MolNFT v1 · #24041 · protein
Crystal structure of soybean beta-conglycinin alpha prime homotrimer
1UIK · Alpha prime subunit of beta-conglycinin: “Crystal structure of soybean beta-conglycinin alpha prime homotrimer”. X-ray diffraction, 1 ligand (MG), 10 pockets (best druggability 0.72). MolNFT v1 #24041 on GenesisL1: 3D structure…
- PDB
- 1UIK
- Type
- protein
- Length
- 1,091 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Alpha prime subunit of beta-conglycinin
- UniProt
- Q7XXT2
- Ligands
- MG
- Pockets
- 10 · best druggability 0.72
Structure
x-ray diffraction · 2 distinct chains · 18% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Alpha prime subunit of beta-conglycinin | protein | 364 | 19% helix, 42% strand | Q7XXT2 |
| B | Alpha prime subunit of beta-conglycinin | protein | 363 | 17% helix, 42% strand | Q7XXT2 |
Ligands and binding sites
- MG · Magnesium ion · metal · 3 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 51 | 0.72 | 0.99 | 15 | empty |
| 2 | 920 | 0.70 | 0.75 | 86 | empty |
| 3 | 51 | 0.69 | 0.97 | 16 | empty |
| 4 | 524 | 0.63 | 0.76 | 67 | empty |
| 5 | 109 | 0.44 | 0.77 | 21 | empty |
Interfaces
3 interfaces between chains.
- A–C · 2542 Ų buried · 25 hydrogen bonds · protein-protein
- B–C · 2541 Ų buried · 29 hydrogen bonds · protein-protein
- A–B · 2526 Ų buried · 29 hydrogen bonds · protein-protein
Compared structures
- 1UIK · Crystal structure of soybean beta-conglycinin alpha prime homotrimer · 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 Q7XXT2
- Elsewhere: RCSB PDB 1UIK · PDBe 1UIK · UniProt Q7XXT2
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