of 06:35, 14 March 2012
Crystal Structure of Human Beta-Tryptase Complexed with a Synthetic Inhibitor with a Tropanylamide Scaffold
Template:ABSTRACT PUBMED 22264487
About this Structure
3v7t is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Liang G, Choi-Sledeski YM, Shum P, Chen X, Poli GB, Kumar V, Minnich A, Wang Q, Tsay J, Sides K, Kang J, Zhang Y. A beta-tryptase inhibitor with a tropanylamide scaffold to improve in vitro stability and to lower hERG channel binding affinity. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1606-10. Epub 2012 Jan 3. PMID:22264487 doi:10.1016/j.bmcl.2011.12.127