| Literature DB >> 29119630 |
Jan Abendroth1,2, Andrew Frando3,4, Isabelle Q Phan2,3, Bart L Staker2,3, Peter J Myler2,3,4,5, Thomas E Edwards1,2, Christoph Grundner3,4.
Abstract
The genome of the human pathogen Mycobacterium tuberculosis (Mtb) encodes ∼4,400 proteins, but one third of them have unknown functions. We solved the crystal structure of Rv3651, a hypothetical protein with no discernible similarity to proteins with known function. Rv3651 has a three-domain architecture that combines one cGMP-specific phosphodiesterases, adenylyl cyclases and FhlA (GAF) domain and two Per-ARNT-Sim (PAS) domains. GAF and PAS domains are sensor domains that are typically linked to signaling effector molecules. Unlike these sensor-effector proteins, Rv3651 is an unusual sensor domain-only protein with highly divergent sequence. The structure suggests that Rv3651 integrates multiple different signals and serves as a scaffold to facilitate signal transfer.Entities:
Keywords: GAF domain; Mycobacterium tuberculosis; PAS domain; proteins of unknown function
Mesh:
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Year: 2017 PMID: 29119630 PMCID: PMC5775179 DOI: 10.1002/pro.3343
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725