Structure of PDB 1we1 Chain C Binding Site BS02
Receptor Information
>1we1 Chain C (length=222) Species:
1148
(Synechocystis sp. PCC 6803) [
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SVNLASQLREGTKKSHSMAENVGFVKCFLKGVVEKNSYRKLVGNLYFVYS
AMEEEMAKFKDHPILSHIYFPELNRKQSLEQDLQFYYGSNWRQEVKISAA
GQAYVDRVRQVAATAPELLVAHSYTRYLGDLSGGQILKKIAQNAMNLHDG
GTAFYEFADIDDEKAFKNTYRQAMNDLPIDQATAERIVDEANDAFAMNMK
MFNELEGNLIKAIGIMVFNSLT
Ligand information
Ligand ID
IPA
InChI
InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3
InChIKey
KFZMGEQAYNKOFK-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 11.02
OC(C)C
CACTVS 3.352
OpenEye OEToolkits 1.7.0
CC(C)O
Formula
C3 H8 O
Name
ISOPROPYL ALCOHOL;
2-PROPANOL
ChEMBL
CHEMBL582
DrugBank
DB02325
ZINC
ZINC000000901159
PDB chain
1we1 Chain C Residue 1007 [
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Receptor-Ligand Complex Structure
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PDB
1we1
Crystal structure of heme oxygenase-1 from cyanobacterium Synechocystis sp. PCC 6803 in complex with heme
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
I69 F71 L74
Binding residue
(residue number reindexed from 1)
I68 F70 L73
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N22 Y50 T126 R127 G130 D131 G135
Catalytic site (residue number reindexed from 1)
N21 Y49 T125 R126 G129 D130 G134
Enzyme Commision number
1.14.14.18
: heme oxygenase (biliverdin-producing).
Gene Ontology
Molecular Function
GO:0004392
heme oxygenase (decyclizing) activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006788
heme oxidation
GO:0006979
response to oxidative stress
GO:0015979
photosynthesis
GO:0042167
heme catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1we1
,
PDBe:1we1
,
PDBj:1we1
PDBsum
1we1
PubMed
15560792
UniProt
P72849
|HO1_SYNY3 Heme oxygenase 1 (Gene Name=pbsA1)
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