2ilp
From Proteopedia
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[[Image:2ilp.png|left|200px]] | [[Image:2ilp.png|left|200px]] | ||
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{{STRUCTURE_2ilp| PDB=2ilp | SCENE= }} | {{STRUCTURE_2ilp| PDB=2ilp | SCENE= }} | ||
===Clostridium botulinum Serotype A Light Chain inhibited by 4-chlorocinnamic hydroxamate=== | ===Clostridium botulinum Serotype A Light Chain inhibited by 4-chlorocinnamic hydroxamate=== | ||
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{{ABSTRACT_PUBMED_17524984}} | {{ABSTRACT_PUBMED_17524984}} | ||
==About this Structure== | ==About this Structure== | ||
- | + | [[2ilp]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Clostridium_botulinum Clostridium botulinum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ILP OCA]. | |
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:017524984</ref><references group="xtra"/> |
[[Category: Bontoxilysin]] | [[Category: Bontoxilysin]] | ||
[[Category: Clostridium botulinum]] | [[Category: Clostridium botulinum]] | ||
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[[Category: Silvaggi, N R.]] | [[Category: Silvaggi, N R.]] | ||
[[Category: Clostridium botulinum neurotoxin]] | [[Category: Clostridium botulinum neurotoxin]] | ||
+ | [[Category: Hydrolase]] | ||
[[Category: Protease inhibitor]] | [[Category: Protease inhibitor]] | ||
[[Category: Substrate specificity]] | [[Category: Substrate specificity]] | ||
[[Category: Substrate switching]] | [[Category: Substrate switching]] | ||
[[Category: Type some]] | [[Category: Type some]] | ||
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- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 13:08:42 2009'' |
Revision as of 13:42, 7 January 2013
Clostridium botulinum Serotype A Light Chain inhibited by 4-chlorocinnamic hydroxamate
Template:ABSTRACT PUBMED 17524984
About this Structure
2ilp is a 2 chain structure with sequence from Clostridium botulinum. Full crystallographic information is available from OCA.
Reference
- Silvaggi NR, Boldt GE, Hixon MS, Kennedy JP, Tzipori S, Janda KD, Allen KN. Structures of Clostridium botulinum Neurotoxin Serotype A Light Chain complexed with small-molecule inhibitors highlight active-site flexibility. Chem Biol. 2007 May;14(5):533-42. PMID:17524984 doi:http://dx.doi.org/10.1016/j.chembiol.2007.03.014