Structure of PDB 1ulj Chain A Binding Site BS02
Receptor Information
>1ulj Chain A (length=425) Species:
101510
(Rhodococcus jostii RHA1) [
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WADADIAELVDERTGRLDPRIYTDEALYEQELERIFGRSWLLMGHETQIP
KAGDFMTNYMGEDPVMVVRQKNGEIRVFLNQCRHRGMRICRADGGNAKSF
TCSYHGWAYDTGGNLVSVPFEEQAFPGLRKEDWGPLQARVETYKGLIFAN
WDADAPDLDTYLGEAKFYMDHMLDRTEAGTEAIPGIQKWVIPCNWKFAAE
QFCSDMYHAGTTSHLSGILAGLPPTEGIQYRATWGGHGSGFYIGDPNLLL
AIMGPKVTEYWTQGPAAEKASERLGSTERGQQLMAQHMTIFPTCSFLPGI
NTIRAWHPRGPNEIEVWAFTVVDADAPEEMKEEYRQQTLRTFSAGGVFEQ
DDGENWVEIQQVLRGHKARSRPFNAEMGLGQTDSDNPDYPGTISYVYSEE
AARGLYTQWVRMMTSPDWAALDATR
Ligand information
Ligand ID
FES
InChI
InChI=1S/2Fe.2S
InChIKey
NIXDOXVAJZFRNF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[Fe]1S[Fe]S1
CACTVS 3.341
OpenEye OEToolkits 1.5.0
S1[Fe]S[Fe]1
Formula
Fe2 S2
Name
FE2/S2 (INORGANIC) CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
1ulj Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1ulj
Crystal Structure of the Terminal Oxygenase Component of Biphenyl Dioxygenase Derived from Rhodococcus sp. Strain RHA1
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
C98 H100 R101 M103 C118 Y120 H121 W123
Binding residue
(residue number reindexed from 1)
C82 H84 R85 M87 C102 Y104 H105 W107
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 D352
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1ulj
,
PDBe:1ulj
,
PDBj:1ulj
PDBsum
1ulj
PubMed
15342255
UniProt
Q53122
|BPHA1_RHOJR Biphenyl 2,3-dioxygenase subunit alpha (Gene Name=bphA1)
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