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3GPX

Sequence-matched MutM Interrogation Complex 4 (IC4)

Summary for 3GPX
Entry DOI10.2210/pdb3gpx/pdb
Related3GPP 3GPU 3GPY 3GQ3 3GQ4 3GQ5
DescriptorDNA glycosylase, DNA (5'-D(*A*GP*GP*TP*AP*GP*AP*CP*TP*CP*GP*GP*AP*CP*GP*C)-3'), DNA (5'-D(*TP*GP*CP*GP*TP*CP*CP*GP*AP*GP*TP*CP*TP*AP*CP*C)-3'), ... (5 entities in total)
Functional Keywordsdna glycosylase, dna repair, damage search, base extrusion, disulfide crosslinking, dna damage, dna-binding, glycosidase, hydrolase, lyase, metal-binding, multifunctional enzyme, zinc-finger, lyase-dna complex, lyase/dna
Biological sourceGeobacillus stearothermophilus (Geobacillus stearothermophilus)
Total number of polymer chains3
Total formula weight38733.29
Authors
Spong, M.C.,Qi, Y.,Verdine, G.L. (deposition date: 2009-03-23, release date: 2009-11-10, Last modification date: 2024-02-21)
Primary citationQi, Y.,Spong, M.C.,Nam, K.,Banerjee, A.,Jiralerspong, S.,Karplus, M.,Verdine, G.L.
Encounter and extrusion of an intrahelical lesion by a DNA repair enzyme.
Nature, 462:762-766, 2009
Cited by
PubMed Abstract: How living systems detect the presence of genotoxic damage embedded in a million-fold excess of undamaged DNA is an unresolved question in biology. Here we have captured and structurally elucidated a base-excision DNA repair enzyme, MutM, at the stage of initial encounter with a damaged nucleobase, 8-oxoguanine (oxoG), nested within a DNA duplex. Three structures of intrahelical oxoG-encounter complexes are compared with sequence-matched structures containing a normal G base in place of an oxoG lesion. Although the protein-DNA interfaces in the matched complexes differ by only two atoms-those that distinguish oxoG from G-their pronounced structural differences indicate that MutM can detect a lesion in DNA even at the earliest stages of encounter. All-atom computer simulations show the pathway by which encounter of the enzyme with the lesion causes extrusion from the DNA duplex, and they elucidate the critical free energy difference between oxoG and G along the extrusion pathway.
PubMed: 20010681
DOI: 10.1038/nature08561
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.78 Å)
Structure validation

236371

数据于2025-05-21公开中

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