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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1993-4-1
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pubmed:abstractText |
The recently solved X-ray structure of the dimerization region ("leucine zipper") of the yeast transcriptional activator GCN4 (O'Shea, E.K., Klemm, J.D., Kim, P.S., Alber, T. Science 254:539-544, 1991) is compared to previously predicted models which had been obtained by a conformational search procedure employing simulated annealing without any knowledge of the crystal coordinates (Nilges, M., Brünger, A.T. Protein Eng. 4:649-659, 1991). During the course of the simulated annealing procedure, the models converged towards the X-ray structure. The averaged root mean square difference between the models and the X-ray structure is 1.26 and 1.75 A for backbone atoms and all nonhydrogen atoms at the dimerization interface, respectively. The local helix-helix crossing angle of the X-ray structure falls within the range predicted by the models; a slight unwinding of the coiled coil toward the N-terminal DNA-binding end of the dimerization region has been correctly predicted. Distance maps between the helices are largely identical. The region around asparagine 20 is asymmetric in the X-structure and in the models. Surface side chain dihedrals showed a large variation in the models although the chi 1, chi 2, chi 3, chi 4 3-fold dihedrals were correctly predicted in 69, 42, 43, and 44% of the cases, respectively. Phenomenological free energies of dimerization of the models show little correlation with the root mean square difference between the models and the X-ray structure.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0887-3585
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
133-46
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:8441750-Computer Simulation,
pubmed-meshheading:8441750-DNA-Binding Proteins,
pubmed-meshheading:8441750-Electrochemistry,
pubmed-meshheading:8441750-Fungal Proteins,
pubmed-meshheading:8441750-Leucine Zippers,
pubmed-meshheading:8441750-Models, Molecular,
pubmed-meshheading:8441750-Molecular Structure,
pubmed-meshheading:8441750-Protein Conformation,
pubmed-meshheading:8441750-Protein Kinases,
pubmed-meshheading:8441750-Saccharomyces cerevisiae Proteins,
pubmed-meshheading:8441750-Thermodynamics,
pubmed-meshheading:8441750-X-Ray Diffraction
|
pubmed:year |
1993
|
pubmed:articleTitle |
Successful prediction of the coiled coil geometry of the GCN4 leucine zipper domain by simulated annealing: comparison to the X-ray structure.
|
pubmed:affiliation |
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06511.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|