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5JR4

Crystal structure of FimH A27V/V163A from E. coli UTI89 bound to FimG N-terminal extension

Summary for 5JR4
Entry DOI10.2210/pdb5jr4/pdb
Related5JQI
DescriptorType 1 fimbiral adhesin FimH, FimG N-terminal extension, GLYCEROL, ... (5 entities in total)
Functional Keywordslectin, immunoglobulin fold, carbohydrate binding protein, sugar binding protein, donor strand exchange
Biological sourceEscherichia coli (strain UTI89 / UPEC)
More
Total number of polymer chains2
Total formula weight30683.21
Authors
Kalas, V.,Hultgren, S.J. (deposition date: 2016-05-05, release date: 2017-02-22, Last modification date: 2024-10-23)
Primary citationKalas, V.,Pinkner, J.S.,Hannan, T.J.,Hibbing, M.E.,Dodson, K.W.,Holehouse, A.S.,Zhang, H.,Tolia, N.H.,Gross, M.L.,Pappu, R.V.,Janetka, J.,Hultgren, S.J.
Evolutionary fine-tuning of conformational ensembles in FimH during host-pathogen interactions.
Sci Adv, 3:e1601944-e1601944, 2017
Cited by
PubMed Abstract: Positive selection in the two-domain type 1 pilus adhesin FimH enhances fitness in urinary tract infection (UTI). We report a comprehensive atomic-level view of FimH in two-state conformational ensembles in solution, composed of one low-affinity tense (T) and multiple high-affinity relaxed (R) conformations. Positively selected residues allosterically modulate the equilibrium between these two conformational states, each of which engages mannose through distinct binding orientations. A FimH variant that only adopts the R state is severely attenuated early in a mouse model of uncomplicated UTI but is proficient at colonizing catheterized bladders in vivo or bladder transitional-like epithelial cells in vitro. Thus, the bladder habitat has barrier(s) to R state-mediated colonization possibly conferred by the terminally differentiated bladder epithelium and/or decoy receptors in urine. Together, our studies reveal the conformational landscape in solution, binding mechanisms, and adhesive strength of an allosteric two-domain adhesin that evolved "moderate" affinity to optimize persistence in the bladder during UTI.
PubMed: 28246638
DOI: 10.1126/sciadv.1601944
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.596 Å)
Structure validation

226707

数据于2024-10-30公开中

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