Structure of PDB 5dly Chain A Binding Site BS02
Receptor Information
>5dly Chain A (length=266) Species:
326423
(Bacillus velezensis FZB42) [
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EIETIVRESEANRIQAQTWFSHPEKSKVSFRYDERETSSIRSISIETFLS
FYSSKFNREPYSVLDIGCGQGQVIQYLNSRFQKIELTGIDSSAQAISSAK
KLGINASFICSNAENIMQYVSKKQDIIFIHLCFGLFKNPIAIVNTLIHLL
SDQSCIYIVDLDRNSLGEGLNTAQSREEEAYLKDQYRASLTMEEFKQLLH
VVTKEQHGVSFHVGNSFIGGFDETSSQFFSLMRNRNLQDALRTSVGEQLK
QSQMPALLHGWIIKNK
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
5dly Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5dly
Insights into methyltransferase specificity and bioactivity of derivatives of the antibiotic plantazolicin.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
Q18 F21 G68 D91 S92 A114 H131 C133 L136 F137
Binding residue
(residue number reindexed from 1)
Q17 F20 G67 D90 S91 A113 H130 C132 L135 F136
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:5dly
,
PDBe:5dly
,
PDBj:5dly
PDBsum
5dly
PubMed
25635336
UniProt
A7Z2A9
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