DEFECT IN MU HEAVY-CHAIN DISEASE PROTEIN GLI
- 1 January 1976
- journal article
- research article
- Vol. 116 (4) , 1194-1195
Abstract
Amino acid sequence studies of [human] .mu.HCD [heavy chain disease] protein GLI reveal the absence of the amino terminal 130 residues. The molecule starts at Ala 131 and contains Cys 140, normally involved in the H chain-L chain disulfide bridges. Except for the deletion and presumably an extra H chain-H chain disulfide bridge involving Cys 140, the remainder of the .mu. chain appears normal.This publication has 2 references indexed in Scilit:
- A Protein SequenatorEuropean Journal of Biochemistry, 1967
- Electrophoretic Heterogeneity of Polypeptide Chains of Specific AntibodiesScience, 1966