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Crystal structure of trastuzumab Fab fragment bearing P-azido-L- phenylalanine

Analyse Crystal structure of trastuzumab Fab fragment bearing P-azido-L- phenylalanine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XHF
Type
protein
Length
861 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polypeptide (L chain); Polypeptide (H chain)
Pockets
10 · best druggability 0.65

Structure

x-ray diffraction · 4 distinct chains · 5% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APolypeptide (L chain)protein2135% helix, 48% strand—
BPolypeptide (H chain)protein2146% helix, 51% strand—
CPolypeptide (L chain)protein2146% helix, 49% strand—
DPolypeptide (H chain)protein2204% helix, 51% strand—

Pockets

10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16660.650.7568empty
23520.550.7537empty
32960.510.7443empty
41610.500.7831empty
51220.400.7524empty

Interfaces

3 interfaces between chains.

  • C–D · 1984 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 1817 Ų buried · 14 hydrogen bonds · protein-protein
  • B–D · 719 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 2 modified (disulfide, nonstandard).

Compared structures

  • 5XHF · Crystal structure of Trastuzumab Fab fragment bearing p-azido-L-phenylalanine · the same entry in another collection · chain A against A, TM-score 1.00

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