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Human ncam, FN3 domains 1 and 2, M610R mutant

Analyse Human ncam, FN3 domains 1 and 2, M610R mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VKX
Type
protein
Length
1,191 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Neural cell adhesion molecule
UniProt
P13591
Ligands
SO4
Pockets
20 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 3% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, D, FNeural cell adhesion moleculeprotein1983% helix, 49% strandP13591
BNeural cell adhesion moleculeprotein1974% helix, 49% strandP13591
ENeural cell adhesion moleculeprotein2023% helix, 48% strandP13591

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 11 copies · chains A, C, E, D, F

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

Pockets

20 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1970.770.9825empty
2950.760.9726empty
3930.760.9727empty
4750.740.9816empty
52960.580.7732empty

Interfaces

12 interfaces between chains.

  • A–B · 1835 Ų buried · 39 hydrogen bonds · protein-protein
  • E–F · 1784 Ų buried · 34 hydrogen bonds · protein-protein
  • C–D · 1736 Ų buried · 34 hydrogen bonds · protein-protein
  • B–E · 765 Ų buried · 11 hydrogen bonds · protein-protein
  • C–F · 727 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 2VKX · Human NCAM, FN3 domains 1 and 2, M610R mutant · the same entry in another collection · chain F against F, TM-score 1.00
  • P13591 · AlphaFold monomer V2.0 prediction for neural cell adhesion molecule 1 (P13591) · a predicted model of the same protein · chain B against A, TM-score 0.66

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