Toxic Proteins from a bacterial pathogen or virus may cause disease (botulinum or tetanus toxin). There are protein such as tumor antigens that can trigger cancer. Tumor suppressor protein p53 is also exist to prevent cancer.
In order for a protein to perform its biological function, it has to be folded in a certain way, because it is not just the chemical composition of the protein, but also its precise shape, which enables it to match the composition and shape of other molecules with which it reacts, or serves as a catalyst. And the real problem is that an incorrectly folded protein not only fails to do what it would otherwise have been able to do for the normal biochemical functioning of the organism, but it also will cause other proteins to become incorrectly folded; it is essentially a catalyst for incorrect folding. So, incorrect folding is a contagious condition, it spreads and incapacitates all the proteins of that type. And since those proteins were needed to perform some vital biological function, the organism will become ill (and will eventually die; prion diseases are eventually fatal, although they take a long time to develop).
PM is first line of defense against pathogens and is in charge of what comes in and out of cell via various channels. If foreign pathogens enter cell they can effect DNA replication, transcription, and several other vital cellular functions. If several cells have faulty PMs then this is where diseases arise such as cancers.
We need proteins to help mend the muscle but if you eat meat not fully cooked then yes.
in the cytoplasm technically, it doesn't. prokaryotes perform anaerobic respiration.
As a general rule, practically all the internal organelles of a cell are covered by a protective membrane, except for one type, which couldn't even be called a real organelle, and those are the Ribosomes. More a macromolecular assemble than a cell organelle, the reason because they aren't membrane-bound is because they can directly interact with the membrane in order to exchange proteins, so, having their own membrane would actually act as a barrier for them to do their job correctly.
Proteins leave to rough endoplasmic reticulum via vesicles that bud off and enter into the Golgi apparatus. Here the proteins undergo further production and some are given cell surface receptors. They then exit the Golgi apparatus via a budding vesicle. That vesicle travels along the microtubules to the plasma membrane, where the vesicle fuses with the plasma membrane. some stay in the membrane as integral proteins and some are released into the area outside of the cell.
No bacterial cell has a nuclear membrane. A bacteria is defined by not having any membrane-bound organelles.
It increases the surface area of the cell membrane. By having more surface area, more matter can be moved in and out of the cell.
True
All proteins have structure.
in the cytoplasm technically, it doesn't. prokaryotes perform anaerobic respiration.
The mother has a 50% chance of passing the defective recessive gene to her daughters who will be carries of the disorder (like their mother).
Defective
1-.015 = .985
Yes plants and animal cell membranes are having macromolecules on them. They are mainly lipids and integral and peripheral proteins. The pattern of this is well explained as "fluid-mossaic model".
can beavers live having a disease
As a general rule, practically all the internal organelles of a cell are covered by a protective membrane, except for one type, which couldn't even be called a real organelle, and those are the Ribosomes. More a macromolecular assemble than a cell organelle, the reason because they aren't membrane-bound is because they can directly interact with the membrane in order to exchange proteins, so, having their own membrane would actually act as a barrier for them to do their job correctly.
As a general rule, practically all the internal organelles of a cell are covered by a protective membrane, except for one type, which couldn't even be called a real organelle, and those are the Ribosomes. More a macromolecular assemble than a cell organelle, the reason because they aren't membrane-bound is because they can directly interact with the membrane in order to exchange proteins, so, having their own membrane would actually act as a barrier for them to do their job correctly.
Proteins leave to rough endoplasmic reticulum via vesicles that bud off and enter into the Golgi apparatus. Here the proteins undergo further production and some are given cell surface receptors. They then exit the Golgi apparatus via a budding vesicle. That vesicle travels along the microtubules to the plasma membrane, where the vesicle fuses with the plasma membrane. some stay in the membrane as integral proteins and some are released into the area outside of the cell.
Cryoglobulins are proteins that precipitate when cold. Cryoglobulinemia is the condition of having these proteins in the blood.