Research workbench
RV2258C-SAH
Analyse RV2258C-SAH in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5F8E
- Type
- protein
- Length
- 1,058 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Methyltransferase
- UniProt
- O53532
- Ligands
- SAH
- Pockets
- 10 · best druggability 0.83
Structure
x-ray diffraction · 3 distinct chains · 52% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Methyltransferase | protein | 353 | 54% helix, 15% strand | O53532 |
| B | Methyltransferase | protein | 350 | 51% helix, 17% strand | O53532 |
| C | Methyltransferase | protein | 355 | 51% helix, 16% strand | O53532 |
Ligands and binding sites
- SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B
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 | 1017 | 0.83 | 0.84 | 84 | empty |
| 2 | 784 | 0.83 | 0.86 | 97 | SAH |
| 3 | 1015 | 0.80 | 0.81 | 91 | SAH |
| 4 | 228 | 0.52 | 0.76 | 39 | empty |
| 5 | 131 | 0.45 | 0.77 | 24 | empty |
Interfaces
2 interfaces between chains.
- A–B · 3821 Ų buried · 52 hydrogen bonds · protein-protein
- B–C · 869 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 modified (oxidation).
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 O53532
- Elsewhere: RCSB PDB 5F8E · PDBe 5F8E · UniProt O53532
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