2gkt
From Proteopedia
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- | [[Image:2gkt.gif|left|200px]] | + | [[Image:2gkt.gif|left|200px]] |
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- | '''Crystal structure of the P14'-Ala32 variant of the N-terminally truncated OMTKY3-del(1-5)''' | + | {{Structure |
+ | |PDB= 2gkt |SIZE=350|CAPTION= <scene name='initialview01'>2gkt</scene>, resolution 1.23Å | ||
+ | |SITE= | ||
+ | |LIGAND= | ||
+ | |ACTIVITY= | ||
+ | |GENE= | ||
+ | }} | ||
+ | |||
+ | '''Crystal structure of the P14'-Ala32 variant of the N-terminally truncated OMTKY3-del(1-5)''' | ||
+ | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
- | 2GKT is a [ | + | 2GKT is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Meleagris_gallopavo Meleagris gallopavo]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GKT OCA]. |
==Reference== | ==Reference== | ||
- | Structural insights into the non-additivity effects in the sequence-to-reactivity algorithm for serine peptidases and their inhibitors., Lee TW, Qasim MA, Laskowski M Jr, James MN, J Mol Biol. 2007 Mar 23;367(2):527-46. Epub 2007 Jan 9. PMID:[http:// | + | Structural insights into the non-additivity effects in the sequence-to-reactivity algorithm for serine peptidases and their inhibitors., Lee TW, Qasim MA, Laskowski M Jr, James MN, J Mol Biol. 2007 Mar 23;367(2):527-46. Epub 2007 Jan 9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17266986 17266986] |
[[Category: Meleagris gallopavo]] | [[Category: Meleagris gallopavo]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: reactive-site loop]] | [[Category: reactive-site loop]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 17:05:50 2008'' |
Revision as of 15:05, 20 March 2008
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Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of the P14'-Ala32 variant of the N-terminally truncated OMTKY3-del(1-5)
Overview
Sequence-to-reactivity algorithms (SRAs) for proteins have the potential of being broadly applied in molecular design. Recently, Laskowski et al. have reported an additivity-based SRA that accurately predicts most of the standard free energy changes of association for variants of turkey ovomucoid third domain (OMTKY3) with six serine peptidases, one of which is streptogrisin B (commonly known as Streptomyces griseus peptidase B, SGPB). Non-additivity effects for residues 18I and 32I, and for residues 20I and 32I of OMTKY3 occurred when the associations with SGPB were predicted using the SRA. To elucidate precisely the mechanics of these non-additivity effects in structural terms, we have determined the crystal structures of the unbound OMTKY3 (with Gly32I as in the wild-type amino acid sequence) at a resolution of 1.16 A, the unbound Ala32I variant of OMTKY3 at a resolution of 1.23 A, and the SGPB:OMTKY3-Ala32I complex (equilibrium association constant K(a)=7.1x10(9) M(-1) at 21(+/-2) C degrees, pH 8.3) at a resolution of 1.70 A. Extensive comparisons with the crystal structure of the unbound OMTKY3 confirm our understanding of some previously addressed non-additivity effects. Unexpectedly, SGPB and OMTKY3-Ala32I form a 1:2 complex in the crystal. Comparison with the SGPB:OMTKY3 complex shows a conformational change in the SGPB:OMTKY3-Ala32I complex, resulting from a hinged rigid-body rotation of the inhibitor caused by the steric hindrance between the methyl group of Ala32IA of the inhibitor and Pro192BE of the peptidase. This perturbs the interactions among residues 18I, 20I, 32I and 36I of the inhibitor, probably resulting in the above non-additivity effects. This conformational change also introduces residue 10I as an additional hyper-variable contact residue to the SRA.
About this Structure
2GKT is a Single protein structure of sequence from Meleagris gallopavo. Full crystallographic information is available from OCA.
Reference
Structural insights into the non-additivity effects in the sequence-to-reactivity algorithm for serine peptidases and their inhibitors., Lee TW, Qasim MA, Laskowski M Jr, James MN, J Mol Biol. 2007 Mar 23;367(2):527-46. Epub 2007 Jan 9. PMID:17266986
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