9SGX image
Deposition Date 2025-08-22
Release Date 2026-06-17
Last Version Date 2026-06-17
Entry Detail
PDB ID:
9SGX
Keywords:
Title:
tbPEX38(65-134) in complex with tbPEX19(1-50)
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Conformers Calculated:
200
Conformers Submitted:
20
Selection Criteria:
structures with the least restraint violations
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:STI1 domain-containing protei
Gene (Uniprot):Tb06.4F7.320, Tb927.6.4000
Chain IDs:B (auth: A)
Chain Length:70
Number of Molecules:1
Biological Source:Trypanosoma brucei brucei
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Peroxin 19
Chain IDs:A (auth: B)
Chain Length:54
Number of Molecules:1
Biological Source:Trypanosoma brucei brucei
Ligand Molecules
Primary Citation
Evolutionary remodeling of a remnant GET pathway factor into PEX38, an essential peroxin.
Proc.Natl.Acad.Sci.USA 123 e2533726123 e2533726123 (2026)
PMID: 41746722 DOI: 10.1073/pnas.2533726123

Abstact

PEX19 is a cytosolic receptor that directs membrane proteins posttranslationally to peroxisomes, as well as to mitochondria, lipid droplets, and the endoplasmic reticulum. A comprehensive Trypanosoma PEX19 interactome analysis uncovered PEX38 as an essential Euglenozoa-specific peroxin. PEX38 contains distinct domains that bind the cochaperone Hip and the PEX3-binding motif of PEX19, suggesting a role in stabilizing membrane proteins and preventing premature membrane docking. PEX38 illustrates functional repurposing in organelle biogenesis. It originated from a remnant of the GET/TRC pathway, typically responsible for the targeting of tail-anchored (TA) proteins to the endoplasmic reticulum. While most components of this machinery are absent in Euglenozoa, PEX38 has been retained and adapted to mediate peroxisomal membrane protein targeting. This evolutionary adaptation is unique to Euglenozoa. Because the PEX19-PEX38 interaction is essential for parasite viability and PEX38 has no human homologs, this complex is a promising therapeutic target against trypanosomatid parasites.

Legend

Protein

Chemical

Disease

Primary Citation of related structures
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