Inactivity of YGL082W in vitro due to impairment of conformational change in the catalytic center loop

• Published in: Science China. Chemistry Vol. 63; no. 2; pp. 237 - 243
• Main Authors: Lu, Lining, Guo, Yu, Wang, Tian, Liang, Lujun, Zhao, Suwen, Wang, Feng, Liu, Lei
• Format: Journal Article
• Language: English
• Published: Beijing Science China Press 01.02.2020; Springer Nature B.V
• Subjects: Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Crosslinking; Crystal structure; Homology; Hydrogen bonds; Hydrolysis; Hypotheses; Molecular dynamics; Mutation; Yeast; X-ray crystal structure; deubiquitinating enzymes (DUB); molecular dynamics; enzymology
• ISSN: 1674-7291; 1869-1870
• DOI: 10.1007/s11426-019-9623-0

MINDY-1 is a recently discovered new family of deubiquitinating enzymes (DUB), but one of its yeast homologs, YGL082W, does not show any DUB activity in vitro . Sequence alignment shows that YGL082W possesses the correct catalytic triad, and yet did not catalyze either the hydrolysis of di-ubiquitin, crosslinking with C-terminally propargylated ubiquitin, or hydrolysis of ubiquitin-7-amino-4-methylcoumarin. After obtaining a crystal structure of the catalytic domain of YGL082W, we identified an interesting difference between the catalytic center loop of YGL082W and that of its human homolog MINDY-1. Because the conformation of the catalytic center loop was previously reported to be important for the deubiquitination activity of MINDY-1, we hypothesized that Glu27 (instead of the corresponding Pro136 in MINDY-1) of the catalytic center loop of YGL082W may impair the conformational change and account for the lack of activity. This hypothesis was supported by homology modeling and molecular dynamics simulations, which showed that the Pro-to-Glu mutation (P136E mutation for MINDY-1) creates a hydrogen bond that inhibits the conformation change of the catalytic center loop of MINDY-1. Further experiments through site-directed mutation validated this hypothesis, showing that the P27E mutation caused MIY1 (a homologous active DUB from yeast) to lose activity.