Structure of PDB 5je4 Chain B Binding Site BS01
Receptor Information
>5je4 Chain B (length=225) Species:
337
(Burkholderia glumae) [
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AAQRAIEVRTIFHMIGDVSGKSVLDLACGFGFFGREIYRRGAAKVVGVDI
SEKMIELAREESRKYGDPLEFHVRDVANMEPLGQFDLVNAAWLFNYADSV
ENLRKMFKVVRASLKPDGKLVAYTVDPDFSLAKGNFAKYGVNVLNERAWG
PGYRHDAEFVTDPPSQFSFYRWSRADYESAIADAGFSHFEWQKPLLEADD
IATHPPGFWDVFQNNCLQTGLVCKP
Ligand information
Ligand ID
SAH
InChI
InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
InChIKey
ZJUKTBDSGOFHSH-WFMPWKQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCSC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CSCCC(C(=O)O)N)O)O)N
CACTVS 3.341
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCSCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CSCC[C@@H](C(=O)O)N)O)O)N
Formula
C14 H20 N6 O5 S
Name
S-ADENOSYL-L-HOMOCYSTEINE
ChEMBL
CHEMBL418052
DrugBank
DB01752
ZINC
ZINC000004228232
PDB chain
5je4 Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5je4
Burkholderia glumae ToxA Is a Dual-Specificity Methyltransferase That Catalyzes the Last Two Steps of Toxoflavin Biosynthesis.
Resolution
1.932 Å
Binding residue
(original residue number in PDB)
R24 A47 C48 F53 D69 I70 D95 V96 A111 Y116
Binding residue
(residue number reindexed from 1)
R4 A27 C28 F33 D49 I50 D75 V76 A91 Y96
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
Biological Process
GO:0032259
methylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5je4
,
PDBe:5je4
,
PDBj:5je4
PDBsum
5je4
PubMed
27070241
UniProt
Q9LBJ0
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