Structure of PDB 3vcc Chain B Binding Site BS02

Receptor Information
>3vcc Chain B (length=385) Species: 481743 (Paenibacillus sp. Y412MC10) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SLNITGIQSDWKVEKIEFAKLTGERARSAGANGRIGVHGKSCTVDIARIT
IDGQTGYGSSIHMTPEWAEDVIGRRLLDLFDDRGRLREAYRLQLEYPVLD
WLGQRQGKPVYDLVSGAHLETGASLVVPCYDTSLYFDDLHLADERAAVAL
MQEEAMQGYAKGQRHFKIKVGRGGRHMPLWEGTKRDIAIVRGISEVAGPA
GKIMIDANNAYNLNLTKEVLAALSDVNLYWLEEAFHEDEALYEDLKEWLG
QRGQNVLIADGEGLASPHLIEWATRGRVDVLQYDIIWPGFTHWMELGEKL
DAHGLRSAPHCYGNAYGIYASGHLSAAVRNFEFVEYDDITIEGMDVSGYR
IENGEIHVPATPGFGIVFDDELVTYLINRSGWSEG
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 chain3vcc Chain B Residue 403 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3vcc CRYSTAL STRUCTURE OF D-Galacturonate Dehydratase from GEOBACILLUS SP. complexed with Mg
Resolution1.64 Å
Binding residue
(original residue number in PDB)
D207 E233 E263
Binding residue
(residue number reindexed from 1)
D206 E232 E262
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) D207 E233 E263 D285 H311
Catalytic site (residue number reindexed from 1) D206 E232 E262 D284 H310
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0016836 hydro-lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0016052 carbohydrate catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:3vcc, PDBe:3vcc, PDBj:3vcc
PDBsum3vcc
PubMed
UniProtD3EID5

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