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4YX9

Crystal structure of the CFTR inhibitory factor Cif bound to tiratricol

Summary for 4YX9
Entry DOI10.2210/pdb4yx9/pdb
Related3KD2
DescriptorCFTR inhibitory factor, [4-(4-HYDROXY-3-IODO-PHENOXY)-3,5-DIIODO-PHENYL]-ACETIC ACID (3 entities in total)
Functional Keywordsinhibitor, enzyme, cif, cftr, epoxide hydrolase, alpha beta hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourcePseudomonas aeruginosa (strain UCBPP-PA14)
Total number of polymer chains4
Total formula weight139146.52
Authors
Bahl, C.D.,Madden, D.R. (deposition date: 2015-03-22, release date: 2015-07-15, Last modification date: 2024-10-16)
Primary citationBahl, C.D.,Hvorecny, K.L.,Bomberger, J.M.,Stanton, B.A.,Hammock, B.D.,Morisseau, C.,Madden, D.R.
Inhibiting an Epoxide Hydrolase Virulence Factor from Pseudomonas aeruginosa Protects CFTR.
Angew.Chem.Int.Ed.Engl., 54:9881-9885, 2015
Cited by
PubMed Abstract: Opportunistic pathogens exploit diverse strategies to sabotage host defenses. Pseudomonas aeruginosa secretes the CFTR inhibitory factor Cif and thus triggers loss of CFTR, an ion channel required for airway mucociliary defense. However, the mechanism of action of Cif has remained unclear. It catalyzes epoxide hydrolysis, but there is no known role for natural epoxides in CFTR regulation. It was demonstrated that the hydrolase activity of Cif is strictly required for its effects on CFTR. A small-molecule inhibitor that protects this key component of the mucociliary defense system was also uncovered. These results provide a basis for targeting the distinctive virulence chemistry of Cif and suggest an unanticipated role of physiological epoxides in intracellular protein trafficking.
PubMed: 26136396
DOI: 10.1002/anie.201503983
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

226707

數據於2024-10-30公開中

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