Basic Information
Gene ID
Potra2n6c15093
Position
chr6:21532102-21539229 (+)
7127bp
Gene Type
gene
Gene Description (Protein Product)
"hydroxymethylglutaryl-CoA lyase
Organism
Also AS Potri.006G036800AT2G26800Potri.006G036800.v4.1

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Potra2n8c17724 Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex
Potra2n6c15348 Belongs to the thiolase family
Potra2n9c19923 citrate synthase

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail


Pathway
KEGG Term Name Description
map04146 Peroxisome Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contribute to many crucial metabolic processes such as fatty acid oxidation, biosynthesis of ether lipids and free radical detoxification. The biogenesis of peroxisomes starts with the early peroxins PEX3, PEX16 and PEX19 and proceeds via several steps. The import of membrane proteins into peroxisomes needs PEX19 for recognition, targeting and insertion via docking at PEX3. Matrix proteins in the cytosol are recognized by peroxisomal targeting signals (PTS) and transported to the docking complex at the peroxisomal membrane. Peroxisomes' deficiencies lead to severe and often fatal inherited peroxisomal disorders (PD). PDs are usually classified in two groups. The first group is disorders of peroxisome biogenesis which include Zellweger syndrome, and the second group is single peroxisomal enzyme deficiencies.
map01100 Metabolic pathways -
map00650 Butanoate metabolism -
map00280 Valine, leucine and isoleucine degradation -