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MTH0212 in complex with ssdna in space group P32

Analyse MTH0212 in complex with ssdna in space group P32 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3G3Y
Type
protein + DNA
Length
517 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Exodeoxyribonuclease; 5'-D(*CP*GP*TP*AP*(UPS)P*TP*AP*CP*G)-3'
EC
3.1.11.2
UniProt
O26314
Ligands
MG
Pockets
3 · best druggability 0.69

Structure

x-ray diffraction · 3 distinct chains · 31% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AExodeoxyribonuclease (EC 3.1.11.2)protein25731% helix, 27% strandO26314
BExodeoxyribonuclease (EC 3.1.11.2)protein25631% helix, 27% strandO26314
I5'-D(*CP*GP*TP*AP*(UPS)P*TP*AP*CP*G)-3'dna4——

Ligands and binding sites

  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17580.690.7664empty
22020.540.7931MG
31310.410.7526MG

Interfaces

2 interfaces between chains.

  • B–I · 455 Ų buried · 12 hydrogen bonds · protein-nucleic
  • A–B · 255 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (nucleotide modification).

Compared structures

  • 3G3Y · Mth0212 in complex with ssDNA in space group P32 · the same entry in another collection · chain A against A, TM-score 1.00
  • O26314 · AlphaFold monomer V2.0 prediction for DNA uridine endonuclease (O26314) · a predicted model of the same protein · chain B against A, TM-score 0.99

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