Aspect

A rare autosomal recessive lysosomal disorder characterized by deficiency of N-aspartyl-beta-glucosaminidase. It is characterized by developmental delays during childhood.

Aspartyl Proteases (Aspartic Endopeptidases) have an acidic residue (aspartate) involved in the catalytic process, have a pH optimum below 5 and catalyze…

A non-essential amino acid in humans, Aspartic Acid has an overall negative charge and plays an important role in the synthesis of…

An enzyme found in the liver, heart, and other tissues. A high level of aspartate transaminase released into the blood may be…

Aspartate aminotransferase, mitochondrial (430 aa, ~48 kDa) is encoded by the human GOT2 gene. This protein plays a role in both the…

Aspartate aminotransferase, cytoplasmic (413 aa, ~46 kDa) is encoded by the human GOT1 gene. This protein is involved in amino acid…