Research workbench
Ternary complex of human DNA polymerase iota with DNA and dttp
Analyse Ternary complex of human DNA polymerase iota with DNA and dttp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2FLL
- Type
- protein + DNA
- Length
- 389 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA primer strand; DNA template strand; DNA polymerase iota
- EC
- 2.7.7.7
- UniProt
- Q9UNA4
- Ligands
- TTP, MG
- Pockets
- 7 · best druggability 0.74
Structure
x-ray diffraction · 3 distinct chains · 44% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| P | DNA primer strand | dna | 7 | — | — |
| T | DNA template strand | dna | 9 | — | — |
| A | DNA polymerase iota (EC 2.7.7.7) | protein | 373 | 44% helix, 19% strand | Q9UNA4 |
Ligands and binding sites
- TTP · Thymidine-5'-triphosphate · ligand · chains P, T, A
- MG · Magnesium ion · metal · 2 copies · chains A, P
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 634 | 0.74 | 0.81 | 52 | empty |
| 2 | 741 | 0.73 | 0.79 | 59 | empty |
| 3 | 373 | 0.70 | 0.82 | 38 | MG, TTP |
| 4 | 91 | 0.44 | 0.79 | 16 | empty |
| 5 | 75 | 0.41 | 0.79 | 13 | empty |
Interfaces
3 interfaces between chains.
- T–A · 743 Ų buried · 15 hydrogen bonds · protein-nucleic
- P–A · 488 Ų buried · 8 hydrogen bonds · protein-nucleic
- P–T · 327 Ų buried · 24 hydrogen bonds · nucleic-nucleic
Modifications
Observed in the structure: 1 modified (nucleotide modification).
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 Q9UNA4
- Elsewhere: RCSB PDB 2FLL · PDBe 2FLL · UniProt Q9UNA4
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