This family of ATPases is structurally related to the pumps that acidify lysosomes and vesicles; however, they usually function in reverse, generating ATP from ADP and Pi using proton gradients across membranes is called F-type pumps.
- The inner membrane of mitochondria and bacterial plasma membranes both contain F type pumps, which are necessary for the generation of ATP.
- It is also known as the ATP synthase complex or Complex V. By letting these protons passively return to the matrix, they use the proton gradient created by the flow of electrons to produce ATP.
- The F1 motor is the ATP turnover motor and,
- In mammals, the F0 motor, which is in charge of ion translocation, has nine subunits, nine of which are likely centered on the membrane's A, B, and C subunits, along with D, E, F2, F6, G2, and 8 subunits.
learn more about ATPases here: brainly.com/question/13914625
#SPJ4
Milk contains a lot of proteins in them it contains calcium protein potassium iodine. Phosphorus. It also contains vitamins b1 and b12.
Answer:
D. 4E-BP1 binding to elF4E prevents loading of the mRNA onto the ribosome.
Explanation
In eukaryotic organisms, the eIF4E translation initiation factor functions by directing the ribosomes to the 5'-terminal cap structure of the messenger RNA (mRNA) in order to start the translation. Moreover, phosphorylation is a posttranslational modification of specific amino acids on proteins that play diverse cellular functions by altering protein stability, location, and/or enzymatic activity. It has been shown that elF4E phosphorylation is increased in response to cellular stimuli that induce translation in the ribosomes (e.g., growth factors, hormones, etc). The eukaryotic translation initiation factor 4E (eIF4E)-binding protein 1 (4E-BP1) is a repressor of mRNA translation which is phosphorylated and inactivated by growth factors and hormones, thereby inhibiting 4E-BP1 binding to elF4E and consequently activating translation.
Frameshift mutation affects codons downstream the point of mutation. The previous order of 3 nucleotide- sequences (codons) is consequently changed. This, therefore, changes the protein coded by the mRNA transcribed by the mutated DNA region. Frameshifts are mostly due to insertion or deletion mutations.
