Ontology highlight
ABSTRACT:
SUBMITTER: De Bruyn P
PROVIDER: S-EPMC8488858 | biostudies-literature | 2021 Oct
REPOSITORIES: biostudies-literature
De Bruyn Pieter P Prolič-Kalinšek Maruša M Vandervelde Alexandra A Malfait Milan M Sterckx Yann G J YGJ Sobott Frank F Hadži San S Pardon Els E Steyaert Jan J Loris Remy R
Acta crystallographica. Section F, Structural biology communications 20210921 Pt 10
paaR2-paaA2-parE2 is a three-component toxin-antitoxin module found in prophage CP-993P of Escherichia coli O157:H7. Transcription regulation of this module occurs via the 123-amino-acid regulator PaaR2, which forms a large oligomeric structure. Despite appearing to be well folded, PaaR2 withstands crystallization, as does its N-terminal DNA-binding domain. Native mass spectrometry was used to screen for nanobodies that form a unique complex and stabilize the octameric structure of PaaR2. One su ...[more]