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MolNFT v1 · #25065 · protein

Mycobacterium smegmatis dps tetragonal form

1VEL · Starvation-induced DNA protecting protein: “Mycobacterium smegmatis dps tetragonal form”. X-ray diffraction, 3 ligands (CD, NA, SO4), 17 pockets (best druggability 0.65). MolNFT v1 #25065 on GenesisL1: 3D structure, binding sites…

PDB
1VEL
Type
protein
Length
983 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Starvation-induced DNA protecting protein
UniProt
Q8VP75
Ligands
CD, NA, SO4
Pockets
17 · best druggability 0.65

Structure

x-ray diffraction · 3 distinct chains · 70% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, D, FStarvation-induced DNA protecting proteinprotein16371% helix, 2% strandQ8VP75
CStarvation-induced DNA protecting proteinprotein16669% helix, 5% strandQ8VP75
EStarvation-induced DNA protecting proteinprotein16570% helix, 4% strandQ8VP75

Ligands and binding sites

  • CD · Cadmium ion · metal · 10 copies · chains A, B, C, E, D, F
  • NA · Sodium ion · metal · 2 copies · chains A, B, C, D, E, F
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15030.650.7746empty
24660.650.7847empty
3610.620.9215NA, SO4
4760.590.8916NA, SO4
5920.430.7917empty

Interfaces

9 interfaces between chains.

  • C–E · 1421 Ų buried · 27 hydrogen bonds · protein-protein
  • D–F · 791 Ų buried · 9 hydrogen bonds · protein-protein
  • A–C · 789 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 789 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 770 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 1VEL · Mycobacterium smegmatis Dps tetragonal form · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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