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Crystal structure of S25-39 Fab unliganded 3

Analyse Crystal structure of S25-39 Fab unliganded 3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7T0I
Type
protein
Length
1,728 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S25-39 Fab heavy chain; S25-39 Fab light chain
Pockets
20 · best druggability 0.76

Structure

x-ray diffraction · 5 distinct chains · 7% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HS25-39 Fab heavy chainprotein2136% helix, 50% strand—
L, A, C, ES25-39 Fab light chainprotein2198% helix, 53% strand—
BS25-39 Fab heavy chainprotein2147% helix, 51% strand—
DS25-39 Fab heavy chainprotein2158% helix, 49% strand—
FS25-39 Fab heavy chainprotein2109% helix, 51% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18960.760.8085empty
25800.710.7962empty
33060.660.8136empty
45820.650.7666empty
5570.640.9418empty

Interfaces

13 interfaces between chains.

  • D–C · 1768 Ų buried · 21 hydrogen bonds · protein-protein
  • B–A · 1683 Ų buried · 14 hydrogen bonds · protein-protein
  • H–L · 1612 Ų buried · 13 hydrogen bonds · protein-protein
  • F–E · 1605 Ų buried · 14 hydrogen bonds · protein-protein
  • H–B · 545 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 7T0I · Crystal structure of S25-39 Fab Unliganded 3 · the same entry in another collection · chain A against A, TM-score 1.00

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