Structure of PDB 4kft Chain D Binding Site BS01
Receptor Information
>4kft Chain D (length=194) Species:
754004
(Sulfolobus turreted icosahedral virus 2) [
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MNPDDIVVLVGRKKSGKSYLIKHYFIPVLKAHKISYIIDDSEYSKFGYNA
TSLSDIVSKQYVVVYDRDFFEKLWQASKLHSKKYGTTVLIIDEAYYHFKY
KQKVTPAIDEALHANRHAGLGLILSTQRVYDLMPIVYKQADLIIMFYTRE
PNELRWISKYISAEAAEKVKTLKQYHFLIYDVNSQTIKIHKPIL
Ligand information
Ligand ID
AGS
InChI
InChI=1S/C10H16N5O12P3S/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(25-10)1-24-28(18,19)26-29(20,21)27-30(22,23)31/h2-4,6-7,10,16-17H,1H2,(H,18,19)(H,20,21)(H2,11,12,13)(H2,22,23,31)/t4-,6-,7-,10-/m1/s1
InChIKey
NLTUCYMLOPLUHL-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=S)(O)O)O)O)N
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=S)[C@@H](O)[C@H]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=S)[CH](O)[CH]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)OP(=O)(O)OP(=S)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(OP(=S)(O)O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C10 H16 N5 O12 P3 S
Name
PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER;
ATP-GAMMA-S;
ADENOSINE 5'-(3-THIOTRIPHOSPHATE);
ADENOSINE 5'-(GAMMA-THIOTRIPHOSPHATE);
ADENOSINE-5'-DIPHOSPHATE MONOTHIOPHOSPHATE
ChEMBL
CHEMBL131890
DrugBank
DB02930
ZINC
ZINC000008295128
PDB chain
4kft Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4kft
The Structure of the NTPase That Powers DNA Packaging into Sulfolobus Turreted Icosahedral Virus 2.
Resolution
2.241 Å
Binding residue
(original residue number in PDB)
K13 K14 G16 K17 S18 Y19 Y186 I204
Binding residue
(residue number reindexed from 1)
K13 K14 G16 K17 S18 Y19 Y175 I193
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.-.-.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:4kft
,
PDBe:4kft
,
PDBj:4kft
PDBsum
4kft
PubMed
23698307
UniProt
D5IEZ9
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