1. Signaling Pathways
  2. Metabolic Enzyme/Protease
  3. Adenosine Deaminase

Adenosine Deaminase (腺苷脱氨酶)

腺苷脱氨酶 (ADA) 是一种嘌呤代谢酶,可催化腺苷和脱氧腺苷不可逆脱氨,分别生成肌苷和脱氧肌苷。这种普遍存在的酶存在于多种微生物、植物和无脊椎动物中。此外,它存在于所有哺乳动物细胞中,在淋巴系统的分化和成熟中起着核心作用。人类有两种不同的腺苷脱氨酶,ADA1 和 ADA2。ADA1 在淋巴细胞功能中起重要作用,ADA1 的遗传突变会导致严重的联合免疫缺陷。ADA2 属于新型腺苷脱氨酶生长因子 (ADGF) 家族,在组织发育中起重要作用。

ADA 在各种疾病中起着关键作用。有趣的是,遗传性 ADA 缺乏和 ADA 过表达都可能导致疾病。一般认为,遗传性 ADA 缺陷是重症联合免疫缺陷病 (SCID) 的主要原因,约占所有 SCID 病例的 15%。相反,ADA 的过表达可能与溶血性贫血、肝癌、乳腺癌等密切相关。

Adenosine deaminase (ADA) is an enzyme of the purine metabolism which catalyzes the irreversible deamination of adenosine and deoxyadenosine to inosine and deoxyinosine, respectively. This ubiquitous enzyme has been found in a wide variety of microorganisms, plants, and invertebrates. In addition, it is present in all mammalian cells that play a central role in the differentiation and maturation of the lymphoid system. Two distinct adenosine deaminases, ADA1 and ADA2, are found in humans. ADA1 has an important role in lymphocyte function and inherited mutations in ADA1 result in severe combined immunodeficiency. ADA2 belongs to the novel family of adenosine deaminase growth factors (ADGFs), which play an important role in tissue development.

ADA plays a critical role in various diseases. Interestingly, Both genetic ADA deficiency and ADA overexpression may cause diseases. Generally appreciated is the notion that inherited genetic ADA deficiency represents the main cause of severe combined immunodeficiency disease (SCID), accounting for about 15% of all SCID cases. Conversely, overexpression of ADA may be closely related to hemolytic anemia, liver cancer, breast cancer, etc.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-A0006R
    Pentostatin (Standard)

    喷司他丁(Standard)

    Inhibitor
    Pentostatin (Standard)是 Pentostatin 的分析标准品。本产品用于研究及分析应用。Pentostatin (CI-825; Deoxycoformycin) 是一种高效,不可逆的腺苷脱氨酶抑制剂,Ki 值为 2.5 pM。
    Pentostatin (Standard)
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