MolNFT v1 · #94630 · protein + DNA
Binary complex of mouse tdt with ssdna
4I2F · DNA nucleotidylexotransferase: “Binary complex of mouse tdt with ssdna”. X-ray diffraction, 3 ligands (MG, NA, ZN), 3 pockets (best druggability 0.72). MolNFT v1 #94630 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 4I2F
- Type
- protein + DNA
- Length
- 362 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA nucleotidylexotransferase; 5'-D(P*AP*AP*AP*AP*A)-3'
- EC
- 2.7.7.31
- UniProt
- P09838
- Ligands
- MG, NA, ZN
- Pockets
- 3 · best druggability 0.72
Structure
x-ray diffraction · 2 distinct chains · 49% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA nucleotidylexotransferase (EC 2.7.7.31) | protein | 358 | 49% helix, 15% strand | P09838 |
| C | 5'-D(P*AP*AP*AP*AP*A)-3' | dna | 4 | — | — |
Ligands and binding sites
- MG · Magnesium ion · metal · chains A, C
- NA · Sodium ion · metal · chains A, C
- ZN · Zinc ion · metal · chains A, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1020 | 0.72 | 0.76 | 76 | MG |
| 2 | 69 | 0.37 | 0.77 | 12 | empty |
| 3 | 56 | 0.34 | 0.78 | 14 | empty |
Interfaces
1 interface between chains.
- A–C · 593 Ų buried · 18 hydrogen bonds · protein-nucleic
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 P09838
- Elsewhere: RCSB PDB 4I2F · PDBe 4I2F · UniProt P09838
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.