Basic Information
Gene ID
Position
GWHASIS00000025:16390046-16396010 (+)
5964bp
Gene Type
gene
Gene Description (Protein Product)
Peroxisome biogenesis protein
Organism
Also AS AT1G48635

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
EVM0032003 Peroxisomal membrane protein
EVM0034925 Belongs to the mitochondrial carrier (TC 2.A.29) family
EVM0031979 Peroxisomal adenine nucleotide carrier
Regulatory gene
EVM0017728 Protein BASIC PENTACYSTEINE7-like
EVM0023251 Protein BASIC PENTACYSTEINE4-like
EVM0028830 Protein BASIC PENTACYSTEINE2-like

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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.