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Designed enzyme RA61 M48K/I72D mutant: form V

Analyse Designed enzyme RA61 M48K/I72D mutant: form V in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7F1L
Type
protein
Length
194 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Engineered retroaldolase
Ligands
CL
Pockets
2 · best druggability 0.45

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 64% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEngineered retroaldolaseprotein1945% helix, 64% strand—

Ligands and binding sites

  • CL · Chloride ion · ion · chains A
  • IMD · Imidazole · additive · chains A

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1880.450.8018IMD
2530.330.7815empty

Compared structures

  • 7F1L · Designed enzyme RA61 M48K/I72D mutant: form V · the same entry in another collection · chain A against A, TM-score 1.00

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