8F5B

Human ABCA4 structure in complex with AMP-PNP

8F5B の概要

• エントリーDOI: 10.2210/pdb8f5b/pdb
• EMDBエントリー: 28864
• 分子名称: Retinal-specific phospholipid-transporting ATPase ABCA4, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
• 機能のキーワード: abc transporter, importer, membrane protein, transport protein
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 258657.82

構造登録者

Scortecci, J.F.,Van Petegem, F.,Molday, R.S. (登録日: 2022-11-13, 公開日: 2023-11-22, 最終更新日: 2024-11-20)

主引用文献

Scortecci, J.F.,Garces, F.A.,Mahto, J.K.,Molday, L.L.,Van Petegem, F.,Molday, R.S.
Structural and functional characterization of the nucleotide-binding domains of ABCA4 and their role in Stargardt disease.
J.Biol.Chem., 300:107666-107666, 2024

PubMed Abstract: ABCA4 is an ATP-binding cassette (ABC) transporter that prevents the buildup of toxic retinoid compounds by facilitating the transport of N-retinylidene-phosphatidylethanolamine across membranes of rod and cone photoreceptor cells. Over 1500 missense mutations in ABCA4, many in the nucleotide-binding domains (NBDs), have been genetically linked to Stargardt disease. Here, we show by cryo-EM that ABCA4 is converted from an open outward conformation to a closed conformation upon the binding of adenylyl-imidodiphosphate. Structural information and biochemical studies were used to further define the role of the NBDs in the functional properties of ABCA4 and the mechanisms by which mutations lead to the loss in activity. We show that ATPase activity in both NBDs is required for the functional activity of ABCA4. Mutations in Walker A asparagine residues cause a severe reduction in substrate-activated ATPase activity due to the loss in polar interactions with residues within the D-loops of the opposing NBD. The structural basis for how disease mutations in other NBD residues, including the R1108C, R2077W, R2107H, and L2027F, affect the structure and function of ABCA4 is described. Collectively, our studies provide insight into the structure and function of ABCA4 and mechanisms underlying Stargardt disease.

PubMed: 39128720
DOI: 10.1016/j.jbc.2024.107666

実験手法

ELECTRON MICROSCOPY (3.95 Å)