Structure of PDB 2og9 Chain B Binding Site BS01
Receptor Information
>2og9 Chain B (length=363) Species:
296591
(Polaromonas sp. JS666) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
PSDRITWVRISSCYLPLATPIMTEIAILFAEIETAGGHQGLGFSYSKRAG
GPGQFAHAREIAPALIGEDPSDIAKLWDKLCWAGASAGRSGLSTQAIGAF
DVALWDLKAKRAGLSLAKLLGSYRDSVRCYNTSGGFLHTPIDQLMVNASA
SIERGIGGIKLKVGQPDGALDIARVTAVRKHLGDAVPLMVDANQQWDRPT
AQRMCRIFEPFNLVWIEEPLDAYDHEGHAALALQFDTPIATGEMLTSAAE
HGDLIRHRAADYLMPDAPRVGGITPFLKIASLAEHAGLMLAPHFAMELHV
HLAAAYPREPWVEHFEWLEPLFNERIEIRDGRMLVPTRPGLGLTLSGQVK
AWTREEAQVGTRP
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
2og9 Chain B Residue 402 [
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
2og9
Crystal Structure of mandelate racemase/muconate lactonizing enzyme from Polaromonas sp. JS666
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
A254 F257
Binding residue
(residue number reindexed from 1)
A232 F235
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S68 T154 K182 K184 D213 N215 E239 G264 E265 M286 D288 H315 F316 A317 E335
Catalytic site (residue number reindexed from 1)
S46 T132 K160 K162 D191 N193 E217 G242 E243 M264 D266 H293 F294 A295 E313
Enzyme Commision number
4.2.1.-
4.2.1.42
: galactarate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008867
galactarate dehydratase activity
GO:0016829
lyase activity
GO:0016836
hydro-lyase activity
GO:0046872
metal ion binding
GO:1990594
L-altrarate dehydratase activity
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2og9
,
PDBe:2og9
,
PDBj:2og9
PDBsum
2og9
PubMed
UniProt
Q12GE3
[
Back to BioLiP
]