Structure of PDB 7vb0 Chain E Binding Site BS01
Receptor Information
>7vb0 Chain E (length=468) Species:
300852
(Thermus thermophilus HB8) [
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LLKKEYTGITYISGPLLFVENAKDLAYGAIVDIKDGTGRVRGGQVIEVSE
EYAVIQVFEETTGLDLATTSVSLVEDVARLGVSKEMLGRRFNGIGKPIDG
LPPITPEKRLPITGLPLNPVARRKPEQFIQTGISTIDVMNTLVRGQKLPI
FSGSGLPANEIAAQIARQATVRPDLSGEGEKEEPFAVVFAAMGITQRELS
YFIQEFERTGALSRSVLFLNKADDPTIERILTPRMALTVAEYLAFEHDYH
VLVILTDMTNYCEALREIGAAREEIPGRRGYPGYMYTDLATIYERAGVVE
GKKGSVTQIPILSMPDDDRTHPIPDLTGYITEGQIQLSRELHRKGIYPPI
DPLPSLSRLMNNGVGKGKTREDHKQVSDQLYSAYANGVDIRKLVAIIGED
ALTENDRRYLQFADAFERFFINQGQQNRSIEESLQIAWALLSMLPQGELK
RISKDHIGKYYGQKLEEI
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
7vb0 Chain E Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
7vb0
Structural snapshots of V/A-ATPase reveal the rotary catalytic mechanism of rotary ATPases.
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
Y331 R360
Binding residue
(residue number reindexed from 1)
Y329 R358
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
Biological Process
GO:0006754
ATP biosynthetic process
GO:0042777
proton motive force-driven plasma membrane ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7vb0
,
PDBe:7vb0
,
PDBj:7vb0
PDBsum
7vb0
PubMed
35260556
UniProt
Q56404
|VATB_THET8 V-type ATP synthase beta chain (Gene Name=atpB)
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