Structure of PDB 7u8p Chain C Binding Site BS01
Receptor Information
>7u8p Chain C (length=600) Species:
9823
(Sus scrofa) [
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TFGYVHGVSGPVVTACDMAGAAMYELVRVGHSELVGEIIRLEGDMATIQV
YEETSGVSVGDPVLRTGKPLSVELGPGIMGAIFDGIQRPLSDISSQTQSI
YIPRGVNVSALSRDVKWEFTPSKNLRVGSHITGGDIYGIVNENSLIKHRI
MLPPRNRGTVTYIAPPGNYDTSDVVLELEFEGVKEKFSMVQVWPVRQVRP
VTEKLPANHPLLTGQRVLDALFPCVQGGTTAIPGAFGCGKTVISQSLSKY
SNSDVIIYVGCGERVNEMSEVLRDFPELTMEVDGKVESIMKRTALVANTS
NMPVAAREASIYTGITLSEYFRDMGYHVSMMANSTSRWAEALREISGRLA
EMPADSGYPAYLGARLASFYERAGRVKCLGNPEREGSVTIVGAVSPPGGD
FSDPVTSATLGIVQVFWGLDKKLAQRKHFPSVNWLISYSKYMRALDEYYD
KHFTEFVPLRTKAKEILQEEEDLAEIVQLVGKASLAETDKITLEVAKLIK
DDFLQQNGYTPYDRFCPFYKTVGMLSNMIAFYDLARRAVETTAQSDNKIT
WSIIREHMGEILYKLSSMKFKDPVKDGEAKIKADYAQLLEDVQNAFRSLE
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
7u8p Chain C Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
7u8p
CryoEM of endogenous mammalian V-ATPase interacting with the TLDc protein mEAK-7.
Resolution
3.7 Å
Binding residue
(original residue number in PDB)
G253 C254 G255 K256 T257 V258 R280 F445 G524 Y525
Binding residue
(residue number reindexed from 1)
G237 C238 G239 K240 T241 V242 R264 F429 G508 Y509
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:0006879
intracellular iron ion homeostasis
GO:0015986
proton motive force-driven ATP synthesis
GO:0036295
cellular response to increased oxygen levels
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0000221
vacuolar proton-transporting V-type ATPase, V1 domain
GO:0005737
cytoplasm
GO:0005764
lysosome
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0030133
transport vesicle
GO:0030665
clathrin-coated vesicle membrane
GO:0031410
cytoplasmic vesicle
GO:0033180
proton-transporting V-type ATPase, V1 domain
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7u8p
,
PDBe:7u8p
,
PDBj:7u8p
PDBsum
7u8p
PubMed
35794005
UniProt
Q29048
|VATA_PIG V-type proton ATPase catalytic subunit A (Gene Name=ATP6V1A)
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