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MolNFT v1 · #125919 · protein

Structure of full length unliganded cody from bacillus subtilis

5LNH · GTP-sensing transcriptional pleiotropic repressor cody: “Structure of full length unliganded cody from bacillus subtilis”. X-ray diffraction, 1 ligand (SO4), 20 pockets (best druggability 0.86). MolNFT v1 #125919 on GenesisL1: 3D…

PDB
5LNH
Type
protein
Length
2,550 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GTP-sensing transcriptional pleiotropic repressor cody
UniProt
P39779
Ligands
SO4
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 53% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, KGTP-sensing transcriptional pleiotropic repressor codyprotein25553% helix, 19% strandP39779

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 12 copies · chains A, H, B, G, C, F, D, E, I, K

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

Pockets

20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16600.860.9060empty
26060.850.9070empty
37700.840.8876empty
47620.840.8869empty
5940.590.8720empty

Interfaces

16 interfaces between chains.

  • I–K · 1439 Ų buried · 13 hydrogen bonds · protein-protein
  • D–F · 1420 Ų buried · 7 hydrogen bonds · protein-protein
  • B–H · 1385 Ų buried · 10 hydrogen bonds · protein-protein
  • C–E · 1379 Ų buried · 10 hydrogen bonds · protein-protein
  • A–G · 1350 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 70 modified (engineered).

Compared structures

  • 5LNH · Structure of full length Unliganded CodY from Bacillus subtilis · the same entry in another collection · chain K against K, TM-score 1.00
  • P39779 · AlphaFold monomer V2.0 prediction for GTP-sensing transcriptional pleiotropic repressor… · a predicted model of the same protein · chain B against A, TM-score 0.89

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