MolNFT v1 · #19384 · protein
Aspartate aminotransferase from escherichia COLI, C191F mutation, with bound maleate
1QIS: “Aspartate aminotransferase from escherichia COLI, C191F mutation, with bound maleate”. X-ray diffraction, 2 ligands (PLP, MAE), 4 pockets (best druggability 0.63). MolNFT v1 #19384 on GenesisL1: 3D structure, binding sites and…
- PDB
- 1QIS
- Type
- protein
- Length
- 396 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Aspartate aminotransferase
- EC
- 2.6.1.1
- UniProt
- P00509
- Ligands
- PLP, MAE
- Pockets
- 4 · best druggability 0.63
Structure
x-ray diffraction · 1 distinct chain · 47% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Aspartate aminotransferase (EC 2.6.1.1) | protein | 396 | 47% helix, 14% strand | P00509 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 192 | 0.63 | 0.83 | 30 | PLP, MAE |
| 2 | 94 | 0.41 | 0.77 | 22 | empty |
| 3 | 55 | 0.30 | 0.76 | 16 | empty |
| 4 | 51 | 0.25 | 0.73 | 15 | empty |
Modifications
Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).
Compared structures
- 1QIS · Aspartate aminotransferase from escherichia COLI, C191F mutation, with bound maleate · the same entry in another collection · chain A against A, TM-score 1.00
- P00509 · AlphaFold monomer V2.0 prediction for aspartate aminotransferase (P00509) · a predicted model of the same protein · chain A against A, TM-score 0.99
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 P00509
- Elsewhere: RCSB PDB 1QIS · PDBe 1QIS · UniProt P00509
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