6B9X image
Deposition Date 2017-10-11
Release Date 2017-11-08
Last Version Date 2023-10-04
Entry Detail
PDB ID:
6B9X
Title:
Crystal structure of Ragulator
Biological Source:
Source Organism(s):
Homo sapiens (Taxon ID: 9606)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.42 Å
R-Value Free:
0.23
R-Value Work:
0.21
R-Value Observed:
0.21
Space Group:
P 61
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Ragulator complex protein LAM
Gene (Uniprot):LAMTOR1
Chain IDs:A
Chain Length:161
Number of Molecules:1
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Ragulator complex protein LAM
Gene (Uniprot):LAMTOR2
Chain IDs:B
Chain Length:126
Number of Molecules:1
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Ragulator complex protein LAM
Gene (Uniprot):LAMTOR3
Chain IDs:C
Chain Length:124
Number of Molecules:1
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Ragulator complex protein LAM
Gene (Uniprot):LAMTOR4
Chain IDs:D
Chain Length:99
Number of Molecules:1
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Hepatitis B virus x interacti
Chain IDs:E
Chain Length:173
Number of Molecules:1
Biological Source:Homo sapiens
Primary Citation
Hybrid Structure of the RagA/C-Ragulator mTORC1 Activation Complex.
Mol. Cell 68 835 846.e3 (2017)
PMID: 29107538 DOI: 10.1016/j.molcel.2017.10.016

Abstact

The lysosomal membrane is the locus for sensing cellular nutrient levels, which are transduced to mTORC1 via the Rag GTPases and the Ragulator complex. The crystal structure of the five-subunit human Ragulator at 1.4 Å resolution was determined. Lamtor1 wraps around the other four subunits to stabilize the assembly. The Lamtor2:Lamtor3 dimer stacks upon Lamtor4:Lamtor5 to create a platform for Rag binding. Hydrogen-deuterium exchange was used to map the Rag binding site to the outer face of the Lamtor2:Lamtor3 dimer and to the N-terminal intrinsically disordered region of Lamtor1. EM was used to reconstruct the assembly of the full-length RagAGTP:RagCGDP dimer bound to Ragulator at 16 Å resolution, revealing that the G-domains of the Rags project away from the Ragulator core. The combined structural model shows how Ragulator functions as a platform for the presentation of active Rags for mTORC1 recruitment, and might suggest an unconventional mechanism for Rag GEF activity.

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