It usually ends up in the Golgi Body which is the shipping department of the cell. From there, it goes to where it is need. Some are enzymes which are needed for chemical reactions in the cell, some are the main ingredient of tears or saliva or mucous to coat the lining of the respiratory tract and other tracts.
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Four 'types' of nucleotide bases - when they are read three-at-a-time - this is considered to be a triplet-codon. Triplet codons are individually related to one specific amino acid, a polypeptide being a short protein.
The chain of amino acids linked together form Protein. Depending on the type and arrangement of aminoacids, different types of proteins are formed. The blueprint for this formation is provided by the genetic material ot the organism where it is being synthesized.
There are two steps to protein synthesis: 1. Transcription - DNA unwinds, mRNA is made on the DNA template, the mRNA leaves the nucleus (through the nuclear pores) and goes to the ribosomes. 2. Translation - The mRNA moves along the ribosome where the information in the mRNA (codons) give the instructions for the sequence of amino acids in the protein that is being made. Once the amino acid sequence (protein, or "polypeptide") is complete, it detaches from the ribosome.
RNA is being translated.
punetas ensenate a estudiar no aserte pendejo. homez
Four 'types' of nucleotide bases - when they are read three-at-a-time - this is considered to be a triplet-codon. Triplet codons are individually related to one specific amino acid, a polypeptide being a short protein.
The chain of amino acids linked together form Protein. Depending on the type and arrangement of aminoacids, different types of proteins are formed. The blueprint for this formation is provided by the genetic material ot the organism where it is being synthesized.
The primary structure of a protein is the unique sequence of amino acids. There are 20 possible amino acids, and the primary structure consists of a string of amino acids held together by peptide bonds. The secondary structure occurs when the amino acid chain becomes coiled or folded in alpha helix or beta pleated sheets. The protein develops its three-dimensional shape in the tertiary structure. Van der Waals interactions, disulfide bonds, hydrophobic interactions, and ionic bonding all impact the tertiary structure. Finally, the quaternary structure is made up of more than one polypeptide chain (a polypeptide chain is the string of amino acids described in the primary structure). Hope this helps!
Urea itself will only break non-covalent bonds, breaking any protein into its basic subunits, polypeptide chains of amino acids. Without mercaptoethanol this would be the end result, and from this you could deduce whether the protein was a dimer, tetramer, etc. Mercaptoethanol is an oxidizing agent which is used to oxidize the disulfide bridge formed between cysteine residues. Oxidation of these sulfur atoms results in the disulfide bridge being broken, further reducing the protein (now polypeptide chains) into its smaller subunits. If successful, all of the collected protein remains should equal the total molecular weight observed in the protein in its entirety.
There are two steps to protein synthesis: 1. Transcription - DNA unwinds, mRNA is made on the DNA template, the mRNA leaves the nucleus (through the nuclear pores) and goes to the ribosomes. 2. Translation - The mRNA moves along the ribosome where the information in the mRNA (codons) give the instructions for the sequence of amino acids in the protein that is being made. Once the amino acid sequence (protein, or "polypeptide") is complete, it detaches from the ribosome.
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The tRNA helps to form amino acid in the cytoplasm during protein synthesis as a specific enzymes for activation and for attaching itself to corresponding tRNA. The tRNA has an anticodon complementry to the appropriate codon of the RNA.
The data is held by RAM(random access memory) or primary memory when it's being processed.
RNA is being translated.
When monosaccharides are joined together by dehydration synthesis then it is called glycosidic linkage, it is a covalent bond. When lipids are being bonded together the bond is called an ester bond. When amino acids are joining together to form a polypeptide then the bonds are called peptide bonds.
The ribosome uses tRNA that matches the current codon (triplet) on the mRNA to append an amino acid to the polypeptide chain. This is done for each triplet on the mRNA, while the ribosome moves towards the 3' end of the mRNA.