The DOI matches its Crossref record; 66 of the 66 references it cites were found in a registry or an index.
Crystal Structure of the Heterodimeric CLOCK:BMAL1 Transcriptional Activator Complex
Open accessAbstract
A Timely Structure: The physiology and behavior of most organisms are inextricably aligned with the day/night cycle. In mammals, these daily rhythms are generated by a circadian clock encoded by transcriptional activators and repressors operating in a feedback loop that takes about 24 hours to complete. A key participant in this loop is a heterodimeric transcriptional activator consisting of the CLOCK and BMAL1 proteins. Huang et al. (p. 189 , published online 31 May; see Perspective by Crane ) determined the crystal structure of a complex containing the PAS domains (implicated in protein-protein interactions) and the basic helix-loop-helix domains (implicated in DNA binding) from each protein. CLOCK and BMAL1 were observed to be tightly intertwined in an unusual asymmetric conformation, which may contribute to the stability and activity of the complex.
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Metadata
- Authors
- Huang, N., Chelliah, Y., Shan, Y., Taylor, C. A., Yoo, S.-H., Partch, C., Green, C. B., Zhang, H., & Takahashi, J. S.
- Venue
- Science
- Published
- 2012-07-13
- Volume
- 337
- Issue
- 6091
- Pages
- 189-194
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2088724035
- Cited by
- 349
- References
- 66
- FWCI
- 9.11
- Type
- journal article
- Language
- en
- Open access
- green
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