9606
TAXONOMY
31983
ChemSpider
Hydrogen Ion
SMILES
C[S+](CC[C@H](N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N
979-92-0
CAS
71-00-1
CAS
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
HMDB0000177
HMDB
C00080
KEGG Compound
Unknown
HMDB0001185
HMDB
1.0
Unknown
CHEBI:15971
ChEBI
1-Methylhistidine synthesis via METTL9-catalyzed methylation
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
C6H9N3O2
L-Histidine
155.06947
SMP0124853
SMPDB
S-Adenosylmethionine
ReactionCatalysis207411
ACTIVATION
HMDB0000939
HMDB
1-Methylhistidine
PW126354
PathWhiz
C7H11N3O2
1-Methylhistidine
169.08513
1.0
2.3.1.85
false
2.3.1.85
L-Histidine + S-Adenosylmethionine → 1-Methylhistidine + Hydrogen Ion + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
Homo sapiens
6038
ChemSpider
L-Histidine
S-ADENOSYLMETHIONINE
BioCyc
1038
PubChem-compound
SMILES
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)C(O)=O
C00135
KEGG Compound
1.0
25246222
PubChem-compound
1.0
C01152
KEGG Compound
HIS
BioCyc
H
Hydrogen Ion
1.007825
6274
PubChem-compound
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
HMDB0059597
HMDB
485-80-3
CAS
SMILES
N[C@@H](CC1=CN=CN1)C(O)=O
C00021
KEGG Compound
CHEBI:16680
ChEBI
CHEBI:50599
ChEBI
332-80-9
CAS
1010
ChemSpider
24762165
PubChem-compound
HMDB0000001
HMDB
1.0
SMILES
CN1C=NC(C[C@H](N)C(O)=O)=C1
83153
ChemSpider
CPD-1823
BioCyc
7020397
PubChem-compound