Propionyl-coenzyme A carboxylase of Mycobacterium smegmatis. An electron microscopic study. Eur J Biochem 1984;140:147-151.Haase FC, Beegen H, Allen SH. Propionyl-coenzyme A carboxylase of Mycobacterium smegmatis. An electron microscopic study. Eur J Biochem 1984;140:147–151....
英文名字 Propionyl Coenzyme A Carboxylase Beta (PCCb) Antibody 供应商 Abbexa 产品货号 abx178117 产品报价 ￥询价/100ul ￥询价/200ul ￥询价/1ml 产品说明书 点击查看 购买方式 银行转账、电汇、支票、现金,在线支付宝及网银支付,或直接与我们电话联系400-6800-868。
产品名称 Propionyl Coenzyme A Carboxylase Beta (PCCB) Antibody (Biotin) 产品货号 Catalogue No: abx337203 产品价格 现货询价,电话:010-67529703 产品规格 Available Options * Size: 20 µg 50 µg 100 µg 200 µg 1 mg 产品品牌 abbexa...
(note that there are very significant clinical phenotypic variations, including asymptomatic cases), but it is also encountered in conjunction with multiple other carboxylase (pyruvate carboxylase, propionyl coenzyme A carboxylase, acetyl coenzyme A carboxylase; see also primary lactic acidosis, propionic ...
Propionyl-CoA carboxylase propionyl Coenzyme A carboxylase, alpha polypeptide Identifiers Symbol PCCA Entrez 5095 HUGO 8653 OMIM 232000 RefSeq NM_000282
Zhou, L. Tong Crystal structure of the alpha(6)beta(6) holoenzyme of propionyl-coenzyme A carboxylase Nature, 466 (2010), pp. 1001-1005 CrossrefView in ScopusGoogle Scholar [8] E.P. Frenkel, R.L. Kitchens Intracellular localization of hepatic propionyl-CoA carboxylase and methylmalonyl-CoA ...
The coenzyme A thioester derivative of propionic acid; an intermediate in the degradation of l-valine, l-isoleucine, l-threonine, l-methionine, and odd-chain fatty acids; a precursor for the synthesis of odd-chain fatty acids; it accumulates in individuals with a deficiency of propionyl-CoA c...
机译:丙酰辅酶A羧化酶;丙酸血症;柠檬酸甲酯;3-羟基丙酸酯; 入库时间 2022-08-21 11:08:49 相似文献 外文文献 中文文献 专利 1. Propionyl Coenzyme A (Propionyl-CoA) Carboxylase in Haloferax mediterranei: Indispensability for Propionyl-CoA Assimilation and Impacts on Global Metabolism [J] . Jin...
glycerol kinase; GPD1, glycerol-3-phosphate dehydrogenase 1; GPD2, glycerol -3-phosphate dehydrogenase 2; ACSS3, acyl CoA synthetase short chain family member 3; PCCA,propionyl CoA carboxylasealpha; PCCB,propionyl CoA carboxylasebeta; MCEE, methylmalonyl CoA epimerase; MUT, methylmalonyl CoA mutase...
The patient was treated with a protein-restricted diet supplemented with a mixture of ketoacid analogues of the essential amino acids, which precipitated ketosis and acidosis. A primary deficiency of propionyl coenzyme A (CoA) carboxylase was subsequently demonstrated. Because disorders of propionate ...