Structure of PDB 3pcd Chain M Binding Site BS01
Receptor Information
>3pcd Chain M (length=233) Species:
303
(Pseudomonas putida) [
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PAQDNSRFVIRDRNWHPKALTPDYKTSIARSPRQALVSIPQSISETTGPN
FSHLGFGAHDHDLLLNFGLPIGERIIVAGRVVDQYGKPVPNTLVEMWQAN
AGGRYRHKNDRYLAPLDPNFGGVGRCLTDSDGYYSFRTIKPGPHPWRNGP
NDWRPAHIHFGISGPSIATKLITQLYFEGDPLIPMCPIVKSIANPEAVQQ
LIAKLDMNNANPMDCLAYRFDIVLRGQRKTHFE
Ligand information
Ligand ID
CO3
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-2
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)([O-])[O-]
ACDLabs 10.04
CACTVS 3.341
[O-]C([O-])=O
Formula
C O3
Name
CARBONATE ION
ChEMBL
DrugBank
DB14531
ZINC
PDB chain
3pcd Chain M Residue 550 [
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Receptor-Ligand Complex Structure
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PDB
3pcd
The axial tyrosinate Fe3+ ligand in protocatechuate 3,4-dioxygenase influences substrate binding and product release: evidence for new reaction cycle intermediates.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
Y408 H447 R457 H460 H462
Binding residue
(residue number reindexed from 1)
Y105 H144 R154 H157 H159
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.13.11.3
: protocatechuate 3,4-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:0018578
protocatechuate 3,4-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0019619
3,4-dihydroxybenzoate catabolic process
GO:0042952
beta-ketoadipate pathway
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3pcd
,
PDBe:3pcd
,
PDBj:3pcd
PDBsum
3pcd
PubMed
9485360
UniProt
P00437
|PCXB_PSEPU Protocatechuate 3,4-dioxygenase beta chain (Gene Name=pcaH)
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