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Crystal structure of the stationary phase survival protein sure from thermus thermophilus HB8

Analyse Crystal structure of the stationary phase survival protein sure from thermus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2E6E
Type
protein
Length
853 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5'-nucleotidase sure
EC
3.1.3.5
UniProt
Q53W92
Pockets
7 · best druggability 0.64

Structure

x-ray diffraction · 4 distinct chains · 28% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A5'-nucleotidase sure (EC 3.1.3.5)protein22127% helix, 35% strandQ53W92
B5'-nucleotidase sure (EC 3.1.3.5)protein21028% helix, 33% strandQ53W92
C5'-nucleotidase sure (EC 3.1.3.5)protein21728% helix, 34% strandQ53W92
D5'-nucleotidase sure (EC 3.1.3.5)protein20529% helix, 32% strandQ53W92

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15870.640.7567empty
25350.630.7553empty
35160.600.7450empty
41790.480.7624empty
5790.460.8225empty

Interfaces

6 interfaces between chains.

  • C–D · 2480 Ų buried · 33 hydrogen bonds · protein-protein
  • A–B · 2441 Ų buried · 40 hydrogen bonds · protein-protein
  • B–D · 755 Ų buried · 0 hydrogen bonds · protein-protein
  • A–D · 498 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 474 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 2E6E · Crystal structure of the stationary phase survival protein SurE from Thermus thermophilus… · the same entry in another collection · chain D against D, TM-score 1.00
  • Q53W92 · AlphaFold monomer V2.0 prediction for 5'-nucleotidase sure (Q53W92) · a predicted model of the same protein · chain C against A, TM-score 0.93

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