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Unliganded 2 crystal structure of S25-26 Fab

Analyse Unliganded 2 crystal structure of S25-26 Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4M93
Type
protein
Length
872 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S25-26 Fab (IGG1K) light chain; S25-26 Fab (IGG1K) heavy chain
Ligands
NAG, CA
Pockets
10 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, CS25-26 Fab (IGG1K) light chainprotein2186% helix, 54% strand—
H, BS25-26 Fab (IGG1K) heavy chainprotein2186% helix, 50% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains H, B
  • CA · Calcium ion · metal · chains B
  • ACT · Acetate ion · additive · 3 copies · chains C, B

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

Pockets

10 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17350.670.7585empty
22850.590.7848ACT
32320.550.7835empty
41550.520.7925empty
53040.510.7337empty

Interfaces

3 interfaces between chains.

  • L–H · 2046 Ų buried · 24 hydrogen bonds · protein-protein
  • C–B · 2042 Ų buried · 20 hydrogen bonds · protein-protein
  • H–C · 552 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 2 glycan, 2 modified (disulfide, N-glycosylation, cyclization).

Compared structures

  • 4M93 · Unliganded 2 crystal structure of S25-26 Fab · the same entry in another collection · chain L against L, TM-score 1.00

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