Structure of PDB 4zsr Chain B Binding Site BS01

Receptor Information
>4zsr Chain B (length=389) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GSFVEMVDNLRGKSGQGYYVEMTVGSPPQTLNILVDTGSSNFAVGAAPHP
FLHRYYQRQLSSTYRDLRKGVYVPYTQGKWEGELGTDLVSIPHGPNVTVR
ANIAAITESDKFFINGSNWEGILGLAYAEIARPDDSLEPFFDSLVKQTHV
PNLFSLQLCGAGFPLNQSEVLASVGGSMIIGGIDHSLYTGSLWYTPIRRE
WYYEVIIVRVEINGQDLKMDCKEYNYDKSIVDSGTTNLRLPKKVFEAAVK
SIKAASSTEKFPDGFWLGEQLVCWQAGTTPWNIFPVISLYLMGEVTNQSF
RITILPQQYLRPVEDVATSQDDCYKFAISQSSTGTVMGAVIMEGFYVVFD
RARKRIGFAVSACHVHDEFRTAAVEGPFVTLDMEDCGYN
Ligand information
Ligand ID4RY
InChIInChI=1S/C17H20ClN3O2S/c18-12-3-1-2-11(6-12)14(22)20-13-4-5-17-9-23-8-16(17,7-13)10-24-15(19)21-17/h1-3,6,13H,4-5,7-10H2,(H2,19,21)(H,20,22)/t13-,16-,17-/m0/s1
InChIKeyXDMHBNONUZHFDP-JQFCIGGWSA-N
SMILES
SoftwareSMILES
CACTVS 3.385NC1=N[C@]23CC[C@@H](C[C@]2(COC3)CS1)NC(=O)c4cccc(Cl)c4
ACDLabs 12.01C=4(SCC21COCC1(CCC(C2)NC(c3cccc(c3)Cl)=O)N=4)N
OpenEye OEToolkits 1.7.6c1cc(cc(c1)Cl)C(=O)N[C@H]2CC[C@]34COC[C@@]3(C2)CSC(=N4)N
CACTVS 3.385NC1=N[C]23CC[CH](C[C]2(COC3)CS1)NC(=O)c4cccc(Cl)c4
OpenEye OEToolkits 1.7.6c1cc(cc(c1)Cl)C(=O)NC2CCC34COCC3(C2)CSC(=N4)N
FormulaC17 H20 Cl N3 O2 S
NameN-[(4aS,6S,8aR)-2-amino-5,6,7,8-tetrahydro-4a,8a-(methanooxymethano)-3,1-benzothiazin-6(4H)-yl]-3-chlorobenzamide
ChEMBL
DrugBank
ZINCZINC000230533706
PDB chain4zsr Chain B Residue 401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB4zsr Preparation and biological evaluation of conformationally constrained BACE1 inhibitors.
Resolution1.65 Å
Binding residue
(original residue number in PDB)
S10 G11 Q12 G13 D32 G34 I110 W115 D228 G230 T232
Binding residue
(residue number reindexed from 1)
S14 G15 Q16 G17 D36 G38 I114 W119 D232 G234 T236
Annotation score1
Binding affinityMOAD: ic50=36.1uM
Enzymatic activity
Catalytic site (original residue number in PDB) D32 S35 N37 A39 Y71 D228 T231
Catalytic site (residue number reindexed from 1) D36 S39 N41 A43 Y75 D232 T235
Enzyme Commision number 3.4.23.46: memapsin 2.
Gene Ontology
Molecular Function
GO:0004190 aspartic-type endopeptidase activity
Biological Process
GO:0006508 proteolysis
Cellular Component
GO:0016020 membrane

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:4zsr, PDBe:4zsr, PDBj:4zsr
PDBsum4zsr
PubMed26001341
UniProtP56817|BACE1_HUMAN Beta-secretase 1 (Gene Name=BACE1)

[Back to BioLiP]