Structure of PDB 7uzi Chain B Binding Site BS01
Receptor Information
>7uzi Chain B (length=602) Species:
10116
(Rattus norvegicus) [
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ESTFGYVHGVSGPVVTACDMAGAAMYELVRVGHSELVGEIIRLEGDMATI
QVYEETSGVSVGDPVLRTGKPLSVELGPGIMGAIFDGIQRPLSDISSQTQ
SIYIPRGVNVSALSRDIKWEFIPSKNLRVGSHITGGDIYGIVNENSLIKH
KIMLPPRSRGSVTYIAPPGNYDASDVVLELEFEGVKEKLSMVQVWPVRQV
RPVTEKLPANHPLLTGQRVLDALFPCVQGGTTAIPGAFGCGKTVISQSLS
KYSNSDVIIYVGCGERGNEMSEVLRDFPELTMEVDGKVESIMKRTALVAN
TSNMPVAAREASIYTGITLSEYFRDMGYHVSMMADSTSRWAEALREISGR
LAEMPADSGYPAYLGARLASFYERAGRVKCLGNPEREGSVSIVGAVSPPG
GDFSDPVTSATLGIVQVFWGLDKKLAQRKHFPSVNWLISYSKYMRALDEY
YDKHFTEFVPLRTKAKEILQEEEDLAEIVQLVGKASLAETDKITLEVAKL
IKDDFLQQNGYTPYDRFCPFYKTVGMLSNMISFYDMARRAVETTAQSDNK
ITWSIIREHMGEILYKLSSMKFKDPVKDGEAKIKADYAQLLEDMQNAFRS
LE
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
7uzi Chain B Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
7uzi
Structure of V-ATPase with NCOA7B
Resolution
3.9 Å
Binding residue
(original residue number in PDB)
G253 C254 G255 K256 T257 V258 R280 F445
Binding residue
(residue number reindexed from 1)
G239 C240 G241 K242 T243 V244 R266 F431
Annotation score
5
Enzymatic activity
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:0015986
proton motive force-driven ATP synthesis
GO:0036295
cellular response to increased oxygen levels
GO:0046034
ATP metabolic process
GO:0097401
synaptic vesicle lumen acidification
GO:1902600
proton transmembrane transport
Cellular Component
GO:0000221
vacuolar proton-transporting V-type ATPase, V1 domain
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0005902
microvillus
GO:0016020
membrane
GO:0016324
apical plasma membrane
GO:0030133
transport vesicle
GO:0030141
secretory granule
GO:0030665
clathrin-coated vesicle membrane
GO:0033176
proton-transporting V-type ATPase complex
GO:0033180
proton-transporting V-type ATPase, V1 domain
GO:0043231
intracellular membrane-bounded organelle
GO:0098850
extrinsic component of synaptic vesicle membrane
GO:1904949
ATPase complex
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Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:7uzi
,
PDBe:7uzi
,
PDBj:7uzi
PDBsum
7uzi
PubMed
UniProt
D4A133
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