<u>Answer</u>:
The two molecules generated by the Krebs cycle that pass their high-energy electrons to the electron transport are NADH and FADH2
<u>Explanation:</u>
The kreb's cycle gives NADH and also the another hydrogen carrier which is termed as FADH2. During the process of the electron transport chain, one NADH gives rise to electrons and also the hydrogen ions, which has enough potential energy that can convert and produce 3 ATP molecules. Again in the electron transport chain the NADH and the FADH2 undergoes oxidation and releases energy in the form of the ATP. The process of generation of the ATP in the electron transport chain(ETC) is also referred as the chemiosmotic phosphorolation.
A. Kinetic energy is the energy of motion. B,C,D all describe situations where there is not movement.
Answer:
Blood
Explanation:
Connective tissue consists of extracellular matrix and cells. The main function of connective tissue is to bind the other tissues together, provide them support and strength. Blood is one of the liquid connective tissue that does not perform such functions. The presence of liquid extracellular matrix (plasma) and formed elements (blood cells) makes it a connective tissue. It serves in the transport of nutrients, gases, wastes, hormones, etc. It also takes part in immune responses but does not strength or support other body tissues.
The correct answer to this could be numerous words. The most broad term that would fit would be the Cosmos. If you are referring to more specific then you might be saying things such as Ionosphere. That is where Sputnik 1, the first satellite, was launched.
Answer:
One of the common genetic disorders is sickle cell anemia, in which 2 recessive alleles must meet to allow for destruction and alteration in the morphology of red blood cells. This usually leads to loss of proper binding of oxygen to hemoglobin and curved, sickle-shaped erythrocytes. The mutation causing this disease occurs in the 6th codon of the HBB gene encoding the hemoglobin subunit β (β-globin), a protein, serving as an integral part of the adult hemoglobin A (HbA), which is a heterotetramer of 2 α chains and 2 β chains that is responsible for binding to the oxygen in the blood. This mutation changes a charged glutamic acid to a hydrophobic valine residue and disrupts the tertiary structure and stability of the hemoglobin molecule. Since in the field of protein intrinsic disorder, charged and polar residues are typically considered as disorder promoting, in opposite to the order-promoting non-polar hydrophobic residues, in this study we attempted to answer a question if intrinsic disorder might have a role in the pathogenesis of sickle cell anemia. To this end, several disorder predictors were utilized to evaluate the presence of intrinsically disordered regions in all subunits of human hemoglobin: α, β, δ, ε, ζ, γ1, and γ2. Then, structural analysis was completed by using the SWISS-MODEL Repository to visualize the outputs of the disorder predictors. Finally, Uniprot STRING and D2P2 were used to determine biochemical interactome and protein partners for each hemoglobin subunit along with analyzing their posttranslational modifications. All these properties were used to determine any differences between the 6 different types of subunits of hemoglobin and to correlate the mutation leading to sickle cell anemia with intrinsic disorder propensity.
Explanation:
