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MolNFT v1 · #139761 · protein

Crystal structure of DREP4 cide domain

5XPC · Dnaation factor-related protein 4: “Crystal structure of DREP4 cide domain”. X-ray diffraction, 3 pockets (best druggability 0.37). MolNFT v1 #139761 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5XPC
Type
protein
Length
433 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dnaation factor-related protein 4
UniProt
Q9V3H0
Pockets
3 · best druggability 0.37

Structure

x-ray diffraction · 5 distinct chains · 28% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADnaation factor-related protein 4protein8527% helix, 27% strandQ9V3H0
BDnaation factor-related protein 4protein8830% helix, 26% strandQ9V3H0
CDnaation factor-related protein 4protein8628% helix, 27% strandQ9V3H0
DDnaation factor-related protein 4protein8729% helix, 26% strandQ9V3H0
EDnaation factor-related protein 4protein8728% helix, 25% strandQ9V3H0

Ligands and binding sites

  • GOL · Glycerol · additive · 12 copies · chains A, B, C, D, E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1710.370.7818GOL
2660.360.7715empty
3950.330.7215empty

Interfaces

4 interfaces between chains.

  • A–B · 623 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 551 Ų buried · 11 hydrogen bonds · protein-protein
  • D–E · 551 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 539 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (additive adduct).

Compared structures

  • 5XPC · Crystal Structure of Drep4 CIDE domain · the same entry in another collection · chain A against A, TM-score 1.00

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