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Structure paper

TitleBiomimetic Design Results in a Potent Allosteric Inhibitor of Dihydrodipicolinate Synthase from Campylobacter jejuni.
Journal, issue, pagesJ. Am. Chem. Soc., Vol. 138, Page 2014-2020, Year 2016
Publish dateNov 30, 2015 (structure data deposition date)
AuthorsSkovpen, Y.V. / Conly, C.J. / Sanders, D.A. / Palmer, D.R.
External linksJ. Am. Chem. Soc. / PubMed:26836694
MethodsX-ray diffraction
Resolution2.2 - 2.35 Å
Structure data

PDB-5f1u:
biomimetic design results in a potent allosteric inhibitor of dihydrodipicolinate synthase from Campylobacter jejuni
Method: X-RAY DIFFRACTION / Resolution: 2.35 Å

PDB-5f1v:
biomimetic design results in a potent allosteric inhibitor of dihydrodipicolinate synthase from Campylobacter jejuni
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-3VN:
(2R,5R)-2,5-diamino-2,5-bis(4-aminobutyl)hexanedioic acid

ChemComp-PG4:
TETRAETHYLENE GLYCOL / precipitant*YM

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-CL:
Unknown entry

ChemComp-PGE:
TRIETHYLENE GLYCOL

ChemComp-HOH:
WATER

ChemComp-GOL:
GLYCEROL

Source
  • campylobacter jejuni (Campylobacter)
KeywordsLYASE/LYASE inhibitor / schiff-base / aldolase / TIM barrel / LYASE-LYASE inhibitor complex

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