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MolNFT v1 · #167855 · protein

Cryo-EM structure of the full-length A39R/PLEXINC1 complex

6VXK · Semaphorin-like protein 139: “Cryo-EM structure of the full-length A39R/PLEXINC1 complex”. Electron microscopy, 1 ligand (NAG), 20 pockets (best druggability 0.82). MolNFT v1 #167855 on GenesisL1: 3D structure, binding sites and…

PDB
6VXK
Type
protein
Length
2,254 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Semaphorin-like protein 139; Plexin-C1
UniProt
Q8JL80, O60486
Ligands
NAG
Pockets
20 · best druggability 0.82

Structure

electron microscopy · 2 distinct chains · 4% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CSemaphorin-like protein 139protein3806% helix, 45% strandQ8JL80
B, DPlexin-C1protein7474% helix, 42% strandO60486

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 18 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19310.820.8374empty
29430.800.8272empty
36080.720.8046empty
45910.710.7940empty
54910.690.8041empty

Interfaces

3 interfaces between chains.

  • C–D · 973 Ų buried · 24 hydrogen bonds · protein-protein
  • A–B · 967 Ų buried · 24 hydrogen bonds · protein-protein
  • A–C · 903 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 34 disulfide, 18 glycan (disulfide, N-glycosylation).

Compared structures

  • 6VXK · Cryo-EM Structure of the full-length A39R/PlexinC1 complex · the same entry in another collection · chain A against A, TM-score 1.00
  • O60486 · AlphaFold monomer V2.0 prediction for plexin-C1 (O60486) · a predicted model of the same protein · chain B against A, TM-score 0.91

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