extracellular enzyme - definição. O que é extracellular enzyme. Significado, conceito
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O que (quem) é extracellular enzyme - definição

Extracellular domain

Extracellular vesicle         
VESICLE THAT IS PART OF THE EXTRACELLULAR REGION
Extracellular vesicles; Apoptotic body
Extracellular vesicles (EVs) are lipid bilayer-delimited particles that are naturally released from almost all types of cell and, unlike a cell, cannot replicate. EVs range in diameter from near the size of the smallest physically possible unilamellar liposome (around 20-30 nanometers) to as large as 10 microns or more, although the vast majority of EVs are smaller than 200 nm.
holoenzyme         
  • recessive]] fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.
  • The energies of the stages of a [[chemical reaction]]. Uncatalysed (dashed line), substrates need a lot of [[activation energy]] to reach a [[transition state]], which then decays into lower-energy products. When enzyme catalysed (solid line), the enzyme binds the substrates (ES), then stabilizes the transition state (ES<sup>‡</sup>) to reduce the activation energy required to produce products (EP) which are finally released.
  • alt=Lysozyme displayed as an opaque globular surface with a pronounced cleft which the substrate depicted as a stick diagram snuggly fits into.
  • 2E2Q}})
  • 1KW0}})
  • alt=A graph showing that reaction rate increases exponentially with temperature until denaturation causes it to decrease again.
  • 4KXV}})
LARGE BIOLOGICAL MOLECULE THAT ACTS AS A CATALYST
Apoenzyme; Holoenzyme; Enzymes; ENZ; Enzyme action; Mechanisms of enzyme action; Enzymatic; Lock-and-key model (enzyme); Enyzme; Enzymology; Biocatalyst; Biocatalysts; Lock and Key Theory; Enzyme-substrate complex; ENZYME STRUCTURE AND FUNCTION; Holoenzymes; Apoenzymes; Enzymatically; Lock and key model; Encyme; Ensyme; Enyme characteristics; Cofactors and coenzymes; Coenzymes and cofactors; Enzymic; Enzyme preparations; Lock-and-key model; Lock and key theory; Enzime; Haloenzyme; Enzyme type; Regulation mechanism; Enzyme regulation; Carbamidase
[?h?l??'?nz??m]
¦ noun Biochemistry a biochemically active compound of an enzyme combined with a coenzyme.
Enzyme         
  • recessive]] fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.
  • The energies of the stages of a [[chemical reaction]]. Uncatalysed (dashed line), substrates need a lot of [[activation energy]] to reach a [[transition state]], which then decays into lower-energy products. When enzyme catalysed (solid line), the enzyme binds the substrates (ES), then stabilizes the transition state (ES<sup>‡</sup>) to reduce the activation energy required to produce products (EP) which are finally released.
  • alt=Lysozyme displayed as an opaque globular surface with a pronounced cleft which the substrate depicted as a stick diagram snuggly fits into.
  • 2E2Q}})
  • 1KW0}})
  • alt=A graph showing that reaction rate increases exponentially with temperature until denaturation causes it to decrease again.
  • 4KXV}})
LARGE BIOLOGICAL MOLECULE THAT ACTS AS A CATALYST
Apoenzyme; Holoenzyme; Enzymes; ENZ; Enzyme action; Mechanisms of enzyme action; Enzymatic; Lock-and-key model (enzyme); Enyzme; Enzymology; Biocatalyst; Biocatalysts; Lock and Key Theory; Enzyme-substrate complex; ENZYME STRUCTURE AND FUNCTION; Holoenzymes; Apoenzymes; Enzymatically; Lock and key model; Encyme; Ensyme; Enyme characteristics; Cofactors and coenzymes; Coenzymes and cofactors; Enzymic; Enzyme preparations; Lock-and-key model; Lock and key theory; Enzime; Haloenzyme; Enzyme type; Regulation mechanism; Enzyme regulation; Carbamidase
·noun An unorganized or unformed ferment, in distinction from an organized or living ferment; a soluble, or chemical, ferment. Ptyalin, pepsin, diastase, and rennet are good examples of enzymes.

Wikipédia

Ectodomain

An ectodomain is the domain of a membrane protein that extends into the extracellular space (the space outside a cell). Ectodomains are usually the parts of proteins that initiate contact with surfaces, which leads to signal transduction. A notable example of an ectodomain is the S protein, commonly known as the spike protein, of the viral particle responsible for the COVID-19 pandemic. The ectodomain region of the spike protein (S) is essential for attachment and eventual entry of the viral protein into the host cell.

Ectodomains play a crucial part in the signaling pathways of viruses. Recent findings have indicated that certain antibodies including the anti-receptor binding domain (anti-RBD) or anti-spike ectodomain (anti-ECD) IgG titers can act as virus neutralization titers (VN titers) which can be identified in individuals with diseases, dyspnea and hospitalizations. In perspective of severe acute respiratory syndrome corona virus 2 (SARS-Cov-2) these specific ectodomains may detect antibody efficacy against SARS-Cov-2, in which VN titers can classify eligible plasma donors. Protective measures against diseases and respiratory conditions can further be advanced through ongoing research on ectodomains. Ectodomain's play a crucial part in the signaling pathways of viruses. In perspective of severe acute respiratory syndrome corona virus 2 (SARS-Cov-2) these specific ectodomains may detect antibody efficacy against SARS-Cov-2, in which VN titers can classify eligible plasma donors. Protective measures against diseases and respiratory conditions can further be advanced through ongoing research on ectodomains.

Ectodomains also interact with membrane systems inducing vesicle aggregation, lipid mixing and liposome leakage which provides information as to how certain viruses spread infection throughout the cellular domain. Specifically, the hepatitis C virus (HCV) utilize a fusion process in which the ectodomain of HCV E2 envelope protein confers fusogenic properties to membrane systems implying HCV infection proceeds throughout the cell through receptor mediated endocytosis. These findings in the role of the ectodomains interacting with target membranes give insight into virus destabilization and mechanism of the fusion of viral and cellular membrane which is yet to be further characterized.