3RZM
Duplex Interrogation by a Direct DNA Repair Protein in the Search of Damage
Summary for 3RZM
Entry DOI | 10.2210/pdb3rzm/pdb |
Related | 3RZG 3RZH 3RZJ 3RZK 3RZL |
Descriptor | Alpha-ketoglutarate-dependent dioxygenase alkB homolog 2, 5'-D(*AP*TP*GP*TP*AP*TP*AP*AP*CP*TP*GP*CP*G)-3', 5'-D(*TP*CP*GP*CP*AP*GP*TP*TP*AP*TP*AP*CP*A)-3', ... (4 entities in total) |
Functional Keywords | protein-dna complex, jelly-roll, demethylase, nucleus, oxidoreductase-dna complex, oxidoreductase/dna |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus: Q6NS38 |
Total number of polymer chains | 3 |
Total formula weight | 31464.13 |
Authors | |
Primary citation | Yi, C.,Chen, B.,Qi, B.,Zhang, W.,Jia, G.,Zhang, L.,Li, C.J.,Dinner, A.R.,Yang, C.G.,He, C. Duplex interrogation by a direct DNA repair protein in search of base damage Nat.Struct.Mol.Biol., 19:671-676, 2012 Cited by PubMed Abstract: ALKBH2 is a direct DNA repair dioxygenase guarding the mammalian genome against N(1)-methyladenine, N(3)-methylcytosine and 1,N(6)-ethenoadenine damage. A prerequisite for repair is to identify these lesions in the genome. Here we present crystal structures of human ALKBH2 bound to different duplex DNAs. Together with computational and biochemical analyses, our results suggest that DNA interrogation by ALKBH2 has two previously unknown features: (i) ALKBH2 probes base-pair stability and detects base pairs with reduced stability, and (ii) ALKBH2 does not have nor need a damage-checking site, which is critical for preventing spurious base cleavage for several glycosylases. The demethylation mechanism of ALKBH2 insures that only cognate lesions are oxidized and reversed to normal bases, and that a flipped, non-substrate base remains intact in the active site. Overall, the combination of duplex interrogation and oxidation chemistry allows ALKBH2 to detect and process diverse lesions efficiently and correctly. PubMed: 22659876DOI: 10.1038/nsmb.2320 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.06 Å) |
Structure validation
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