7beq
From Proteopedia
MicroED structure of the MyD88 TIR domain higher-order assembly
Structural highlights
DiseaseMYD88_HUMAN Defects in MYD88 are the cause of MYD88 deficiency (MYD88D) [MIM:612260; also known as recurrent pyogenic bacterial infections due to MYD88 deficiency. Patients suffer from autosomal recessive, life-threatening, often recurrent pyogenic bacterial infections, including invasive pneumococcal disease, and die between 1 and 11 months of age. Surviving patients are otherwise healthy, with normal resistance to other microbes, and their clinical status improved with age.[1] [2] FunctionMYD88_HUMAN Adapter protein involved in the Toll-like receptor and IL-1 receptor signaling pathway in the innate immune response. Acts via IRAK1, IRAK2, IRF7 and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Increases IL-8 transcription. Involved in IL-18-mediated signaling pathway. Activates IRF1 resulting in its rapid migration into the nucleus to mediate an efficient induction of IFN-beta, NOS2/INOS, and IL12A genes (By similarity).[3] [4] [5] [6] See AlsoReferences
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Categories: Homo sapiens | Large Structures | Abbey B | Aquila A | Clabbers MTB | Croll TI | Darmanin C | Gambin Y | Holmes S | Hunter DJB | Hunter MS | Kobe B | Liang M | Malde AK | Muusse TW | Nanson JD | Rahaman MH | Sierecki E | Thygesen SJ | Vajjhala P | Ve T | Xu H | Yoon CH | Zatsepin NA | Zhao J