Structure of PDB 5je5 Chain A Binding Site BS01
Receptor Information
>5je5 Chain A (length=243) Species:
337
(Burkholderia glumae) [
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TTARYDSIGGLFEDFTQSAAQRAIEVRTIFHMIGDVSGKSVLDLACGFGF
FGREIYRRGAAKVVGVDISEKMIELAREESRKYGDPLEFHVRDVANMEPL
GQFDLVNAAWLFNYADSVENLRKMFKVVRASLKPDGKLVAYTVDPDFSLA
KGNFAKYGVNVLNERAWGPGYRHDAEFVTDPPSQFSFYRWSRADYESAIA
DAGFSHFEWQKPLLEADDIATHPPGFWDVFQNNCLQTGLVCKP
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
5je5 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5je5
Burkholderia glumae ToxA Is a Dual-Specificity Methyltransferase That Catalyzes the Last Two Steps of Toxoflavin Biosynthesis.
Resolution
1.564 Å
Binding residue
(original residue number in PDB)
Y7 F14 R24 A47 C48 G49 F53 D69 I70 D95 V96 A111 Y116
Binding residue
(residue number reindexed from 1)
Y5 F12 R22 A45 C46 G47 F51 D67 I68 D93 V94 A109 Y114
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:5je5
,
PDBe:5je5
,
PDBj:5je5
PDBsum
5je5
PubMed
27070241
UniProt
Q9LBJ0
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