Structure of PDB 5jdy Chain B Binding Site BS01
Receptor Information
>5jdy Chain B (length=241) Species:
337
(Burkholderia glumae) [
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ARFDSIGGLFEDFTQSAAQRAIEVRTIFHMIGDVSGKSVLDLACGFGFFG
REIYRRGAAKVVGVDISEKMIELAREESRKYGDPLEFHVRDVANMEPLGQ
FDLVNAAWLFNYADSVENLRKMFKVVRASLKPDGKLVAYTVDPDFSLAKG
NFAKYGVNVLNERAWGPGYRHDAEFVTDPPSQFSFYRWSRADYESAIADA
GFSHFEWQKPLLEADDIATHPPGFWDVFQNNCLQTGLVCKP
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
5jdy Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5jdy
Burkholderia glumae ToxA Is a Dual-Specificity Methyltransferase That Catalyzes the Last Two Steps of Toxoflavin Biosynthesis.
Resolution
1.77 Å
Binding residue
(original residue number in PDB)
F7 F14 R24 A47 C48 G49 D69 I70 V96 Y116
Binding residue
(residue number reindexed from 1)
F3 F10 R20 A43 C44 G45 D65 I66 V92 Y112
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
View graph for
Biological Process
External links
PDB
RCSB:5jdy
,
PDBe:5jdy
,
PDBj:5jdy
PDBsum
5jdy
PubMed
27070241
UniProt
Q9LBJ0
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