1yu6: Difference between revisions

Revision as of 08:34, 29 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:1yu6.png

Template:STRUCTURE 1yu6

Crystal Structure of the Subtilisin Carlsberg:OMTKY3 ComplexCrystal Structure of the Subtilisin Carlsberg:OMTKY3 Complex

Template:ABSTRACT PUBMED 15858268

About this StructureAbout this Structure

1YU6 is a Protein complex structure of sequences from Bacillus licheniformis and Meleagris gallopavo. Full crystallographic information is available from OCA.

ReferenceReference

Structure of the subtilisin Carlsberg-OMTKY3 complex reveals two different ovomucoid conformations., Maynes JT, Cherney MM, Qasim MA, Laskowski M Jr, James MN, Acta Crystallogr D Biol Crystallogr. 2005 May;61(Pt 5):580-8. Epub 2005, Apr 20. PMID:15858268

Page seeded by OCA on Tue Jul 29 08:34:58 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-[[Image:1yu6.gif|left|200px]]
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-'''Crystal Structure of the Subtilisin Carlsberg:OMTKY3 Complex'''
+===Crystal Structure of the Subtilisin Carlsberg:OMTKY3 Complex===
-==Overview==
+<!--
-One of the most studied protein proteinase inhibitors is the turkey ovomucoid third domain, OMTKY3. This inhibitor contains a reactive-site loop (Lys13I-Arg21I) that binds in a nearly identical manner to all studied serine proteinases, regardless of their clan or specificity. The crystal structure of OMTKY3 bound to subtilisin Carlsberg (CARL) has been determined. There are two complete copies of the complexes in the crystallographic asymmetric unit. Whereas the two enzyme molecules are virtually identical [0.16 A root-mean-square difference (r.m.s.d.) for 274 C(alpha) atoms], the two inhibitor molecules show dramatic differences between one another (r.m.s.d. = 2.4 A for 50 C(alpha) atoms). When compared with other proteinase-bound OMTKY3 molecules, these inhibitors show even larger differences. This work facilitates a re-evaluation of the importance of certain ovomucoid residues in proteinase binding and explains why additivity and sequence-based binding-prediction methods fail for the CARL-OMTKY3 complex.
+The line below this paragraph, {{ABSTRACT_PUBMED_15858268}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 15858268 is the PubMed ID number.
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+{{ABSTRACT_PUBMED_15858268}}
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 [[Category: Protease]]
 [[Category: Protein proteinase inhibitor]]
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