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Structure of a human glycosylphosphatidylinositol (gpi) transamidase

Analyse Structure of a human glycosylphosphatidylinositol (gpi) transamidase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7W72
Type
protein
Length
2,398 residues
Chains
5
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphatidylinositol glycan anchor biosynthesis class U protein; Gpi transamidase…
EC
3.-.-.-
UniProt
Q9H490, Q96S52, Q969N2, Q92643, O43292
Ligands
8JY, NAG, BMA, CA
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 5 distinct chains · 42% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
UPhosphatidylinositol glycan anchor biosynthesis class U proteinprotein42071% helix, 0% strandQ9H490
SGpi transamidase component pig-Sprotein53340% helix, 17% strandQ96S52
TGpi transamidase component pig-Tprotein52717% helix, 34% strandQ969N2
KGpi-anchor transamidase (EC 3.-.-.-)protein33026% helix, 15% strandQ92643
AGlycosylphosphatidylinositol anchor attachment 1 proteinprotein58855% helix, 11% strandO43292

Ligands and binding sites

  • 8JY · [2-[[(2~{R})-2-hexanoyloxy-3-[(~{E})-hex-3-enoxy]propoxy]-oxidanyl-phosphoryl]oxy-3,4,5,6-tetrakis(oxidanyl)phenyl] (2~{E},4~{E})-hepta-2,4-dienoate · ligand · chains U, T
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, S, T
  • BMA · beta-D-mannopyranose · sugar
  • CA · Calcium ion · metal · chains K

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110880.870.88127empty
28610.860.87123empty
32080.830.9631empty
43300.790.8932empty
51310.780.9630empty

Interfaces

9 interfaces between chains.

  • S–K · 2632 Ų buried · 26 hydrogen bonds · protein-protein
  • U–T · 2470 Ų buried · 22 hydrogen bonds · protein-protein
  • T–K · 2330 Ų buried · 35 hydrogen bonds · protein-protein
  • T–A · 1527 Ų buried · 15 hydrogen bonds · protein-protein
  • S–T · 1485 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 3 glycan, 1 covalent (disulfide, N-glycosylation, covalent ligand).

Compared structures

  • 7W72 · Structure of a human glycosylphosphatidylinositol (GPI) transamidase · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9H490 · AlphaFold monomer V2.0 prediction for phosphatidylinositol glycan anchor biosynthesis… · a predicted model of the same protein · chain U against A, TM-score 0.99
  • O43292 · AlphaFold monomer V2.0 prediction for glycosylphosphatidylinositol anchor attachment 1… · a predicted model of the same protein · chain A against A, TM-score 0.98
  • Q969N2 · AlphaFold monomer V2.0 prediction for gpi transamidase component pig-T (Q969N2) · a predicted model of the same protein · chain T against A, TM-score 0.92
  • Q96S52 · AlphaFold monomer V2.0 prediction for gpi transamidase component pig-S (Q96S52) · a predicted model of the same protein · chain S against A, TM-score 0.90
  • Q92643 · AlphaFold monomer V2.0 prediction for gpi-anchor transamidase (Q92643) · a predicted model of the same protein · chain K against A, TM-score 0.81

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