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Search results 501 to 527 out of 527 for Acox1

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Type Details Score
Publication
First Author: Houten SM
Year: 2012
Journal: J Lipid Res
Title: Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acids.
Volume: 53
Issue: 7
Pages: 1296-303
Publication
First Author: Ferdinandusse S
Year: 2005
Journal: J Biol Chem
Title: Developmental changes of bile acid composition and conjugation in L- and D-bifunctional protein single and double knockout mice.
Volume: 280
Issue: 19
Pages: 18658-66
Publication
First Author: Ranea-Robles P
Year: 2021
Journal: Kidney360
Title: Peroxisomal L-bifunctional protein (EHHADH) deficiency causes male-specific kidney hypertrophy and proximal tubular injury in mice.
Volume: 2
Issue: 9
Pages: 1441-1454
Genotype
Symbol: Ehhadh/Ehhadh Hsd17b4/Hsd17b4
Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Ehhadh/Ehhadh
Background: involves: 129P2/OlaHsd * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
Publication
First Author: Hayashi H
Year: 1998
Journal: J Biol Chem
Title: Molecular characterization of a glyoxysomal long chain acyl-CoA oxidase that is synthesized as a precursor of higher molecular mass in pumpkin.
Volume: 273
Issue: 14
Pages: 8301-7
Publication
First Author: Pedersen L
Year: 2005
Journal: J Mol Biol
Title: Acyl-CoA oxidase 1 from Arabidopsis thaliana. Structure of a key enzyme in plant lipid metabolism.
Volume: 345
Issue: 3
Pages: 487-500
Publication
First Author: Nakade Y
Year: 2017
Journal: PLoS One
Title: Conophylline inhibits non-alcoholic steatohepatitis in mice.
Volume: 12
Issue: 6
Pages: e0178436
Publication
First Author: Arguin G
Year: 2017
Journal: Sci Rep
Title: The loss of P2X7 receptor expression leads to increase intestinal glucose transit and hepatic steatosis.
Volume: 7
Issue: 1
Pages: 12917
Publication
First Author: Yoo HS
Year: 2015
Journal: J Toxicol Environ Health A
Title: Comparative analysis of the relationship between trichloroethylene metabolism and tissue-specific toxicity among inbred mouse strains: liver effects.
Volume: 78
Issue: 1
Pages: 15-31
Protein
Organism: Mus musculus/domesticus
Length: 83  
Fragment?: true
Protein Domain
Type: Domain
Description: Acyl-CoA oxidase (ACO) acts on CoA derivatives of fatty acids with chain lengths from 8 to 18. It catalyses the first and rate-determining step of the peroxisomal beta-oxidation of fatty acids [].Acyl-CoA oxidase is a homodimer and the polypeptide chain of the subunit is folded into the N-terminal alpha-domain, beta-domain, and C-terminal alpha-domain []. Functional differences between the peroxisomal acyl-CoA oxidases and the mitochondrial acyl-CoA dehydrogenases are attributed to structural differences in the FAD environments []. Experimental data indicate that, in the pumpkin, the expression patternof ACOX is very similar to that of the glyoxysomal enzyme 3-ketoacyl-CoA thiolase []. In humans, defects in ACOX1 are the cause of pseudoneonatal adrenoleukodystrophy, also known as peroxisomal acyl-CoA oxidase deficiency. Pseudo-NALD is a peroxisomal single-enzyme disorder. Clinical features include mental retardation, leukodystrophy, seizures, mild hepatomegaly and hearing deficit. Pseudo-NALD is characterised by increased plasma levels of very-long chain fatty acids due to a decrease in, or absence of, peroxisome acyl-CoA oxidase activity, despite the peroxisomes being intact and functioning.This entry represents the Acyl-CoA oxidase C-terminal.
Protein Domain
Type: Family
Description: Acyl-CoA oxidase (ACO) acts on CoA derivatives of fatty acids with chain lengths from 8 to 18. It catalyses the first and rate-determining step of the peroxisomal beta-oxidation of fatty acids and a major producer of hydrogen peroxide (H2O2) [, ].Acyl-CoA oxidase is a homodimer and the polypeptide chain of the subunit is folded into the N-terminal alpha-domain, beta-domain, and C-terminal alpha-domain [, ]. Functional differences between the peroxisomal acyl-CoA oxidases and the mitochondrial acyl-CoA dehydrogenases are attributed to structural differences in the FAD environments []. Experimental data indicate that in the pumpkin, the expression pattern of ACOX is very similar to that of the glyoxysomal enzyme 3-ketoacyl-CoA thiolase []. In humans, defects in ACOX1 are the cause of pseudoneonatal adrenoleukodystrophy, also known as peroxisomal acyl-CoA oxidase deficiency. Clinical features include mental retardation, leukodystrophy, seizures, mild hepatomegaly and hearing deficit. Pseudo-NALD is characterised by increased plasma levels of very-long chain fatty acids due to a decrease in, or absence of, peroxisome acyl-CoA oxidase activity, despite the peroxisomes being intact and functioning [].
Protein
Organism: Mus musculus/domesticus
Length: 143  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 700  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 632  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 661  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 681  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 647  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 681  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 625  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 685  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 673  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 697  
Fragment?: false
Publication
First Author: Nakajima Y
Year: 2002
Journal: J Biochem
Title: Three-dimensional structure of the flavoenzyme acyl-CoA oxidase-II from rat liver, the peroxisomal counterpart of mitochondrial acyl-CoA dehydrogenase.
Volume: 131
Issue: 3
Pages: 365-74
Protein
Organism: Mus musculus/domesticus
Length: 201  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 499  
Fragment?: true