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

3USX

Crystal structure of PGRP-S complexed with Myristic Acid at 2.28 A resolution

Summary for 3USX
Entry DOI10.2210/pdb3usx/pdb
Related3C2X
DescriptorPeptidoglycan recognition protein 1, MYRISTIC ACID, GLYCEROL, ... (4 entities in total)
Functional Keywordsimmune response, secreted, antimicrobial, pgrp-s, antibiotic, peptidoglycan binding, immune system
Biological sourceCamelus dromedarius (camel)
Cellular locationSecreted (By similarity): Q9GK12
Total number of polymer chains4
Total formula weight76366.30
Authors
Yamini, S.,Sharma, P.,Sinha, M.,Kaur, P.,Sharma, S.,Singh, T.P. (deposition date: 2011-11-24, release date: 2012-01-11, Last modification date: 2024-11-13)
Primary citationSharma, P.,Yamini, S.,Dube, D.,Singh, A.,Mal, G.,Pandey, N.,Sinha, M.,Singh, A.K.,Dey, S.,Kaur, P.,Mitra, D.K.,Sharma, S.,Singh, T.P.
Structural basis of the binding of fatty acids to peptidoglycan recognition protein, PGRP-S through second binding site
Arch.Biochem.Biophys., 529:1-10, 2013
Cited by
PubMed Abstract: Short peptidoglycan recognition protein (PGRP-S) is a member of the mammalian innate immune system. PGRP-S from Camelus dromedarius (CPGRP-S) has been shown to bind to lipopolysaccharide (LPS), lipoteichoic acid (LTA) and peptidoglycan (PGN). Its structure consists of four molecules A, B, C and D with ligand binding clefts situated at A-B and C-D contacts. It has been shown that LPS, LTA and PGN bind to CPGRP-S at C-D contact. The cleft at the A-B contact indicated features that suggested a possible binding of fatty acids including mycolic acid of Mycobacterium tuberculosis. Therefore, binding studies of CPGRP-S were carried out with fatty acids, butyric acid, lauric acid, myristic acid, stearic acid and mycolic acid which showed affinities in the range of 10(-5) to 10(-8) M. Structure determinations of the complexes of CPGRP-S with above fatty acids showed that they bound to CPGRP-S in the cleft at the A-B contact. The flow cytometric studies showed that mycolic acid induced the production of pro-inflammatory cytokines, TNF-α and IFN-γ by CD3+ T cells. The concentrations of cytokines increased considerably with increasing concentrations of mycolic acid. However, their levels decreased substantially on adding CPGRP-S.
PubMed: 23149273
DOI: 10.1016/j.abb.2012.11.001
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.28 Å)
Structure validation

247947

PDB entries from 2026-01-21

PDB statisticsPDBj update infoContact PDBjnumon