| Health / Medical Topics |
S-Beta Thalassemia
A disorder characterized by the body's inability to synthesize beta-globin chains, leading to the formation of abnormal hemoglobin and anemia. This inherited autosomal recessive blood disorder is caused by germline mutation of the HBB gene. (NCI Thesaurus)
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An allyl-S compound with the structure C=CCSSCC(N)C(O)O.
An allyl-S compound with the structure C=CCSCC(N)C(O)O.
An allyl-S compound with the structure C=CCSCC(N)C(O)O.
S-adenosylmethionine decarboxylase proenzyme (334 aa, ~38 kDa) is encoded by the human AMD1 gene. This protein is involved in polyamine metabolism. …
The active sulfonium form of methionine that is formed when methionine reacts with ATP and which acts as a methyl group donor…
An amino acid derivative and an intermediate in the synthesis of cysteine and adenosine. S-adenosylhomocysteine (SAH) is formed upon S-adenosylmethionine (SAM)-dependent methylation…
