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TitleDesign, Synthesis, and Mechanism of Fluorine-substituted Cyclohexene Analogues of GAMA-Aminobutyric Acid (GABA) as Selective Ornithine Aminotransferase Inactivators
Journal, issue, pagesTo Be Published
Publish dateDec 10, 2019 (structure data deposition date)
AuthorsZhu, W. / Doubleday, P.T. / Catlin, D.S. / Weerawarna, P. / Butrin, A. / Shen, S. / Kelleher, N.L. / Liu, D. / Silverman, R.B.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution1.9 - 2.25 Å
Structure data

PDB-6v8c:
Design, Synthesis, and Mechanism of Fluorine-substituted Cyclohexene Analogues of GAMA-Aminobutyric Acid (GABA) as Selective Ornithine Aminotransferase Inactivators
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-6v8d:
Design, Synthesis, and Mechanism of Fluorine-substituted Cyclohexene Analogues of GAMA-Aminobutyric Acid (GABA) as Selective Ornithine Aminotransferase Inactivators
Method: X-RAY DIFFRACTION / Resolution: 2.25 Å

Chemicals

ChemComp-PLP:
PYRIDOXAL-5'-PHOSPHATE

ChemComp-QRM:
3-aminocyclohexa-1,3-diene-1-carboxylic acid

ChemComp-HOH:
WATER

ChemComp-O78:
(3Z)-3-iminocyclohex-1-ene-1-carboxylic acid

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Human Ornithine Aminotransferase (hOAT) / Mechanism Based Inactivator / PLP Hepatocellular Carcinoma (HCC)

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