MolNFT v1 · #187926 · protein
GATOR1-rag-ragulator - gap complex
7T3B · RAS-related GTP-binding protein C: “GATOR1-rag-ragulator - gap complex”. Electron microscopy, 2 ligands (GDP, AF3), 20 pockets (best druggability 0.80). MolNFT v1 #187926 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7T3B
- Type
- protein
- Length
- 2,892 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- RAS-related GTP-binding protein C; Gator complex protein NPRL2; Gator complex protein…
- EC
- 3.6.5.-
- UniProt
- Q9HB90, Q8WTW4, O75140, Q9UHA4, Q9Y2Q5, O43504, Q0VGL1, Q6IAA8, Q12980, Q7L523
- Ligands
- GDP, AF3
- Pockets
- 20 · best druggability 0.80
Structure
electron microscopy · 10 distinct chains · 35% helix, 20% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| E | RAS-related GTP-binding protein C (EC 3.6.5.-) | protein | 305 | 39% helix, 14% strand | Q9HB90 |
| B | Gator complex protein NPRL2 | protein | 362 | 38% helix, 16% strand | Q8WTW4 |
| A | Gator complex protein DEPDC5 | protein | 989 | 26% helix, 23% strand | O75140 |
| H | Ragulator complex protein LAMTOR3 | protein | 120 | 37% helix, 29% strand | Q9UHA4 |
| G | Ragulator complex protein LAMTOR2 | protein | 124 | 41% helix, 27% strand | Q9Y2Q5 |
| J | Ragulator complex protein LAMTOR5 | protein | 91 | 26% helix, 35% strand | O43504 |
| I | Ragulator complex protein LAMTOR4 | protein | 89 | 20% helix, 30% strand | Q0VGL1 |
| F | Ragulator complex protein LAMTOR1 | protein | 111 | 50% helix, 0% strand | Q6IAA8 |
| C | Gator complex protein NPRL3 | protein | 405 | 45% helix, 18% strand | Q12980 |
| D | RAS-related GTP-binding protein a | protein | 296 | 40% helix, 22% strand | Q7L523 |
Ligands and binding sites
- GDP · Guanosine-5'-diphosphate · ligand · 2 copies · chains E, B, D
- AF3 · Aluminum fluoride · ligand · 2 copies · chains E, B, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 176 | 0.80 | 0.96 | 31 | empty |
| 2 | 799 | 0.78 | 0.82 | 88 | empty |
| 3 | 482 | 0.75 | 0.83 | 69 | GDP |
| 4 | 688 | 0.74 | 0.80 | 69 | empty |
| 5 | 921 | 0.74 | 0.78 | 99 | empty |
Interfaces
21 interfaces between chains.
- B–C · 2009 Ų buried · 18 hydrogen bonds · protein-protein
- B–A · 1903 Ų buried · 6 hydrogen bonds · protein-protein
- E–D · 1562 Ų buried · 20 hydrogen bonds · protein-protein
- H–G · 1397 Ų buried · 25 hydrogen bonds · protein-protein
- H–F · 1142 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 covalent (covalent ligand).
Compared structures
- 7T3B · GATOR1-RAG-RAGULATOR - GAP Complex · the same entry in another collection · chain D against D, TM-score 1.00
- O75140 · AlphaFold monomer V2.0 prediction for gator complex protein DEPDC5 (O75140) · a predicted model of the same protein · chain A against A, TM-score 0.98
- Q7L523 · AlphaFold monomer V2.0 prediction for RAS-related GTP-binding protein a (Q7L523) · a predicted model of the same protein · chain D against A, TM-score 0.97
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q9HB90
- Every structure of UniProt Q8WTW4
- Every structure of UniProt O75140
- Every structure of UniProt Q9UHA4
- Every structure of UniProt Q9Y2Q5
- Every structure of UniProt O43504
- Every structure of UniProt Q0VGL1
- Every structure of UniProt Q6IAA8
- Every structure of UniProt Q12980
- Every structure of UniProt Q7L523
- Elsewhere: RCSB PDB 7T3B · PDBe 7T3B · UniProt Q9HB90 · UniProt Q8WTW4 · UniProt O75140 · UniProt Q9UHA4 · UniProt Q9Y2Q5 · UniProt O43504 · UniProt Q0VGL1 · UniProt Q6IAA8 · UniProt Q12980 · UniProt Q7L523
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