Structure of PDB 2cdu Chain B Binding Site BS02
Receptor Information
>2cdu Chain B (length=449) Species:
1625
(Fructilactobacillus sanfranciscensis) [
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MKVIVVGCTHAGTFAVKQTIADHPDADVTAYEMNDNISFLSCGIALYLGK
EIKNNDPRGLFYSSPEELSNLGANVQMRHQVTNVDPETKTIKVKDLITNE
EKTEAYDKLIMTTGSKPTVPPIPGIDSSRVYLCKNYNDAKKLFEEAPKAK
TITIIGSGYIGAELAEAYSNQNYNVNLIDGHERVLYKYFDKEFTDILAKD
YEAHGVNLVLGSKVAAFEEVDDEIITKTLDGKEIKSDIAILCIGFRPNTE
LLKGKVAMLDNGAIITDEYMHSSNRDIFAAGDSAAVHYNPTNSNAYIPLA
TNAVRQGRLVGLNLTEDKVKDMGTQSSSGLKLYGRTYVSTGINTALAKAN
NLKVSEVIIADNYRPEFMLSTDEVLMSLVYDPKTRVILGGALSSMHDVSQ
SANVLSVCIQNKNTIDDLAMVDMLFQPQFDRPFNYLNILGQAAQAQADK
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
2cdu Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
2cdu
The Crystal Structure of Nad(P)H Oxidase from Lactobacillus Sanfranciscensis: Insights Into the Conversion of O(2) Into Two Water Molecules by the Flavoenzyme.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
I160 D179 G180 H181 Y188 K213 V214 I243 G244
Binding residue
(residue number reindexed from 1)
I160 D179 G180 H181 Y188 K213 V214 I243 G244
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H10 I37 S41 C42 V304
Catalytic site (residue number reindexed from 1)
H10 I37 S41 C42 V304
Enzyme Commision number
1.6.-.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:2cdu
,
PDBe:2cdu
,
PDBj:2cdu
PDBsum
2cdu
PubMed
16893166
UniProt
Q9F1X5
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