Assessment of predicted enzymatic activity of α‐ <i>N</i> ‐acetylglucosaminidase variants of unknown significance for CAGI 2016

Wyatt T. Clark(BioMarin (United States)), Laura Kasak(University of Tartu), Constantina Bakolitsa(University of California, Berkeley), Zhiqiang Hu(University of California, Berkeley), Gaia Andreoletti(University of California, Berkeley), Giulia Babbi(University of Bologna), Yana Bromberg(Rutgers, The State University of New Jersey), Rita Casadio(University of Bologna), Roland L. Dunbrack(Fox Chase Cancer Center), Lukas Folkman(ETH Zurich), Colby T. Ford(University of North Carolina at Charlotte), David T. Jones(The London College), Panagiotis Katsonis(Baylor College of Medicine), Kunal Kundu(Advanced Bioscience Laboratories (United States)), Olivier Lichtarge(Baylor College of Medicine), Pier Luigi Martelli(University of Tartu), Sean D. Mooney(Buck Institute for Research on Aging), Conor Nodzak(University of North Carolina at Charlotte), Lipika R. Pal(Advanced Bioscience Laboratories (United States)), Predrag Radivojac(Indiana University Bloomington), Castrense Savojardo(University of Bologna), Xinghua Shi(University of North Carolina at Charlotte), Yaoqi Zhou(Indiana Clinical and Translational Sciences Institute), Aneeta Uppal(University of North Carolina at Charlotte), Qifang Xu(Fox Chase Cancer Center), Yizhou Yin(Advanced Bioscience Laboratories (United States)), Vikas Pejaver(Indiana University Bloomington), Meng Wang(Peking University), Liping Wei(Peking University), John Moult(Advanced Bioscience Laboratories (United States)), Guoying Karen Yu(BioMarin (United States)), Steven E. Brenner(University of California, Berkeley), Jonathan H. LeBowitz(BioMarin (United States))
Human Mutation
July 25, 2019
Cited by 25Open Access
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Abstract

The NAGLU challenge of the fourth edition of the Critical Assessment of Genome Interpretation experiment (CAGI4) in 2016, invited participants to predict the impact of variants of unknown significance (VUS) on the enzymatic activity of the lysosomal hydrolase α-N-acetylglucosaminidase (NAGLU). Deficiencies in NAGLU activity lead to a rare, monogenic, recessive lysosomal storage disorder, Sanfilippo syndrome type B (MPS type IIIB). This challenge attracted 17 submissions from 10 groups. We observed that top models were able to predict the impact of missense mutations on enzymatic activity with Pearson's correlation coefficients of up to .61. We also observed that top methods were significantly more correlated with each other than they were with observed enzymatic activity values, which we believe speaks to the importance of sequence conservation across the different methods. Improved functional predictions on the VUS will help population-scale analysis of disease epidemiology and rare variant association analysis.


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