Structure of PDB 4ymg Chain B Binding Site BS01
Receptor Information
>4ymg Chain B (length=239) [
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LGSILPFNEETADRVSAYCEKNSHGIPDALVEHWEWTRTRFPDADKMSSR
LQGSWMIFTARDRKPKRILEIGCYSGYSALAWYEGTRDTKAEIVTLEYSP
KMIAASREAFKKYGVGDRVKLIEGPAENTLKTLEGEFDLIFVDANKDGYA
GYVKTILDQGLLSANGIILCDNVFARGLTIGPDCAPWLNDHVRPYWNGCG
QALDKFSAGLMEDPRIDVLLLPVFDGVTQIRWKDGAQRA
Ligand information
Ligand ID
SAM
InChI
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27-/m0/s1
InChIKey
MEFKEPWMEQBLKI-FCKMPRQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.341
C[S+](CC[CH](N)C([O-])=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S@@+](CC[C@@H](C(=O)[O-])N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
ACDLabs 10.04
[O-]C(=O)C(N)CC[S+](C)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H22 N6 O5 S
Name
S-ADENOSYLMETHIONINE
ChEMBL
CHEMBL1235831
DrugBank
ZINC
PDB chain
4ymg Chain B Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
4ymg
Structure and Biophysical Characterization of the S-Adenosylmethionine-dependent O-Methyltransferase PaMTH1, a Putative Enzyme Accumulating during Senescence of Podospora anserina.
Resolution
1.899 Å
Binding residue
(original residue number in PDB)
S49 G73 Y75 S79 E98 Y99 P126 A127 E128 D144 A145 N146 Y153
Binding residue
(residue number reindexed from 1)
S48 G72 Y74 S78 E97 Y98 P125 A126 E127 D143 A144 N145 Y152
Annotation score
4
Binding affinity
MOAD
: Kd=21uM
Enzymatic activity
Catalytic site (original residue number in PDB)
D144 K147 D172 N173
Catalytic site (residue number reindexed from 1)
D143 K146 D171 N172
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008171
O-methyltransferase activity
GO:0008757
S-adenosylmethionine-dependent methyltransferase activity
Biological Process
GO:0032259
methylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:4ymg
,
PDBe:4ymg
,
PDBj:4ymg
PDBsum
4ymg
PubMed
25979334
UniProt
Q9HGR1
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