Found 131 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
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
152 434 6gxaA Crystal structure of schistosoma mansoni hdac8 complexed with an hydroxamate 2
145 427 6gxuA Crystal structure of schistosoma mansoni hdac8 complexed with an hydroxamate 3
153 434 6gxwA Crystal structure of schistosoma mansoni hdac8 complexed with an hydroxamate 4
143 369 6g3oA Crystal structure of human hdac2 in complex with (r)-6-[3,4-dioxo-2-(4-trifluoromethoxy-phenylamino)-cyclobut-1-enylamino]-heptanoic acid hydroxyamide
28 100 6ceeA Crystal structure of fragment 3-(1-methyl-2-oxo-1,2-dihydroquinoxalin-3-yl)propionic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
29 101 6ce8A Crystal structure of fragment 2-(benzo[d]thiazol-2-yl)acetic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
28 100 6cecA Crystal structure of fragment 3-(3-methoxy-2-quinoxalinyl)propanoic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
28 99 6cedA Crystal structure of fragment 3-(3-methyl-4-oxo-3,4-dihydroquinazolin-2-yl)propanoic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
29 100 6cefA Crystal structure of fragment 3-(1,3-benzothiazol-2-yl)propanoic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
30 101 6ce6A Structure of hdac6 zinc-finger ubiquitin binding domain soaked with 3,3'-(benzo[1,2-d:5,4-d']bis(thiazole)-2,6-diyl)dipropionic acid
28 99 6ceaA Crystal structure of fragment 3-(quinolin-2-yl)propanoic acid bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain
133 361 5vi6A Crystal structure of histone deacetylase 8 in complex with trapoxin a
133 365 5bwzA Crystal structure of s39e hdac8 in complex with droxinostat
32 99 5b8dA Crystal structure of a low occupancy fragment candidate (n-(4-methyl-1,3-thiazol-2-yl)propanamide) bound adjacent to the ubiquitin binding pocket of the hdac6 zinc-finger domain
137 380 5a2sA Potent, selective and cns-penetrant tetrasubstituted cyclopropane class iia histone deacetylase (hdac) inhibitors
119 385 4cbtA Design, synthesis, and biological evaluation of potent and selective class iia hdac inhibitors as a potential therapy for huntington's disease
135 380 4cbyA Design, synthesis, and biological evaluation of potent and selective class iia hdac inhibitors as a potential therapy for huntington's disease
120 369 4bkxB The structure of hdac1 in complex with the dimeric elm2-sant domain of mta1 from the nurd complex
137 369 4a69A Structure of hdac3 bound to corepressor and inositol tetraphosphate
134 386 3znrA Hdac7 bound with inhibitor tmp269
134 386 3znsA Hdac7 bound with tfmo inhibitor tmp942
0 17 3v31B Crystal structure of the peptide bound complex of the ankyrin repeat domains of human ankra2