Structure of PDB 4k8g Chain A Binding Site BS01
Receptor Information
>4k8g Chain A (length=386) Species:
279238
(Novosphingobium aromaticivorans DSM 12444) [
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HMKITAARVIITCPGRNFVTLKIETDQGVYGIGDATLNGRELSVVAYLQE
HVAPCLIGMDPRRIEDIWQYVYRGAYWRRGPVTMRAIAAVDMALWDIKAK
MAGMPLYQLLGGRSRDGIMVYGHANGSDIAETVEAVGHYIDMGYKAIRAQ
TGVPGIKSLPSVTGWDTRKALNYVPKLFEELRKTYGFDHHLLHDGHHRYT
PQEAANLGKMLEPYQLFWLEDCTPAENQEAFRLVRQHTVTPLAVGEIFNT
IWDAKDLIQNQLIDYIRATVVGAGGLTHLRRIADLASLYQVRTGCHGATD
LSPVTMGCALHFDTWVPNFGIQEYMRHTEETDAVFPHDYWFEKGELFVGE
TPGHGVDIDEELAAKYPYKPAYLPVARLEDGTMWNW
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
4k8g Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
4k8g
Crystal structure of D-Mannonate dehydratase from Novosphingobium aromaticivorans mutant (V161A, R163A, K165G, L166A, Y167G, Y168A, E169G)
Resolution
1.25 Å
Binding residue
(original residue number in PDB)
D210 E236 E262
Binding residue
(residue number reindexed from 1)
D194 E220 E246
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G121 R147 Q149 D210 H212 E236 G261 E262 R283 T285 H312 E339 W402
Catalytic site (residue number reindexed from 1)
G122 R148 Q150 D194 H196 E220 G245 E246 R267 T269 H296 E323 W386
Enzyme Commision number
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
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4k8g
,
PDBe:4k8g
,
PDBj:4k8g
PDBsum
4k8g
PubMed
UniProt
A4XF23
|MAND_NOVAD D-mannonate dehydratase (Gene Name=manD)
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