Research workbench
Crystal structure of human aminopeptidase a
Analyse Crystal structure of human aminopeptidase a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4KX7
- Type
- protein
- Length
- 875 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Glutamyl aminopeptidase
- EC
- 3.4.11.7
- UniProt
- Q07075
- Ligands
- NAG, ZN
- Pockets
- 8 · best druggability 0.73
Structure
x-ray diffraction · 1 distinct chain · 46% helix, 21% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Glutamyl aminopeptidase (EC 3.4.11.7) | protein | 875 | 46% helix, 21% strand | Q07075 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 15 copies · chains A
- ZN · Zinc ion · metal · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
8 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 249 | 0.73 | 0.88 | 54 | empty |
| 2 | 234 | 0.66 | 0.84 | 37 | empty |
| 3 | 69 | 0.64 | 0.93 | 19 | empty |
| 4 | 171 | 0.61 | 0.84 | 22 | empty |
| 5 | 152 | 0.61 | 0.84 | 32 | empty |
Modifications
Observed in the structure: 8 glycan, 1 disulfide (N-glycosylation, disulfide).
Compared structures
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 Q07075
- Elsewhere: RCSB PDB 4KX7 · PDBe 4KX7 · UniProt Q07075
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.