Basic Information
Gene ID
AALBA5B460882
Position
aalba5_s00029832:18312-19144 (+)
832bp
Gene Type
gene
Gene Description (Protein Product)
radicals which are normally produced within the cells and which are toxic to biological systems
Organism
Also AS AT3G10920

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
AALBA5B984506 Mitochondrial ribosomal death-associated protein 3
AALBA5B848409 Peroxiredoxin Q, chloroplastic
AALBA5B630255 Ribosomal protein S14
Regulatory gene
AALBA5B057320 Protein BASIC PENTACYSTEINE2-like
AALBA5B1014427 GATA transcription factor
AALBA5B1038335 B3 domain-containing transcription factor

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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.