7PBK

Vibriophage phiVC8 family A DNA polymerase (DpoZ), two conformations: thumb-exo open and thumb-exo closed

7PBK の概要

• エントリーDOI: 10.2210/pdb7pbk/pdb
• 分子名称: DNA polymerase I (2 entities in total)
• 機能のキーワード: phivc8, pola, dpoz, thumb-exo open, thumb-exo closed, viral protein
• 由来する生物種: Vibrio phage phiVC8
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 145685.52

構造登録者

Czernecki, D.,Hu, H.,Romoli, F.,Delarue, M. (登録日: 2021-08-02, 公開日: 2021-11-17, 最終更新日: 2024-01-31)

主引用文献

Czernecki, D.,Hu, H.,Romoli, F.,Delarue, M.
Structural dynamics and determinants of 2-aminoadenine specificity in DNA polymerase DpoZ of vibriophage phi VC8.
Nucleic Acids Res., 49:11974-11985, 2021

PubMed Abstract: All genetic information in cellular life is stored in DNA copolymers composed of four basic building blocks (ATGC-DNA). In contrast, a group of bacteriophages belonging to families Siphoviridae and Podoviridae has abandoned the usage of one of them, adenine (A), replacing it with 2-aminoadenine (Z). The resulting ZTGC-DNA is more stable than its ATGC-DNA counterpart, owing to the additional hydrogen bond present in the 2-aminoadenine:thymine (Z:T) base pair, while the additional amino group also confers resistance to the host endonucleases. Recently, two classes of replicative proteins found in ZTGC-DNA-containing phages were characterized and one of them, DpoZ from DNA polymerase A (PolA) family, was shown to possess significant Z-vs-A specificity. Here, we present the crystallographic structure of the apo form of DpoZ of vibriophage ϕVC8, composed of the 3'-5' exonuclease and polymerase domains. We captured the enzyme in two conformations that involve the tip of the thumb subdomain and the exonuclease domain. We highlight insertions and mutations characteristic of ϕVC8 DpoZ and its close homologues. Through mutagenesis and functional assays we suggest that the preference of ϕVC8 DpoZ towards Z relies on a polymerase backtracking process, more efficient when the nascent base pair is A:T than when it is Z:T.

PubMed: 34751404
DOI: 10.1093/nar/gkab955

実験手法

X-RAY DIFFRACTION (2.8 Å)