Fujisawa H, Yonesaki T, Minagawa T
Nucleic Acids Res. 1985 Oct 25;13(20):7473-81. doi: 10.1093/nar/13.20.7473.
We have determined the nucleotide sequence of the uvsX gene of bacteriophage T4 which is involved in DNA recombination and damage repair, and whose product catalyzes in vitro reactions related to recombination process in analogous manners to E. coli recA gene product. The coding region consisted of 1170 nucleotides directing the synthesis of a polypeptide of 390 amino acids in length with a calculated molecular weight of 43,760. Amino acid composition, the sequence of seven NH2-terminal amino acids and molecular weight of the protein deduced from the nucleotide sequence were consistent with the data from the analysis of the purified uvsX protein. The nucleotide sequence and the deduced amino acid sequence were compared with those of the recA gene. Although a significant homology was not found in the nucleotide sequences, the amino acid sequences included 23% of identical and 15% of conservatively substituted residues.
我们已经确定了噬菌体T4的uvsX基因的核苷酸序列,该基因参与DNA重组和损伤修复,其产物以与大肠杆菌recA基因产物类似的方式催化与重组过程相关的体外反应。编码区由1170个核苷酸组成,指导合成长度为390个氨基酸的多肽,计算分子量为43760。从核苷酸序列推导的蛋白质的氨基酸组成、七个NH2末端氨基酸的序列和分子量与纯化的uvsX蛋白的分析数据一致。将核苷酸序列和推导的氨基酸序列与recA基因的序列进行了比较。虽然在核苷酸序列中未发现显著的同源性,但氨基酸序列包含23%的相同残基和15%的保守取代残基。