Structure of PDB 4dfu Chain B Binding Site BS02
Receptor Information
>4dfu Chain B (length=297) Species:
37734
(Enterococcus casseliflavus) [
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TYTFDQVEKAIEQLYPDFTINTIEISGEGNDCIAYEINRDFIFKFPKHSR
GSTNLFNEVNILKRIHNKLPLPIPEVVFTGMPSETYQMSFAGFTKIKGVP
LTPLLLNNLPKQSQNQAAKDLARFLSELHSINISGFKSNLVLDFREKINE
DNKKIKKLLSRELKGPQMKKVDDFYRDILENEIYFKYYPCLIHNDFSSDH
ILFDTEKNTICGIIDFGDAAISDPDNDFISLMEDDEEYGMEFVSKILNHY
KHKDIPTVLEKYRMKEKYWSFEKIIYGKEYGYMDWYEEGLNEIRSIK
Ligand information
Ligand ID
KAN
InChI
InChI=1S/C18H36N4O11/c19-2-6-10(25)12(27)13(28)18(30-6)33-16-5(21)1-4(20)15(14(16)29)32-17-11(26)8(22)9(24)7(3-23)31-17/h4-18,23-29H,1-3,19-22H2/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-/m1/s1
InChIKey
SBUJHOSQTJFQJX-NOAMYHISSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC[CH]1O[CH](O[CH]2[CH](N)C[CH](N)[CH](O[CH]3O[CH](CO)[CH](O)[CH](N)[CH]3O)[CH]2O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04
O(C2C(O)C(OC1OC(CN)C(O)C(O)C1O)C(N)CC2N)C3OC(C(O)C(N)C3O)CO
OpenEye OEToolkits 1.5.0
C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CN)O)O)O)O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)N)O)N
OpenEye OEToolkits 1.5.0
C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N
Formula
C18 H36 N4 O11
Name
KANAMYCIN A
ChEMBL
CHEMBL1384
DrugBank
DB01172
ZINC
ZINC000008214590
PDB chain
4dfu Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4dfu
A small molecule discrimination map of the antibiotic resistance kinome.
Resolution
1.98 Å
Binding residue
(original residue number in PDB)
D197 S199 D220 E235 E238 W271 Y278
Binding residue
(residue number reindexed from 1)
D195 S197 D218 E233 E236 W269 Y276
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:4dfu
,
PDBe:4dfu
,
PDBj:4dfu
PDBsum
4dfu
PubMed
22195561
UniProt
O68183
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