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Literature summary for 1.14.15.3 extracted from

  • Hardwick, J.P.
    Cytochrome P450 omega hydroxylase (CYP4) function in fatty acid metabolism and metabolic diseases (2008), Biochem. Pharmacol., 75, 2263-2275.
    View publication on PubMed

Application

Application Comment Organism
drug development CYP4A may be a therapeutic target in the control of inflammatory, vascular, and liver diseases, as well as peroxisome disorders of fatty acid metabolism Mus musculus
drug development CYP4A may be a therapeutic target in the control of inflammatory, vascular, and liver diseases, as well as peroxisome disorders of fatty acid metabolism Homo sapiens

Cloned(Commentary)

Cloned (Comment) Organism
baculovirus expressed human CYP4A11 Homo sapiens

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.228
-
arachidonic acid
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-
Mus musculus
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
hepatocyte
-
Homo sapiens
-
kidney CYP4A11 is one of the major kidney CYP4 P450s Homo sapiens
-
liver
-
Mus musculus
-
liver
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
arachidonic acid + NAD(P)H + H+ + O2
-
Mus musculus (5Z,8Z,11Z,14Z)-20-hydroxyeicosa-5,8,11,14-tetraenoic acid + NAD(P)+ + H2O
-
?
arachidonic acid + NAD(P)H + H+ + O2 the rate of metabolism by CYPA11 P450 is 10-100fold less as compared to lauric acid Homo sapiens (5Z,8Z,11Z,14Z)-20-hydroxyeicosa-5,8,11,14-tetraenoic acid + NAD(P)+ + H2O
-
?
lauric acid + NAD(P)H + H+ + O2 CYPA11 P450 efficiently and selectively omega-hydroxylates lauric acid Homo sapiens 12-hydroxydodecanoic acid + NAD(P)+ + H2O
-
?
additional information CYP4A prefers to metabolize medium chain fatty acids (C10-C16) Homo sapiens ?
-
?
additional information CYP4A prefers to metabolize medium chain fatty acids (C10–C16) Mus musculus ?
-
?
palmitic acid + NAD(P)H + H+ + O2 CYPA11 P450 shows less selectivity in the metabolism of palmitic acid where both omega and omega-1 products are produced Homo sapiens 16-hydroxyhexadecanoic acid + NAD(P)+ + H2O
-
?
stearic acid + NAD(P)H + H+ + O2
-
Homo sapiens ? + NAD(P)+ + H2O
-
?

Synonyms

Synonyms Comment Organism
CYP4 P450
-
Mus musculus
CYP4 P450
-
Homo sapiens
CYP4A
-
Mus musculus
CYP4A
-
Homo sapiens
CYP4A10
-
Mus musculus
CYP4A14
-
Mus musculus
CYPA11 P450
-
Homo sapiens
cytochrome P450 omega hydroxylase
-
Mus musculus
cytochrome P450 omega hydroxylase
-
Homo sapiens

Cofactor

Cofactor Comment Organism Structure
NAD(P)H
-
Homo sapiens

Expression

Organism Comment Expression
Homo sapiens in humans, the CYP4A11 gene is not induced by peroxisome proliferators down
Homo sapiens CYP4A gene is altered in both lipid and inflammatory disorders, modest 2fold induction of the CYP4A11 gene by peroxisome proliferator in primary human hepatocytes up
Mus musculus induction of CYP4A genes by starvation (60-700fold), by peroxisome proliferators (30-70fold), ethanol, high fat diet (2.5-100fold), and in diabetes and steatohepatitis. Dramatic induction of both the mouse CYP4A10 and CYP4A14 genes in CYP2E1 knockout mice, which accounts for the increased reactive oxygen species that induce lipid peroxidation up

General Information

General Information Comment Organism
malfunction several diseases are genetically linked to the expression of CYP4 gene polymorphic variants, which may link human susceptibility to diseases of lipid metabolism and the activation and resolution phases of inflammation Homo sapiens
metabolism CYP4A functions in liver fatty acid metabolism Homo sapiens
metabolism CYP4A functions in liver fatty acid metabolism. Increased expression of the CYP4A omega hydroxylase during steatohepatitis and their induction in animals fed a high fat diet suggest they may play a pivotal role in preventing lipotoxicity, and may be responsible for induction of oxidative stress and progression to steatohepatitis. Omega-hydroxylation of the CYP2C arachidonic acid metabolite epoxyeicosatrienonic acid to omega-hydroxylated eicosatrienoic acid can induce peroxisome proliferation in rodents Mus musculus