Search
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/18:2(9Z,11Z)/a-13:0)[rac]
smpdb.ca/view/SMP0371326MetabolicLast, cardiolipin synthase catalyzes the synthesis of cardiolipin by transferring a phosphatidyl group from a second CDP-diacylglycerol to PG. It requires a divalent metal cation cofactor.
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-13:0/18:2(9Z,11Z))[rac]
smpdb.ca/view/SMP0371344MetabolicLast, cardiolipin synthase catalyzes the synthesis of cardiolipin by transferring a phosphatidyl group from a second CDP-diacylglycerol to PG. It requires a divalent metal cation cofactor.
Glutamyl aminopeptidase
go.drugbank.com/bio_entities/BE0002271TargetHumansRegulates central hypertension through its calcium-modulated preference to cleave N-terminal acidic residues from peptides such as angiotensin II
Synonyms: AP-A, Aminopeptidase AProbable peptidoglycan D,D-transpeptidase PenA
go.drugbank.com/bio_entities/BE0003621TargetNeisseria gonorrhoeaeCatalyzes cross-linking of the peptidoglycan cell wall at the division septum.
Polypeptides: Probable peptidoglycan D,D-transpeptidase PenAUncharacterized MFS-type transporter EfpA
go.drugbank.com/bio_entities/BE0009715TargetMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)Synonyms: Efflux protein AFever
go.drugbank.com/conditions/DBCOND0020923Drugs: Acetaminophen · Acetylsalicylic acid · Ascorbic acid · Brompheniramine · Caffeine · Chlorpheniramine +20 moreSynonyms: Has a temperatureCardiolipin Biosynthesis (Barth Syndrome)
smpdb.ca/view/SMP0074684DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164). … Last, cardiolipin synthase catalyzes the synthesis of cardiolipin by transferring a phosphatidyl group from a second CDP-diacylglycerol to PG. It requires a divalent metal cation cofactor.
Febrile Illness Acute
go.drugbank.com/conditions/DBCOND0059951Drugs: AcetaminophenSynonyms: Has a temperatureVitamin A Deficiency
smpdb.ca/view/SMP0125788DiseaseVitamin A deficiency can be caused by many causes. A defect in the BCMO1 gene which codes for beta,beta-carotene 15,15’-monooxygenase is one of them. … A defect in this enzyme results in decrease of levels of retinal and vitamin A in serum; Signs and symptoms include night blindness, poor adaptation to darkness, dry skin and hair.
Vitamin A Deficiency
smpdb.ca/view/SMP0000336DiseaseVitamin A deficiency can be caused by many causes. A defect in the BCMO1 gene which codes for beta,beta-carotene 15,15’-monooxygenase is one of them. … A defect in this enzyme results in decrease of levels of retinal and vitamin A in serum; Signs and symptoms include night blindness, poor adaptation to darkness, dry skin and hair.