|
115
|
314
|
3tf3A |
Crystal structure of metal-free human arginase i |
|
138
|
374
|
5li3A |
Crystal structure of hdac-like protein from p. aeruginosa in complex with a photo-switchable inhibitor. |
|
118
|
305
|
5ji5A |
Crystal structure of a histone deacetylase superfamily protein from burkholderia phymatumphymatum |
|
124
|
369
|
5icnB |
Hdac1:mta1 in complex with inositol-6-phosphate and a novel peptide inhibitor based on histone h4 |
|
117
|
310
|
5hjaA |
Crystal structure of leishmania mexicana arginase in complex with inhibitor abhdp |
|
118
|
298
|
5cevA |
Arginase from bacillus caldevelox, l-lysine complex |
|
133
|
365
|
5bwzA |
Crystal structure of s39e hdac8 in complex with droxinostat |
|
137
|
380
|
5a2sA |
Potent, selective and cns-penetrant tetrasubstituted cyclopropane class iia histone deacetylase (hdac) inhibitors |
|
114
|
341
|
4zuqA |
Crystal structure of acetylpolyamine amidohydrolase from mycoplana ramosa in complex with a hydroxamate inhibitor |
|
125
|
344
|
4q41A |
Crystal structure of schistosoma mansoni arginase in complex with l-lysine |
|
119
|
316
|
4dz4A |
X-ray crystal structure of a hypothetical agmatinase from burkholderia thailandensis |
|
153
|
434
|
4cqfA |
Crystal structure of schistosoma mansoni hdac8 complexed with a mercaptoacetamide inhibitor |
|
152
|
434
|
4bz7A |
Crystal structure of schistosoma mansoni hdac8 complexed with m344 |
|
112
|
298
|
4cevA |
Arginase from bacillus caldevelox, l-ornithine complex |
|
144
|
426
|
4bz8A |
Crystal structure of schistosoma mansoni hdac8 complexed with j1038 |
|
152
|
434
|
4bz6A |
Crystal structure of schistosoma mansoni hdac8 complexed with saha |
|
148
|
434
|
4bz5A |
Crystal structure of schistosoma mansoni hdac8 |
|
135
|
380
|
4cbyA |
Design, synthesis, and biological evaluation of potent and selective class iia hdac inhibitors as a potential therapy for huntington's disease |
|
152
|
434
|
4bz9A |
Crystal structure of schistosoma mansoni hdac8 complexed with j1075 |
|
119
|
385
|
4cbtA |
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 |
|
112
|
314
|
3thhA |
Crystal structure of the co2+2-hai-abh complex |
|
117
|
314
|
3theA |
Crystal structure of co2+2-hai (ph 8.5) |
|
115
|
314
|
3thjA |
Crystal structure of the co2+2-hai-l-orn complex |
|
114
|
314
|
3th7A |
Crystal structure of unliganded co2+2-hai (ph 7.0) |
|
114
|
313
|
3sjtA |
Crystal structure of human arginase i in complex with the inhibitor me-abh, resolution 1.60 a, twinned structure |
|
119
|
314
|
3skkA |
Crystal structure of human arginase i in complex with the inhibitor fabh, resolution 1.70 a, twinned structure |
|
130
|
364
|
3sfhA |
Crystal structure of human hdac8 inhibitor complex, an amino acid derived inhibitor |
|
118
|
390
|
3sl0A |
Crystal structure of p. falciparum arginase complexed with 2-amino-6-borono-2-(difluoromethyl)hexanoic acid |
|
119
|
390
|
3sl1A |
Crystal structure of p. falciparum arginase complexed with 2-amino-6-borono-2-methylhexanoic acid |
|
125
|
364
|
3sffA |
Crystal structure of human hdac8 inhibitor complex, an amino acid derived inhibitor |
|
131
|
364
|
3rqdA |
Ideal thiolate-zinc coordination geometry in depsipeptide binding to histone deacetylase 8 |
|
106
|
314
|
3rlaA |
Altering the binuclear manganese cluster of arginase diminishes thermostability and catalytic function |
|
134
|
365
|
5thuA |
Crystal structure of g304a hdac8 in complex with m344 |
|
132
|
362
|
5thvA |
Crystal structure of g305a hdac8 in complex with m344 |
|
129
|
366
|
5thtA |
Crystal structure of g303a hdac8 in complex with m344 |
|
138
|
364
|
5thsA |
Crystal structure of g302a hdac8 in complex with m344 |
|
107
|
314
|
5rlaA |
Altering the binuclear manganese cluster of arginase diminishes thermostability and catalytic function |
|
145
|
368
|
5iwgA |
Hdac2 with ligand brd4884 |
|
144
|
369
|
5ix0A |
Hdac2 with ligand brd7232 |
|
294
|
744
|
5g0iA |
Crystal structure of danio rerio hdac6 cd1 and cd2 (linker cleaved) in complex with nexturastat a |
|
290
|
756
|
5g0jA |
Crystal structure of danio rerio hdac6 cd1 and cd2 (linker intact) in complex with nexturastat a |
|
105
|
311
|
5hj9A |
Crystal structure of leishmania mexicana arginase in complex with inhibitor abhpe |
|
142
|
370
|
5g1cA |
Structure of hdac like protein from bordetella alcaligenes bound the photoswitchable pyrazole inhibitor cew395 |
|
139
|
369
|
5g11A |
Pseudomonas aeruginosa hdah bound to pfsaha. |
|
139
|
371
|
5g1bA |
Bordetella alcaligenes hdah native |
|
135
|
368
|
5g17A |
Bordetella alcaligenes hdah (t101a) bound to 9,9,9-trifluoro-8,8- dihydroxy-n-phenylnonanamide. |
