Shao H, Lou L, Pandey A, Verderame M F, Siever D A, Dixit V M
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109.
J Biol Chem. 1995 Feb 24;270(8):3467-70. doi: 10.1074/jbc.270.8.3467.
We have isolated a murine cDNA encoding a ligand for the Cek7 receptor protein-tyrosine kinase (RPTK), a member of the Eph/Eck RPTK subfamily. Sequence analysis predicts an open reading frame of 209 amino acids with a predicted molecular mass of 24 kDa. The Cek7 ligand shows a 48% sequence identity at the protein level to B61, a ligand for the related Eck RPTK, 30% to the Cek5 ligand, 59% to the recently cloned Ehk1-L, and identity to ELF-1, a recently described ligand for the Mek4 and Sek RPTKs. The expressed Cek7 ligand is functionally active as it induces autophosphorylation of the Cek7 RPTK.
我们已经分离出一种小鼠cDNA,它编码Cek7受体蛋白酪氨酸激酶(RPTK)的配体,Cek7属于Eph/Eck RPTK亚家族成员。序列分析预测其开放阅读框为209个氨基酸,预测分子量为24 kDa。Cek7配体在蛋白质水平上与相关的Eck RPTK的配体B61有48%的序列同一性,与Cek5配体有30%的同一性,与最近克隆的Ehk1-L有59%的同一性,并且与最近描述的Mek4和Sek RPTKs的配体ELF-1相同。表达的Cek7配体具有功能活性,因为它能诱导Cek7 RPTK的自身磷酸化。