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1scn
From Proteopedia
(Difference between revisions)
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[[Image:1scn.png|left|200px]] | [[Image:1scn.png|left|200px]] | ||
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{{STRUCTURE_1scn| PDB=1scn | SCENE= }} | {{STRUCTURE_1scn| PDB=1scn | SCENE= }} | ||
| - | ===INACTIVATION OF SUBTILISIN CARLSBERG BY N-(TERT-BUTOXYCARBONYL-ALANYL-PROLYL-PHENYLALANYL)-O- | + | ===INACTIVATION OF SUBTILISIN CARLSBERG BY N-(TERT-BUTOXYCARBONYL-ALANYL-PROLYL-PHENYLALANYL)-O-BENZOL HYDROXYLAMINE: FORMATION OF COVALENT ENZYME-INHIBITOR LINKAGE IN THE FORM OF A CARBAMATE DERIVATIVE=== |
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| - | (as it appears on PubMed at http://www.pubmed.gov), where 8068694 is the PubMed ID number. | ||
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{{ABSTRACT_PUBMED_8068694}} | {{ABSTRACT_PUBMED_8068694}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1scn]] is a 1 chain structure of [[Subtilisin]] with sequence from [http://en.wikipedia.org/wiki/Bacillus_licheniformis Bacillus licheniformis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SCN OCA]. | |
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| + | ==See Also== | ||
| + | *[[Subtilisin|Subtilisin]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:008068694</ref><references group="xtra"/> |
[[Category: Bacillus licheniformis]] | [[Category: Bacillus licheniformis]] | ||
[[Category: Subtilisin]] | [[Category: Subtilisin]] | ||
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[[Category: Ringe, D.]] | [[Category: Ringe, D.]] | ||
[[Category: Steinmetz, A C.U.]] | [[Category: Steinmetz, A C.U.]] | ||
| - | + | [[Category: Hydrolase-hydrolase inhibitor complex]] | |
| - | + | [[Category: Serine proteinase]] | |
Revision as of 03:10, 27 July 2012
Contents |
INACTIVATION OF SUBTILISIN CARLSBERG BY N-(TERT-BUTOXYCARBONYL-ALANYL-PROLYL-PHENYLALANYL)-O-BENZOL HYDROXYLAMINE: FORMATION OF COVALENT ENZYME-INHIBITOR LINKAGE IN THE FORM OF A CARBAMATE DERIVATIVE
Template:ABSTRACT PUBMED 8068694
About this Structure
1scn is a 1 chain structure of Subtilisin with sequence from Bacillus licheniformis. Full crystallographic information is available from OCA.
See Also
Reference
- Steinmetz AC, Demuth HU, Ringe D. Inactivation of subtilisin Carlsberg by N-((tert-butoxycarbonyl)alanylprolylphenylalanyl)-O-benzoylhydroxyl- amine: formation of a covalent enzyme-inhibitor linkage in the form of a carbamate derivative. Biochemistry. 1994 Aug 30;33(34):10535-44. PMID:8068694
