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The catalytic core of RAD2 (complex I)

Analyse The catalytic core of RAD2 (complex I) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Q0R
Type
protein + DNA
Length
574 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA repair protein RAD2; DNA (5'-D(*CP*TP*GP*AP*GP*TP*CP*AP*GP*AP*GP*CP*AP*AP*A)- 3')
EC
3.1.-.-
UniProt
P07276
Pockets
7 · best druggability 0.43

Structure

x-ray diffraction · 3 distinct chains · 50% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADNA repair protein RAD2 (EC 3.1.-.-)protein29351% helix, 11% strandP07276
BDNA repair protein RAD2 (EC 3.1.-.-)protein27750% helix, 11% strandP07276
DDNA (5'-D(*CP*TP*GP*AP*GP*TP*CP*AP*GP*AP*GP*CP*AP*AP*A)- 3')dna4——

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11070.430.7723empty
21500.430.7533empty
31110.420.7722empty
41190.380.7319empty
51080.340.7213empty

Interfaces

2 interfaces between chains.

  • A–B · 554 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 172 Ų buried · 6 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 24 modified (engineered).

Compared structures

  • 4Q0R · The catalytic core of Rad2 (complex I) · the same entry in another collection · chain A against A, TM-score 1.00
  • P07276 · AlphaFold monomer V2.0 prediction for DNA repair protein RAD2 (P07276) · a predicted model of the same protein · chain B against A, TM-score 0.97

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