AASS (GeneName), Alpha-aminoadipic semialdehyde synthase, mitochondrial (ProteinName), AASS_HUMAN.
Product Name:
Human AASS/ Alpha-aminoadipic semialdehyde synthase, mitochondrial ELISA Kit
Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Alternative:
LKR/SDH
Detection Method:
ELISA
Specificity:
Natural and recombinant human Alpha-aminoadipic semialdehyde synthase, mitochondrial
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
Cell Biology
- Data
- Citations
- Publication
- Sequence / 3D
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General Annotation
Sub Unit:
Homodimer.
Function:
Bifunctional enzyme that catalyzes the first two steps in lysine degradation. The N-terminal and the C-terminal contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively.
Subcellular Location:
Mitochondrion
This product has not yet been referenced specifically in any publications.
[1].
"Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia."
[2].
"Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia."
[3].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."
[5].
"The enzymology of lysine catabolism in rice seeds--isolation, characterization, and regulatory properties of a lysine 2-oxoglutarate reductase/saccharopine dehydrogenase bifunctional polypeptide."
[6].
"FBXL13 directs the proteolysis of CEP192 to regulate centrosome homeostasis and cell migration."
[7].
"Architecture of the human interactome defines protein communities and disease networks."
[8].
"Response Element Composition Governs Correlations between Binding Site Affinity and Transcription in Glucocorticoid Receptor Feed-forward Loops."
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