Research workbench
Crystal structure of banana lectin H84T mutant
Analyse Crystal structure of banana lectin H84T mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4PIU
- Type
- protein
- Length
- 283 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ripening-associated protein
- UniProt
- O22321
- Ligands
- NA
- Pockets
- 1 · best druggability 0.39
Structure
x-ray diffraction · 2 distinct chains · 0% helix, 70% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Ripening-associated protein | protein | 141 | 0% helix, 71% strand | O22321 |
| B | Ripening-associated protein | protein | 142 | 0% helix, 69% strand | O22321 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 68 | 0.39 | 0.79 | 16 | GOL |
Interfaces
1 interface between chains.
- A–B · 785 Ų buried · 16 hydrogen bonds · protein-protein
Compared structures
- 4PIU · Crystal structure of banana lectin H84T mutant · the same entry in another collection · chain A against A, TM-score 1.00
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 O22321
- Elsewhere: RCSB PDB 4PIU · PDBe 4PIU · UniProt O22321
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