Structure of PDB 3vcc Chain B Binding Site BS01
Receptor Information
>3vcc Chain B (length=385) Species:
481743
(Paenibacillus sp. Y412MC10) [
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SLNITGIQSDWKVEKIEFAKLTGERARSAGANGRIGVHGKSCTVDIARIT
IDGQTGYGSSIHMTPEWAEDVIGRRLLDLFDDRGRLREAYRLQLEYPVLD
WLGQRQGKPVYDLVSGAHLETGASLVVPCYDTSLYFDDLHLADERAAVAL
MQEEAMQGYAKGQRHFKIKVGRGGRHMPLWEGTKRDIAIVRGISEVAGPA
GKIMIDANNAYNLNLTKEVLAALSDVNLYWLEEAFHEDEALYEDLKEWLG
QRGQNVLIADGEGLASPHLIEWATRGRVDVLQYDIIWPGFTHWMELGEKL
DAHGLRSAPHCYGNAYGIYASGHLSAAVRNFEFVEYDDITIEGMDVSGYR
IENGEIHVPATPGFGIVFDDELVTYLINRSGWSEG
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
3vcc Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
3vcc
CRYSTAL STRUCTURE OF D-Galacturonate Dehydratase from GEOBACILLUS SP. complexed with Mg
Resolution
1.64 Å
Binding residue
(original residue number in PDB)
E234 E238 D261
Binding residue
(residue number reindexed from 1)
E233 E237 D260
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D207 E233 E263 D285 H311
Catalytic site (residue number reindexed from 1)
D206 E232 E262 D284 H310
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016836
hydro-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0016052
carbohydrate catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3vcc
,
PDBe:3vcc
,
PDBj:3vcc
PDBsum
3vcc
PubMed
UniProt
D3EID5
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