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Crystal structure of human exonuclease 1 EXO1 (wt) in complex with 5' recessed-end DNA (riv)

Analyse Crystal structure of human exonuclease 1 EXO1 (wt) in complex with 5'… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5V06
Type
protein + DNA
Length
371 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Exonuclease 1; DNA (5'-D(*CP*GP*CP*TP*AP*GP*TP*CP*GP*AP*CP*AP*T)-3'); DNA…
EC
3.1.-.-
UniProt
Q9UQ84
Ligands
MN, NA
Pockets
4 · best druggability 0.75

Structure

x-ray diffraction · 3 distinct chains · 47% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ZExonuclease 1 (EC 3.1.-.-)protein34847% helix, 12% strandQ9UQ84
ADNA (5'-D(*CP*GP*CP*TP*AP*GP*TP*CP*GP*AP*CP*AP*T)-3')dna13——
BDNA (5'-D(P*TP*CP*GP*AP*CP*TP*AP*GP*CP*G)-3')dna10——

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 3 copies · chains Z, B
  • NA · Sodium ion · metal · chains Z, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19620.750.7958empty
21070.520.8321MN
31360.440.7718empty
4590.290.7415empty

Interfaces

3 interfaces between chains.

  • Z–A · 678 Ų buried · 14 hydrogen bonds · protein-nucleic
  • Z–B · 547 Ų buried · 16 hydrogen bonds · protein-nucleic
  • A–B · 474 Ų buried · 51 hydrogen bonds · nucleic-nucleic

Compared structures

  • 5V06 · Crystal structure of human exonuclease 1 Exo1 (WT) in complex with 5' recessed-end DNA… · the same entry in another collection · chain Z against Z, TM-score 1.00
  • Q9UQ84 · AlphaFold monomer V2.0 prediction for exonuclease 1 (Q9UQ84) · a predicted model of the same protein · chain Z against A, TM-score 0.99

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