Structure of PDB 5knc Chain C Binding Site BS01
Receptor Information
>5knc Chain C (length=586) Species:
768486
(Enterococcus hirae ATCC 9790) [
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MQIGKIIKVSGPLVMAENMSEASIQDMCLVGDLGVIGEIIEMRQDVASIQ
VYEETSGIGPGEPVRSTGEALSVELGPGIISQMFDGIQRPLDTFMEVTQS
NFLGRGVQLPALDHEKQWWFEATIEEGTEVSAGDIIGYVDETKIIQHKIM
VPNGIKGTVQKIESGSFTIDDPICVIETEQGLKELTMMQKWPVRRGRPIK
QKLNPDVPMITGQRVIDTFFPVTKGGAAAVPGPFGAGKTVVQHQIAKWSD
VDLVVYVGCGERGNEMTDVVNEFPELIDPNTGESLMERTVLIANTSNMPV
AAREASIYTGITIAEYFRDMGYDVAIMADSTSRWAEALREMSGRLEEMPG
DEGYPAYLGSRLAEYYERSGRVIALGSDQREGSITAISAVSPSGGDISEP
VTQNTLRVVKVFWGLDSSLAQKRHFPSINWIQSYSLYSTEVGRYMDQILQ
QDWSDMVTEGMRILQEEEQLNEIVRLVGIDSLSDNDRLTLEVAKSIREDY
LQQNAFDDVDTFTSREKQFNMLKVILTFGKEARKALSLGAYFNEIMEGTV
AVRERISRSKYIPEEELAKISSINEEIKETIQLIVS
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
5knc Chain C Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
5knc
Crystal structures of the ATP-binding and ADP-release dwells of the V1 rotary motor
Resolution
3.015 Å
Binding residue
(original residue number in PDB)
G235 A236 G237 K238 T239 V240 F425 A505 F506
Binding residue
(residue number reindexed from 1)
G235 A236 G237 K238 T239 V240 F425 A505 F506
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K238 E261 R262 L436
Catalytic site (residue number reindexed from 1)
K238 E261 R262 L436
Enzyme Commision number
7.2.2.1
: Na(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0046932
sodium-transporting ATP synthase activity, rotational mechanism
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
GO:0046961
proton-transporting ATPase activity, rotational mechanism
GO:0046962
sodium-transporting ATPase activity, rotational mechanism
Biological Process
GO:0006814
sodium ion transport
GO:0035725
sodium ion transmembrane transport
GO:0042777
proton motive force-driven plasma membrane ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0045259
proton-transporting ATP synthase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5knc
,
PDBe:5knc
,
PDBj:5knc
PDBsum
5knc
PubMed
27807367
UniProt
Q08636
|NTPA_ENTHA V-type sodium ATPase catalytic subunit A (Gene Name=ntpA)
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