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3BTZ

Crystal structure of human ABH2 cross-linked to dsDNA

Summary for 3BTZ
Entry DOI10.2210/pdb3btz/pdb
Related2FD8 2IUW 3BTX 3BTY 3BU0 3BUC
DescriptorAlpha-ketoglutarate-dependent dioxygenase alkB homolog 2, DNA (5'-D(*AP*GP*GP*TP*GP*AP*(2YR)P*AP*AP*TP*GP*CP*G)-3'), DNA (5'-D(*DTP*DCP*DGP*DCP*DAP*DTP*DTP*DAP*DTP*DCP*DAP*DCP*DC)-3'), ... (4 entities in total)
Functional Keywordsprotein/dna interaction, human dioxygenase, cross-link, dna repair, dna damage, iron, metal-binding, nucleus, oxidoreductase, oxidoreductase-dna complex, oxidoreductase/dna
Biological sourceHomo sapiens (human)
Cellular locationNucleus: Q6NS38
Total number of polymer chains3
Total formula weight30964.59
Authors
Yang, C.-G.,Yi, C.,He, C. (deposition date: 2007-12-31, release date: 2008-04-22, Last modification date: 2024-11-13)
Primary citationYang, C.G.,Yi, C.,Duguid, E.M.,Sullivan, C.T.,Jian, X.,Rice, P.A.,He, C.
Crystal structures of DNA/RNA repair enzymes AlkB and ABH2 bound to dsDNA.
Nature, 452:961-965, 2008
Cited by
PubMed Abstract: Escherichia coli AlkB and its human homologues ABH2 and ABH3 repair DNA/RNA base lesions by using a direct oxidative dealkylation mechanism. ABH2 has the primary role of guarding mammalian genomes against 1-meA damage by repairing this lesion in double-stranded DNA (dsDNA), whereas AlkB and ABH3 preferentially repair single-stranded DNA (ssDNA) lesions and can repair damaged bases in RNA. Here we show the first crystal structures of AlkB-dsDNA and ABH2-dsDNA complexes, stabilized by a chemical cross-linking strategy. This study reveals that AlkB uses an unprecedented base-flipping mechanism to access the damaged base: it squeezes together the two bases flanking the flipped-out one to maintain the base stack, explaining the preference of AlkB for repairing ssDNA lesions over dsDNA ones. In addition, the first crystal structure of ABH2, presented here, provides a structural basis for designing inhibitors of this human DNA repair protein.
PubMed: 18432238
DOI: 10.1038/nature06889
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3 Å)
Structure validation

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数据于2025-06-25公开中

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