Fibrinogen alpha chain

纤维蛋白原α链

Homo sapiensTaxon: 9606

3D-structureAdaptive immunityAlternative splicingAmyloidAmyloidosisBlood coagulationCalciumCoiled coilDirect protein sequencingDisease variantDisulfide bondGlycoprotein+11

序列长度

866

氨基酸

分子量

95.0 kDa

理论值

实验结构

PDB 条目

功能描述

Cleaved by the protease thrombin to yield monomers which, together with fibrinogen beta (FGB) and fibrinogen gamma (FGG), polymerize to form an insoluble fibrin matrix. Fibrin has a major function in hemostasis as one of the primary components of blood clots. In addition, functions during the early stages of wound repair to stabilize the lesion and guide cell migration during re-epithelialization. Was originally thought to be essential for platelet aggregation, based on in vitro studies using anticoagulated blood. However, subsequent studies have shown that it is not absolutely required for thrombus formation in vivo. Enhances expression of SELP in activated platelets via an ITGB3-dependent pathway. Maternal fibrinogen is essential for successful pregnancy. Fibrin deposition is also associated with infection, where it protects against IFNG-mediated hemorrhage. May also facilitate the immune response via both innate and T-cell mediated pathways

被蛋白酶凝血酶裂解产生单体，与纤维蛋白原β (FGB) 和纤维蛋白原γ (FGG) 一起聚合形成不溶性纤维蛋白基质。纤维蛋白作为血栓的主要成分之一，具有止血的主要功能。此外，在伤口修复的早期阶段发挥作用，稳定病变并在上皮化过程中引导细胞迁移。根据使用抗凝血液的体外研究，最初被认为对于血小板聚集至关重要。然而，随后的研究表明，它并不是体内血栓形成所绝对需要的。通过 ITGB3 依赖性途径增强活化血小板中 SELP 的表达。母体纤维蛋白原对于成功妊娠至关重要。纤维蛋白沉积也与感染有关，可以防止 IFNG 介导的出血。还可能通过先天和 T 细胞介导的途径促进免疫反应

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定位与分布

组织特异性

Detected in blood plasma (at protein level)

相关疾病

Congenital afibrinogenemia

Rare autosomal recessive disorder is characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen.

Amyloidosis, hereditary systemic 2

A form of hereditary systemic amyloidosis, a disorder characterized by amyloid deposition in multiple tissues resulting in a wide clinical spectrum. AMYLD2 is an autosomal dominant form characterized by deposition of amyloid preferentially in the glomeruli of the kidney. It clinically presents with hypertension, proteinuria, and finally azotemia. Involvement of liver and spleen may be seen in advanced cases, but heavy glomerular deposition without significant medium sized vessel involvement is characteristic of the disease.

Dysfibrinogenemia, congenital

A disorder characterized by qualitative abnormalities (dysfibrinogenemia) of the circulating fibrinogen. Affected individuals are frequently asymptomatic, but some patients have bleeding diathesis, thromboembolic complications, or both. In some cases, dysfibrinogenemia is associated with low circulating fibrinogen levels (hypodysfibrinogenemia).

氨基酸序列

MFSMRIVCLVLSVVGTAWTADSGEGDFLAEGGGVRGPRVVERHQSACKDSDWPFCSDEDW
NYKCPSGCRMKGLIDEVNQDFTNRINKLKNSLFEYQKNNKDSHSLTTNIMEILRGDFSSA
NNRDNTYNRVSEDLRSRIEVLKRKVIEKVQHIQLLQKNVRAQLVDMKRLEVDIDIKIRSC
RGSCSRALAREVDLKDYEDQQKQLEQVIAKDLLPSRDRQHLPLIKMKPVPDLVPGNFKSQ

FASTA 格式 · 866 个氨基酸 · 分子量 95.0 kDa