Research workbench
Mobm relaxase domain (mobv; MOB_PRE) bound to plasmid PMV158 orit DNA (22NT). mn-bound crystal structure at pH 4.6
Analyse Mobm relaxase domain (mobv; MOB_PRE) bound to plasmid PMV158 orit DNA (22NT).… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4LVI
- Type
- protein + DNA
- Length
- 212 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Plasmid recombination enzyme; Actttat oligonucleotide; Ataaagtatagtgtg oligonucleotide
- UniProt
- P13925
- Ligands
- MN
- Pockets
- 3 · best druggability 0.66
Structure
x-ray diffraction · 3 distinct chains · 44% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Plasmid recombination enzyme | protein | 190 | 44% helix, 18% strand | P13925 |
| B | Actttat oligonucleotide | dna | 7 | — | — |
| C | Ataaagtatagtgtg oligonucleotide | dna | 15 | — | — |
Ligands and binding sites
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 | 109 | 0.66 | 0.90 | 19 | empty |
| 2 | 188 | 0.44 | 0.74 | 26 | empty |
| 3 | 54 | 0.26 | 0.73 | 16 | empty |
Interfaces
3 interfaces between chains.
- A–C · 1740 Ų buried · 47 hydrogen bonds · protein-nucleic
- A–B · 330 Ų buried · 4 hydrogen bonds · protein-nucleic
- B–C · 301 Ų buried · 24 hydrogen bonds · nucleic-nucleic
Compared structures
- 4LVI · MobM Relaxase Domain (MOBV; Mob_Pre) bound to plasmid pMV158 oriT DNA (22nt). Mn-bound… · the same entry in another collection · chain A against A, TM-score 1.00
- P13925 · AlphaFold monomer V2.0 prediction for plasmid recombination enzyme (P13925) · a predicted model of the same protein · chain A against A, TM-score 1.00
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 P13925
- Elsewhere: RCSB PDB 4LVI · PDBe 4LVI · UniProt P13925
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