EC Number |
Inhibitors |
Structure |
---|
2.1.1.10 | more |
no product inhibition by L-methionine below 0.5 mM, no inhibition by EDTA |
|
2.1.1.10 | more |
relative inhibition of human BHMT (EC 2.1.1.5) and human BHMT-2 activities by methyl donor substrates determined |
|
2.1.1.10 | EDTA |
1 mM, 26% inhibition |
|
2.1.1.10 | EDTA |
complete inhibition, reversible by addition of excess of Zn2+ |
|
2.1.1.10 | S-adenosyl-L-methionine |
weak inhibitor of, does not inhibit BHMT (EC 2.1.1.5), not inhibited by betaine |
|
2.1.1.10 | S-adenosyl-L-methionine |
product inhibition above 0.25 mM |
|
2.1.1.10 | S-adenosyl-L-homocysteine |
product inhibition |
|
2.1.1.10 | L-methionine |
product inhibition |
|
2.1.1.10 | L-methionine |
no inhibition with D-isomer; product inhibition |
|
2.1.1.10 | L-methionine |
strong product inhibition |
|