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Don inactivated escherichia COLI glutamine phosphoribosylpyrophosphate (prpp) amidotransferase

Analyse Don inactivated escherichia COLI glutamine phosphoribosylpyrophosphate (prpp)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ECG
Type
protein
Length
992 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutamine phosphoribosylpyrophosphate amidotransferase
EC
2.4.2.14
UniProt
P00496
Ligands
PIN, ONL
Pockets
14 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutamine phosphoribosylpyrophosphate amidotransferase (EC 2.4.2.14)protein49234% helix, 23% strandP00496
BGlutamine phosphoribosylpyrophosphate amidotransferase (EC 2.4.2.14)protein50035% helix, 24% strandP00496

Ligands and binding sites

  • PIN · Piperazine-N,N'-bis(2-ethanesulfonic acid) · ligand · 6 copies · chains A, B
  • ONL · 5-oxo-L-norleucine · ligand · 2 copies · chains A, B

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

Pockets

14 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19720.850.8693PIN
21320.690.9034ONL
31190.680.9039ONL
41210.600.8530empty
52480.590.7924empty

Interfaces

1 interface between chains.

  • A–B · 2861 Ų buried · 33 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 1ECG · Don inactivated escherichia COLI glutamine phosphoribosylpyrophosphate (prpp)… · the same entry in another collection · chain A against A, TM-score 1.00

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