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1WB9

Crystal Structure of E. coli DNA Mismatch Repair enzyme MutS, E38T mutant, in complex with a G.T mismatch

Summary for 1WB9
Entry DOI10.2210/pdb1wb9/pdb
Related1E3M 1NG9 1OH5 1OH6 1OH7 1OH8 1W7A 1WBB 1WBD
DescriptorDNA MISMATCH REPAIR PROTEIN MUTS, 5'-D(*AP*GP*CP*TP*GP*CP*CP*AP*GP*GP *CP*AP*CP*CP*AP*GP*TP*G)-3', 5'-D(*AP*CP*TP*GP*GP*TP*GP*CP*TP*TP *GP*GP*CP*AP*GP*CP*T)-3', ... (6 entities in total)
Functional Keywordsdna-binding, atp-binding, dna binding, dna repair, mismatch recognition
Biological sourceESCHERICHIA COLI
More
Total number of polymer chains4
Total formula weight190365.17
Authors
Natrajan, G.,Georgijevic, D.,Lebbink, J.H.G.,Winterwerp, H.H.K.,de Wind, N.,Sixma, T.K. (deposition date: 2004-10-31, release date: 2006-01-18, Last modification date: 2023-12-13)
Primary citationLebbink, J.H.G.,Georgijevic, D.,Natrajan, G.,Fish, A.,Winterwerp, H.H.K.,Sixma, T.K.,De Wind, N.
Dual Role of Muts Glutamate 38 in DNA Mismatch Discrimination and in the Authorization of Repair.
Embo J., 25:409-, 2006
Cited by
PubMed Abstract: MutS plays a critical role in DNA mismatch repair in Escherichia coli by binding to mismatches and initiating repair in an ATP-dependent manner. Mutational analysis of a highly conserved glutamate, Glu38, has revealed its role in mismatch recognition by enabling MutS to discriminate between homoduplex and mismatched DNA. Crystal structures of MutS have shown that Glu38 forms a hydrogen bond to one of the mismatched bases. In this study, we have analyzed the crystal structures, DNA binding and the response to ATP binding of three Glu38 mutants. While confirming the role of the negative charge in initial discrimination, we show that in vivo mismatch repair can proceed even when discrimination is low. We demonstrate that the formation of a hydrogen bond by residue 38 to the mismatched base authorizes repair by inducing intramolecular signaling, which results in the inhibition of rapid hydrolysis of distally bound ATP. This allows formation of the stable MutS-ATP-DNA clamp, a key intermediate in triggering downstream repair events.
PubMed: 16407973
DOI: 10.1038/SJ.EMBOJ.7600936
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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数据于2025-12-03公开中

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