Structure of PDB 3i4k Chain H Binding Site BS01
Receptor Information
>3i4k Chain H (length=370) Species:
1718
(Corynebacterium glutamicum) [
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DLTIQKVESRILDVPLIRPHGFATTTSTEQHILLVSVHLENGVIGYGEGV
VPGGPWWGGESVETMKALVDGYLAPVLIGRAVSELAGIMADLERVVARAR
YAKAAVDVAMHDAWARSLNVPVRDLLGGTVRDKVDVTWALGVLPLDVAVA
EIEERIEEFGNRSFKLKMGAGDPAEDTRRVAELAREVGDRVSLRIDINAR
WDRRTALHYLPILAEAGVELFEQPTPADDLETLREITRRTNVSVMADESV
WTPAEALAVVKAQAADVIALKTTKHGGLLESKKIAAIAEAGGLACHGATS
LEGPIGTAASLQFAASTKAISYGTELFGPQLLKDTYIVQEFEYKDGQVAI
PQGPGLGVDVDMDKVNFYTR
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
3i4k Chain H Residue 385 [
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Receptor-Ligand Complex Structure
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PDB
3i4k
Crystal structure of Muconate lactonizing enzyme from Corynebacterium glutamicum
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
D200 E226 D251
Binding residue
(residue number reindexed from 1)
D196 E222 D247
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H24 V55 G58 G91 A143 K169 K171 D200 N202 E226 D251 E252 S253 A273 K275 T276 A302 T303 S304 T328 E329 L330
Catalytic site (residue number reindexed from 1)
H20 V51 G54 G87 A139 K165 K167 D196 N198 E222 D247 E248 S249 A269 K271 T272 A298 T299 S300 T324 E325 L326
Enzyme Commision number
5.5.1.1
: muconate cycloisomerase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016853
isomerase activity
GO:0018849
muconate cycloisomerase activity
GO:0018850
chloromuconate cycloisomerase activity
GO:0030145
manganese ion binding
GO:0046872
metal ion binding
Biological Process
GO:0009056
catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3i4k
,
PDBe:3i4k
,
PDBj:3i4k
PDBsum
3i4k
PubMed
UniProt
Q8NN12
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