Structure of PDB 5iqg Chain D Binding Site BS01
Receptor Information
>5iqg Chain D (length=301) Species:
1280
(Staphylococcus aureus) [
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RYDDNATNVKAMKYLIEHYFDNFKVDSIEIIGSGYDSVAYLVNNEYIFKT
KFSTNKKKGYAKEKAIYNFLNTNLETNVKIPNIEYSYISDELSILGYKEI
KGTFLTPEIYSTMSEEEQNLLKRDIASFLRQMHGLDYTDISECTIDNKQN
VLEEYILLRETIYNDLTDIEKDYIESFMERLNATTVFEGKKCLCHNDFSC
NHLLLDGNNRLTGIIDFGDSGIIDEYCDFIYLLEDSEEEIGTNFGEDILR
MYGNIDIEKAKEYQDIVEEYYPIETIVYGIKNIKQEFIENGRKEIYKRTY
K
Ligand information
Ligand ID
GDP
InChI
InChI=1S/C10H15N5O11P2/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(25-9)1-24-28(22,23)26-27(19,20)21/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
QGWNDRXFNXRZMB-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H15 N5 O11 P2
Name
GUANOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL384759
DrugBank
DB04315
ZINC
ZINC000008215481
PDB chain
5iqg Chain D Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
5iqg
Antibiotic Binding Drives Catalytic Activation of Aminoglycoside Kinase APH(2)-Ia.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
G211 I224 K226 Y274 I277 F281 I392 D393
Binding residue
(residue number reindexed from 1)
G34 I47 K49 Y97 I100 F104 I215 D216
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.1.-
2.7.1.190
: aminoglycoside 2''-phosphotransferase.
External links
PDB
RCSB:5iqg
,
PDBe:5iqg
,
PDBj:5iqg
PDBsum
5iqg
PubMed
27161980
UniProt
P0A0C1
|AACA_STAAU Bifunctional AAC/APH (Gene Name=aacA-aphD)
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