Research workbench
Post-catalytic nicked complex of human DNA polymerase mu with 1-nt gapped substrate containing template 8OG and newly incorporated AMP
Analyse Post-catalytic nicked complex of human DNA polymerase mu with 1-nt gapped… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6P1S
- Type
- protein + DNA
- Length
- 343 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA-directed DNA/RNA polymerase mu; DNA (5'-D(*CP*GP*GP*CP*(8OG)P*TP*AP*CP*G)-3')…
- EC
- 2.7.7.7
- UniProt
- Q9NP87
- Ligands
- ATP, NA, MN, CL
- Pockets
- 2 · best druggability 0.72
Structure
x-ray diffraction · 4 distinct chains · 52% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA-directed DNA/RNA polymerase mu (EC 2.7.7.7) | protein | 325 | 52% helix, 15% strand | Q9NP87 |
| T | DNA (5'-D(*CP*GP*GP*CP*(8OG)P*TP*AP*CP*G)-3') | dna | 9 | — | — |
| P | DNA/RNA (5'-D(*CP*GP*TP*A)-R(P*A)-3') | dna | 5 | — | — |
| D | DNA (5'-D(P*GP*CP*CP*G)-3') | dna | 4 | — | — |
Ligands and binding sites
- ATP · Adenosine-5'-triphosphate · ligand · chains A, P
- NA · Sodium ion · metal · 2 copies · chains A, P
- MN · Manganese (II) ion · metal · chains A, P
- CL · Chloride ion · ion · 2 copies · chains A, T, D
- EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · chains A
- EDO · 1,2-ethanediol · additive · chains A, T, P
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1094 | 0.72 | 0.76 | 54 | ATP, NA |
| 2 | 85 | 0.44 | 0.81 | 13 | empty |
Interfaces
5 interfaces between chains.
- A–T · 699 Ų buried · 19 hydrogen bonds · protein-nucleic
- A–P · 595 Ų buried · 21 hydrogen bonds · protein-nucleic
- A–D · 366 Ų buried · 16 hydrogen bonds · protein-nucleic
- T–P · 253 Ų buried · 16 hydrogen bonds · nucleic-nucleic
- T–D · 196 Ų buried · 15 hydrogen bonds · nucleic-nucleic
Modifications
Observed in the structure: 1 modified (nucleotide modification).
Compared structures
- 6P1S · Post-catalytic nicked complex of human DNA Polymerase Mu with 1-nt gapped substrate… · the same entry in another collection · chain A against A, TM-score 1.00
- Q9NP87 · AlphaFold monomer V2.0 prediction for DNA-directed DNA/RNA polymerase mu (Q9NP87) · a predicted model of the same protein · chain A against A, TM-score 0.99
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 Q9NP87
- Elsewhere: RCSB PDB 6P1S · PDBe 6P1S · UniProt Q9NP87
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