
Apolipoprotein B-100
Homo sapiensTaxon: 9606
4563
アミノ酸
515.5 kDa
理論値
8
PDB エントリー
2
記録済み
機能記述
関連疾患
Hypobetalipoproteinemia, familial, 1
A disorder of lipid metabolism characterized by less than 5th percentile age- and sex-specific levels of low density lipoproteins, and dietary fat malabsorption. Clinical presentation may vary from no symptoms to severe gastrointestinal and neurological dysfunction similar to abetalipoproteinemia.
Hypercholesterolemia, familial, 2
A form of hypercholesterolemia, a disorder of lipoprotein metabolism characterized by elevated serum low-density lipoprotein (LDL) cholesterol levels, which result in excess deposition of cholesterol in tissues and leads to xanthelasma, xanthomas, accelerated atherosclerosis and increased risk of premature coronary heart disease. FHCL2 inheritance is autosomal dominant.
アミノ酸配列
MDPPRPALLALLALPALLLLLLAGARAEEEMLENVSLVCPKDATRFKHLRKYTYNYEAES SSGVPGTADSRSATRINCKVELEVPQLCSFILKTSQCTLKEVYGFNPEGKALLKKTKNSE EFAAAMSRYELKLAIPEGKQVFLYPEKDEPTYILNIKRGIISALLVPPETEEAKQVLFLD TVYGNCSTHFTVKTRKGNVATEISTERDLGQCDRFKPIRTGISPLALIKGMTRPLSTLIS
FASTA 形式 · 4563 アミノ酸 · 分子量 515.5 kDa
実験構造
8 PDB エントリー翻訳後修飾
- •Palmitoylated; structural requirement for proper assembly of the hydrophobic core of the lipoprotein particle