Structure of PDB 6c5u Chain D Binding Site BS01
Receptor Information
>6c5u Chain D (length=291) Species:
1280
(Staphylococcus aureus) [
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DDNATNVKAMKYLIEHYFDNFKVDSIEIIGSGYDSVAYLVNNEYIFKTKF
SYAKEKAIYNFLNTNLETNVKIPNIEYSYISDELSILGYKEIKGTFLTPE
IYSTMSEEEQNLLKRDIASFLRQMHGLDYTDISECTIDNKQNVLEEYILL
RETIYNDLTDIEKDYIESFMERLNATTVFEGKKCLCHNDFSCNHLLLDGN
NRLTGIIDFGDSGIIDEYCDFIYLLEDSEEEIGTNFGEDILRMYGNIDIE
KAKEYQDIVEEYYPIETIVYGIKNIKQEFIENGRKEIYKRT
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
6c5u Chain D Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
6c5u
Plasticity of Aminoglycoside Binding to Antibiotic Kinase APH(2′′)-Ia.
Resolution
2.41 Å
Binding residue
(original residue number in PDB)
I224 K226 Y274 I277 F281 H379 I392 D393
Binding residue
(residue number reindexed from 1)
I45 K47 Y89 I92 F96 H194 I207 D208
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.-
2.7.1.190
: aminoglycoside 2''-phosphotransferase.
External links
PDB
RCSB:6c5u
,
PDBe:6c5u
,
PDBj:6c5u
PDBsum
6c5u
PubMed
29661878
UniProt
P0A0C1
|AACA_STAAU Bifunctional AAC/APH (Gene Name=aacA-aphD)
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