Structure of PDB 4trz Chain A Binding Site BS01
Receptor Information
>4trz Chain A (length=388) Species:
9606
(Homo sapiens) [
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FVEMVDNLRGKSGQGYYVEMTVGSPPQTLNILVDTGSSNFAVGAAPHPFL
HRYYQRQLSSTYRDLRKGVYVPYTQGKWEGELGTDLVSIPHGPNVTVRAN
IAAITESDKFFINGSNWEGILGLAYAEIARPDDSLEPFFDSLVKQTHVPN
LFSLQLCGAGFPLNQSEVLASVGGSMIIGGIDHSLYTGSLWYTPIRREWY
YEVIIVRVEINGQDLKMDCKEYNYDKSIVDSGTTNLRLPKKVFEAAVKSI
KAASSTEKFPDGFWLGEQLVCWQAGTTPWNIFPVISLYLMGEVTNQSFRI
TILPQQYLRPVEDVATSQDDCYKFAISQSSTGTVMGAVIMEGFYVVFDRA
RKRIGFAVSACHVHDEFRTAAVEGPFVTLDMEDCGYNI
Ligand information
>4trz Chain D (length=4) Species:
32630
(synthetic construct) [
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EIPc
Receptor-Ligand Complex Structure
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PDB
4trz
Evaluation of transition-state mimics in a superior BACE1 cleavage sequence as peptide-mimetic BACE1 inhibitors
Resolution
3.25 Å
Binding residue
(original residue number in PDB)
G72 Q73 G74 D93 G95 Y132 Q134 F169 I171 Y259 D289 G291 T292 T293 N294 R296
Binding residue
(residue number reindexed from 1)
G13 Q14 G15 D34 G36 Y73 Q75 F110 I112 Y200 D230 G232 T233 T234 N235 R237
Enzymatic activity
Catalytic site (original residue number in PDB)
D93 S96 N98 A100 Y132 D289 T292
Catalytic site (residue number reindexed from 1)
D34 S37 N39 A41 Y73 D230 T233
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4trz
,
PDBe:4trz
,
PDBj:4trz
PDBsum
4trz
PubMed
26264846
UniProt
P56817
|BACE1_HUMAN Beta-secretase 1 (Gene Name=BACE1)
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