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Crystal structure of ixodes scapularis glutaminyl cyclase with D238A mutation

Analyse Crystal structure of ixodes scapularis glutaminyl cyclase with D238A mutation in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7D1H
Type
protein
Length
326 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutaminyl-peptide cyclotransferase
EC
2.3.2.5
UniProt
B7QK46
Ligands
ZN
Pockets
2 · best druggability 0.48

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutaminyl-peptide cyclotransferase (EC 2.3.2.5)protein32638% helix, 19% strandB7QK46

Ligands and binding sites

  • ZN · Zinc ion · metal · chains A

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11530.480.7721empty
21140.440.7824empty

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 7D1H · Crystal structure of Ixodes scapularis glutaminyl cyclase with D238A mutation · the same entry in another collection · chain A against A, TM-score 1.00
  • B7QK46 · AlphaFold monomer V2.0 prediction for glutaminyl-peptide cyclotransferase (B7QK46) · a predicted model of the same protein · chain A against A, TM-score 1.00

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