Structure of PDB 3cb3 Chain B Binding Site BS02

Receptor Information
>3cb3 Chain B (length=361) Species: 296591 (Polaromonas sp. JS666) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SDRITWVRISSCYLPLATPIMTEIAILFAEIETAGGHQGLGFSYSKRAGG
PGQFAHAREIAPALIGEDPSDIAKLWDKLCWAGASAGRSGLSTQAIGAFD
VALWDLKAKRAGLSLAKLLGSYRDSVRCYNTSGGFLHTPIDQLMVNASAS
IERGIGGIKLKVGQPDGALDIARVTAVRKHLGDAVPLMVDANQQWDRPTA
QRMCRIFEPFNLVWIEEPLDAYDHEGHAALALQFDTPIATGEMLTSAAEH
GDLIRHRAADYLMPDAPRVGGITPFLKIASLAEHAGLMLAPHFAMELHVH
LAAAYPREPWVEHFEWLEPLFNERIEIRDGRMLVPTRPGLGLTLSGQVKA
WTREEAQVGTR
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain3cb3 Chain B Residue 503 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure 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]
PDB3cb3 Crystal structure of L-Talarate dehydratase from Polaromonas sp. JS666 complexed with Mg and L-glucarate.
Resolution2.0 Å
Binding residue
(original residue number in PDB)
A252 F255
Binding residue
(residue number reindexed from 1)
A231 F234
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) S66 T152 K180 K182 D211 N213 E237 G262 E263 M284 D286 H313 F314 A315 E333
Catalytic site (residue number reindexed from 1) S45 T131 K159 K161 D190 N192 E216 G241 E242 M263 D265 H292 F293 A294 E312
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:3cb3, PDBe:3cb3, PDBj:3cb3
PDBsum3cb3
PubMed
UniProtQ12GE3

[Back to BioLiP]