Structure of PDB 6q45 Chain L Binding Site BS01
Receptor Information
>6q45 Chain L (length=459) Species:
190304
(Fusobacterium nucleatum subsp. nucleatum ATCC 25586) [
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NKGTITQIISAVVDIAFKDELPAIYNALKVKLEDKELVLEVEQHLGNNVV
RTVAMDSTDGLKRGMEVIDTGKPITIPVGKAVLGRILNVLGEPVDNQGPL
NAETFLPIHREAPEFDDLETETEIFETGIKVIDLLAPYIKGGKIGLFGGA
GVGKTVLIMELINNIAKGHGGISVFAGVGERTREGRDLYGEMTESGVITK
TALVYGQMNEPPGARLRVALTGLTVAENFRDKDGQDVLLFIDNIFRFTQA
GSEVSALLGRIPSAVGYQPNLATEMGALQERITSTKSGSITSVQAVYVPA
DDLTDPAPATTFSHLDATTVLSRNIASLGIYPAVDPLDSTSKALSEDVVG
KEHYEVARKVQEVLQRYKELQDIIAILGMDELSDEDKLTVSRARKIERFF
SQPFSVAEQFTGMEGKYVPVKETIRGFREILEGKHDDIPEQAFLYVGTIE
EAVAKSKDL
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
6q45 Chain L Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
6q45
Structure of F1-ATPase from the obligate anaerobe Fusobacterium nucleatum.
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
G152 G154 K155 T156 V157 Y332 F405 F411
Binding residue
(residue number reindexed from 1)
G151 G153 K154 T155 V156 Y331 F404 F410
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K155 E181 R182 K343
Catalytic site (residue number reindexed from 1)
K154 E180 R181 K342
Enzyme Commision number
7.1.2.2
: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
GO:0046961
proton-transporting ATPase activity, rotational mechanism
Biological Process
GO:0006754
ATP biosynthetic process
GO:0015986
proton motive force-driven ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005886
plasma membrane
GO:0045259
proton-transporting ATP synthase complex
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6q45
,
PDBe:6q45
,
PDBj:6q45
PDBsum
6q45
PubMed
31238823
UniProt
Q8RGE2
|ATPB_FUSNN ATP synthase subunit beta (Gene Name=atpD)
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