about
P688
The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patternsLate-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutationsDifferences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiencyOxidative damage to mitochondrial complex I due to peroxynitrite: identification of reactive tyrosines by mass spectrometryGenomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductaseRewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and Neurogenesis
P921
Q22008460-9469161C-DF41-4AB6-BDD0-917B9DB4B63AQ24290607-6FD97C9D-B706-4077-8FE9-0F3832E038EFQ24294235-737E8C30-85F9-43E7-A555-64F22B71FC83Q24306549-2D8247D1-7E90-460D-9ED9-9B013202BA34Q24307861-404FB584-17E1-4BBD-9F55-ADE3ADA9E849Q24315917-E61C5CFE-D26C-4045-9B7C-DC9EFAFE9996Q90180281-C1420331-23CC-4BF9-A7F7-44D7C360F04C
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
NADH:ubiquinone oxidoreductase core subunit S8
@en
NADH:ubiquinone oxidoreductase core subunit S8
@nl
type
label
NADH:ubiquinone oxidoreductase core subunit S8
@en
NADH:ubiquinone oxidoreductase core subunit S8
@nl
altLabel
CI-23kD
@en
NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase)
@en
NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial
@en
NADH-ubiquinone oxidoreductase 23 kDa subunit
@en
NDUFS8
@en
TYKY subunit
@en
complex I 23kDa subunit
@en
complex I-23kD
@en
prefLabel
NADH:ubiquinone oxidoreductase core subunit S8
@en
NADH:ubiquinone oxidoreductase core subunit S8
@nl
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