Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

8OUK

Arf GTPase from the asgard Hodarchaea : HodArfR1 bound to GTP

Summary for 8OUK
Entry DOI10.2210/pdb8ouk/pdb
DescriptorArf GTPase, GUANOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordsarf gtpases, asgaard archaea, signaling protein
Biological sourceAsgard group
Total number of polymer chains1
Total formula weight20760.49
Authors
Menetrey, J.,Jackson, C.,Dacks, J.,Elias, M.,Vargova, R. (deposition date: 2023-04-23, release date: 2024-05-01, Last modification date: 2025-02-12)
Primary citationVargova, R.,Chevreau, R.,Alves, M.,Courbin, C.,Terry, K.,Legrand, P.,Elias, M.,Menetrey, J.,Dacks, J.B.,Jackson, C.L.
The Asgard archaeal origins of Arf family GTPases involved in eukaryotic organelle dynamics.
Nat Microbiol, 10:495-508, 2025
Cited by
PubMed Abstract: The evolution of eukaryotes is a fundamental event in the history of life. The closest prokaryotic lineage to eukaryotes, the Asgardarchaeota, encode proteins previously found only in eukaryotes, providing insight into their archaeal ancestor. Eukaryotic cells are characterized by endomembrane organelles, and the Arf family GTPases regulate organelle dynamics by recruiting effector proteins to membranes upon activation. The Arf family is ubiquitous among eukaryotes, but its origins remain elusive. Here we report a group of prokaryotic GTPases, the ArfRs, which are widely present in Asgardarchaeota. Phylogenetic analyses reveal that eukaryotic Arf family proteins arose from the ArfR group. Expression of representative Asgardarchaeota ArfR proteins in yeast and X-ray crystallographic studies show that ArfR GTPases possess the mechanism of membrane binding and structural features unique to Arf family proteins. Our results indicate that Arf family GTPases originated in the archaeal ancestor of eukaryotes, consistent with aspects of the endomembrane system evolving early in eukaryogenesis.
PubMed: 39849086
DOI: 10.1038/s41564-024-01904-6
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

237735

数据于2025-06-18公开中

PDB statisticsPDBj update infoContact PDBjnumon