Hemilä H, Koivula T T, Palva I
Department of Public Health, University of Helsinki, Finland.
Biochim Biophys Acta. 1994 Jan 3;1210(2):249-53. doi: 10.1016/0005-2760(94)90129-5.
We have sequenced a gene from Bacillus acidocaldarius which encodes an open reading frame (ORF3) of 310 amino acids. The ORF3 was found to be related to the mammalian hormone-sensitive lipase (HSL). Searching the protein data base revealed five other bacterial proteins related to the HSL. Upon further sequence comparisons this HSL-group was found to be related to the family of carboxylesterases, and to a family of lipases (lipoprotein, hepatic and pancreatic lipases). The evolutionary relationship of these serine-dependent hydrolytic enzymes has not been studied previously, and it has not been known that these proteins belong to the same superfamily. Finally, the alignment of the HSL with the bacterial proteins allowed us to infer the location of the hormone-sensitive regulatory domain of the HSL-protein.
我们对嗜酸热硫化叶菌中的一个基因进行了测序,该基因编码一个由310个氨基酸组成的开放阅读框(ORF3)。发现ORF3与哺乳动物激素敏感脂肪酶(HSL)相关。搜索蛋白质数据库发现了另外五种与HSL相关的细菌蛋白。通过进一步的序列比较,发现这个HSL家族与羧酸酯酶家族以及脂肪酶家族(脂蛋白脂肪酶、肝脂肪酶和胰脂肪酶)相关。这些丝氨酸依赖性水解酶的进化关系以前尚未研究过,而且此前也不知道这些蛋白质属于同一个超家族。最后,通过将HSL与细菌蛋白进行比对,我们能够推断出HSL蛋白激素敏感调节域的位置。