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Lac repressor engineered to bind sucralose, sucralose-bound tetramer

Analyse Lac repressor engineered to bind sucralose, sucralose-bound tetramer in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RZT
Type
protein
Length
1,192 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lac repressor
UniProt
C9QQT3
Ligands
RRY, RRJ
Pockets
15 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CLac repressorprotein30146% helix, 17% strandC9QQT3
B, DLac repressorprotein29546% helix, 18% strandC9QQT3

Ligands and binding sites

  • RRY · 1,6-dichloro-1,6-dideoxy-beta-D-fructofuranose · ligand · 4 copies · chains A, B, C, D
  • RRJ · 4-chloro-4-deoxy-alpha-D-galactopyranose · ligand · 4 copies · chains A, B, C, D

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

Pockets

15 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11210.810.9829empty
23130.790.8947RRY, RRJ
31190.780.9723empty
43070.780.8942RRY, RRJ
52980.780.8943RRY, RRJ

Interfaces

6 interfaces between chains.

  • A–B · 2244 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 2205 Ų buried · 13 hydrogen bonds · protein-protein
  • B–D · 787 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 455 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 93 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4RZT · Lac repressor engineered to bind sucralose, sucralose-bound tetramer · the same entry in another collection · chain A against A, TM-score 1.00

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