Sickle-cell disease is a disorder that results in malformed hemoglobin molecules. What is the result of this in terms of hemoglobin function? Multiple Choice Hemoglobin has a reduced ability to bind to and transport oxygen in red blood cells. Hemoglobin has an increased ability to bind to and transport oxygen in red blood cells. Hemoglobin has an increased ability to bind to and transport carbon dioxide in red blood cells. White blood cells begin to pick up hemoglobin molecules instead and this decreases their ability to function in the immune system as intended.

idk but if i had to take an educated guess i’d say a c d

Cuz i said so. which gives it to b

Proteins are the workhorses of the cell, controlling virtually every reaction within as well as providing structure and serving as signals to other cells. proteins are long chains of  amino acids  , and the exact sequence of the amino acids determines the final structure and function of the protein. instructions for that sequence are encoded in  genes  . to make a particular protein, a messenger ribonucleic acid (mrna) copy is made from the gene (in the process called  transcription  ), and the mrna is transported to the  ribosome  . protein synthesis, also called  translation  , begins when the two ribosomal subunits link onto the mrna. this step, called initiation, is followed by elongation, in which successive amino acids are added to the growing chain, brought in by transfer rnas (trnas). in this step, the ribosome reads the  nucleotides  of mrna three by three, in units called  codons  , and matches each to three nucleotides on the trna, called the anticodon. finally, during termination, the ribosome unbinds from the mrna, and the  amino acid  chain goes on to be processed and folded to make the final, functional protein