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4HDV

Crystal structure of S. pombe ATL1 in complex with damaged DNA containing 2,6-diaminopurine

Summary for 4HDV
Entry DOI10.2210/pdb4hdv/pdb
Related4HDU
DescriptorAlkyltransferase-like protein 1, 5'-D(*GP*CP*CP*AP*TP*GP*(1AP)P*CP*TP*AP*GP*TP*A)-3', 5'-D(*CP*TP*AP*CP*TP*AP*GP*CP*CP*AP*TP*GP*G)-3', ... (4 entities in total)
Functional Keywordsalkyltransferase, dna repair, nucleotide excision repair, ner, base repair, dna damage, guanine, alkylation, dna binding protein-dna complex, dna binding protein/dna
Biological sourceSchizosaccharomyces pombe (Fission yeast)
Total number of polymer chains3
Total formula weight21604.62
Authors
Tubbs, J.L.,Tainer, J.A. (deposition date: 2012-10-02, release date: 2012-12-26, Last modification date: 2023-09-20)
Primary citationWilkinson, O.J.,Latypov, V.,Tubbs, J.L.,Millington, C.L.,Morita, R.,Blackburn, H.,Marriott, A.,McGown, G.,Thorncroft, M.,Watson, A.J.,Connolly, B.A.,Grasby, J.A.,Masui, R.,Hunter, C.A.,Tainer, J.A.,Margison, G.P.,Williams, D.M.
Alkyltransferase-like protein (Atl1) distinguishes alkylated guanines for DNA repair using cation-{pi} interactions.
Proc.Natl.Acad.Sci.USA, 109:18755-18760, 2012
Cited by
PubMed Abstract: Alkyltransferase-like (ATL) proteins in Schizosaccharomyces pombe (Atl1) and Thermus thermophilus (TTHA1564) protect against the adverse effects of DNA alkylation damage by flagging O(6)-alkylguanine lesions for nucleotide excision repair (NER). We show that both ATL proteins bind with high affinity to oligodeoxyribonucleotides containing O(6)-alkylguanines differing in size, polarity, and charge of the alkyl group. However, Atl1 shows a greater ability than TTHA1564 to distinguish between O(6)-alkylguanine and guanine and in an unprecedented mechanism uses Arg69 to probe the electrostatic potential surface of O(6)-alkylguanine, as determined using molecular mechanics calculations. An unexpected consequence of this feature is the recognition of 2,6-diaminopurine and 2-aminopurine, as confirmed in crystal structures of respective Atl1-DNA complexes. O(6)-Alkylguanine and guanine discrimination is diminished for Atl1 R69A and R69F mutants, and S. pombe R69A and R69F mutants are more sensitive toward alkylating agent toxicity, revealing the key role of Arg69 in identifying O(6)-alkylguanines critical for NER recognition.
PubMed: 23112169
DOI: 10.1073/pnas.1209451109
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.702 Å)
Structure validation

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건을2024-11-06부터공개중

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