Structure of PDB 5jdz Chain B Binding Site BS01
Receptor Information
>5jdz Chain B (length=220) Species:
337
(Burkholderia glumae) [
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QRAIEVRTIFHMIGDVSGKSVLDLACGFGFFGREIYRRGAAKVVGVDISE
KMIELAREESRKYGDPLEFHVRDVANMEPLGQFDLVNAAWLFNYADSVEN
LRKMFKVVRASLKPDGKLVAYTVDPDFSLAKGNFAKYGVNVLNERAWGPG
YRHDAEFVPSQFSFYRWSRADYESAIADAGFSHFEWQKPLLEADDIATHP
PGFWDVFQNNCLQTGLVCKP
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
5jdz Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5jdz
Burkholderia glumae ToxA Is a Dual-Specificity Methyltransferase That Catalyzes the Last Two Steps of Toxoflavin Biosynthesis.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
R24 A47 C48 F53 D69 I70 D95 V96 A111 W112 Y116
Binding residue
(residue number reindexed from 1)
R2 A25 C26 F31 D47 I48 D73 V74 A89 W90 Y94
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:5jdz
,
PDBe:5jdz
,
PDBj:5jdz
PDBsum
5jdz
PubMed
27070241
UniProt
Q9LBJ0
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