Research workbench
Replication of N2,3-ethenoguanine by DNA polymerases
Analyse Replication of N2,3-ethenoguanine by DNA polymerases in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3V6K
- Type
- protein + DNA
- Length
- 722 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA polymerase IV; DNA (5'-D(P*GP*AP*AP*GP*GP*AP*TP*TP*CP*(2DT))-3'); DNA…
- EC
- 2.7.7.7
- UniProt
- Q97W02
- Ligands
- CA, MG, NA
- Pockets
- 10 · best druggability 0.82
Structure
x-ray diffraction · 5 distinct chains · 41% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA polymerase IV (EC 2.7.7.7) | protein | 342 | 42% helix, 23% strand | Q97W02 |
| J | DNA polymerase IV (EC 2.7.7.7) | protein | 333 | 39% helix, 21% strand | Q97W02 |
| P, K | DNA (5'-D(P*GP*AP*AP*GP*GP*AP*TP*TP*CP*(2DT))-3') | dna | 10 | — | — |
| B | DNA (5'-D(*TP*CP*AP*CP*(EFG)P*GP*AP*AP*TP*CP*CP*TP*TP*C)- 3') | dna | 14 | — | — |
| M | DNA (5'-D(*TP*CP*AP*CP*(EFG)P*GP*AP*AP*TP*CP*CP*TP*TP*C)- 3') | dna | 13 | — | — |
Ligands and binding sites
- CA · Calcium ion · metal · 7 copies · chains A, P, J, K
- MG · Magnesium ion · metal · 4 copies · chains A, P, J, K
- NA · Sodium ion · metal · 4 copies · chains P, 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, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 974 | 0.82 | 0.84 | 96 | MG, CA |
| 2 | 905 | 0.82 | 0.84 | 66 | MG |
| 3 | 451 | 0.72 | 0.82 | 45 | empty |
| 4 | 500 | 0.71 | 0.81 | 42 | empty |
| 5 | 338 | 0.67 | 0.81 | 50 | empty |
Interfaces
7 interfaces between chains.
- A–B · 1067 Ų buried · 17 hydrogen bonds · protein-nucleic
- J–M · 847 Ų buried · 15 hydrogen bonds · protein-nucleic
- J–K · 695 Ų buried · 16 hydrogen bonds · protein-nucleic
- A–P · 674 Ų buried · 14 hydrogen bonds · protein-nucleic
- A–J · 573 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 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 Q97W02
- Elsewhere: RCSB PDB 3V6K · PDBe 3V6K · UniProt Q97W02
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