Ontology highlight
ABSTRACT:
SUBMITTER: Tyndall JD
PROVIDER: S-EPMC3433185 | biostudies-literature | 2012 Sep
REPOSITORIES: biostudies-literature
Tyndall Joel D A JD Lue Hongqi H Rutledge Malcolm T MT Bernhagen Jurgen J Hampton Mark B MB Wilbanks Sigurd M SM
Acta crystallographica. Section F, Structural biology and crystallization communications 20120829 Pt 9
Macrophage migration inhibitory factor is irreversibly inhibited via covalent modification by phenethyl isothiocyanate, a naturally occurring compound with anti-inflammatory and anticancer properties. The structure of the modified protein obtained from X-ray diffraction data to 1.64 Å resolution is presented. The inhibitor sits within a deep hydrophobic pocket between subunits of the homotrimer and is highly ordered. The secondary structure of macrophage migratory inhibitory factor is unchanged ...[more]