Apolipoprotein A-II explained

Symbol:ApoA-II
ApoA-II
Pfam:PF04711
Interpro:IPR006801
Scop:1l6k

Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[1] It is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. ApoA-II regulates many steps in HDL metabolism, and its role in coronary heart disease is unclear. [2] Remarkably, defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.[3]

Interactions

ApoA-II has been shown to interact with phospholipid transfer protein.[4]

Further reading

Notes and References

  1. Tsao YK, Wei CF, Robberson DL, Gotto AM, Chan L . Isolation and characterization of the human apolipoprotein A-II gene. Electron microscopic analysis of RNA:DNA hybrids, nucleotide sequence, identification of a polymorphic MspI site, and general structural organization of apolipoprotein genes . The Journal of Biological Chemistry . 260 . 28 . 15222–31 . Dec 1985 . 10.1016/S0021-9258(18)95725-X . 2415515 . free .
  2. Tailleux . Anne . Duriez . Patrick . Fruchart . Jean-Charles . Clavey . Véronique . September 2002 . Apolipoprotein A-II, HDL metabolism and atherosclerosis . Atherosclerosis . 164 . 1 . 1–13 . 10.1016/s0021-9150(01)00751-1 . 0021-9150 . 12119188.
  3. Web site: Entrez Gene: APOA2 apolipoprotein A-II.
  4. Pussinen PJ, Jauhiainen M, Metso J, Pyle LE, Marcel YL, Fidge NH, Ehnholm C . Binding of phospholipid transfer protein (PLTP) to apolipoproteins A-I and A-II: location of a PLTP binding domain in the amino terminal region of apoA-I . Journal of Lipid Research . 39 . 1 . 152–61 . Jan 1998 . 10.1016/S0022-2275(20)34211-5 . 9469594 . free .