1T64, 1T67, 1T69, 1VKG, 1W22, 2V5W, 2V5X, 3EW8, 3EWF, 3EZP, 3EZT, 3F06, 3F07, 3F0R, 3MZ3, 3MZ4, 3MZ6, 3MZ7, 3RQD, 3SFF, 3SFH, 4QA0, 4QA1, 4QA2, 4QA3, 4QA4, 4QA5, 4QA6, 4QA7, 4RN0, 4RN1, 4RN2, 5DC7, 5D1D, 5D1C, 5DC8, 5D1B, 5DC5, 5DC6, 5BWZ5586970315ENSG00000147099ENSMUSG00000067567Q9BY41Q8VH37NM_018486NM_027382NM_001313742NP_060956NP_001300671NP_081658Histone deacetylase 8 is an enzyme that in humans is encoded by the HDAC8 gene.1t64: Crystal Structure of human HDAC8 complexed with Trichostatin A1t67: Crystal Structure of Human HDAC8 complexed with MS-3441t69: Crystal Structure of human HDAC8 complexed with SAHA1vkg: Crystal Structure of Human HDAC8 complexed with CRA-191561w22: CRYSTAL STRUCTURE OF INHIBITED HUMAN HDAC8 Histone deacetylase 8 is an enzyme that in humans is encoded by the HDAC8 gene. Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation / deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class I of the histone deacetylase/acuc/apha family. It has histone deacetylase activity and represses transcription when tethered to a promoter. Histone deacetylase 8 is involved in skull morphogenesis and metabolic control of the ERR-alpha / PGC1-alpha transcriptional complex. HDAC8 has been linked to number of disease states notably to acute myeloid leukemia and is related to actin cytoskeleton in smooth muscle cells. siRNA targeting HDAC8 showed anticancer effects. Inhibition of HDAC8 induced apoptosis has been observed in T cell lymphomas. In addition the HDAC8 enzyme has been implicated in the pathogenesis of neuroblastoma. Therefore, there has been interest in developing HDAC8 selective inhibitors. This article incorporates text from the United States National Library of Medicine, which is in the public domain.