Structure of PDB 3ojn Chain D Binding Site BS01
Receptor Information
>3ojn Chain D (length=359) Species:
47914
(Brevibacterium fuscum) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
EIPKPVAPAPDILRCAYAELVVTDLAKSRNFYVDVLGLHVSYEDENQIYL
RSFEEFIHHNLVLTKGPVAALKAMAFRVRTPEDVDKAEAYYQELGCRTER
RKDGFVKGIGDALRVEDPLGFPYEFFFETTHVERLHMRYDLYSAGELVRL
DHFNQVTPDVPRGRKYLEDLGFRVTEDIQDDEGTTYAAWMHRKGTVHDTA
LTGGNGPRLHHVAFSTHEKHNIIQICDKMGALRISDRIERGPGRHGVSNA
FYLYILDPDNHRIEIYTQDYYTGDPDNPTITWNVHDNQRRDWWGNPVVPS
WYTEASKVLDLDGNVQEIIERTDDSELEVTIGADGFSFTRAGDEDGSYHG
QASKGFKLG
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
3ojn Chain D Residue 500 [
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
3ojn
A hyperactive cobalt-substituted extradiol-cleaving catechol dioxygenase.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
H155 H214 E267
Binding residue
(residue number reindexed from 1)
H152 H211 E264
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H155 H200 H214 H248 Y257 E267
Catalytic site (residue number reindexed from 1)
H152 H197 H211 H245 Y254 E264
Enzyme Commision number
1.13.11.15
: 3,4-dihydroxyphenylacetate 2,3-dioxygenase.
Gene Ontology
Molecular Function
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
View graph for
Molecular Function
External links
PDB
RCSB:3ojn
,
PDBe:3ojn
,
PDBj:3ojn
PDBsum
3ojn
PubMed
21153851
UniProt
Q45135
[
Back to BioLiP
]