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| - | [[Image:1dhj.gif|left|200px]] | + | {{Seed}} |
| | + | [[Image:1dhj.png|left|200px]] |
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| | {{STRUCTURE_1dhj| PDB=1dhj | SCENE= }} | | {{STRUCTURE_1dhj| PDB=1dhj | SCENE= }} |
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| - | '''LONG-RANGE STRUCTURAL EFFECTS IN A SECOND-SITE REVERTANT OF A MUTANT DIHYDROFOLATE REDUCTASE'''
| + | ===LONG-RANGE STRUCTURAL EFFECTS IN A SECOND-SITE REVERTANT OF A MUTANT DIHYDROFOLATE REDUCTASE=== |
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| - | ==Overview==
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| - | X-ray crystal structures have been determined for a second-site revertant (Asp-27-->Ser, Phe-137-->Ser; D27S/F137S) and both component single-site mutants of Escherichia coli dihydrofolate reductase. The primary D27S mutation, located in the substrate binding pocket, greatly reduces catalytic activity as compared to the wild-type enzyme. The additional F137S mutation, which partially restores catalytic activity, is located on the surface of the molecule, well outside of the catalytic center and approximately 15 A from residue 27. Comparison of kinetic data for the single-site F137S mutant, specifically constructed as a control, and for the double-mutant enzymes indicates that the effects of the F137S and D27S mutations on catalysis are nonadditive. This result suggests that the second-site mutation might mediate its effects through a structural perturbation propagated along the polypeptide backbone. To investigate the mechanism by which the F137S substitution elevates the catalytic activity of D27S we have determined the structure of the D27S/F137S double mutant. We also present a rerefined structure for the original D27S mutant and a preliminary structural interpretation for the F137S single-site mutant. We find that while either single mutant shows little more than a simple side-chain substitution, the double mutant undergoes an extended structural perturbation, which is propagated between these two widely separated sites via the helix alpha B.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_8265622}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 8265622 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_8265622}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Kraut, J.]] | | [[Category: Kraut, J.]] |
| | [[Category: Oxidoreductase]] | | [[Category: Oxidoreductase]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 13:51:16 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 23:04:32 2008'' |
Revision as of 20:04, 30 June 2008
Template:STRUCTURE 1dhj
LONG-RANGE STRUCTURAL EFFECTS IN A SECOND-SITE REVERTANT OF A MUTANT DIHYDROFOLATE REDUCTASE
Template:ABSTRACT PUBMED 8265622
About this Structure
1DHJ is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.
Reference
Long-range structural effects in a second-site revertant of a mutant dihydrofolate reductase., Brown KA, Howell EE, Kraut J, Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11753-6. PMID:8265622
Page seeded by OCA on Mon Jun 30 23:04:32 2008
