Structure of PDB 1uli Chain E Binding Site BS01
Receptor Information
>1uli Chain E (length=425) Species:
101510
(Rhodococcus jostii RHA1) [
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WADADIAELVDERTGRLDPRIYTDEALYEQELERIFGRSWLLMGHETQIP
KAGDFMTNYMGEDPVMVVRQKNGEIRVFLNQCRHRGMRICRADGGNAKSF
TCSYHGWAYDTGGNLVSVPFEEQAFPGLRKEDWGPLQARVETYKGLIFAN
WDADAPDLDTYLGEAKFYMDHMLDRTEAGTEAIPGIQKWVIPCNWKFAAE
QFCSDMYHAGTTSHLSGILAGLPTEGIQYRATWGGHGSGFYIGDPNLLLA
IMGPKVTEYWTQGPAAEKASERLGSTERGQQLMAQHMTIFPTCSFLPGIN
TIRAWHPRGPNEIEVWAFTVVDADAPEEMKEEYRQQTLRTFSAGGVFEQD
DGENWVEIQQVLRGHKARSRPFNAEMGLGQTDSDNPDYPGTISYVYSEEA
ARGLYTQWVRMMTSPDWAALDATRP
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
1uli Chain E Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1uli
Crystal Structure of the Terminal Oxygenase Component of Biphenyl Dioxygenase Derived from Rhodococcus sp. Strain RHA1
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Q217 H224 H230 D378
Binding residue
(residue number reindexed from 1)
Q201 H208 H214 D351
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H121 D221 H224 H230 D378
Catalytic site (residue number reindexed from 1)
H105 D205 H208 H214 D351
Enzyme Commision number
1.14.12.18
: biphenyl 2,3-dioxygenase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0005515
protein 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:1uli
,
PDBe:1uli
,
PDBj:1uli
PDBsum
1uli
PubMed
15342255
UniProt
Q53122
|BPHA1_RHOJR Biphenyl 2,3-dioxygenase subunit alpha (Gene Name=bphA1)
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