Research workbench
Structure of PSB29 at 1.55A
Analyse Structure of PSB29 at 1.55A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5MLF
- Type
- protein
- Length
- 1,421 residues
- Chains
- 7
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein THF1
- UniProt
- Q8DJT8
- Ligands
- HG
- Pockets
- 16 · best druggability 0.82
Structure
x-ray diffraction · 1 distinct chain · 67% helix, 2% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, G, F | Protein THF1 | protein | 203 | 67% helix, 2% strand | Q8DJT8 |
Ligands and binding sites
- HG · Mercury (II) ion · metal · 7 copies · chains A, B, C, D, E, G, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
16 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 841 | 0.82 | 0.84 | 91 | empty |
| 2 | 788 | 0.81 | 0.84 | 98 | empty |
| 3 | 735 | 0.76 | 0.81 | 65 | empty |
| 4 | 225 | 0.70 | 0.86 | 40 | empty |
| 5 | 194 | 0.69 | 0.87 | 39 | empty |
Interfaces
13 interfaces between chains.
- A–B · 521 Ų buried · 7 hydrogen bonds · protein-protein
- C–F · 520 Ų buried · 6 hydrogen bonds · protein-protein
- A–D · 519 Ų buried · 6 hydrogen bonds · protein-protein
- C–D · 511 Ų buried · 7 hydrogen bonds · protein-protein
- A–E · 506 Ų buried · 6 hydrogen bonds · protein-protein
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 Q8DJT8
- Elsewhere: RCSB PDB 5MLF · PDBe 5MLF · UniProt Q8DJT8
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