gopubmed logo
 
find other proteinsAll proteins
GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

ND5 NADH dehydrogenase, subunit 5 (complex I)

ND5, NADH dehydrogenase subunit 5
Top mentioned proteins: ND4, DiI, ND6, CAN, HAD
Papers on ND5
Graphical Representation and Similarity Analysis of Protein Sequences Based on Fractal Interpolation.
New
Zhou et al., In Ieee/acm Trans Comput Biol Bioinform, Jan 2016
Nine different species from Nicotinamide adenine dinucleotide (NADH) dehydrogenase 5 (ND5) protein sequences were tested as an example to demonstrate our method.
Complete mitochondrial genome of Aulonocara stuartgranti (Flavescent peacock cichlid).
New
Gao et al., Shenzhen, China. In Mitochondrial Dna, Jan 2016
ATP8 and ATP6 genes overlap by nine nucleotides, ND5 and ND6 genes by four nucleotides, and ND4L and ND4 genes share six nucleotides.
The complete mitochondrial genome of the Greater Mouse-Eared bat, Myotis myotis (Chiroptera: Vespertilionidae).
New
Teeling et al., Dublin, Ireland. In Mitochondrial Dna, Jan 2016
All protein-coding genes start with the ATG start codon, except for ND2, ND3, and ND5 which begin with ATT or ATA.
The complete mitochondrial genome of Acanthosaura lepidogaster (Squamata: Agamidae).
New
Lin et al., Hangzhou, China. In Mitochondrial Dna, Jan 2016
We constructed a phylogeny that included for 10 species of Leiolepidinae lizards and one outgroup Leiocephalus personatus constructed in BEAST, based on 15 mitochondrial genes (12S, 16S, ND1, ND2, COI, COII, ATP8, ATP6, COIII, ND3, ND4L, ND4, ND5, ND6, and cytochrome b).
The complete mitochondrial genome of Hequ Tibetan Mastiff Canis lupus familiaris (Carnivora: Canidae).
New
Lu et al., Lanzhou, China. In Mitochondrial Dna, Jan 2016
AGA for CYTB, TAA for ATP6, ATP8, COX1, COX2, ND1, ND4L, ND5 and ND6, and an incomplete stop codon T for COX3, ND2, ND3 and ND4.
The complete mitochondrial genome of the black star fat minnow (Rhynchocypris semotilus), an endemic and endangered fish of Korea.
New
Kim et al., Inch'ŏn, South Korea. In Mitochondrial Dna, Jan 2016
Four overlapping regions in ATP8/ATP6, ATP6/COX3, ND4L/ND4, and ND5/ND6, among the 13 PCGs were found.
The complete mitochondrial genome of the drill (Mandrillus leucophaeus).
New
Zhao et al., Shenzhen, China. In Mitochondrial Dna, Jan 2016
All PCGs share the start codon ATG except ND2(ATC), ND3(ATT) and ND5(ATA).
A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease.
New
Rahman et al., London, United Kingdom. In Plos One, Dec 2015
Complete sequence analysis of muscle mtDNA using the MitoChip resequencing chip in all four cases demonstrated significant variation in mtDNA, including a pathogenic MT-ND5 mutation in one patient.
A new species of moray eel (Anguilliformes: Muraenidae) from Taiwan, with comments on related elongate unpatterned species.
Chen et al., Kuala Lumpur, Malaysia. In Zootaxa, 2014
Phylogenetic relationships of the nine species were examined using nucleotide sequence data from partial sequences of mitochondrial ND5 gene (600 bp), and seven species form COI (600 bp).
The mitochondrial RNA-binding protein GRSF1 localizes to RNA granules and is required for posttranscriptional mitochondrial gene expression.
Impact
Shoubridge et al., Montréal, Canada. In Cell Metab, 2013
GRSF1 preferentially binds RNAs transcribed from three contiguous genes on the light strand of mtDNA, the ND6 mRNA, and the long noncoding RNAs for cytb and ND5, each of which contains multiple consensus binding sequences.
Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigree.
GeneRIF
Yan et al., Hangzhou, China. In Gene, 2012
Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigree
Molecular identification of Diphyllobothrium latum and a brief review of diphyllobothriosis in China.
Review
Jia et al., Lanzhou, China. In Acta Parasitol, 2012
Species identity was confirmed by molecular characterization of the 18S rDNA partial sequence, complete sequences of internal transcribed spacers (ITSs) and 5.8S rDNA, and partial sequences of mitochondrial cytochrome c oxidase subunit 1 (cox1) and mitochondrial NADH dehydrogenase subunit 5 (nad5).
Mitochondrial DNA mutations in respiratory complex-I in never-smoker lung cancer patients contribute to lung cancer progression and associated with EGFR gene mutation.
GeneRIF
Sidransky et al., Baltimore, United States. In J Cell Physiol, 2012
Mitochondrial DNA mutations in respiratory complex-I in never-smoker lung cancer patients contribute to lung cancer progression in association with EGFR gene mutation.
Nonsynonymous variants in mt-Nd2, mt-Nd4, and mt-Nd5 are linked to effects on oxidative phosphorylation and insulin sensitivity in rat conplastic strains.
GeneRIF
Pravenec et al., Praha, Czech Republic. In Physiol Genomics, 2012
Inherited variation mt-Nd2, mt-Nd4, and mt-Nd5 can influence glucose and lipid metabolism when expressed on the nuclear genetic background of the SHR strain.
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms.
Review
Papa et al., Bari, Italy. In Adv Exp Med Biol, 2011
Examples of complex I dysfunction are herein presented: homozygous mutations in the nuclear NDUFS1 and NDUFS4 genes for structural components of complex I; an autosomic recessive form of encephalopathy associated with enhanced proteolytic degradation of complex I; familial cases of Parkinson associated to mutations in the PINK1 and Parkin genes, in particular, homoplasmic mutations in the ND5 and ND6 mitochondrial genes of the complex I, coexistent with mutation in the PINK1 gene.
[The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].
GeneRIF
Guan et al., Wenzhou, China. In Yi Chuan, 2011
ND4 G11696A and ND5 T12338C mutation is likely associated with Leber's hereditary optic neuropathy in two Chinese families
[Mitochondrial ND5 as the causative gene of Leight syndrome].
GeneRIF
Jin et al., Beijing, China. In Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2010
Patients with ND5*13513 G to A mutation may have a characteristic clinical course and ND5 *13513 G to A might be a preferential candidate mutation of Leigh syndrome.
Mitochondrial respiratory dysfunction and mutations in mitochondrial DNA in PINK1 familial parkinsonism.
Review
Piccoli et al., Bari, Italy. In J Bioenerg Biomembr, 2009
Sequence analysis of the overall mtDNA revealed coexistence with the PINK1 mutation of homoplasmic point mutations in the ND5 and ND6 genes of complex I.
Mitochondrial DNA-Associated Leigh Syndrome and NARP
Review
Rahman et al., Seattle, United States. In Unknown Journal, 2003
MT-ATP6, MT-TL1, MT-TK, MT-TW, MT-TV, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND5, MT-ND6, and MT-CO3 are the mitochondrial genes in which pathogenic variants are known to cause mtDNA-associated Leigh syndrome.
MELAS
Review
Hirano et al., Seattle, United States. In Unknown Journal, 2001
Mutations in MT-TL1 or other mtDNA genes, particularly MT-ND5, can also cause this disorder.
share on facebooktweetadd +1mail to friends