Structure of PDB 3o4k Chain A Binding Site BS01
Receptor Information
>3o4k Chain A (length=171) Species:
9838
(Camelus dromedarius) [
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EDPPACGSIVPRREWRALASECRERLTRPVRYVVVSHTAGSHCDTPASCA
QQAQNVQSYHVRNLGWCDVGYNFLIGEDGLVYEGRGWNIKGAHAGPTWNP
ISIGISFMGNYMNRVPPPRALRAAQNLLACGVALGALRSNYEVKGHRDVQ
PTLSPGDRLYEIIQTWSHYRA
Ligand information
Ligand ID
LTC
InChI
InChI=1S/C39H70N2O13/c1-5-7-9-11-12-13-14-15-16-17-18-20-22-31(45)52-28(24-49-30(44)21-19-10-8-6-2)25-50-39-36(48)37(34(46)29(23-42)53-39)54-38-33(41-27(4)43)35(47)32(40)26(3)51-38/h14-15,26,28-29,32-39,42,46-48H,5-13,16-25,40H2,1-4H3,(H,41,43)/b15-14-/t26-,28-,29-,32+,33-,34-,35+,36-,37+,38+,39+/m1/s1
InChIKey
PANDRCFROUDETH-PVQRVOPISA-N
SMILES
Software
SMILES
ACDLabs 11.02
O=C(NC2C(O)C(N)C(OC2OC1C(O)C(OC(OCC(OC(=O)CCCCC\C=C/CCCCCCC)COC(=O)CCCCCC)C1O)CO)C)C
OpenEye OEToolkits 1.7.0
CCCCCCCC=CCCCCCC(=O)OC(COC1C(C(C(C(O1)CO)O)OC2C(C(C(C(O2)C)N)O)NC(=O)C)O)COC(=O)CCCCCC
CACTVS 3.352
CCCCCCCC=CCCCCCC(=O)O[CH](CO[CH]1O[CH](CO)[CH](O)[CH](O[CH]2O[CH](C)[CH](N)[CH](O)[CH]2NC(C)=O)[CH]1O)COC(=O)CCCCCC
OpenEye OEToolkits 1.7.0
CCCCCCCC=CCCCCCC(=O)O[C@@H](CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O[C@H]2[C@@H]([C@H]([C@H]([C@H](O2)C)N)O)NC(=O)C)O)COC(=O)CCCCCC
CACTVS 3.352
CCCCCCC\C=C/CCCCCC(=O)O[C@@H](CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](C)[C@H](N)[C@H](O)[C@H]2NC(C)=O)[C@H]1O)COC(=O)CCCCCC
Formula
C39 H70 N2 O13
Name
(2S)-1-({3-O-[2-(acetylamino)-4-amino-2,4,6-trideoxy-beta-D-galactopyranosyl]-alpha-D-glucopyranosyl}oxy)-3-(heptanoyloxy)propan-2-yl (7Z)-pentadec-7-enoate;
Lipoteichoic acid
ChEMBL
DrugBank
ZINC
ZINC000098209129
PDB chain
3o4k Chain C Residue 172 [
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Receptor-Ligand Complex Structure
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PDB
3o4k
Structural basis of recognition of pathogen-associated molecular patterns and inhibition of proinflammatory cytokines by camel peptidoglycan recognition protein
Resolution
2.11 Å
Binding residue
(original residue number in PDB)
R31 N140 E142
Binding residue
(residue number reindexed from 1)
R31 N140 E142
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=7.62,Kd=24nM
Enzymatic activity
Catalytic site (original residue number in PDB)
Y71 T152
Catalytic site (residue number reindexed from 1)
Y71 T152
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008745
N-acetylmuramoyl-L-alanine amidase activity
GO:0016019
peptidoglycan immune receptor activity
GO:0042834
peptidoglycan binding
Biological Process
GO:0001818
negative regulation of cytokine production
GO:0009253
peptidoglycan catabolic process
GO:0016045
detection of bacterium
GO:0042742
defense response to bacterium
GO:0045087
innate immune response
GO:0050830
defense response to Gram-positive bacterium
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3o4k
,
PDBe:3o4k
,
PDBj:3o4k
PDBsum
3o4k
PubMed
21454594
UniProt
Q9GK12
|PGRP1_CAMDR Peptidoglycan recognition protein 1 (Gene Name=PGLYRP1)
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