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PMID: 19836329 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Structure and signaling mechanism of Per-ARNT-Sim domains.

Structure (London, England : 1993) ·Vol. 17 ·No. 10 ·2009-10-14 ·Pages 1282-94

Möglich A, Ayers RA, Moffat K

Abstract

Per-ARNT-Sim (PAS) domains serve as versatile sensor and interaction modules in signal transduction proteins. PAS sensors detect chemical and physical stimuli and regulate the activity of functionally diverse effector domains. In contrast to this chemical, physical, and functional diversity, the structure of the core of PAS domains is broadly conserved and comprises a five-stranded antiparallel beta sheet and several alpha helices. Signals originate within the conserved core and generate structural and dynamic changes predominantly within the beta sheet, from which they propagate via amphipathic alpha-helical and coiled-coil linkers at the N or C termini of the core to the covalently attached effector domain. Effector domains are typically dimeric; their activity appears to be largely regulated by signal-dependent changes in quaternary structure and dynamics. The signaling mechanisms of PAS and other signaling domains share common features, and these commonalities can be exploited to enable structure-based design of artificial photosensors and chemosensors.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Humans Models, Molecular Molecular Sequence Data Protein Serine-Threonine Kinases/chemistry,metabolism Protein Structure, Tertiary Signal Transduction
Chemicals
PAS domain kinases Protein Serine-Threonine Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Möglich Andreas
Department of Biochemistry and Molecular Biology, Institute for Biophysical Dynamics, University of Chicago, 929 East 57th Street, Chicago, IL 60637, USA.
Ayers Rebecca A
Moffat Keith
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Article Info
Journal
Structure (London, England : 1993)
Abbr.
Structure
ISSN
1878-4186
Published
2009-10-14
Pages
1282-94
Language
English
Region
United States
NLM ID
101087697
PMCID
PMC3092527
Subset
IM
Grants
NCRR NIH HHS · P41 RR007707 · United States
NCRR NIH HHS · P41 RR007707-130233 · United States
NIGMS NIH HHS · GM 036452 · United States
NIGMS NIH HHS · R37 GM036452 · United States
NIGMS NIH HHS · R01 GM036452-24 · United States
NIGMS NIH HHS · R01 GM036452 · United States
NCRR NIH HHS · P41 RR007707-17 · United States
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