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

9IBO

VC0430/VcGluP bound to glutamate

Summary for 9IBO
Entry DOI10.2210/pdb9ibo/pdb
DescriptorTAXI family TRAP transporter solute-binding subunit, SODIUM ION, GLUTAMIC ACID, ... (4 entities in total)
Functional Keywordstaxi trap secreted, transport protein
Biological sourceVibrio cholerae
Total number of polymer chains1
Total formula weight32610.48
Authors
Jimmy, S.,Sondermann, H. (deposition date: 2025-02-13, release date: 2025-12-24)
Primary citationPotapova, A.,Oguchi, R.,Jimmy, S.,Evans, C.R.,Yarrington, K.D.,Winans, J.B.,Piepoli, S.,Older, E.A.,Schakel, O.F.,Wetherington, M.T.,Garvey, W.,Floyd, K.A.,Vinogradov, E.,Yunker, P.J.,Sanchez, L.M.,Nadell, C.D.,Limoli, D.H.,Dietrich, L.E.P.,Sondermann, H.,Yildiz, F.H.
Vibrio cholerae biofilm matrix assembly and growth are shaped by a glutamate-specific TAXI/TRAP protein.
Proc.Natl.Acad.Sci.USA, 122:e2504869122-e2504869122, 2025
Cited by
PubMed Abstract: Biofilms are critical for the environmental persistence, survival, and infectivity of , the causative agent of cholera. Here, we find that GluP, a glutamate-specific TRAP-TAXI protein, is an uncharacterized matrix component that plays a critical role in biofilm architecture. Loss of GluP reduces biofilm corrugation, expands colony size, and disperses cells from microcolonies, arguing that this factor maintains biofilm structure and organization. While GluP does not affect the abundance or localization of known matrix proteins, its absence reduces exopolysaccharide (VPS) production. We determined the crystal structure of GluP, which revealed that GluP binds glutamate, and its biofilm-related phenotypes depend on this binding capability. We further examined the role of GluP in growth under defined conditions where L-glutamate serves as a carbon source, nitrogen source, or both. GluP-deficient strains specifically showed reduced growth when glucose was the carbon source and glutamate the nitrogen source. This defect is dependent on glutamate binding by GluP and highlights its role in coordinating nutrient acquisition and biofilm formation. Importantly, both biofilm assembly and growth defects occurred independently of the predicted membrane component of the Glu TRAP-TAXI system, GluQM. These findings indicate that GluP plays a dual role in biofilm assembly and growth, providing insight into its functional importance in physiology.
PubMed: 41364770
DOI: 10.1073/pnas.2504869122
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.08 Å)
Structure validation

250359

PDB entries from 2026-03-11

PDB statisticsPDBj update infoContact PDBjnumon