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Crystal structure analysis of the glycotransferase of kitacinnamycin

Analyse Crystal structure analysis of the glycotransferase of kitacinnamycin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6J31
Type
protein
Length
1,582 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
KCN28; Dbb-dsg-val-mea-val-gly-gly-dva-dle
Ligands
BG9
Pockets
16 · best druggability 0.82

Structure

x-ray diffraction · 4 distinct chains · 45% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKCN28protein38545% helix, 15% strand—
BKCN28protein38745% helix, 15% strand—
C, DKCN28protein38745% helix, 15% strand—
E, F, G, HDbb-dsg-val-mea-val-gly-gly-dva-dleprotein90% helix, 0% strand—

Ligands and binding sites

  • BG9 · (2E,2'E)-3,3'-(1,2-phenylene)di(prop-2-enoic acid) · ligand · 4 copies · chains A, E, B, F, C, G, D, H

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

Pockets

16 pockets found on a 1 Å grid, 13 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110560.820.83105BG9
210430.820.8395BG9
311450.810.8298BG9
411440.770.7995BG9
52430.610.8152empty

Interfaces

8 interfaces between chains.

  • A–C · 1204 Ų buried · 18 hydrogen bonds · protein-protein
  • D–H · 746 Ų buried · 10 hydrogen bonds · protein-protein
  • C–G · 729 Ų buried · 4 hydrogen bonds · protein-protein
  • A–E · 720 Ų buried · 10 hydrogen bonds · protein-protein
  • B–F · 719 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 d-amino, 8 modified, 4 covalent (D-amino acid, nonstandard, covalent ligand).

Compared structures

  • 6J31 · Crystal Structure Analysis of the Glycotransferase of kitacinnamycin · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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