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The ligand-free structure of E COLI btuf, the periplasmic binding protein for vitamin B12

Analyse The ligand-free structure of E COLI btuf, the periplasmic binding protein for… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1N4D
Type
protein
Length
471 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Vitamin B12 transport protein btuf
UniProt
P37028
Pockets
4 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVitamin B12 transport protein btufprotein24442% helix, 11% strandP37028
BVitamin B12 transport protein btufprotein22740% helix, 12% strandP37028

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14130.650.7849empty
23630.590.7642empty
3780.330.7415empty
4650.320.7513empty

Modifications

Observed in the structure: 4 modified, 1 disulfide (engineered, disulfide).

Compared structures

  • 1N4D · The Ligand-Free Structure of E coli BtuF, the Periplasmic Binding Protein for Vitamin B12 · the same entry in another collection · chain A against A, TM-score 1.00
  • P37028 · AlphaFold monomer V2.0 prediction for vitamin B12-binding protein (P37028) · a predicted model of the same protein · chain B against A, TM-score 0.96

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