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MolNFT v1 · #136949 · protein

Crystal structure of smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed with SF354

5V8T · Ubiquitin-like protein SMT3,PEPTIDYL-prolyl cis-trans…: “Crystal structure of smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed…”. X-ray diffraction, 2 ligands (8ZV, MG), 3 pockets (best…

PDB
5V8T
Type
protein
Length
382 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin-like protein SMT3,PEPTIDYL-prolyl cis-trans isomerase
EC
5.2.1.8
UniProt
Q12306, A0A069BB90
Ligands
8ZV, MG
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 13% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BUbiquitin-like protein SMT3,PEPTIDYL-prolyl cis-trans isomerase (EC 5.2.1.8)protein19113% helix, 38% strandQ12306, A0A069BB90

Ligands and binding sites

  • 8ZV · 2-{[3,5-bis(2-methoxyethoxy)benzene-1-carbonyl]amino}ethyl (2S)-1-(benzylsulfonyl) piperidine-2-carboxylate · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · chains A, B
  • FMT · Formic acid · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16860.710.77428ZV
22610.600.7924empty
31390.560.8231empty

Interfaces

1 interface between chains.

  • A–B · 317 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5V8T · Crystal structure of SMT fusion Peptidyl-prolyl cis-trans isomerase from Burkholderia… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q12306 · AlphaFold monomer V2.0 prediction for ubiquitin-like protein SMT3 (Q12306) · a predicted model of the same protein · chain A against A, TM-score 0.40

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