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4MEA

Crystal structure of the Cif epoxide hydrolase from Acinetobacter nosocomialis

Summary for 4MEA
Entry DOI10.2210/pdb4mea/pdb
Related3KD2 4MEB
DescriptorPredicted protein (2 entities in total)
Functional Keywordsalpha/beta hydrolase fold, epoxide hydrolase, secreted, hydrolase
Biological sourceAcinetobacter sp. RUH2624
Total number of polymer chains2
Total formula weight73715.72
Authors
Bahl, C.D.,Madden, D.R. (deposition date: 2013-08-25, release date: 2014-02-05, Last modification date: 2023-09-20)
Primary citationBahl, C.D.,Hvorecny, K.L.,Bridges, A.A.,Ballok, A.E.,Bomberger, J.M.,Cady, K.C.,O'Toole, G.A.,Madden, D.R.
Signature motifs identify an acinetobacter cif virulence factor with epoxide hydrolase activity.
J.Biol.Chem., 289:7460-7469, 2014
Cited by
PubMed Abstract: Endocytic recycling of the cystic fibrosis transmembrane conductance regulator (CFTR) is blocked by the CFTR inhibitory factor (Cif). Originally discovered in Pseudomonas aeruginosa, Cif is a secreted epoxide hydrolase that is transcriptionally regulated by CifR, an epoxide-sensitive repressor. In this report, we investigate a homologous protein found in strains of the emerging nosocomial pathogens Acinetobacter nosocomialis and Acinetobacter baumannii ("aCif"). Like Cif, aCif is an epoxide hydrolase that carries an N-terminal secretion signal and can be purified from culture supernatants. When applied directly to polarized airway epithelial cells, mature aCif triggers a reduction in CFTR abundance at the apical membrane. Biochemical and crystallographic studies reveal a dimeric assembly with a stereochemically conserved active site, confirming our motif-based identification of candidate Cif-like pathogenic EH sequences. Furthermore, cif expression is transcriptionally repressed by a CifR homolog ("aCifR") and is induced in the presence of epoxides. Overall, this Acinetobacter protein recapitulates the essential attributes of the Pseudomonas Cif system and thus may facilitate airway colonization in nosocomial lung infections.
PubMed: 24474692
DOI: 10.1074/jbc.M113.518092
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

238895

數據於2025-07-16公開中

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