期刊
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS
卷 68, 期 -, 页码 962-964出版社
INT UNION CRYSTALLOGRAPHY
DOI: 10.1107/S1744309112032435
关键词
REV1; REV3; REV7; translesion DNA synthesis
资金
- KAKENHI [18770091, 20770089, 22770109]
- Protein 3000 Project
- Targeted Proteins Research Program (TPRP)
- Grants-in-Aid for Scientific Research [22770109, 18770091, 24657076, 23121524, 20770089] Funding Source: KAKEN
REV1, REV3 and REV7 are pivotal proteins in translesion DNA synthesis that allows DNA synthesis to continue even in the presence of DNA damage. REV1 and REV3 are error-prone DNA polymerases, while REV7 acts as an adaptor protein that links them together. A ternary complex of the C-terminal domain of human REV1 in complex with REV7 bound to a REV3 fragment has been crystallized. The crystals belonged to space group P3121, with unit-cell parameters a = b = 74.7, c = 124.5 angstrom.
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