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Native structure of xometc at pH 5.2

Analyse Native structure of xometc at pH 5.2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IXS
Type
protein
Length
733 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cystathionine gamma-lyase-like protein
EC
4.4.1.1
UniProt
Q5H4T8
Ligands
CO3
Pockets
8 · best druggability 0.54

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACystathionine gamma-lyase-like protein (EC 4.4.1.1)protein36139% helix, 16% strandQ5H4T8
BCystathionine gamma-lyase-like protein (EC 4.4.1.1)protein37241% helix, 16% strandQ5H4T8

Ligands and binding sites

  • CO3 · Carbonate ion · ion · chains B
  • GOL · Glycerol · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12110.540.7826empty
2690.470.8314empty
3560.450.8313empty
41180.400.7523empty
5750.330.7622CO3

Interfaces

1 interface between chains.

  • A–B · 1500 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (cofactor).

Compared structures

  • 4IXS · Native structure of xometc at ph 5.2 · the same entry in another collection · chain A against A, TM-score 1.00

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