First Crystal Structure of a Nonstructural Hepatitis E Viral Protein Identifies a Putative Novel Zinc-Binding Protein
Author(s) -
Andrew Proudfoot,
Anastasia Hyrina,
Meghan Holdorf,
Andreas O. Frank,
Dirksen E. Bussiere
Publication year - 2019
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.00170-19
Subject(s) - biology , virology , ns3 , hepatitis e virus , protease , zinc finger , structural protein , viral structural protein , virus , protein structure , viral replication , hepatitis c virus , genetics , enzyme , viral entry , biochemistry , gene , transcription factor , genotype
Hepatitis E virus (HEV) is an emerging virus found predominately in developing countries; it causes an estimated 20 million infections, which result in approximately 57,000 deaths a year. Although it is known that the nonstructural proteins of HEV ORF1 are expressed as a single transcript, there is debate as to whether ORF1 functions as a single polyprotein or if it is processed into separate domains via a viral or endogenous cellular protease. Here we present the first structural and biophysical characterization of an HEV nonstructural protein using a construct that has partially overlapping boundaries with the predicted putative cysteine protease.
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