Structural and Functional Analysis of Disease-Linked p97 ATPase Mutant Complexes

نویسندگان

چکیده

IBMPFD/ALS is a genetic disorder caused by single amino acid mutation on the p97 ATPase, promoting ATPase activity and cofactor dysregulation. The disease mechanism underlying malfunction remains unclear. To understand how alters regulation, we assembled full-length p97R155H with its p47 first visualized their structures using single-particle cryo-EM. More than one-third of population was dodecameric form. Nucleotide presence dissociates dodecamer into two hexamers for highly elevated function. N-domains mutant all show up configurations in ADP- or ATP?S-bound states. Our functional structural analyses showed that binding likely to impact activities via changing conformations arginine fingers. These underline dysregulation miscommunication between modules p97R155H.

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ژورنال

عنوان ژورنال: International Journal of Molecular Sciences

سال: 2021

ISSN: ['1661-6596', '1422-0067']

DOI: https://doi.org/10.3390/ijms22158079