MolNFT v1 · #13107 · protein
Structure of human glutamate dehydrogenase-apo form
1L1F · Glutamate dehydrogenase 1: “Structure of human glutamate dehydrogenase-apo form”. X-ray diffraction, 20 pockets (best druggability 0.90). MolNFT v1 #13107 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1L1F
- Type
- protein
- Length
- 2,976 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Glutamate dehydrogenase 1
- EC
- 1.4.1.3
- UniProt
- P00367
- Pockets
- 20 · best druggability 0.90
Structure
x-ray diffraction · 1 distinct chain · 49% helix, 13% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F | Glutamate dehydrogenase 1 (EC 1.4.1.3) | protein | 496 | 49% helix, 13% strand | P00367 |
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 | 1093 | 0.90 | 0.92 | 127 | empty |
| 2 | 1100 | 0.90 | 0.92 | 129 | empty |
| 3 | 1103 | 0.90 | 0.92 | 146 | empty |
| 4 | 983 | 0.89 | 0.90 | 63 | empty |
| 5 | 1082 | 0.89 | 0.90 | 91 | empty |
Interfaces
15 interfaces between chains.
- D–E · 1711 Ų buried · 32 hydrogen bonds · protein-protein
- A–B · 1682 Ų buried · 29 hydrogen bonds · protein-protein
- B–F · 1682 Ų buried · 32 hydrogen bonds · protein-protein
- C–E · 1680 Ų buried · 31 hydrogen bonds · protein-protein
- A–F · 1676 Ų buried · 31 hydrogen bonds · protein-protein
Compared structures
- 1L1F · Structure of human glutamate dehydrogenase-apo form · the same entry in another collection · chain F against F, TM-score 1.00
- P00367 · AlphaFold monomer V2.0 prediction for glutamate dehydrogenase 1, mitochondrial (P00367) · a predicted model of the same protein · chain B against A, TM-score 0.91
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 P00367
- Elsewhere: RCSB PDB 1L1F · PDBe 1L1F · UniProt P00367
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