Research workbench
Crystal structure of human transthyretin variant A25T in complex with thyroxine (T4)
Analyse Crystal structure of human transthyretin variant A25T in complex with thyroxine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3OZK
- Type
- protein
- Length
- 231 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Transthyretin
- UniProt
- P02766
- Ligands
- T44
- Pockets
- 3 · best druggability 0.36
Structure
x-ray diffraction · 2 distinct chains · 6% helix, 51% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Transthyretin | protein | 116 | 6% helix, 51% strand | P02766 |
| B | Transthyretin | protein | 115 | 7% helix, 51% strand | P02766 |
Ligands and binding sites
- T44 · 3,5,3',5'-tetraiodo-L-thyronine · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 67 | 0.36 | 0.78 | 16 | empty |
| 2 | 85 | 0.33 | 0.74 | 19 | empty |
| 3 | 63 | 0.33 | 0.76 | 14 | empty |
Interfaces
1 interface between chains.
- A–B · 913 Ų buried · 20 hydrogen bonds · protein-protein
Compared structures
- 3OZK · Crystal structure of human transthyretin variant A25T in complex with thyroxine (T4) · 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 P02766
- Elsewhere: RCSB PDB 3OZK · PDBe 3OZK · UniProt P02766
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