3F1W

Crystal structure of a mutant proliferating cell nuclear antigen that blocks translesion synthesis

3F1W の概要

• エントリーDOI: 10.2210/pdb3f1w/pdb
• 分子名称: Proliferating cell nuclear antigen (1 entity in total)
• 機能のキーワード: dna binding, dna clamp, dna damage, dna repair, dna replication, dna-binding, nucleus, ubl conjugation, replication
• 由来する生物種: Saccharomyces cerevisiae (brewer's yeast,lager beer yeast,yeast)
• 細胞内の位置: Nucleus: P15873
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 28974.08

構造登録者

Freudenthal, B.D.,Ramaswamy, S.,Washington, M.T. (登録日: 2008-10-28, 公開日: 2008-12-23, 最終更新日: 2023-09-06)

主引用文献

Freudenthal, B.D.,Ramaswamy, S.,Hingorani, M.M.,Washington, M.T.
Structure of a Mutant Form of Proliferating Cell Nuclear Antigen That Blocks Translesion DNA Synthesis.
Biochemistry, 47:13354-13361, 2008

PubMed Abstract: Proliferating cell nuclear antigen (PCNA) is a homotrimeric protein that functions as a sliding clamp during DNA replication. Several mutant forms of PCNA that block translesion DNA synthesis have been identified in genetic studies in yeast. One such mutant protein (encoded by the rev6-1 allele) is a glycine to serine substitution at residue 178, located at the subunit interface of PCNA. To improve our understanding of how this substitution interferes with translesion synthesis, we have determined the X-ray crystal structure of the PCNA G178S mutant protein. This substitution has little effect on the structure of the domain in which the substitution occurs. Instead, significant, local structural changes are observed in the adjacent subunit. The most notable difference between mutant and wild-type structures is in a single, extended loop (comprising amino acid residues 105-110), which we call loop J. In the mutant protein structure, loop J adopts a very different conformation in which the atoms of the protein backbone have moved by as much as 6.5 A from their positions in the wild-type structure. To improve our understanding of the functional consequences of this structural change, we have examined the ability of this mutant protein to stimulate nucleotide incorporation by DNA polymerase eta (pol eta). Steady state kinetic studies show that while wild-type PCNA stimulates incorporation by pol eta opposite an abasic site, the mutant PCNA protein actually inhibits incorporation opposite this DNA lesion. These results show that the position of loop J in PCNA plays an essential role in facilitating translesion synthesis.

PubMed: 19053247
DOI: 10.1021/bi8017762

実験手法

X-RAY DIFFRACTION (2.901 Å)