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Crystal structure of the mutb F164L mutant from crystals soaked with isomaltulose

Analyse Crystal structure of the mutb F164L mutant from crystals soaked with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4GIA
Type
protein
Length
1,110 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sucrose isomerase
EC
5.4.11.99
UniProt
Q2PS28
Ligands
CA
Pockets
11 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASucrose isomerase (EC 5.4.11.99)protein55434% helix, 19% strandQ2PS28
BSucrose isomerase (EC 5.4.11.99)protein55634% helix, 18% strandQ2PS28

Ligands and binding sites

  • CA · Calcium ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 12 copies · chains A, B
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11150.790.9724GOL
21200.780.9722TRS, GOL
3620.740.9919empty
4560.730.9916empty
53080.600.7835GOL

Interfaces

1 interface between chains.

  • A–B · 229 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4GIA · Crystal structure of the MUTB F164L mutant from crystals soaked with isomaltulose · the same entry in another collection · chain A against A, TM-score 1.00

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