Structure of PDB 4ylh Chain A Binding Site BS01
Receptor Information
>4ylh Chain A (length=421) Species:
55952
(Streptomyces toyocaensis) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
DGLWAALTEAAASVEKLLATLPEHGARSSAERAEIAAAHDAARALRVRFL
DTHADAVYDRLTDHRRVHLRLAELVEAAATAFPGLVPTQQQLAVERSLPQ
AAKEGHEIDQGIFLRAVLRSPLAGPHLLDAMLRPTPRALELLPEFVRTGE
VEMEAVHLERRDGVARLTMCRDDRLNAEDGQQVDDMETAVDLALLDPGVR
VGLLRGGVMSHPRYRGKRVFSAGINLKYLSQGGISLVDFLMRRELGYIHK
LVRGVLTNDDRPGWWHSPRIEKPWVAAVDGFAIGGGAQLLLVFDRVLASS
DAYFSLPAAKEGIIPGAANLRLGRFAGPRVSRQVILEGRRIWAKEPEARL
LVDEVVEPDELDAAIERSLTRLDGDAVLANRRMLNLADESPDGFRAYMAE
FALMQALRLYGHDVIDKVGRF
Ligand information
Ligand ID
XE
InChI
InChI=1S/Xe
InChIKey
FHNFHKCVQCLJFQ-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Xe]
Formula
Xe
Name
XENON
ChEMBL
CHEMBL1236802
DrugBank
DB13453
ZINC
PDB chain
4ylh Chain A Residue 501 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
4ylh
Oxygen diffusion pathways in a cofactor-independent dioxygenase.
Resolution
2.58 Å
Binding residue
(original residue number in PDB)
A298 L302 L317
Binding residue
(residue number reindexed from 1)
A287 L291 L306
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
I235 G296 Q299 A319
Catalytic site (residue number reindexed from 1)
I224 G285 Q288 A308
Enzyme Commision number
1.13.11.80
: (3,5-dihydroxyphenyl)acetyl-CoA 1,2-dioxygenase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0042802
identical protein binding
Biological Process
GO:0006635
fatty acid beta-oxidation
GO:0017000
antibiotic biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4ylh
,
PDBe:4ylh
,
PDBj:4ylh
PDBsum
4ylh
PubMed
26508997
UniProt
Q8KLK7
|DPGC_STRTO (3,5-dihydroxyphenyl)acetyl-CoA 1,2-dioxygenase (Gene Name=BU52_01220)
[
Back to BioLiP
]