Structure of PDB 6jko Chain A Binding Site BS01
Receptor Information
>6jko Chain A (length=376) Species:
1447716
(Bifidobacterium catenulatum PV20-2) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GMLWDYAQPVTIRFGKGRAMEIKDIAEAMGLHDGIMVTPKFFVDSGEAQR
LIDASDGAVSTVFTDFSPNPDVTEVDACAEIIRKNHCEFVVAMGGGSAMD
VSKAAASICLTDDSIADYHGTGKAMPQKHLPIIALPTTAGTGSEVTCVSV
LTNRKLGKKAPIVSDGFFPSVAIVDPELTYSVPPKITASTGMDVLSQAIE
GFWSKGHQPICDSCAAHAAKLVFKYLPIAVAEPHNEEAREKMCEASVIAG
LAFTLPKTTSSHACSFPLTNIHGIPHGEACGLTLDYFARINKDAQHGRVQ
EFARGIGFKDVDAMADAIHDLKVRIGMRTGLKDLNLTEEQIADLVRISRH
PNLYNNPVEITDDMLDTMYHYLASTD
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
6jko Chain A Residue 401 [
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
6jko
Identification and characterization of a new sulfoacetaldehyde reductase from the human gut bacteriumBifidobacterium kashiwanohense.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D192 H261 H275
Binding residue
(residue number reindexed from 1)
D193 H262 H276
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004022
alcohol dehydrogenase (NAD+) activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:6jko
,
PDBe:6jko
,
PDBj:6jko
PDBsum
6jko
PubMed
31123167
UniProt
A0A0A7I0A5
[
Back to BioLiP
]