Structure of PDB 5luh Chain A Binding Site BS04
Receptor Information
>5luh Chain A (length=264) Species:
90371
(Salmonella enterica subsp. enterica serovar Typhimurium) [
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TLSIPPSIQCQTEAACRLITRVTGDTLRAIHLYGSAVAGGLKPNSDIDLL
VTICQPLTEAQRATLMQELLALSSPPGASAEKRALQVTVVLYSQLVPWCF
PPSREMQFGEWLREDICQGIYEPAQQDWDMVLLITQILETSIPLKGERAE
RLFTPAPAAQLLKALRYPLDLWQSTADVQGDEYHIVLTLARIWYTLSTGR
FTSKDAAADWLLPQLPEDYAATLRAAQREYLGLEQQDWHILLPAVVRFVD
FAKAHIPTQFTHHH
Ligand information
Ligand ID
SRY
InChI
InChI=1S/C21H39N7O12/c1-5-21(36,4-30)16(40-17-9(26-2)13(34)10(31)6(3-29)38-17)18(37-5)39-15-8(28-20(24)25)11(32)7(27-19(22)23)12(33)14(15)35/h4-18,26,29,31-36H,3H2,1-2H3,(H4,22,23,27)(H4,24,25,28)/t5-,6-,7+,8-,9-,10-,11+,12-,13-,14+,15+,16-,17-,18-,21+/m0/s1
InChIKey
UCSJYZPVAKXKNQ-HZYVHMACSA-N
SMILES
Software
SMILES
CACTVS 3.385
CN[CH]1[CH](O)[CH](O)[CH](CO)O[CH]1O[CH]2[CH](O[CH](C)[C]2(O)C=O)O[CH]3[CH](O)[CH](O)[CH](NC(N)=N)[CH](O)[CH]3NC(N)=N
OpenEye OEToolkits 1.7.5
[H]/N=C(/N)\N[C@@H]1[C@H]([C@@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2[C@@H]([C@]([C@@H](O2)C)(C=O)O)O[C@H]3[C@H]([C@@H]([C@H]([C@@H](O3)CO)O)O)NC)N/C(=N\[H])/N)O
CACTVS 3.385
CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@H]2[C@@H](O[C@@H](C)[C@]2(O)C=O)O[C@H]3[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]3NC(N)=N
OpenEye OEToolkits 1.7.5
CC1C(C(C(O1)OC2C(C(C(C(C2O)O)NC(=N)N)O)NC(=N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O
ACDLabs 10.04
O=CC3(O)C(OC1OC(C(O)C(O)C1NC)CO)C(OC2C(NC(=[N@H])N)C(O)C(NC(=[N@H])N)C(O)C2O)OC3C
Formula
C21 H39 N7 O12
Name
STREPTOMYCIN;
STREPTOMYCIN A
ChEMBL
CHEMBL372795
DrugBank
DB01082
ZINC
ZINC000008214681
PDB chain
5luh Chain A Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
5luh
Structural mechanism of AadA, a dual-specificity aminoglycoside adenylyltransferase fromSalmonella enterica.
Resolution
1.73 Å
Binding residue
(original residue number in PDB)
Q87 W112 W173 D178 D182 H185
Binding residue
(residue number reindexed from 1)
Q86 W111 W172 D177 D181 H184
Annotation score
4
Binding affinity
MOAD
: Kd=11uM
Enzymatic activity
Enzyme Commision number
2.7.7.47
: streptomycin 3''-adenylyltransferase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0009012
aminoglycoside 3''-adenylyltransferase activity
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
GO:0070566
adenylyltransferase activity
Biological Process
GO:0046677
response to antibiotic
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5luh
,
PDBe:5luh
,
PDBj:5luh
PDBsum
5luh
PubMed
29871922
UniProt
Q8ZPX9
|S3AD_SALTY Aminoglycoside (3'') (9) adenylyltransferase (Gene Name=aadA)
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