Research workbench
Zn substituted E. COLI aminopeptidase P
Analyse Zn substituted E. COLI aminopeptidase P in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2BHB
- Type
- protein
- Length
- 440 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Xaa-pro aminopeptidase
- EC
- 3.4.11.9
- UniProt
- P15034
- Ligands
- ZN, MG
- Pockets
- 3 · best druggability 0.51
Structure
x-ray diffraction · 1 distinct chain · 40% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Xaa-pro aminopeptidase (EC 3.4.11.9) | protein | 440 | 40% helix, 19% strand | P15034 |
Ligands and binding sites
- ZN · Zinc ion · metal · 4 copies · chains A
- MG · Magnesium ion · metal · chains A
- FLC · Citrate anion · additive · chains A
- MRD · (4R)-2-methylpentane-2,4-diol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 222 | 0.51 | 0.76 | 35 | empty |
| 2 | 99 | 0.44 | 0.79 | 21 | MRD |
| 3 | 66 | 0.30 | 0.74 | 16 | empty |
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 P15034
- Elsewhere: RCSB PDB 2BHB · PDBe 2BHB · UniProt P15034
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