Ontology highlight
ABSTRACT:
SUBMITTER: Luo A
PROVIDER: S-EPMC6550000 | biostudies-literature | 2019 May
REPOSITORIES: biostudies-literature
Luo An A Li Xinbo X Zhang Xuecheng X Zhan Huadong H Du Hewei H Zhang Yubo Y Peng Xiongbo X
Royal Society open science 20190501 5
Heat-shock protein of 90 kDa (Hsp90) is a key molecular chaperone involved in folding the synthesized protein and controlling protein quality. Conformational dynamics coupled to ATPase activity in N-terminal domain is essential for Hsp90's function. However, the relevant process is still largely unknown in plant Hsp90s, especially those required for plant embryogenesis which is inextricably tied up with human survival. Here, AtHsp90.6, a member of Hsp90 family in <i>Arabidopsis</i>, was firstly ...[more]