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Klebsiella pneumoniae BLRP1 with FMN and cyclic digmp, no metal ions

Analyse Klebsiella pneumoniae BLRP1 with FMN and cyclic digmp, no metal ions in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3GFY
Type
protein
Length
746 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Klebsiella pneumoniae BLRP1
UniProt
A6T8V8
Ligands
C2E, FMN
Pockets
16 · best druggability 0.69

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKlebsiella pneumoniae BLRP1protein37239% helix, 24% strandA6T8V8
BKlebsiella pneumoniae BLRP1protein37442% helix, 24% strandA6T8V8

Ligands and binding sites

  • C2E · 9,9'-[(2r,3r,3as,5s,7ar,9r,10r,10as,12s,14ar)-3,5,10, 12-tetrahydroxy-5,12-dioxidooctahydro-2H,7H-difuro[3, 2-D:3',2'-J][1,3,7,9,2, 8]tetraoxadiphosphacyclododecine-2,9-diyl]bis(2-amino-1,9-dihydro-6H-purin-6-one) · ligand · 2 copies · chains A, B
  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B

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

Pockets

16 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1580.690.9719empty
2590.660.9518empty
31710.650.8520FMN
41530.640.8620FMN
52990.630.8033empty

Interfaces

1 interface between chains.

  • A–B · 2240 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 3GFY · Klebsiella pneumoniae BlrP1 with FMN and cyclic diGMP, no metal ions · the same entry in another collection · chain A against A, TM-score 1.00

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