Structure of PDB 3bqb Chain Z Binding Site BS01

Receptor Information
>3bqb Chain Z (length=282) Species: 273057 (Saccharolobus solfataricus P2) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MKLFRVVKRGYYISYAILDNSTIIRLDEDPIKALMRYSENKEVLGDRVTG
IDYQSLLKSFQINDIRITKPIDPPEVWGSGISYENVAKILGKTIYEKVYD
AVRPEIFFKATPNRCVGHGEAIAVRSDSEWTLPEPELAVVLDSNGKILGY
TIMDDVSARDLEAENPLYLPQSKIYAGCCAFGPVIVTSDEIKNPYSLDIT
LKIVREGRVFFEGSVNTNKMRRKIEEQIQYLIRDNPIPDGTILTTGTAIV
PGRDKGLKDEDIVEITISNIGTLITPVKKRRK
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 chain3bqb Chain Z Residue 294 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3bqb Structural insight into substrate binding and catalysis of a novel 2-keto-3-deoxy-D-arabinonate dehydratase illustrates common mechanistic features of the FAH superfamily
Resolution2.7 Å
Binding residue
(original residue number in PDB)
E143 E145 D164
Binding residue
(residue number reindexed from 1)
E134 E136 D155
Annotation score1
Enzymatic activity
Enzyme Commision number 4.2.1.141: 2-dehydro-3-deoxy-D-arabinonate dehydratase.
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0003824 catalytic activity
GO:0016829 lyase activity
GO:0016836 hydro-lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0019571 D-arabinose catabolic process
GO:0051289 protein homotetramerization

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Molecular Function

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Biological Process
External links
PDB RCSB:3bqb, PDBe:3bqb, PDBj:3bqb
PDBsum3bqb
PubMed18448118
UniProtQ97UA0|KDAD_SACS2 2-dehydro-3-deoxy-D-arabinonate dehydratase (Gene Name=kdaD)

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