Found 1377 chains in Genus chains table. Displaying 801 - 850. Applied filters: Proteins

Search results query: Asp

Total Genus Sequence Length pdb Title
83 330 5p04A Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 51
83 330 5ozlA Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 32
82 330 5ojeA Endothiapepsin with ligand vsk-b24
85 330 5og7A Endothiapepsin in complex with hydrazide fragment
88 337 5n71A Crystal structure of mature cathepsin d from the tick ixodes ricinus (ircd1)
86 337 5n7qA Crystal structure of mature cathepsin d from the tick ixodes ricinus (ircd1) in complex with the inhibitor pepstatin a
94 361 5n7nA Crystal structure of cathepsin d zymogen from the tick ixodes ricinus (ircd1)
86 330 5lwtA Endothiapepsin in complex with a methoxylated derivative of fragment 177
84 330 5mb5A Cocktail experiment c: fragments 103 and 171 in complex with endothiapepsin
84 330 5lwuA Structure resulting from an endothiapepsin crystal soaked with a dimeric derivative of fragment 177
88 329 4z22A Structure of plasmepsin ii from plasmodium falciparum complexed with inhibitor dr718a
93 387 5kqfA (4~{s},6~{s})-4-[2,4-bis(fluoranyl)phenyl]-4-methyl-6-pyrimidin-5-yl-5,6-dihydro-1,3-thiazin-2-amine (compound 12) bound to bace1
86 330 5hcoA Endothiapepsin in complex with hydrazide
106 390 5hdxA Bace-1 in complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(4-ethoxy-5-fluoro-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
108 390 5he4A Bace-1 in complex with (4ar,7as)-7a-(2,6-difluorophenyl)-6-(5-fluoro-4-methoxy-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
103 390 5hduA Bace-1 incomplex with (7ar)-7a-(4-(3-cyanophenyl)thiophen-2-yl)-6-(5-fluoro-4-methoxypyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
106 390 5he5A Bace-1 in complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4-methyl-6-(methylamino)pyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
81 330 4zeaA Endothiapepsin in complex with fragment b91
103 390 5hdvA Bace-1 incomplex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4-methoxy-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
87 330 5hctA Endothiapepsin in complex with biacylhydrazone
101 388 5i3vA Crystal structure of bace1 in complex with aminoquinoline compound 1
105 390 5he7A Bace-1 in complex with (4ar,7as)-7a-(2,4-difluorophenyl)-6-(5-fluoro-4-methoxy-6-methylpyrimidin-2-yl)-2-imino-3-methyloctahydro-4h-pyrrolo[3,4-d]pyrimidin-4-one
103 390 5hdzA Bace-1 in complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4-methyl-6-(methylthio)pyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
105 390 5hd0A Bace-1 in complex with (7ar)-7a-(4-(3-cyanophenyl)thiophen-2-yl)-6-(5-fluoropyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium
98 390 5f01A Crystal structure of bace-1 in complex with (1sr,2sr)-2-((r)-2-amino-5,5-difluoro-4-methyl-5,6-dihydro-4h-1,3-oxazin-4-yl)-n-(3-chloroquinolin-8-yl)cyclopropanecarboxamide
107 390 4zsrA Bace crystal structure with tricyclic aminothiazine inhibitor
101 389 4zsmA Bace crystal structure with bicyclic aminothiazine fragment
99 390 5f00A Crystal structure of bace-1 in complex with 5-[3-[(3-chloro-8-quinolyl)amino]phenyl]-5-methyl-2,6-dihydro-1,4-oxazin-3-amine
88 387 5enmA Compound 10
106 390 4zspA Bace crystal structure with bicyclic aminothiazine inhibitor
90 387 5enkA Compound 18
99 389 4zsqA Bace crystal structure with tricyclic aminothiazine inhibitor
73 330 5er1E A rational approach to the design of antihypertensives. x-ray studies of complexes between aspartic proteinases and aminoalcohol renin inhibitors
101 390 5ezzA Crystal structure of bace-1 in complex with (4s)-4-[3-(5-chloro-3-pyridyl)phenyl]-4-[4-(difluoromethoxy)-3-methyl-phenyl]-5h-oxazol-2-amine
80 330 5er2E High-resolution x-ray diffraction study of the complex between endothiapepsin and an oligopeptide inhibitor. the analysis of the inhibitor binding and description of the rigid body shift in the enzyme
89 325 5aprE Structures of complexes of rhizopuspepsin with pepstatin and other statine-containing inhibitors
85 330 5dr0A Endothiapepsin in complex with fragment 203
84 330 5dr7A Endothiapepsin in complex with fragment 311
83 330 5dpzA Endothiapepsin in complex with fragment 31
84 330 5dr3A Endothiapepsin in complex with fragment 333
82 330 5dq1A Endothiapepsin in complex with fragment 34
86 330 5dr8A Endothiapepsin in complex with fragment 330
86 330 5dr1A Endothiapepsin in complex with fragment 278
84 330 5dr4A Endothiapepsin in complex with fragment 231
100 388 5dqcA Co-crystal of bace1 with compound 0211
83 330 5dq2A Endothiapepsin in complex with fragment 48
85 330 5dq5A Endothiapepsin in complex with fragment 209
85 330 5dq4A Endothiapepsin in complex with fragment 66
100 389 4zpfA Bace1 in complex with 8-(3-((1-aminopropan-2-yl)oxy)benzyl)-4-(cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-one
98 389 4zpgA Bace1 in complex with 8-benzyl-4-(cyclohexylamino)-1-(3-fluorophenyl)-7-methyl-1,3,8-triazaspiro[4.5]dec-3-en-2-one