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The crystal structure of a post-reactive cognate DNA-eco ri complex at 2.50 a in the presence of MN2+ ion

Analyse The crystal structure of a post-reactive cognate DNA-eco ri complex at 2.50 a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QPS
Type
protein + DNA
Length
274 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5'-D(*TP*CP*GP*CP*GP*)-3'; 5'-D(*AP*AP*TP*TP*CP*GP*CP*GP*)-3'; Endonuclease ecori
UniProt
P00642
Ligands
MN
Pockets
2 · best druggability 0.35

Structure

x-ray diffraction · 3 distinct chains · 34% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
M5'-D(*TP*CP*GP*CP*GP*)-3'dna5——
N5'-D(*AP*AP*TP*TP*CP*GP*CP*GP*)-3'dna8——
AEndonuclease ecoriprotein26134% helix, 20% strandP00642

Ligands and binding sites

  • MN · Manganese (II) ion · metal · chains N, A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1900.350.7418empty
2750.340.7618empty

Interfaces

3 interfaces between chains.

  • N–A · 574 Ų buried · 14 hydrogen bonds · protein-nucleic
  • M–A · 298 Ų buried · 8 hydrogen bonds · protein-nucleic
  • M–N · 110 Ų buried · 3 hydrogen bonds · nucleic-nucleic

Compared structures

  • 1QPS · The crystal structure of a post-reactive cognate DNA-eco ri complex at 2.50 a in the… · the same entry in another collection · chain M against M, TM-score 1.00
  • P00642 · AlphaFold monomer V2.0 prediction for type-2 restriction enzyme ecori (P00642) · a predicted model of the same protein · chain A against A, TM-score 0.99

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