Structure of PDB 3w3a Chain M Binding Site BS01
Receptor Information
>3w3a Chain M (length=457) Species:
300852
(Thermus thermophilus HB8) [
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EYTGITYISGPLLFVENAKDLAYGAIVDIKDGTGRVRGGQVIEVSEEYAV
IQVFEETTGLDLATTSVSLVEDVARLGVSKEMLGRRFNGIGKPIDGLPPI
TPEKRLPITGLPLNPVARRKPEQFIQTGISTIDVMNTLVRGQKLPIFSGS
GLPANEIAAQIARQATVRPDLSGEGEKEEPFAVVFAAMGITQRELSYFIQ
EFERTGALSRSVLFLNKADDPTIERILTPRMALTVAEYLAFEHDYHVLVI
LTDMTNYCEALREIGAAREEIPGRRGYPGYMYTDLATIYERAGVVEGKKG
SVTQIPILSMPDDDRTHPIPDLTGYITEGQIQLSRELHRKGIYPPIDPLP
SLSRLMNNGVGKGKTREDHKQVSDQLYSAYANGVDIRKLVAIIGEDALTE
NDRRYLQFADAFERFFINQGQQNRSIEESLQIAWALLSMLPQGELKRISK
DHIGKYY
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=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)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
3w3a Chain K Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
3w3a
Origin of Asymmetry at the Intersubunit Interfaces of V1-ATPase from Thermusthermophilus
Resolution
3.9 Å
Binding residue
(original residue number in PDB)
R360 N363
Binding residue
(residue number reindexed from 1)
R354 N357
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
A160 I196 T197 R360
Catalytic site (residue number reindexed from 1)
A154 I190 T191 R354
Enzyme Commision number
3.6.3.14
: Transferred entry: 7.1.2.2.
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:3w3a
,
PDBe:3w3a
,
PDBj:3w3a
PDBsum
3w3a
PubMed
23639357
UniProt
Q56404
|VATB_THET8 V-type ATP synthase beta chain (Gene Name=atpB)
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