Structure and functionality of a multimeric human COQ7:COQ9 complex-Reference-Cited by-同舟云学术

Structure and functionality of a multimeric human COQ7:COQ9 complex

Published:2022-11 Issue:22 Volume:82 Page:4307-4323.e10
ISSN:1097-2765
Container-title:Molecular Cell
language:en
Short-container-title:Molecular Cell

Author:

Manicki Mateusz,Aydin Halil,Abriata Luciano A.,Overmyer Katherine A.,Guerra Rachel M.,Coon Joshua J.,Dal Peraro Matteo,Frost Adam,Pagliarini David J.^ORCID

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference106 articles.

1. GROMACS: high performance molecular simulations through multi-level parallelism from laptops to supercomputers;Abraham;SoftwareX,2015

2. Phospholipid ebb and flow makes mitochondria go;Acoba;J. Cell Biol.,2020

3. Real-space refinement in PHENIX for cryo-EM and crystallography;Afonine;Acta Crystallogr.,2018

4. Identification of Coq11, a new coenzyme Q biosynthetic protein in the CoQ-synthome in Saccharomyces cerevisiae;Allan;J. Biol. Chem.,2015

5. The Ferritin-like superfamily: evolution of the biological iron storeman from a rubrerythrin-like ancestor;Andrews;Biochim. Biophys. Acta,2010

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