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Structure 2012-07-03

Structural Insights into the Role of Domain Flexibility in Human DNA Ligase IV

Takashi Ochi, Qian Wu, Dimitri Y. Chirgadze, J. Günter Grossmann, Victor M. Bolanos-Garcia, Tom L. Blundell

文献索引:Structure 20(7) , 1212-22, (2012)

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摘要

Knowledge of the architecture of DNA ligase IV (LigIV) and interactions with XRCC4 and XLF-Cernunnos is necessary for understanding its role in the ligation of double-strand breaks during nonhomologous end joining. Here we report the structure of a subdomain of the nucleotidyltrasferase domain of human LigIV and provide insights into the residues associated with LIG4 syndrome. We use this structural information together with the known structures of the BRCT/XRCC4 complex and those of LigIV orthologs to interpret small-angle X-ray scattering of LigIV in complex with XRCC4 and size exclusion chromatography of LigIV, XRCC4, and XLF-Cernunnos. Our results suggest that the flexibility of the catalytic region is limited in a manner that affects the formation of the LigIV/XRCC4/XLF-Cernunnos complex.

相关化合物

结构式 名称/CAS号 全部文献
T4 DNA连接酶 结构式 T4 DNA连接酶
CAS:9015-85-4