Structure of PDB 3p93 Chain B Binding Site BS01
Receptor Information
>3p93 Chain B (length=388) Species:
158080
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LKIRDAYTIVTCPGRNFVTLKIVTESGTHGIGDATLNGREMAVAAYLDEH
VVPALIGRDAGRIEDTWQYLYRGAYWRRGPVTMTAIAAVDMALWDIKAKA
AGMPLYQLLGGKSRERVMTYAHCTGQTIEDCLGEVARHVELGYRAVRVQS
GVPGEPADSSLPAEHVWSTEKYLNHAPKLFAAVRERFGDDLHVLHDVHHR
LTPIEAARLGKAVEPYHLFWLEDCVPAENQESLRLIREHTTTPLAIGEVF
NSIHDCRELIQNQWIDYIRMPLTHGGGITAMRRVADLASLYHVRTGFHGP
TDLSPVCLGAAIHFDTWVPNFGIQEHMPHTDETDAVFPHDYRFEDGHFLA
GESPGHGVDIDEELAAKYPYERASLPVNRLEDGTLWHW
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
3p93 Chain B Residue 406 [
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Receptor-Ligand Complex Structure
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PDB
3p93
CRYSTAL STRUCTURE OF D-MANNONATE DEHYDRATASE FROM CHROMOHALOBACTER SALEXIGENS complexed with MG,D-Mannonate and 2-keto-3-deoxy-D-Gluconate
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D213 E239 E265
Binding residue
(residue number reindexed from 1)
D196 E222 E248
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H124 R149 Q151 D213 H215 E239 G264 E265 R286 P288 H315 G316 E342 W405
Catalytic site (residue number reindexed from 1)
H122 R147 Q149 D196 H198 E222 G247 E248 R269 P271 H298 G299 E325 W388
Enzyme Commision number
4.2.1.-
4.2.1.39
: gluconate dehydratase.
4.2.1.8
: mannonate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008927
mannonate dehydratase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
GO:0047929
gluconate 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:3p93
,
PDBe:3p93
,
PDBj:3p93
PDBsum
3p93
PubMed
UniProt
Q1QT89
|DMGD_CHRSD D-galactonate dehydratase family member ManD (Gene Name=manD)
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