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Crystal structure of CALG1, calicheamicin glycostyltransferase, tdp bound form

Analyse Crystal structure of CALG1, calicheamicin glycostyltransferase, tdp bound form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OTG
Type
protein
Length
391 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CALG1
UniProt
Q8KNF2
Ligands
TYD, CL
Pockets
1 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACALG1protein39149% helix, 14% strandQ8KNF2

Ligands and binding sites

  • TYD · Thymidine-5'-diphosphate · ligand · chains A
  • CL · Chloride ion · ion · 5 copies · chains A

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18670.820.8496TYD, CL

Modifications

Observed in the structure: 3 modified (engineered).

Compared structures

  • 3OTG · Crystal Structure of CalG1, Calicheamicin Glycostyltransferase, TDP bound form · the same entry in another collection · chain A against A, TM-score 1.00

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