Structure of PDB 2xsv Chain A Binding Site BS02
Receptor Information
>2xsv Chain A (length=309) Species:
40216
(Acinetobacter radioresistens) [
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HHHHNRQQIDALVKQMNVDTAKGPVDERIQQVVVRLLGDLFQAIEDLDIQ
PSEVWKGLEYLTDAGQANELGALAAGLGLEHYLDLRADEADAKAGITGGT
PRTIEGPLYVAGAPESVGFARMDDGSESDKVDTLIIEGTVTDTEGNIIEG
AKVEVWHANSLGNYSFFDKSQSDFNLRRTILTDVNGKYVALTTMPVGYGC
PPEGTTQALLNKLGRHGNRPSHVHYFVSAPGYRKLTTQFNIEGDEYLWDD
FAFATRDGLVATATDVTDEAEIARRELDKPFKHITFNVELVKEAEAAPSS
EVERRRASA
Ligand information
Ligand ID
PIE
InChI
InChI=1S/C43H81O13P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-37(45)55-35(34-54-57(51,52)56-43-41(49)39(47)38(46)40(48)42(43)50)33-53-36(44)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,35,38-43,46-50H,3-16,19-34H2,1-2H3,(H,51,52)/p-1/b18-17+/t35-,38-,39-,40+,41-,42-,43-/m1/s1
InChIKey
PDLAMJKMOKWLAJ-OJERQSHOSA-M
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCCCCCCCCCCCCCCC(=O)OC[C@H](CO[P@](=O)([O-])OC1[C@@H]([C@H](C([C@H]([C@H]1O)O)O)O)O)OC(=O)CCCCCCC\C=C\CCCCCCCC
OpenEye OEToolkits 1.5.0
CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OC1C(C(C(C(C1O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCC
CACTVS 3.341
CCCCCCCCCCCCCCCC(=O)OC[C@H](CO[P]([O-])(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C\CCCCCCCC
ACDLabs 10.04
O=C(OCC(OC(=O)CCCCCCC/C=C/CCCCCCCC)COP([O-])(=O)OC1C(O)C(O)C(O)C(O)C1O)CCCCCCCCCCCCCCC
CACTVS 3.341
CCCCCCCCCCCCCCCC(=O)OC[CH](CO[P]([O-])(=O)O[CH]1[CH](O)[CH](O)[CH](O)[CH](O)[CH]1O)OC(=O)CCCCCCCC=CCCCCCCCC
Formula
C43 H80 O13 P
Name
1,2-DIACYL-SN-GLYCERO-3-PHOSPHOINOSITOL
ChEMBL
DrugBank
DB02144
ZINC
PDB chain
2xsv Chain A Residue 1308 [
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Receptor-Ligand Complex Structure
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PDB
2xsv
X-Ray Crystallography, Mass Spectrometry and Single Crystal Microspectrophotometry: A Multidisciplinary Characterization of Catechol 1,2 Dioxygenase.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
E50 K53 Y57 L58 D60 A71 T202 A205
Binding residue
(residue number reindexed from 1)
E53 K56 Y60 L61 D63 A74 T205 A208
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.13.11.1
: catechol 1,2-dioxygenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005506
iron ion binding
GO:0008199
ferric iron binding
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0018576
catechol 1,2-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0009712
catechol-containing compound metabolic process
GO:0019614
catechol-containing compound catabolic process
GO:0042952
beta-ketoadipate pathway
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2xsv
,
PDBe:2xsv
,
PDBj:2xsv
PDBsum
2xsv
PubMed
20869471
UniProt
Q9F103
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