Found 1855 chains in Genus chains table. Displaying 901 - 950. Applied filters: Proteins

Search results query: Cathepsin D, subunit A; domain 1

Total Genus Sequence Length pdb Title
100 403 4i0fA Design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors
15 99 4j55A Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 with the potent antiviral inhibitor grl-02031
95 389 4ivsA Crystal structure of bace1 with its inhibitor
101 403 4i0jA Spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors
97 388 4i0hA Spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors.
100 390 4j1cA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((s)-2-amino-5,5-difluoro-4-fluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
101 390 4j17A Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((s)-2-amino-4-difluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
101 400 4i10A Structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates
96 390 4j1hA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((4s,6r)-2-amino-4-methyl-6-trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
102 390 4j0vA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((4r,5r)-2-amino-5-fluoro-4-methyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
94 399 4i1cA Design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors
19 99 4jecA Joint neutron and x-ray structure of per-deuterated hiv-1 protease in complex with clinical inhibitor amprenavir
16 99 4j5jA Crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20 in complex with amprenavir
104 403 4i11A Structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates.
99 403 4i0eA Design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors
107 402 4jpeA Spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors
95 390 4j1iA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((4r,5r,6r)-2-amino-5-fluoro-4-methyl-6-trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
100 390 4j0tA Crystal structure of bace-1 in complex with 5-ethoxy-pyridine-2-carboxylic acid [3-((r)-2-amino-5,5-difluoro-4-methyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
103 388 4i0iA Spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors
105 402 4jpcA Spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors
98 390 4j1fA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((4s,6s)-2-amino-4-methyl-6-trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
103 390 4j1eA Crystal structure of bace-1 in complex with 5-cyano-pyridine-2-carboxylic acid [3-((4s,6s)-2-amino-4-fluoromethyl-6-trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide
98 403 4i0gA Design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors
15 99 4hvpA Structure of complex of synthetic hiv-1 protease with a substrate-based inhibitor at 2.3 angstroms resolution
104 390 4h3jA Structure of bace bound to 2-fluoro-5-(5-(2-imino-3-methyl-4-oxo-6-phenyloctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl)thiophen-2-yl)benzonitrile
19 99 4hlaA Crystal structure of wild type hiv-1 protease in complex with darunavir
103 390 4h3fA Structure of bace bound to 3-(5-((7ar)-2-imino-6-(6-methoxypyridin-2-yl)-3-methyl-4-oxooctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl)thiophen-3-yl)benzonitrile
20 99 4he9A Crystal structure of hiv-1 protease mutants i54m complexed with inhibitor grl-0519
20 99 4hegA Crystal structure of hiv-1 protease mutants r8q complexed with inhibitor grl-0519
104 390 4h3iA Structure of bace bound to 3-(5-((7ar)-2-imino-6-(3-methoxypyridin-2-yl)-3-methyl-4-oxooctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl)thiophen-3-yl)benzonitrile
19 99 4hdfA Crystal structure of hiv-1 protease mutants v82a complexed with inhibitor grl-0519
19 99 4hdpA Crystal structure of hiv-1 protease mutants i50v complexed with inhibitor grl-0519
18 99 4hdbA Crystal structure of hiv-1 protease mutants d30n complexed with inhibitor grl-0519
106 390 4h3gA Structure of bace bound to 2-((7ar)-7a-(4-(3-cyanophenyl)thiophen-2-yl)-2-imino-3-methyl-4-oxohexahydro-1h-pyrrolo[3,4-d]pyrimidin-6(2h)-yl)nicotinonitrile
103 390 4ha5A Structure of bace bound to (s)-3-(5-(2-imino-1,4-dimethyl-6-oxohexahydropyrimidin-4-yl)thiophen-3-yl)benzonitrile
17 99 4gzfA Multi-drug resistant hiv-1 protease 769 variant with reduced lrf peptide
15 99 4gyeA Mdr 769 hiv-1 protease in complex with reduced p1f
103 389 4h1eA Structure of bace-1 bound to (7ar)-6-benzoyl-7a-(4-(3-cyanophenyl)thiophen-2-yl)-3-methyl-4-oxohexahydro-1h-pyrrolo[3,4-d]pyrimidin-2(3h)-iminium
82 340 4gj5A Crystal structure of renin in complex with nvp-amq838 (compound 5)
85 339 4gj6A Crystal structure of renin in complex with nvp-ayz832 (compound 6a)
16 99 4gb2A Hiv-1 protease (mutant q7k l33i l63i) in complex with a bicyclic pyrrolidine inhibitor
88 340 4gj8A Crystal structure of renin in complex with pkf909-724 (compound 3)
82 340 4gjbA Crystal structure of renin in complex with nvp-bbv031 (compound 6)
103 389 4gmiA Bace-1 in complex with hea-type macrocyclic inhibitor, mv078571
88 339 4gj7A Crystal structure of renin in complex with nvp-bca079 (compound 12a)
103 387 4gidA Structure of beta-secretase complexed with inhibitor
83 338 4gj9A Crystal structure of renin in complex with gp055321 (compound 4)
89 340 4gjaA Crystal structure of renin in complex with nvp-ayl747 (compound 5)
88 340 4gjcA Crystal structure of renin in complex with nvp-bch965 (compound 9)
87 339 4gjdA Crystal structure of renin in complex with nvp-bgq311 (compound 12)