The growth and differentiation of normal cells are controlled by protein-tyrosine kinases, which serve as receptors for a wide variety external signals. Small protein modules called Src homology 2 (SH2) SH3 domains mediate protein-protein interactions in signaling pathways that triggered tyrosine kinases. SH2 domain, module around 100 amino acids, is present kinase targets within the cell. recr...

Microtubules are dynamic structures regulated by post-translational modifications called a tubulin code. The pictured jester's cap ‘n’ bells resembles disassembling microtubules—a catastrophe—with the illustrating C-terminal tyrosine on tubulins. One is replaced our chemical proteomics probe, which being attached tubulin-tyrosine ligase. juggling amino acids of proteins animate tyrosination cyc...

Liquid-liquid phase separation (LLPS) between tyrosine- and arginine-rich peptides are of biological importance. To understand the interactions proteins in condensed close analogy to complex coacervation, we run multiple umbrella calculations oligomers containing tyrosine (pY) arginine (pR). We find pR-pY complexation be energetically driven. Metadynamics simulations on monomers suggest that th...

Supplementation of tyrosine, non-essential amino acid, and precursor catecholamine was found to ameliorate the heat-induced alterations in latencies event-related potential P300 contingent negative variation. Here we present effect tyrosine supplementation on heat stress (exposure ambient temperature 45 oC relative humidity 30 %) induced behavior (attention, mood) levels plasma monoamines. Ten ...

Fate of tyrosine self assembly from dimer formation to photoluminescent and magnetically active ternary nanocomposite containing nanotubes.

background: tyrosinemia type 1 is an autosomal recessive metabolic disorder, which typically affects liver and kidneys. it is caused by a defect in fumarylacetoacetate hydrolase or fumarylacetoacetase (fah) enzyme, the final enzyme in the tyrosine degradation pathway. the disease typically manifests as early onset type in early infancy with acute hepatic crisis with hepatomegaly and bleeding te...

acute lymphoblastic leukemia(all) is due to early stage arrest of lymphoblast development. the translocation of philadelphia (ph) chromosome occurs as a result of the bcr-abl fusion gene, which constitutively produced activated tyrosine kinase. this gene fusion is an important indicator for prognosis in all and is associated with poor overall survival and remission duration. bcr-abl could inter...