Structure of PDB 3no1 Chain D Binding Site BS01
Receptor Information
>3no1 Chain D (length=350) Species:
312284
(marine actinobacterium PHSC20C1) [
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LTITRIETIPMVARATIVTRVHTDAGIIGEAYTGDEHETMFDIDRIIHEE
LAPTLIGQDAMAIERLWDSGYKVTFDILRDRRLGLVALAAVNTAIWDAVG
KALKMPLWKLWGGYRNELPMIAIGGYYGEPLGSIADEMHNYQELGLAGVK
FKVGGLSAAEDAARITAAREAAGDDFIICIDANQGYKPAVAVDLSRRIAD
LNIRWFEEPVEWHNDKRSMRDVRYQGSVPVCAGQTEFSASGCRDLMETGA
IDVCNFDSSWSGGPTAWLRTAAIATSYDVQMGHHEEPQVSTHLLASQPHG
TIAECFHPDRDPFWWNMITNRPKLNNGTLTLSDRPGLGWDLNWDYIDQYR
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
3no1 Chain D Residue 397 [
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Receptor-Ligand Complex Structure
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PDB
3no1
Crystal Structure of Mandelate racemase/muconate lactonizing enzyme from a Marine actinobacterium in complex with magnesium
Resolution
2.16 Å
Binding residue
(original residue number in PDB)
D215 E241 Q268
Binding residue
(residue number reindexed from 1)
D181 E207 Q234
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D69 I157 K184 K186 I214 D215 A216 N217 E241 G267 Q268 N289 D291 H318 E319 E320 E338 D343
Catalytic site (residue number reindexed from 1)
D35 I123 K150 K152 I180 D181 A182 N183 E207 G233 Q234 N255 D257 H284 E285 E286 E304 D309
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:3no1
,
PDBe:3no1
,
PDBj:3no1
PDBsum
3no1
PubMed
UniProt
A4AFX2
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