Structure of PDB 4x5r Chain B Binding Site BS01
Receptor Information
>4x5r Chain B (length=158) Species:
83333
(Escherichia coli K-12) [
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FACKTANGTAIPIGGGSANVYVNLAPVVNVGQNLVVDLSTQIFCHNDYPE
TITDYVTLQRGSAYGGVLSNFSGTVKYSGSSYPFPTTSETPRVVYNSRTD
KPWPVALYLTPVSSAGGVAIKAGSLIAVLILRQTNNYNSDDFQFVWNIYA
NNDVVVPT
Ligand information
Ligand ID
3XO
InChI
InChI=1S/C21H26ClN3O8/c1-24-4-6-25(7-5-24)15-14(17(28)18(15)29)23-10-2-3-12(11(22)8-10)32-21-20(31)19(30)16(27)13(9-26)33-21/h2-3,8,13,16,19-21,23,26-27,30-31H,4-7,9H2,1H3/t13-,16-,19+,20+,21+/m1/s1
InChIKey
OVFSRWMGARZIAS-YVNBQAQUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.9.2
CN1CCN(CC1)C2=C(C(=O)C2=O)Nc3ccc(c(c3)Cl)OC4C(C(C(C(O4)CO)O)O)O
ACDLabs 12.01
O=C2C(N1CCN(C)CC1)=C(C2=O)Nc4ccc(OC3OC(C(O)C(O)C3O)CO)c(Cl)c4
CACTVS 3.385
CN1CCN(CC1)C2=C(Nc3ccc(O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)c(Cl)c3)C(=O)C2=O
OpenEye OEToolkits 1.9.2
CN1CCN(CC1)C2=C(C(=O)C2=O)Nc3ccc(c(c3)Cl)O[C@@H]4[C@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
CACTVS 3.385
CN1CCN(CC1)C2=C(Nc3ccc(O[CH]4O[CH](CO)[CH](O)[CH](O)[CH]4O)c(Cl)c3)C(=O)C2=O
Formula
C21 H26 Cl N3 O8
Name
2-chloro-4-{[2-(4-methylpiperazin-1-yl)-3,4-dioxocyclobut-1-en-1-yl]amino}phenyl alpha-D-mannopyranoside
ChEMBL
CHEMBL2177628
DrugBank
ZINC
ZINC000103074417
PDB chain
4x5r Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4x5r
The Tyrosine Gate of the Bacterial Lectin FimH: A Conformational Analysis by NMR Spectroscopy and X-ray Crystallography.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
F1 I13 N46 D47 Y48 I52 D54 Q133 N135 D140
Binding residue
(residue number reindexed from 1)
F1 I13 N46 D47 Y48 I52 D54 Q133 N135 D140
Annotation score
1
Binding affinity
MOAD
: Kd=14nM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0007155
cell adhesion
Cellular Component
GO:0009289
pilus
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Biological Process
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Cellular Component
External links
PDB
RCSB:4x5r
,
PDBe:4x5r
,
PDBj:4x5r
PDBsum
4x5r
PubMed
25940742
UniProt
P08191
|FIMH_ECOLI Type 1 fimbrin D-mannose specific adhesin (Gene Name=fimH)
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