Structure of PDB 4fgx Chain A Binding Site BS01
Receptor Information
>4fgx Chain A (length=374) Species:
9606
(Homo sapiens) [
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SFVEMVDNLRGKSGQGYYVEMTVGSPPQTLNILVDTGSSNFAVGAAPHPF
LHRYYQRQLSSTYRDLRKGVYVPYTQGAWAGELGTDLVSIPHGPNVTVRA
NIAAITESDKFFINGSNWEGILGLAYAEIARPDDSLEPFFDSLVKQTHVP
NLFSLQLCGASVGGSMIIGGIDHSLYTGSLWYTPIRREWYYEVIIVRVEI
NGQDLKMDCKEYNYDKSIVDSGTTNLRLPKKVFEAAVKSIKAASSTEKFP
DGFWLGEQLVCWQAGTTPWNIFPVISLYLMGEVTNQSFRITILPQQYLRP
VESQDDCYKFAISQSSTGTVMGAVIMEGFYVVFDRARKRIGFAVSACHVH
DEFRTAAVEGPFVTLDMEDCGYNI
Ligand information
>4fgx Chain B (length=7) [
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AVQFLAF
Receptor-Ligand Complex Structure
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PDB
4fgx
Cyanobacterial Peptides as a Prototype for the Design of Potent beta-Secretase Inhibitors and the Development of Selective Chemical Probes for Other Aspartic Proteases
Resolution
1.59 Å
Binding residue
(original residue number in PDB)
G59 Q60 D80 P118 Y119 T120 F156 W163 I174 K272 D276 G278 T279 T280 R283
Binding residue
(residue number reindexed from 1)
G14 Q15 D35 P73 Y74 T75 F111 W118 I129 K216 D220 G222 T223 T224 R227
Enzymatic activity
Catalytic site (original residue number in PDB)
D80 S83 N85 A87 Y119 D276 T279
Catalytic site (residue number reindexed from 1)
D35 S38 N40 A42 Y74 D220 T223
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:4fgx
,
PDBe:4fgx
,
PDBj:4fgx
PDBsum
4fgx
PubMed
23181502
UniProt
P56817
|BACE1_HUMAN Beta-secretase 1 (Gene Name=BACE1)
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