Structure of PDB 2xso Chain K Binding Site BS02
Receptor Information
>2xso Chain K (length=433) Species:
266265
(Paraburkholderia xenovorans LB400) [
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NWTPEAIRGLVDQEKGLLDPRIYADQSLYELELERVFGRSWLLLGHESHV
PETGDFLATYMGEDPVVMVRQKDKSIKVFLNQCRHRGMRICRSDAGNAKA
FTCSYHGWAYDIAGKLVNVPFEKEAFFDKAEWGPLQARVATYKGLVFANW
DVQAPDLETYLGDARPYMDVMLDRTPAGTVAIGGMQKWVIPCNWKFAAEQ
FCSDMYHAGTTTHLSGILAGIPPEMDLSQAQIPTKGNQFRAAWGGHGSGW
YVDEPGSLLAVMGPKVTQYWTEGPAAELAEQRLGHTGMPVRRMVGQHMTI
FPTCSFLPAMNNIRIWHPRGPNEIEVWAFTLVDADAPAEIKEEYRRHNIR
NFSAGGVFEQDDGENWVEIQKGLRGYKAKSQPLNAQMGLGRSQTGHPDFP
GNVGYVYAEEAARGMYHHWMRMMSEPSWATLKP
Ligand information
Ligand ID
FE2
InChI
InChI=1S/Fe/q+2
InChIKey
CWYNVVGOOAEACU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Fe+2]
CACTVS 3.341
[Fe++]
Formula
Fe
Name
FE (II) ION
ChEMBL
DrugBank
DB14510
ZINC
PDB chain
2xso Chain K Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
2xso
Structural Insight Into the Expanded Pcb-Degrading Abilities of a Biphenyl Dioxygenase Obtained by Directed Evolution.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
H233 H239 D388
Binding residue
(residue number reindexed from 1)
H207 H213 D362
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H123 D230 H233 H239 D388
Catalytic site (residue number reindexed from 1)
H106 D204 H207 H213 D362
Enzyme Commision number
1.14.12.18
: biphenyl 2,3-dioxygenase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0018687
biphenyl 2,3-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
GO:0051537
2 iron, 2 sulfur cluster binding
Biological Process
GO:0009056
catabolic process
GO:0044237
cellular metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2xso
,
PDBe:2xso
,
PDBj:2xso
PDBsum
2xso
PubMed
21073881
UniProt
P37333
|BPHA_PARXL Biphenyl dioxygenase subunit alpha (Gene Name=bphA)
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