post krebs protein

Protein metabolism

Amino acid synthesis is the set of biochemical processes (metabolic pathways) by which the amino acids are produced.  They are considered as the building blocks for the synthesis of proteins.

Protein metabolism includes all various biochemical processes responsible for:

  • The synthesis of proteins [transcription, translation, and post translational modifications] and amino acids (anabolism),
  • the degradation of proteins (catabolism) into absorbable monomers for further degradation or reassembly.

Health conditions related to protein metabolism are generally caused by the amount of dietary protein consumed. Examples of protein metabolism disorders include: Phenylketonuria (PKU), Maple Syrup Urine Disease (MSUD), Tyrosinemia and Homocystinuria.

AMSBIO is offering an extensive range of products involved in this metabolic pathway:

Alpha Ketoglutarate
Glutamine Synthetase
Alpha Ketoacid
Aminotransferase
Aminoacyl-Trna-Synthetase
Pepsin
Lysine
Leucine
Alanine
Glutamine
Peptidase
Trypsin
Arginine
Asparagine
Aspartate
Cysteine
Protease
Chymotrypsin
Glutamic Acid
Glycine
Histidine
Methionine
Endopeptidase
Glutamate
Proline
Serine
Valine
Phenylalanine
Carboxypeptidase
Aspartic Acid
Isoleucine
Threonine
Tryptophan
Tyrosine
Aminopeptidase
Blood Ammonia
Total Amino Acids
Albumin (ALB)
Hydroxyproline (HYP)
Protein Carbonyl
Homocysteine (HCY)
Biuret Protein
Bradford Protein
Total Carbonyl
Bca Protein
Gamma-Aminobutyric Acid (GABA)
Ornithine
Citrulline
post krebs nucleotide

Nucleotide Metabolism

Nucleic acids are polynucleotides serving serve as the main energy donors for cellular processes.

Nucleic acid metabolism consists of synthesis and degradation of nucleic acids:

  • Ribonucleic acid (RNA) : it is a linear nucleotide chain containing the guanine (G), uracil (U), adenine (A), cytosine (C) bases. RNA is synthesized from DNA by an enzyme known as RNA polymerase during a process called transcription. There are three distinct phases of RNA metabolism : transcription, translation and degradation.
  • Deoxyribonucleic acid (DNA): it is a complementary double chain, nucleotide chain with specific base pairing (adenine and thymine, guanine and cytosine). There three main processes (Replication, repair, and recombination) of DNAmetabolism carried out by specialized machinery within the cell.

Disorders that involve abnormalities of nucleotide metabolism range from relatively common diseases. These include hyperuricemia, acute renal failure, renal stones, gout, unexplained neurologic deficits etc. Hyperuricemia and gout, are due to an increased production or impaired excretion of a metabolic end product of purine metabolism (uric acid).

AMSBIO is offering an extensive range of products involved in this metabolic pathway:

Guanine
Adenine
Cytosine
Thymine
Adenosine Triphosphate (ATP)
Guanosine Triphosphate (GTP)
Uridine Triphosphate (UTP)
Deoxyribonucleic Acid (DNA)
Ribonucleic Acid (RNA)
Uracil
Cyclic Guanosine Monophosphate (cGMP)
Cyclic Adenosine Monophosphate (cAMP)
Purine
Pyrimidine
Nucleoside Diphosphate
Nucleoside Triphosphate
Pyrophosphate
Ribose 5-Phosphate
Carbamoyl Transferase
Orotate
Dihydroorotate
Amidotransferase
Hypoxanthine
Xanthine Oxidase
Inosine
HGPRT
Hypoxanthine-Guanine Phosphoribosyltransferase
Adenosine Deaminase
5-Phospho-?-D-Ribosyl 1-Pyrophosphate (PRPP)
Phosphoribosyl 1-Pyrophosphate
Ribonucleoside
6-Phosphogluconate
Glucose 6-Phosphate
Phosphogluconolactonase
CTP Synthase
Nucleoside Diphosphate Kinase
Orotate Phosphoribosyltransferase
Carbamoyl Phosphate
Beta-Ureidopropionase
Beta Alanine
Amidophosphoribosyltransferase
Inosine Monophosphate (IMP)
Adenylosuccinate Lyase
Fumarate
Adenine Phosphoribosyltransferase (APRT)
Adenylosuccinate Synthase
AMP Deaminase
GMP Synthase
GMP Reductase
Nuclease
Nucleotidase
Purine Nucleoside Phosphorylase