Structure of PDB 7p2y Chain D Binding Site BS01
Receptor Information
>7p2y Chain D (length=463) Species:
400667
(Acinetobacter baumannii ATCC 17978) [
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SSGRIIQIIGAVIDVEFERTSVPKIYDALQVDGTETTLEVQQQLGDGVVR
TIAMGSTEGLKRGLTVTSTNAPISVPVGTATLGRIMDVLGRPIDEAGPVA
TEERLPIHRQAPSYAEQAASTDLLETGIKVIDLLCPFAKGGKVGLFGGAG
VGKTVNMMELINNIAKAHSGLSVFAGVGERTREGNDFYHEMKDSNVLDKV
AMVYGQMNEPPGNRLRVALTGLTMAEYFRDEKDENGKGRDVLLFVDNIYR
YTLAGTEVSALLGRMPSAVGYQPTLAEEMGVLQERITSTKSGSITSIQAV
YVPADDLTDPSPATTFAHLDATVVLSRDIASSGIYPAIDPLDSTSRQLDP
LVVGQEHYEIARAVQNVLQRYKELKDIIAILGMDELAEEDKLVVYRARKI
QRFFSQPFHVAEVFTGAPGKLVPLKETIRGFKGLLAGEYDHIPEQAFYMV
GGIDEVIAKAEKL
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
7p2y Chain D Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
7p2y
Structure of ATP synthase from ESKAPE pathogen Acinetobacter baumannii.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
G151 V152 G153 K154 T155 V156 Y336 F409 F415
Binding residue
(residue number reindexed from 1)
G150 V151 G152 K153 T154 V155 Y335 F408 F414
Annotation score
5
Enzymatic activity
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)
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Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:7p2y
,
PDBe:7p2y
,
PDBj:7p2y
PDBsum
7p2y
PubMed
35171679
UniProt
A3M144
|ATPB_ACIBT ATP synthase subunit beta (Gene Name=atpD)
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