Schwarz E, Oesterhelt D, Reinke H, Beyreuther K, Dimroth P
Max-Planck-Institut für Biochemie, Martinsried, Federal Republic of Germany.
J Biol Chem. 1988 Jul 15;263(20):9640-5.
The gene encoding the alpha-subunit of the Na+ pump oxalacetate decarboxylase of Klebsiella pneumoniae was cloned and sequenced. The deduced primary structure of the protein was confirmed by protein sequencing of about 30% of the polypeptide chain. The gene has a GC content of 67% and codes for 596 amino acids. The N-terminal methionine is removed in the mature protein which has a calculated molecular mass of 63,600 daltons. The protein consists of two different domains that are connected by a stretch of amino acid residues susceptible to proteolytic cleavage. Limited proteolysis of the native enzyme with trypsin produced fragments of about 51 kDa and 10.2 kDa, the latter of which started with valine 491 and contained the biotin prosthetic group. Peptide sequencing indicated binding of the biotin prosthetic group to lysine 561, 35 residues from the C terminus. The decarboxylase contains an extended alanine- and proline-rich region (positions 502-532) on the N-terminal side of the 10.2-kDa biotin domain. This sequence includes a total of 16 alanine and 9 proline residues.
肺炎克雷伯菌钠泵草酰乙酸脱羧酶α亚基的编码基因被克隆并测序。通过对约30%的多肽链进行蛋白质测序,证实了该蛋白质推导的一级结构。该基因的GC含量为67%,编码596个氨基酸。成熟蛋白中N端的甲硫氨酸被去除,其计算分子量为63,600道尔顿。该蛋白质由两个不同的结构域组成,它们由一段易受蛋白水解切割的氨基酸残基相连。用胰蛋白酶对天然酶进行有限的蛋白水解产生了约51 kDa和10.2 kDa的片段,后者从缬氨酸491开始,包含生物素辅基。肽段测序表明生物素辅基与赖氨酸561结合,赖氨酸561位于C端35个残基处。脱羧酶在10.2 kDa生物素结构域的N端一侧含有一个延伸的富含丙氨酸和脯氨酸的区域(位置502 - 532)。该序列总共包括16个丙氨酸和9个脯氨酸残基。