8IIP
Complex form of MsmUdgX H109Q mutant and uracil- obtained from uracil DNA (ttUtt) post its cleavage by MsmUdgX H109Q
Summary for 8IIP
Entry DOI | 10.2210/pdb8iip/pdb |
Descriptor | Type-4 uracil-DNA glycosylase, IRON/SULFUR CLUSTER, URACIL, ... (5 entities in total) |
Functional Keywords | udgx, h109q, uracil, complex, protein, dna binding protein |
Biological source | Mycolicibacterium smegmatis MC2 155 |
Total number of polymer chains | 1 |
Total formula weight | 22347.62 |
Authors | Aroli, S. (deposition date: 2023-02-24, release date: 2023-06-21, Last modification date: 2024-05-29) |
Primary citation | Aroli, S.,Woo, E.J.,Gopal, B.,Varshney, U. Mutational and structural analyses of UdgX: insights into the active site pocket architecture and its evolution. Nucleic Acids Res., 51:6554-6565, 2023 Cited by PubMed Abstract: UdgX excises uracil from uracil-containing DNA to concurrently form a covalent bond with the resulting AP-DNA. Structurally, UdgX is highly similar to family-4 UDGs (F4-UDGs). However, UdgX is unique in possessing a flexible R-loop (105KRRIH109). Among the class-defining motifs, while its motif A (51GEQPG55) diverged to possess Q53 in place of A53/G53 in F4-UDGs, motif B [178HPS(S/A)(L/V)(L/V)R184] has remained unchanged. Previously, we proposed an SN1 mechanism resulting in a covalent bond between H109 and AP-DNA. In this study, we investigated several single/double mutants of UdgX. The H109A, H109S, H109G, H109Q, H109C and H109K mutants gain conventional UDG activity to varying levels. The crystal structures of UdgX mutants show topological changes in their active sites, rationalizing their UDG activities. The E52Q, E52N and E52A mutants reveal that E52 forms a catalytic dyad with H109 to enhance its nucleophilicity. The Q53A mutant supports that UdgX specific evolution of Q53 occurred essentially to stabilize the R-loop conformation. The R184A mutation (motif B) supports the role of R184 in substrate-binding. Taken together, the structural, bioinformatics, and mutational studies suggest that UdgX diverged from F4-UDGs, and the emergence of the characteristic R-loop in UdgX is functionally assisted by A53/G53 to Q53 changes in motif A. PubMed: 37283083DOI: 10.1093/nar/gkad486 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.63 Å) |
Structure validation
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