Structure of PDB 3es8 Chain A Binding Site BS01
Receptor Information
>3es8 Chain A (length=387) Species:
182710
(Oceanobacillus iheyensis) [
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MKITDLELHAVGIPRHTGFVNKHVIVKIHTDEGLTGIGEMSDFSHLPLYS
VDLHDLKQGLLSILLGQNPFDLMKINKELTDNFPETMYYYEKGSFIRNGI
DNALHDLCAKYLDISVSDFLGGRVKEKIKVCYPIFRHRFSEEVESNLDVV
RQKLEQGFDVFRLYVGKNLDADEEFLSRVKEEFGSRVRIKSYDFSHLLNW
KDAHRAIKRLTKYDLGLEMIESPAPRNDFDGLYQLRLKTDYPISEHVWSF
KQQQEMIKKDAIDIFNISPVFIGGLTSAKKAAYAAEVASKDVVLGTTQEL
SVGTAAMAHLGCSLTNINHTSDPTGPELYVGDVVKNRVTYKDGYLYAPDR
SVKGLGIELDESLLAKYQVPDLSWDNVTVHQLQDRTA
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
3es8 Chain A Residue 393 [
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Receptor-Ligand Complex Structure
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PDB
3es8
Computation-facilitated assignment of the function in the enolase superfamily: a regiochemically distinct galactarate dehydratase from Oceanobacillus iheyensis .
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
D42 H45 T297
Binding residue
(residue number reindexed from 1)
D42 H45 T297
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D42 H45 Y90 P133 R162 Y164 Y192 D193 F194 M219 E221 S244 E245 H246 S268 G295 T296 T297 S321 D322
Catalytic site (residue number reindexed from 1)
D42 H45 Y90 P133 R162 Y164 Y192 D193 F194 M219 E221 S244 E245 H246 S268 G295 T296 T297 S321 D322
Enzyme Commision number
4.2.1.158
: galactarate dehydratase (D-threo-forming).
Gene Ontology
Molecular Function
GO:0016829
lyase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:3es8
,
PDBe:3es8
,
PDBj:3es8
PDBsum
3es8
PubMed
19883118
UniProt
Q8EMJ9
|GALRD_OCEIH Galactarate dehydratase (D-threo-forming) (Gene Name=OB2843)
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