Structure of PDB 7tmt Chain E Binding Site BS01
Receptor Information
>7tmt Chain E (length=593) Species:
4932
(Saccharomyces cerevisiae) [
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YGAIYSVSGPVVIAENMIGCAMYELVKVGHDNLVGEVIRIDGDKATIQVY
EETAGLTVGDPVLRTGKPLSVELGPGLMETIYDGIQRPLKAIKEESQSIY
IPRGIDTPALDRTIKWQFTPGKFQVGDHISGGDIYGSVFENSLISSHKIL
LPPRSRGTITWIAPAGEYTLDEKILEVEFDGKKSDFTLYHTWPVRVPRPV
TEKLSADYPLLTGQRVLDALFPCVQGGTTCIPGAFGCGKTVISQSLSKYS
NSDAIIYVGCGERGNEMAEVLMEFPELYTEMSGTKEPIMKRTTLVANTSN
MPVAAREASIYTGITLAEYFRDQGKNVSMIADSSSRWAEALREISGRLGE
MPADQGFPAYLGAKLASFYERAGKAVALGSPDRTGSVSIVAAVSPAGGDF
SDPVTTATLGITQVFWGLDKKLAQRKHFPSINTSVSYSKYTNVLNKFYDS
NYPEFPVLRDRMKEILSNAEELEQVVQLVGKSALSDSDKITLDVATLIKE
DFLQQNGYSTYDAFCPIWKTFDMMRAFISYHDEAQKAVANGANWSKLADS
TGDVKHAVSSSKFFEPSRGEKEVHGEFEKLLSTMQERFAESTD
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
7tmt Chain E Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
7tmt
Coordinated conformational changes in the V 1 complex during V-ATPase reversible dissociation.
Resolution
3.8 Å
Binding residue
(original residue number in PDB)
G259 C260 G261 K262 T263 V264 F451 P452 N529 G530 Y531
Binding residue
(residue number reindexed from 1)
G236 C237 G238 K239 T240 V241 F428 P429 N506 G507 Y508
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:0015986
proton motive force-driven ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0000329
fungal-type vacuole membrane
GO:0005774
vacuolar membrane
GO:0012505
endomembrane system
GO:0016020
membrane
GO:0033180
proton-transporting V-type ATPase, V1 domain
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:7tmt
,
PDBe:7tmt
,
PDBj:7tmt
PDBsum
7tmt
PubMed
35469063
UniProt
B3LH69
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