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3RZM

Duplex Interrogation by a Direct DNA Repair Protein in the Search of Damage

Summary for 3RZM
Entry DOI10.2210/pdb3rzm/pdb
Related3RZG 3RZH 3RZJ 3RZK 3RZL
DescriptorAlpha-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 Keywordsprotein-dna complex, jelly-roll, demethylase, nucleus, oxidoreductase-dna complex, oxidoreductase/dna
Biological sourceHomo sapiens (human)
Cellular locationNucleus: Q6NS38
Total number of polymer chains3
Total formula weight31464.13
Authors
Yi, C.,Chen, B.,Qi, B.,Zhang, W.,Jia, G.,Zhang, L.,Li, C.,Dinner, A.,Yang, C.,He, C. (deposition date: 2011-05-11, release date: 2012-06-06, Last modification date: 2023-11-01)
Primary citationYi, 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: 22659876
DOI: 10.1038/nsmb.2320
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.06 Å)
Structure validation

226707

数据于2024-10-30公开中

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