Found 255 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: Arginase; Chain A

Total Genus Sequence Length pdb Title
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
144 426 4bz8A Crystal structure of schistosoma mansoni hdac8 complexed with j1038
152 434 4bz7A Crystal structure of schistosoma mansoni hdac8 complexed with m344
112 298 4cevA Arginase from bacillus caldevelox, l-ornithine complex
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
152 434 4bz6A Crystal structure of schistosoma mansoni hdac8 complexed with saha
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 3znsA Hdac7 bound with tfmo inhibitor tmp942
134 386 3znrA Hdac7 bound with inhibitor tmp269
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
118 390 3sl0A Crystal structure of p. falciparum arginase complexed with 2-amino-6-borono-2-(difluoromethyl)hexanoic acid
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
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
106 314 3rlaA Altering the binuclear manganese cluster of arginase diminishes thermostability and catalytic function
131 364 3rqdA Ideal thiolate-zinc coordination geometry in depsipeptide binding to histone deacetylase 8
134 365 5thuA Crystal structure of g304a 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
132 362 5thvA Crystal structure of g305a 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
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
294 744 5g0iA Crystal structure of danio rerio hdac6 cd1 and cd2 (linker cleaved) in complex with nexturastat a
135 368 5g17A Bordetella alcaligenes hdah (t101a) bound to 9,9,9-trifluoro-8,8- dihydroxy-n-phenylnonanamide.
142 370 5g0xA Pseudomonas aeruginosa hdah bound to acetate.
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.