Structure of PDB 6wm4 Chain A Binding Site BS01
Receptor Information
>6wm4 Chain A (length=600) Species:
9606
(Homo sapiens) [
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TFGYVHGVSGPVVTACDMAGAAMYELVRVGHSELVGEIIRLEGDMATIQV
YEETSGVSVGDPVLRTGKPLSVELGPGIMGAIFDGIQRPLSDISSQTQSI
YIPRGVNVSALSRDIKWDFTPCKNLRVGSHITGGDIYGIVSENSLIKHKI
MLPPRNRGTVTYIAPPGNYDTSDVVLELEFEGVKEKFTMVQVWPVRQVRP
VTEKLPANHPLLTGQRVLDALFPCVQGGTTAIPGAFGCGKTVISQSLSKY
SNSDVIIYVGCGERGNEMSEVLRDFPELTMEVDGKVESIMKRTALVANTS
NMPVAAREASIYTGITLSEYFRDMGYHVSMMADSTSRWAEALREISGRLA
EMPADSGYPAYLGARLASFYERAGRVKCLGNPEREGSVSIVGAVSPPGGD
FSDPVTSATLGIVQVFWGLDKKLAQRKHFPSVNWLISYSKYMRALDEYYD
KHFTEFVPLRTKAKEILQEEEDLAEIVQLVGKASLAETDKITLEVAKLIK
DDFLQQNGYTPYDRFCPFYKTVGMLSNMIAFYDMARRAVETTAQSDNKIT
WSIIREHMGDILYKLSSMKFKDPLKDGEAKIKSDYAQLLEDMQNAFRSLE
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
6wm4 Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
6wm4
Structures of a Complete Human V-ATPase Reveal Mechanisms of Its Assembly.
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
F252 G253 G255 K256 T257 V258 F445
Binding residue
(residue number reindexed from 1)
F236 G237 G239 K240 T241 V242 F429
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K256 E279 R280 K456
Catalytic site (residue number reindexed from 1)
K240 E263 R264 K440
Enzyme Commision number
7.1.2.2
: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
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:0007035
vacuolar acidification
GO:0007042
lysosomal lumen acidification
GO:0015986
proton motive force-driven ATP synthesis
GO:0016241
regulation of macroautophagy
GO:0036295
cellular response to increased oxygen levels
GO:0046034
ATP metabolic process
GO:0048388
endosomal lumen acidification
GO:0051452
intracellular pH reduction
GO:0061795
Golgi lumen acidification
GO:0097401
synaptic vesicle lumen acidification
GO:1902600
proton transmembrane transport
Cellular Component
GO:0000139
Golgi membrane
GO:0000221
vacuolar proton-transporting V-type ATPase, V1 domain
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005764
lysosome
GO:0005765
lysosomal membrane
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0005902
microvillus
GO:0010008
endosome membrane
GO:0016020
membrane
GO:0016324
apical plasma membrane
GO:0016469
proton-transporting two-sector ATPase complex
GO:0030133
transport vesicle
GO:0030141
secretory granule
GO:0030665
clathrin-coated vesicle membrane
GO:0031090
organelle membrane
GO:0031410
cytoplasmic vesicle
GO:0033176
proton-transporting V-type ATPase complex
GO:0033180
proton-transporting V-type ATPase, V1 domain
GO:0043231
intracellular membrane-bounded organelle
GO:0070062
extracellular exosome
GO:0098850
extrinsic component of synaptic vesicle membrane
GO:1904949
ATPase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6wm4
,
PDBe:6wm4
,
PDBj:6wm4
PDBsum
6wm4
PubMed
33065002
UniProt
P38606
|VATA_HUMAN V-type proton ATPase catalytic subunit A (Gene Name=ATP6V1A)
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