Arlaud G J, Willis A C, Gagnon J
Biochem J. 1987 Feb 1;241(3):711-20. doi: 10.1042/bj2410711.
The amino acid sequence of human C1r A chain was determined, from sequence analysis performed on fragments obtained from C1r autolytic cleavage, cleavage of methionyl bonds, tryptic cleavages at arginine and lysine residues, and cleavages by staphylococcal proteinase. The polypeptide chain has an N-terminal serine residue and contains 446 amino acid residues (Mr 51,200). The sequence data allow chemical characterization of fragments alpha (positions 1-211), beta (positions 212-279) and gamma (positions 280-446) yielded from C1r autolytic cleavage, and identification of the two major cleavage sites generating these fragments. Position 150 of C1r A chain is occupied by a modified amino acid residue that, upon acid hydrolysis, yields erythro-beta-hydroxyaspartic acid, and that is located in a sequence homologous to the beta-hydroxyaspartic acid-containing regions of Factor IX, Factor X, protein C and protein Z. Sequence comparison reveals internal homology between two segments (positions 10-78 and 186-257). Two carbohydrate moieties are attached to the polypeptide chain, both via asparagine residues at positions 108 and 204. Combined with the previously determined sequence of C1r B chain [Arlaud & Gagnon (1983) Biochemistry 22, 1758-1764], these data give the complete sequence of human C1r.
通过对C1r自溶裂解片段、甲硫氨酰键裂解、精氨酸和赖氨酸残基处的胰蛋白酶裂解以及葡萄球菌蛋白酶裂解产物进行序列分析,确定了人C1r A链的氨基酸序列。该多肽链具有一个N端丝氨酸残基,包含446个氨基酸残基(Mr 51,200)。序列数据允许对C1r自溶裂解产生的片段α(第1 - 211位)、β(第212 - 279位)和γ(第280 - 446位)进行化学表征,并确定产生这些片段的两个主要裂解位点。C1r A链的第150位被一个修饰的氨基酸残基占据,该残基在酸水解时产生赤藓糖-β-羟基天冬氨酸,并且位于与因子IX、因子X、蛋白C和蛋白Z的含β-羟基天冬氨酸区域同源的序列中。序列比较揭示了两个片段(第10 - 78位和第186 - 257位)之间的内部同源性。两个碳水化合物部分通过第108位和第204位的天冬酰胺残基连接到多肽链上。结合先前确定的C1r B链序列[Arlaud & Gagnon (1983) Biochemistry 22, 1758 - 1764],这些数据给出了人C1r的完整序列。