Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

8CA4

Cryo-EM structure NDUFS4 knockout complex I from Mus musculus heart (Class 2 N-domain).

Summary for 8CA4
Entry DOI10.2210/pdb8ca4/pdb
Related8C2S 8CA1 8CA3
EMDB information16517
DescriptorNADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial, NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial, NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, ... (8 entities in total)
Functional Keywordsnadh ubiquinone oxidoreductase, complex i, oxidoreductase
Biological sourceMus musculus (house mouse)
More
Total number of polymer chains5
Total formula weight182718.26
Authors
Yin, Z.,Bridges, H.R.,Agip, A.N.A.,Hirst, J. (deposition date: 2023-01-24, release date: 2023-12-20, Last modification date: 2024-10-16)
Primary citationYin, Z.,Agip, A.A.,Bridges, H.R.,Hirst, J.
Structural insights into respiratory complex I deficiency and assembly from the mitochondrial disease-related ndufs4 -/- mouse.
Embo J., 43:225-249, 2024
Cited by
PubMed Abstract: Respiratory complex I (NADH:ubiquinone oxidoreductase) is essential for cellular energy production and NAD homeostasis. Complex I mutations cause neuromuscular, mitochondrial diseases, such as Leigh Syndrome, but their molecular-level consequences remain poorly understood. Here, we use a popular complex I-linked mitochondrial disease model, the ndufs4 mouse, to define the structural, biochemical, and functional consequences of the absence of subunit NDUFS4. Cryo-EM analyses of the complex I from ndufs4 mouse hearts revealed a loose association of the NADH-dehydrogenase module, and discrete classes containing either assembly factor NDUFAF2 or subunit NDUFS6. Subunit NDUFA12, which replaces its paralogue NDUFAF2 in mature complex I, is absent from all classes, compounding the deletion of NDUFS4 and preventing maturation of an NDUFS4-free enzyme. We propose that NDUFAF2 recruits the NADH-dehydrogenase module during assembly of the complex. Taken together, the findings provide new molecular-level understanding of the ndufs4 mouse model and complex I-linked mitochondrial disease.
PubMed: 38177503
DOI: 10.1038/s44318-023-00001-4
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.25 Å)
Structure validation

227344

数据于2024-11-13公开中

PDB statisticsPDBj update infoContact PDBjnumon