Zorzato F, Fujii J, Otsu K, Phillips M, Green N M, Lai F A, Meissner G, MacLennan D H
Banting and Best Department of Medical Research, University of Toronto, C. H. Best Institute, Ontario, Canada.
J Biol Chem. 1990 Feb 5;265(4):2244-56.
We have cloned cDNAs encoding the rabbit and human forms of the Ca2+ release channel of sarcoplasmic reticulum. The human cDNA encodes a protein of 5032 amino acids, with a molecular weight of 563,584, which is made without an NH2-terminal signal sequence. Amino acid substitutions between rabbit and human sequences were noted in 163 positions and deletions or insertions in eight regions accounted for additional sequence differences between the two proteins. Analysis of the sequence indicates that 10 potential transmembrane sequences in the COOH-terminal fifth of the molecule and two additional, potential transmembrane sequences nearer to the center of the molecule could contribute to the formation of the Ca2+ conducting pore. The remainder of the molecule is hydrophilic and presumably constitutes the cytoplasmic domain of the protein. A 114-120 amino acid motif is repeated four times in the protein, in residues 841-954, 955-1068, 2725-2844, and 2845-2958 and a 16 amino acid part of the motif is repeated twice more in residues 1344-1359 and 1371-1386. Although the channel is modulated by Ca2+, ATP, and calmodulin, no clear high affinity Ca2(+)-binding domain of the EF hand type and no clear high affinity ATP-binding domain were detected in the primary sequence. An acidic sequence in residues 1872-1923 contains 79% glutamate or aspartate residues and this sequence is a potential low affinity Ca2(+)-binding site. Several potential calmodulin-binding sites were observed in the sequence, in the region 2800 to 3050.
我们已经克隆出了编码兔和人肌浆网Ca2+释放通道的cDNA。人cDNA编码一种由5032个氨基酸组成的蛋白质,分子量为563,584,其合成时没有NH2末端信号序列。兔和人序列之间在163个位置存在氨基酸替换,八个区域的缺失或插入导致了这两种蛋白质之间的额外序列差异。序列分析表明,分子COOH末端五分之一处的10个潜在跨膜序列以及更靠近分子中心的另外两个潜在跨膜序列可能有助于形成Ca2+传导孔。分子的其余部分是亲水性的,推测构成了该蛋白质的胞质结构域。一个114 - 120个氨基酸的基序在蛋白质中重复了四次,分别位于841 - 954、955 - 1068、2725 - 2844和2845 - 2958位,该基序的一个16个氨基酸的部分在1344 - 1359和1371 - 1386位又重复了两次。尽管该通道受Ca2+、ATP和钙调蛋白调节,但在一级序列中未检测到明确的EF手型高亲和力Ca2(+)-结合结构域和明确的高亲和力ATP结合结构域。1872 - 1923位的一个酸性序列含有79%的谷氨酸或天冬氨酸残基,该序列是一个潜在的低亲和力Ca2(+)-结合位点。在2800至3050区域的序列中观察到了几个潜在的钙调蛋白结合位点。