Found 153 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 3.5.1.98

Total Genus Sequence Length pdb Title
155 672 6z6oB Hdac-tc
157 672 6z6hB Hdac-dc
148 672 6z6fB Hdac-pc
156 661 6z6pK Hdac-pc-nuc
165 661 6z6oA Hdac-tc
151 672 6z6pL Hdac-pc-nuc
151 661 6z6fA Hdac-pc
165 661 6z6hA Hdac-dc
124 369 7ao9B Structure of the core mta1/hdac1/mbd2 nurd deacetylase complex
127 363 7jvwA Crystal structure of human histone deacetylase 8 (hdac8) g320r mutation complexed with m344
148 368 7kbgA Structure of human hdac2 in complex with a 2-substituted benzamide inhibitor (compound 20)
134 365 7jvuA Crystal structure of human histone deacetylase 8 (hdac8) i45t mutation complexed with saha
137 369 7kbhA Structure of human hdac2 in complex with a 2-substituted benzamide inhibitor (compound 16)
131 362 7jvvA Crystal structure of human histone deacetylase 8 (hdac8) e66d/y306f double mutation complexed with a tetrapeptide substrate
124 369 7ao8B Structure of the mta1/hdac1/mbd2 nurd deacetylase complex
124 369 7aoaB Structure of the extended mta1/hdac1/mbd2/rbbp4 nurd deacetylase complex
147 368 6xebA Structure of human hdac2 in complex with ketone inhibitor (compound e)
148 368 6xecA Structure of human hdac2 in complex with ketone inhibitor (compound o)
109 369 6z2kC The structure of the tetrameric hdac1/mideas/dnttip1 midac deacetylase complex
64 369 6z2jC The structure of the dimeric hdac1/mideas/dnttip1 midac deacetylase complex
147 368 6wbzA Structure of human hdac2 in complex with an ethyl ketone inhibitor containing a spiro-bicyclic group
145 367 6wbwA Structure of human hdac2 in complex with an ethyl ketone inhibitor
5 23 1tqeX Mechanism of recruitment of class ii histone deacetylases by myocyte enhancer factor-2
148 432 6hu1A Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 10
147 434 6hsgA Crystal structure of schistosoma mansoni hdac8 h292m mutant complexed with ncc-149
146 432 6hszA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 2
149 434 6htiA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 6
148 434 6ht8A Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 3
155 434 6hshA Crystal structure of schistosoma mansoni hdac8 complexed with quisinostat
150 434 6httA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 7
144 423 6hthA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 5
152 434 6hu3A Crystal structure of schistosoma mansoni hdac8 complexed with a triazole hydroxamate inhibitor
131 364 6hskA Crystal structure of a human hdac8 l6 loop mutant complexed with quisinostat
149 434 6hu2A Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 11
151 434 6hsfA Crystal structure of schistosoma mansoni hdac8 mutant h292m complexed with pci-34051
150 434 6hrqA Crystal structure of schistosoma mansoni hdac8 complexed with ncc-149
148 424 6hu0A Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 9
149 434 6htgA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 4
144 434 6hqyA Crystal structure of schistosoma mansoni hdac8 complexed with pci-34051
149 434 6htzA Crystal structure of schistosoma mansoni hdac8 complexed with a benzohydroxamate inhibitor 8
128 385 6fyzA Development and characterization of a cns-penetrant benzhydryl hydroxamic acid class iia histone deacetylase inhibitor
131 399 5zopG Crystal structure of histone deacetylase 4 (hdac4) in complex with a smrt corepressor sp2 fragment
138 402 5zooG Crystal structure of histone deacetylase 4 (hdac4) in complex with a smrt corepressor sp1 fragment
149 434 6fu1A Crystal structure of schistosoma mansoni hdac8 complexed with a n-alkyl hydroxamate
198 627 5ikkA Structure of the histone deacetylase clr3
30 100 5kh7A Crystal structure of fragment (3-[6-oxo-3-(3-pyridinyl)-1(6h)-pyridazinyl]propanoic acid) bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
30 101 5kh3A Crystal structure of fragment (3-(5-chloro-1,3-benzothiazol-2-yl)propanoic acid) bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
124 369 5icnB Hdac1:mta1 in complex with inositol-6-phosphate and a novel peptide inhibitor based on histone h4
234 722 5eduA Crystal structure of human histone deacetylase 6 catalytic domain 2 in complex with trichostatin a
149 434 6gx3A Crystal structure of schistosoma mansoni hdac8 complexed with an hydroxamate 1