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Structure of cntnw N149L in the intermediate 1 state

Analyse Structure of cntnw N149L in the intermediate 1 state in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5L27
Type
protein
Length
1,212 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nucleoside permease
UniProt
G4CRQ5
Ligands
6ZL
Pockets
20 · best druggability 0.88

Structure

x-ray diffraction · 3 distinct chains · 73% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANucleoside permeaseprotein41573% helix, 0% strandG4CRQ5
BNucleoside permeaseprotein41174% helix, 0% strandG4CRQ5
CNucleoside permeaseprotein38671% helix, 0% strandG4CRQ5

Ligands and binding sites

  • 6ZL · 2-{[(4-O-alpha-D-glucopyranosyl-beta-D-glucopyranosyl) oxy]methyl}-2-octyldecyl 4-O-alpha-D-glucopyranosyl-beta-D-glucopyranoside · ligand · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17310.880.9143empty
25860.810.8651empty
31010.760.9624empty
45120.750.8348empty
56220.740.8081empty

Interfaces

3 interfaces between chains.

  • A–B · 1280 Ų buried · 3 hydrogen bonds · protein-protein
  • B–C · 1240 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 1234 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5L27 · Structure of CNTnw N149L in the intermediate 1 state · the same entry in another collection · chain A against A, TM-score 1.00

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