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Structure of full-length CD20 in complex with obinutuzumab Fab

Analyse Structure of full-length CD20 in complex with obinutuzumab Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6Y9A
Type
protein
Length
775 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
B-lymphocyte antigen CD20; Obinutuzumab Fab heavy chain; Obinutuzumab Fab light chain
UniProt
P11836
Pockets
19 · best druggability 0.77

Structure

electron microscopy · 3 distinct chains · 23% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BB-lymphocyte antigen CD20protein16970% helix, 0% strandP11836
HObinutuzumab Fab heavy chainprotein2186% helix, 43% strand—
LObinutuzumab Fab light chainprotein2195% helix, 45% strand—

Pockets

19 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19540.770.7976empty
21690.740.9140empty
31790.730.8936empty
41290.720.9137empty
53020.720.8542empty

Interfaces

5 interfaces between chains.

  • H–L · 1821 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 1366 Ų buried · 4 hydrogen bonds · protein-protein
  • A–H · 331 Ų buried · 4 hydrogen bonds · protein-protein
  • B–H · 272 Ų buried · 3 hydrogen bonds · protein-protein
  • A–L · 238 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 6Y9A · Structure of full-length CD20 in complex with Obinutuzumab Fab · the same entry in another collection · chain A against A, TM-score 1.00
  • P11836 · AlphaFold monomer V2.0 prediction for B-lymphocyte antigen CD20 (P11836) · a predicted model of the same protein · chain A against A, TM-score 0.92

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