Structure of PDB 4hnc Chain B Binding Site BS01
Receptor Information
>4hnc Chain B (length=351) Species:
303
(Pseudomonas putida) [
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EVLITGLRTRAVNVPLAYPVHGTAPLVLIDLATSAGVVGHSYLFAYTPVA
LKSLKQLLDDMAAMIVNEPLAPVSLEAMLAKRFSLAGYTGLIRMAAAGID
MAAWDALGKVHETPLVKLLGANARPVQAYDSHSLDGVKLATERAVTAAEL
GFRAVKTCIGYPALDQDLAVVRSIRQAVGDDFGIMVDYNQSLDVPAAIKR
SQALQQEGVTWIEEPTLQHDYEGHQRIQSKLNVPVQMGENWLGPEEMFKA
LSIGASRLAMPDAMKIGGVTGWIRASALAQQFGIPMSSHLFQEISAHLLA
ATPTAHWLERLDLAGSVIEPTLTFEGGNAVIPDLPGVGIIWREKEIGKYL
V
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
4hnc Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4hnc
Potent inhibition of mandelate racemase by a fluorinated substrate-product analogue with a novel binding mode.
Resolution
1.889 Å
Binding residue
(original residue number in PDB)
D195 E221 E247
Binding residue
(residue number reindexed from 1)
D187 E213 E239
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
V22 S139 K164 C166 D195 N197 E221 G246 E247 D270 M294 H297 L298 F299 A313 E317
Catalytic site (residue number reindexed from 1)
V20 S131 K156 C158 D187 N189 E213 G238 E239 D262 M286 H289 L290 F291 A305 E309
Enzyme Commision number
5.1.2.2
: mandelate racemase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016836
hydro-lyase activity
GO:0016853
isomerase activity
GO:0018838
mandelate racemase activity
GO:0046872
metal ion binding
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
GO:0018924
mandelate metabolic process
GO:0019596
mandelate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4hnc
,
PDBe:4hnc
,
PDBj:4hnc
PDBsum
4hnc
PubMed
24472022
UniProt
P11444
|MANR_PSEPU Mandelate racemase (Gene Name=mdlA)
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