1k5r: Difference between revisions
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|PDB= 1k5r |SIZE=350|CAPTION= <scene name='initialview01'>1k5r</scene> | |PDB= 1k5r |SIZE=350|CAPTION= <scene name='initialview01'>1k5r</scene> | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=NH2:AMINO GROUP'>NH2</scene> | |LIGAND= <scene name='pdbligand=ESD:(2-AMINO-ETHYLSULFANYL)-ACETIC+ACID'>ESD</scene>, <scene name='pdbligand=NH2:AMINO+GROUP'>NH2</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
|DOMAIN= | |||
|RELATEDENTRY=[[1jmq|1JMQ]], [[1eom|1EOM]], [[1eg3|1EG3]], [[1eg4|1EG4]], [[1i5h|1I5H]] | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1k5r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1k5r OCA], [http://www.ebi.ac.uk/pdbsum/1k5r PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1k5r RCSB]</span> | |||
}} | }} | ||
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[[Category: Toepert, F.]] | [[Category: Toepert, F.]] | ||
[[Category: Volkmer-Engert, R.]] | [[Category: Volkmer-Engert, R.]] | ||
[[Category: beta-sheet protein]] | [[Category: beta-sheet protein]] | ||
[[Category: stability of beta sheet]] | [[Category: stability of beta sheet]] | ||
| Line 37: | Line 39: | ||
[[Category: yap65]] | [[Category: yap65]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:43:54 2008'' | ||
Revision as of 21:43, 30 March 2008
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| Ligands: | , | ||||||
| Related: | 1JMQ, 1EOM, 1EG3, 1EG4, 1I5H
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| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
YAP65 WW domain S24-Amino-Ethylsulfanyl-Acetic Acid mutant
OverviewOverview
Chemical synthesis allows the incorporation of nonnatural amino acids into proteins that may provide previously untried probes of their folding pathway and thermodynamic stability. We have used a flexible thioether linker as a loop mimetic in the human yes kinase-associated protein (YAP 65) WW domain, a three-stranded, 44-residue, beta-sheet protein. This linkage avoids problems of incorporating sequences that constrain loops to the extent that they significantly change the nature of the denatured state with concomitant effects on the folding kinetics. An NMR solution structure shows that the thioether linker had little effect on the global fold of the domain, although the loop is apparently more dynamic. The thioether variants are destabilized by up to 1.4 kcal/mol (1 cal = 4.18 J). Preliminary Phi-value analysis showed that the first loop is highly structured in the folding transition state, and the second loop is essentially unstructured. These data are consistent with results from simulated unfolding and detailed protein-engineering studies of structurally homologous WW domains. Previously, Phi-value analysis was limited to studying side-chain interactions. The linkers used here extend the protein engineering method directly to secondary-structure interactions.
About this StructureAbout this Structure
1K5R is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.
ReferenceReference
Using flexible loop mimetics to extend phi-value analysis to secondary structure interactions., Ferguson N, Pires JR, Toepert F, Johnson CM, Pan YP, Volkmer-Engert R, Schneider-Mergener J, Daggett V, Oschkinat H, Fersht A, Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13008-13. Epub 2001 Oct 30. PMID:11687614
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