Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

6Y45

Crystal Structure of the H33A variant of RsrR

Summary for 6Y45
Entry DOI10.2210/pdb6y45/pdb
DescriptorRrf2 family transcriptional regulator, FE2/S2 (INORGANIC) CLUSTER, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (7 entities in total)
Functional Keywordsredox sensor, iron sulfur cluster, transcription
Biological sourceStreptomyces venezuelae (strain ATCC 10712 / CBS 650.69 / DSM 40230 / JCM 4526 / NBRC 13096 / PD 04745)
Total number of polymer chains4
Total formula weight71238.58
Authors
Rohac, R.,Volbeda, A.,Fontecilla-Camps, J.C. (deposition date: 2020-02-19, release date: 2020-03-04, Last modification date: 2024-01-24)
Primary citationCrack, J.C.,Amara, P.,Volbeda, A.,Mouesca, J.M.,Rohac, R.,Pellicer Martinez, M.T.,Huang, C.Y.,Gigarel, O.,Rinaldi, C.,Le Brun, N.E.,Fontecilla-Camps, J.C.
Electron and Proton Transfers Modulate DNA Binding by the Transcription Regulator RsrR.
J.Am.Chem.Soc., 142:5104-5116, 2020
Cited by
PubMed Abstract: The [FeS]-RsrR gene transcription regulator senses the redox status in bacteria by modulating DNA binding, while its cluster cycles between +1 and +2 states-only the latter binds DNA. We have previously shown that RsrR can undergo remarkable conformational changes involving a 100° rotation of tryptophan 9 between exposed () and buried () states. Here, we have used the chemical modification of Trp9, site-directed mutagenesis, and crystallographic and computational chemical studies to show that (i) the and states correspond to oxidized and reduced RsrR, respectively, (ii) His33 is protonated in the state due to a change in its p caused by cluster reduction, and (iii) Trp9 rotation is conditioned by the response of its dipole moment to environmental electrostatic changes. Our findings illustrate a novel function of protonation resulting from electron transfer.
PubMed: 32078310
DOI: 10.1021/jacs.9b12250
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.68 Å)
Structure validation

234136

PDB entries from 2025-04-02

PDB statisticsPDBj update infoContact PDBjnumon