Structure of PDB 5iqa Chain B Binding Site BS01
Receptor Information
>5iqa Chain B (length=299) Species:
1280
(Staphylococcus aureus) [
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YDDNATNVKAMKYLIEHYFDNFKVDSIEIIGSGYDSVAYLVNNEYIFKTK
FSKKKGYAKEKAIYNFLNTNLETNVKIPNIEYSYISDELSILGYKEIKGT
FLTPEIYSTMSEEEQNLLKRDIASFLRQMHGLDYTDISECTIDNKQNVLE
EYILLRETIYNDLTDIEKDYIESFMERLNATTVFEGKKCLCHNDFSCNHL
LLDGNNRLTGIIDFGDSGIIDEYCDFIYLLEDSEEEIGTNFGEDILRMYG
NIDIEKAKEYQDIVEEYYPIETIVYGIKNIKQEFIENGRKEIYKRTYKD
Ligand information
Ligand ID
GNP
InChI
InChI=1S/C10H17N6O13P3/c11-10-13-7-4(8(19)14-10)12-2-16(7)9-6(18)5(17)3(28-9)1-27-32(25,26)29-31(23,24)15-30(20,21)22/h2-3,5-6,9,17-18H,1H2,(H,25,26)(H3,11,13,14,19)(H4,15,20,21,22,23,24)/t3-,5-,6-,9-/m1/s1
InChIKey
UQABYHGXWYXDTK-UUOKFMHZSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)NP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)N[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[CH](O)[CH]3O
Formula
C10 H17 N6 O13 P3
Name
PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER
ChEMBL
CHEMBL1233085
DrugBank
DB02082
ZINC
ZINC000037868676
PDB chain
5iqa Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
5iqa
Antibiotic Binding Drives Catalytic Activation of Aminoglycoside Kinase APH(2)-Ia.
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
S214 I224 K226 Y274 I277 F281 H379 I392 D393
Binding residue
(residue number reindexed from 1)
S36 I46 K48 Y94 I97 F101 H199 I212 D213
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.-
2.7.1.190
: aminoglycoside 2''-phosphotransferase.
External links
PDB
RCSB:5iqa
,
PDBe:5iqa
,
PDBj:5iqa
PDBsum
5iqa
PubMed
27161980
UniProt
P0A0C1
|AACA_STAAU Bifunctional AAC/APH (Gene Name=aacA-aphD)
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