Search results query: Asp

Found 1377 chains in Genus chains table. Displaying 1101 - 1150. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
98	388	3k5gA	Human bace-1 complex with bjc060
100	389	3inhA	Bace1 with the aminohydantoin compound r-58
101	389	3iviA	Design and synthesis of potent bace-1 inhibitors with cellular activity: structure-activity relationship of p1 substituents
96	389	3indA	Bace1 with the aminohydantoin compound 29
105	389	3ivhA	Design and synthesis of potent bace-1 inhibitors with cellular activity: structure-activity relationship of p1 substituents
103	387	3in4A	Bace1 with compound 38
103	387	3in3A	Bace1 with compound 30
103	389	3infA	Bace1 with the aminohydantoin compound 37
93	388	3ixjA	Crystal structure of beta-secretase 1 in complex with selective beta-secretase 1 inhibitor
100	388	3ineA	Bace1 with the aminohydantoin compound s-34
94	388	3ixkA	Potent beta-secretase 1 inhibitor
100	388	3igbA	Bace-1 with compound 3
91	390	3hvgA	Structure of bace (beta secretase) in complex with ev0
97	389	3hw1A	Structure of bace (beta secretase) in complex with ligand ev2
91	388	3i25A	Potent beta-secretase 1 hydroxyethylene inhibitor
97	388	3h0bA	Discovery of aminoheterocycles as a novel beta-secretase inhibitor class
88	337	3gw5A	Crystal structure of human renin complexed with a novel inhibitor
81	325	3fnsA	Crystal structure of histo-aspartic protease (hap) from plasmodium falciparum
100	339	3fv3A	Secreted aspartic protease 1 from candida parapsilosis in complex with pepstatin a
89	337	3g72A	Design and preparation of potent, non-peptidic, bioavailable renin inhibitors
89	338	3g70A	Design and preparation of potent, non-peptidic, bioavailable renin inhibitors
86	341	3g6zA	Design and preparation of potent, non-peptidic, bioavailable renin inhibitors
79	326	3fnuA	Crystal structure of kni-10006 bound histo-aspartic protease (hap) from plasmodium falciparum
84	329	3f9qA	Re-refinement of uncomplexed plasmepsin ii from plasmodium falciparum.
95	387	3fktA	Crystal structure of human beta secretase complexed with spiropiperdine iminohydantoin inhibitor
65	323	3fntA	Crystal structure of pepstatin a bound histo-aspartic protease (hap) from plasmodium falciparum
78	330	3er5E	The active site of aspartic proteinases
96	389	3exoA	Crystal structure of bace1 bound to inhibitor
78	330	3er3E	The active site of aspartic proteinases
79	329	3emyA	Crystal structure of trichoderma reesei aspartic proteinase complexed with pepstatin a
96	388	3duyA	Crystal structure of human beta-secretase in complex with nvp-afj144
98	388	3dv5A	Crystal structure of human beta-secretase in complex with nvp-bav544
95	388	3dv1A	Crystal structure of human beta-secretase in complex with nvp-arv999
92	388	3dm6A	Beta-secretase 1 complexed with statine-based inhibitor
79	338	3d91A	Human renin in complex with remikiren
104	390	3cibA	Structure of bace bound to sch727596
84	392	3ckrA	Crystal structure of bace-1 in complex with inhibitor
83	323	3cmsA	Engineering enzyme sub-site specificity: preparation, kinetic characterization and x-ray analysis at 2.0-angstroms resolution of val111phe site-mutated calf chymosin
104	390	3cicA	Structure of bace bound to sch709583
93	392	3ckpA	Crystal structure of bace-1 in complex with inhibitor
103	390	3cidA	Structure of bace bound to sch726222
80	329	3c9xA	Crystal structure of trichoderma reesei aspartic proteinase
98	391	3buhA	Bace-1 complexed with compound 4
91	388	3bugA	Bace-1 complexed with compound 3
95	391	3bufA	Bace-1 complexed with compound 2
93	391	3braA	Bace-1 complexed with compound 1
89	325	3aprE	Binding of a reduced peptide inhibitor to the aspartic proteinase from rhizopus chinensis. implications for a mechanism of action
85	323	3appA	Structure and refinement of penicillopepsin at 1.8 angstroms resolution
98	389	2zjmA	Crystal structure of the human bace1 catalytic domain in complex with n-[1-(5-chloro-2-isopropoxy-3-methoxy-benzyl)-piperidin-4-yl]-2-(4-sulfamoyl-phenoxy)-acetamide
88	387	2zhsA	Crystal structure of bace1 at ph 4.0