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

Found 1855 chains in Genus chains table. Displaying 1101 - 1150. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
106	390	3lpkA	Structure of bace bound to sch747123
22	116	3liqA	Crystal structure of htlv protease complexed with the inhibitor, kni-10673
21	116	3lixA	Crystal structure of htlv protease complexed with the inhibitor kni-10729
24	116	3livA	Crystal structure of htlv protease complexed with the inhibitor kni-10683
105	390	3l5fA	Structure of bace bound to sch736201
100	386	3l38A	Bace1 in complex with the aminopyridine compound 44
89	387	3kyrA	Bace-1 in complex with a norstatine type inhibitor
102	390	3l5cA	Structure of bace bound to sch723871
98	387	3l3aA	Bace-1 with the aminopyridine compound 32
103	390	3l5dA	Structure of bace bound to sch723873
104	390	3l59A	Structure of bace bound to sch710413
107	390	3l5eA	Structure of bace bound to sch736062
104	395	3l58A	Structure of bace bound to sch589432
103	390	3l5bA	Structure of bace bound to sch713601
17	99	3kfpA	Hiv protease (pr) with inhibitor tl-3 bound, and dmsos in exo site
16	99	3kfnA	Hiv protease (pr) with inhibitor tl-3 and fragment hit 4d9 by soaking
104	395	3kmyA	Structure of bace bound to sch12472
15	99	3kdbA	Crystal structure of hiv-1 protease (q7k, l33i, l63i) in complex with kni-10006
43	203	3kt5A	Crystal structure of n88s mutant hiv-1 protease
87	337	3km4A	Optimization of orally bioavailable alkyl amine renin inhibitors
15	99	3kf0A	Hiv protease with fragment 4d9 bound
104	390	3kn0A	Structure of bace bound to sch708236
15	99	3kdcA	Crystal structure of hiv-1 protease (q7k, l33i, l63i) in complex with kni-10074
46	203	3kt2A	Crystal structure of n88d mutant hiv-1 protease
17	99	3kddA	Crystal structure of hiv-1 protease (q7k, l33i, l63i) in complex with kni-10265
104	395	3kmxA	Structure of bace bound to sch346572
17	99	3kfsA	Hiv protease (pr) dimer with inhibitor tl-3 bound and fragment 2f4 in the outside/top of flap
43	203	3ka2A	Crystal structure of chemically synthesized 203 amino acid 'covalent dimer' [l-ala;gly51']hiv-1 protease molecule complexed with mvt-101 reduced isostere inhibitor at 1.4 a resolution
18	99	3kfrA	Hiv protease (pr) dimer with inhibitor tl-3 bound and fragment 1f1 in the outside/top of flap
18	99	3k4vC	New crystal form of hiv-1 protease/saquinavir structure reveals carbamylation of n-terminal proline
17	99	3k4vA	New crystal form of hiv-1 protease/saquinavir structure reveals carbamylation of n-terminal proline
16	99	3jw2A	Hiv-1 protease mutant g86s with darunavir
98	388	3k5gA	Human bace-1 complex with bjc060
97	388	3k5cA	Human bace-1 complex with nb-216
20	99	3jvyA	Hiv-1 protease mutant g86a with darunavir
92	388	3k5dA	Crystal structure of bace-1 in complex with ahm178
91	338	3k1wA	New classes of potent and bioavailable human renin inhibitors
93	388	3k5fA	Human bace-1 complex with ayh011
19	99	3jvwA	Hiv-1 protease mutant g86a with symmetric inhibitor dmp323
103	387	3in4A	Bace1 with compound 38
103	387	3in3A	Bace1 with compound 30
101	389	3iviA	Design and synthesis of potent bace-1 inhibitors with cellular activity: structure-activity relationship of p1 substituents
103	389	3infA	Bace1 with the aminohydantoin compound 37
105	389	3ivhA	Design and synthesis of potent bace-1 inhibitors with cellular activity: structure-activity relationship of p1 substituents
100	389	3inhA	Bace1 with the aminohydantoin compound r-58
96	389	3indA	Bace1 with the aminohydantoin compound 29
94	388	3ixkA	Potent beta-secretase 1 inhibitor
100	388	3ineA	Bace1 with the aminohydantoin compound s-34
93	388	3ixjA	Crystal structure of beta-secretase 1 in complex with selective beta-secretase 1 inhibitor
18	99	3ixoA	Crystal structure of uncomplexed hiv_1 protease subtype a