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Yfib-yfir complexed with gmp

Analyse Yfib-yfir complexed with gmp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5Y61
Type
protein
Length
552 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Yfir; Yfib
UniProt
Q9I4L4, Q9I4L6
Ligands
5GP
Pockets
8 · best druggability 0.60

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CYfirprotein15335% helix, 24% strandQ9I4L4
B, DYfibprotein12343% helix, 17% strandQ9I4L6

Ligands and binding sites

  • 5GP · Guanosine-5'-monophosphate · ligand · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12170.600.8127empty
21860.570.8125empty
3500.450.8516empty
4860.360.7618empty
5770.320.7417empty

Interfaces

3 interfaces between chains.

  • C–D · 1681 Ų buried · 20 hydrogen bonds · protein-protein
  • A–B · 1676 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 752 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 5Y61 · YfiB-YfiR complexed with GMP · the same entry in another collection · chain A against A, TM-score 1.00

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