SCO1/YBR037C Literature Guide Help

Other names published for SCO1: PET161, YBR037C

SCO1 - Non-Fungal Related Genes/Proteins (20)

ReferenceOther Genes Addressed
Steinebrunner I, et al.  (2011) HCC1, the Arabidopsis homologue of the yeast mitochondrial copper chaperone SCO1, is essential for embryonic development. J Exp Bot 62(1):319-30
Szklarczyk R and Huynen MA  (2009) Expansion of the human mitochondrial proteome by intra- and inter-compartmental protein duplication. Genome Biol 10(11):R135
Khalimonchuk O, et al.  (2007) Evidence for a pro-oxidant intermediate in the assembly of cytochrome oxidase. J Biol Chem 282(24):17442-9
Cobine PA, et al.  (2006) The P174L mutation in human Sco1 severely compromises Cox17-dependent metallation but does not impair copper binding. J Biol Chem 281(18):12270-6
Andruzzi L, et al.  (2005) Spectroscopic studies of metal binding and metal selectivity in Bacillus subtilis BSco, a Homologue of the Yeast Mitochondrial Protein Sco1p. J Am Chem Soc 127(47):16548-58
Horng YC, et al.  (2005) Human Sco1 and Sco2 function as copper-binding proteins. J Biol Chem 280(40):34113-22
Imriskova-Sosova I, et al.  (2005) Characterization of the redox and metal binding activity of BsSco, a protein implicated in the assembly of cytochrome c oxidase. Biochemistry 44(51):16949-56
Williams JC, et al.  (2005) Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" protein. J Biol Chem 280(15):15202-11
Ye Q, et al.  (2005) Identification of a disulfide switch in BsSco, a member of the Sco family of cytochrome c oxidase assembly proteins. Biochemistry 44(8):2934-42
Balatri E, et al.  (2003) Solution structure of Sco1: a thioredoxin-like protein Involved in cytochrome c oxidase assembly. Structure 11(11):1431-43
Shoubridge EA  (2001) Cytochrome c oxidase deficiency. Am J Med Genet 106(1):46-52
Chinenov YV  (2000) Cytochrome c oxidase assembly factors with a thioredoxin fold are conserved among prokaryotes and eukaryotes. J Mol Med (Berl) 78(5):239-42
Jaksch M, et al.  (2000) Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency. Hum Mol Genet 9(5):795-801
Mattatall NR, et al.  (2000) Characterization of YpmQ, an accessory protein required for the expression of cytochrome c oxidase in Bacillus subtilis. J Biol Chem 275(37):28802-9
Paret C, et al.  (2000) The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase. Biochem Biophys Res Commun 279(2):341-7
Robinson BH  (2000) Human cytochrome oxidase deficiency. Pediatr Res 48(5):581-5
Papadopoulou LC, et al.  (1999) Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nat Genet 23(3):333-7
Paret C, et al.  (1999) Human members of the SCO1 gene family: complementation analysis in yeast and intracellular localization. FEBS Lett 447(1):65-70
Petruzzella V, et al.  (1998) Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain. Genomics 54(3):494-504
Buggy J and Bauer CE  (1995) Cloning and characterization of senC, a gene involved in both aerobic respiration and photosynthesis gene expression in Rhodobacter capsulatus. J Bacteriol 177(23):6958-65