Structure of PDB 4cp9 Chain C Binding Site BS03
Receptor Information
>4cp9 Chain C (length=121) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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AWKGEVLANNEAGQVTSIIYNPGDVITIVAAGWASYGPTQKWGPQGDREH
PDQGLICHDAFCGALVMKIGNSGTIPVNTGLFRWVAPNNVQGAITLIYND
VPGTYGNNSGSFSVNIGKDQS
Ligand information
Ligand ID
CN8
InChI
InChI=1S/C22H32N8O3S/c1-3-24-21(32)19-10-15(12-26-19)27-22(33)18(23-2)11-16-13-30(29-28-16)9-8-25-20(31)14-4-6-17(34)7-5-14/h4-7,13,15,18-19,23,26,34H,3,8-12H2,1-2H3,(H,24,32)(H,25,31)(H,27,33)/t15-,18-,19-/m0/s1
InChIKey
VTNMGGUGQYETGZ-SNRMKQJTSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CCNC(=O)[C@@H]1C[C@@H](CN1)NC(=O)[C@H](Cc2cn(nn2)CCNC(=O)c3ccc(cc3)S)NC
CACTVS 3.385
CCNC(=O)[CH]1C[CH](CN1)NC(=O)[CH](Cc2cn(CCNC(=O)c3ccc(S)cc3)nn2)NC
CACTVS 3.385
CCNC(=O)[C@@H]1C[C@@H](CN1)NC(=O)[C@H](Cc2cn(CCNC(=O)c3ccc(S)cc3)nn2)NC
OpenEye OEToolkits 1.7.6
CCNC(=O)C1CC(CN1)NC(=O)C(Cc2cn(nn2)CCNC(=O)c3ccc(cc3)S)NC
ACDLabs 12.01
O=C(NCC)C3NCC(NC(=O)C(NC)Cc1nnn(c1)CCNC(=O)c2ccc(S)cc2)C3
Formula
C22 H32 N8 O3 S
Name
(4S)-N-ethyl-4-{[N-methyl-3-(1-{2-[(4-sulfanylbenzoyl)amino]ethyl}-1H-1,2,3-triazol-4-yl)-L-alanyl]amino}-L-prolinamide
ChEMBL
DrugBank
ZINC
ZINC000213028450
PDB chain
4cp9 Chain C Residue 1125 [
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Receptor-Ligand Complex Structure
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PDB
4cp9
A Leca Ligand Identified from a Galactoside-Conjugate Array Inhibits Host Cell Invasion by Pseudomonas Aeruginosa.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
H50 P51
Binding residue
(residue number reindexed from 1)
H50 P51
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0030246
carbohydrate binding
Biological Process
GO:0007157
heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
Cellular Component
GO:0005737
cytoplasm
GO:0009986
cell surface
GO:0042597
periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:4cp9
,
PDBe:4cp9
,
PDBj:4cp9
PDBsum
4cp9
PubMed
25044671
UniProt
Q05097
|PA1L_PSEAE PA-I galactophilic lectin (Gene Name=lecA)
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