spinqualitylabelsall models ACAT/SOAT 6l47 Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

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Contents 1 Introduction 2 Structure 2.1 Overall Structure 2.2 Important Residues 2.3 Important Interactions 3 Proposed Mechanism 3.1 Active Site 3.2 Binding Pocket 3.3 Tunnels 4 Disease 5 Relevance 6 Structural highlights

Introduction

We used an article on ACAT. ^[3] We also used an article on SOAT. ^[4]

Acyl-coenzyme A: cholesterol acyltransferase (ACAT), also known as Human Sterol O-acyltransferase (hSOAT) is an enzyme that catalyzes the reaction between long chain fatty acyl CoA and intracellular cholesterol to form the more hydrophobic cholesteryl ester for cholesterol storage. Cholesteryl ester is the primary form of how cholesterol is stored in multiple types of cells and transported through the circulatory system. ACAT is an endoplasmic reticulum membrane protein, and ACAT is a part of the MBOAT (membrane-bound O-acyltransferase) family, which also includes acyl-coenzyme A: diacylglycerol acyltransferase (DGAT) and ghrelin O-acyltransferase (GOAT).

There have been two ACAT isoforms discovered in mammals, ACAT1 and ACAT2 and they are predominantly located in different parts of the body. ACAT1 is mainly found in the liver, kidneys, adrenal glands and macrophages, whereas ACAT2 is found only in the intestines and liver.

Structure

Overall Structure

ACAT is a tetramer composed of a dimer of a dimer, but is able to perform its function solely as a . There are 9 transmembrane helices in each domain which create a tunnel for the active site. There are also three helices found on the intracellular side (IH1, IH2, and IH3) and one helix on the extracellular side (EH1). The active site contains three tunnels – the transmembrane tunnel for cholesterol entrance, the cytosolic tunnel for acyl-CoA entrance, and the lumen tunnel for cholesterol ester exit. ACAT also has an amino-terminal cytosolic domain (NTD) that is important for tetramerization of this protein.

Important Residues

Histidine

Important Interactions

Proposed Mechanism

Active Site

Binding Pocket

Tunnels

Disease

Other Protopedia Page

Relevance

Structural highlights

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