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1.8 ångström resolution crystal structure of K135M mutant of transaldolase B (tala) from francisella tularensis in complex with fructose 6-phosphate

Analyse 1.8 ångström resolution crystal structure of K135M mutant of transaldolase B… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TE9
Type
protein
Length
623 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transaldolase
EC
2.2.1.2
UniProt
Q5NFX0
Ligands
F6R, PO4
Pockets
5 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 58% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATransaldolase (EC 2.2.1.2)protein31057% helix, 13% strandQ5NFX0
BTransaldolase (EC 2.2.1.2)protein31358% helix, 12% strandQ5NFX0

Ligands and binding sites

  • F6R · Fructose -6-phosphate · ligand · chains A
  • PO4 · Phosphate ion · ion · chains B
  • PGE · Triethylene glycol · additive · 6 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12540.870.9928empty
21840.540.7932PO4
31610.530.8034F6R
4650.280.7312empty
5520.250.7311PGE

Interfaces

1 interface between chains.

  • A–B · 852 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 3TE9 · 1.8 Angstrom Resolution Crystal Structure of K135M Mutant of Transaldolase B (TalA) from… · the same entry in another collection · chain A against A, TM-score 1.00

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