MolNFT v1 · #139196 · protein
Crystal structure of tmp bound thymidylate kinase from thermus thermophilus HB8
5X86: “Crystal structure of tmp bound thymidylate kinase from thermus thermophilus HB8”. X-ray diffraction, 3 ligands (TMP, MG, CL), 4 pockets (best druggability 0.54). MolNFT v1 #139196 on GenesisL1: 3D structure, binding sites and…
- PDB
- 5X86
- Type
- protein
- Length
- 375 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Thymidylate kinase
- EC
- 2.7.4.9
- UniProt
- Q5SHX3
- Ligands
- TMP, MG, CL
- Pockets
- 4 · best druggability 0.54
Structure
x-ray diffraction · 2 distinct chains · 53% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | Thymidylate kinase (EC 2.7.4.9) | protein | 187 | 55% helix, 15% strand | Q5SHX3 |
| A | Thymidylate kinase (EC 2.7.4.9) | protein | 188 | 52% helix, 15% strand | Q5SHX3 |
Ligands and binding sites
- TMP · Thymidine-5'-phosphate · ligand · 2 copies · chains B, A
- MG · Magnesium ion · metal · 8 copies · chains B, A
- CL · Chloride ion · ion · 2 copies · chains B, A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 266 | 0.54 | 0.76 | 29 | MG, TMP |
| 2 | 131 | 0.50 | 0.80 | 19 | TMP |
| 3 | 56 | 0.40 | 0.81 | 15 | empty |
| 4 | 59 | 0.37 | 0.79 | 14 | empty |
Interfaces
1 interface between chains.
- B–A · 1060 Ų buried · 13 hydrogen bonds · protein-protein
Compared structures
- 5X86 · Crystal structure of TMP bound thymidylate kinase from thermus thermophilus HB8 · the same entry in another collection · chain B against B, TM-score 1.00
- Q5SHX3 · AlphaFold monomer V2.0 prediction for thymidylate kinase (Q5SHX3) · a predicted model of the same protein · chain B against A, TM-score 0.98
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 Q5SHX3
- Elsewhere: RCSB PDB 5X86 · PDBe 5X86 · UniProt Q5SHX3
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