ORC1:H4K20Me2-nucleosome [nucleoplasm]

Stable Identifier
R-HSA-9749192
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
25689043 A Meier-Gorlin syndrome mutation impairs the ORC1-nucleosome association

Song, J, Gozani, O, Zhang, W, Sankaran, S

ACS Chem Biol 2015
22398447 The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome

Song, J, Gozani, O, Patel, DJ, Cheung, P, Chen, JK, Yamazoe, S, Ishibe-Murakami, S, Kuo, AJ

Nature 2012
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