Structure of PDB 3rk1 Chain A Binding Site BS01
Receptor Information
>3rk1 Chain A (length=221) Species:
186497
(Pyrococcus furiosus DSM 3638) [
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ADVAVLYSGGKDSNYALYWAIKNRFSVKFLVTMVSENEESYMYHTINANL
TDLQARALGIPLVKGFTQGEKEKEVEDLKRVLSGLKIQGIVAGALASKYQ
RKRIEKVAKELGLEVYTPDAKEYMRELLNLGFKIMVVGVSAYGLDESWLG
RILDESALEELITLNEKYKVHVAGEGGEFETFVLDMPLFKYKIVVDKAKK
VWEPCTSSGKLIIEEAHLESK
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
3rk1 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
3rk1
A large conformational change in the putative ATP pyrophosphatase PF0828 induced by ATP binding.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
L10 S12 G14 K15 D16 S17 M37 Y47 H48 G97 Q104 E188 T189
Binding residue
(residue number reindexed from 1)
L6 S8 G10 K11 D12 S13 M33 Y43 H44 G93 Q100 E180 T181
Annotation score
5
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0017178
diphthine-ammonia ligase activity
Biological Process
GO:0017183
protein histidyl modification to diphthamide
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Molecular Function
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Biological Process
External links
PDB
RCSB:3rk1
,
PDBe:3rk1
,
PDBj:3rk1
PDBsum
3rk1
PubMed
22102225
UniProt
Q8U2K6
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