Identify this molecule

Identify this molecule

A health disorder that builds up certain amount of fatty acids in spleen and liver.

A rare genetic disorder that is caused by the absence of an enzyme breaking down fatty acids.

A health condition with high level of lipids in the blood.

A disease caused by defects in the 13 genes, and is one of four related diseases known as peroxisome biogenesis disorders.

A rare inherited condition caused by fatty acid enzyme malfunction.

In beta oxidation of FA, supply the enzyme that catalyzed the reaction: Fatty acyl-CoA -> Trans-delta2-Enoyl-CoA

In beta oxidation of FA, supply the enzyme that catalyzed the reaction: Trans-delta2-Enoyl-CoA -> L-beta-hydroxyacyl-CoA

In beta oxidation of FA, supply the enzyme that catalyzed the reaction: L-beta-hydroxyacyl-CoA -> beta-ketoacyl-CoA

In beta oxidation of FA, supply the enzyme that catalyzed the reaction: beta-ketoacyl-CoA -> Fatty acyl-CoA

In beta oxidation of FA, What is the type of reaction involved in Step 1?

In beta oxidation of FA, What is the type of reaction involved in Step 2?

In beta oxidation of FA, What is the type of reaction involved in Step 3?

In beta oxidation of FA, What is the type of reaction involved in Step 4?

In beta oxidation of FA, the extra step involved in unsaturated FA is isomerization of cis double bond to trans double bond.

Short chain FA, are carried directly into the mitochondrial matrix while Long chain FA needs a carrier to be transported into the matrix.

Synthesis starts with reaction of three molecules of acetyl CoA to form the six carbon compound HMG-CoA.

2 molecules of ATP are lost in activation of saturated FA, stearic acid before beta oxidation.