Structure of PDB 1jct Chain B Binding Site BS01
Receptor Information
>1jct Chain B (length=442) Species:
562
(Escherichia coli) [
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FTTPVVTEMQVIPVAGHDSMLMNLSGAHAPFFTRNIVIIKDNSGHTGVGE
IPGGEKIRKTLEDAIPLVVGKTLGEYKNVLTLVRNTFADRDAGGRGLQTF
DLRTTIHVVTGIEAAMLDLLGQHLGVNVASLLGDGQQRSEVEMLGYLFFV
GNRKATPLPYQSQPDDSCDWYRLRHEEAMTPDAVVRLAEAAYEKYGFNDF
KLKGGVLAGEEEAESIVALAQRFPQARITLDPNGAWSLNEAIKIGKYLKG
SLAYAEDPCGAEQGFSGREVMAEFRRATGLPTATNMIATDWRQMGHTLSL
QSVDIPLADPHFWTMQGSVRVAQMCHEFGLTWGSHSLNHFDISLAMFTHV
AAAAPGKITAIDTHWIWQEGNQRLTKEPFEIKGGLVQVPEKPGLGVEIDM
DQVMKAHELYQKHGLGARDDAMGMQYLIPGWTFDNKRPCMVR
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1jct Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1jct
Evolution of enzymatic activities in the enolase superfamily: identification of the general acid catalyst in the active site of D-glucarate dehydratase from Escherichia coli.
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
D235 E260 N289
Binding residue
(residue number reindexed from 1)
D231 E256 N285
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K205 K207 D235 N237 E260 N289 M290 D313 H339 L341 I365
Catalytic site (residue number reindexed from 1)
K201 K203 D231 N233 E256 N285 M286 D309 H335 L337 I361
Enzyme Commision number
4.2.1.40
: glucarate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008872
glucarate dehydratase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0019394
glucarate catabolic process
GO:0042838
D-glucarate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1jct
,
PDBe:1jct
,
PDBj:1jct
PDBsum
1jct
PubMed
11513584
UniProt
P0AES2
|GUDD_ECOLI Glucarate dehydratase (Gene Name=gudD)
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