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4R8Y

BACE-1 in complex with (R)-4-(2-cyclohexylethyl)-4-(((R)-1-(2-cyclopentylacetyl)pyrrolidin-3-yl)methyl)-1-methyl-5-oxoimidazolidin-2-iminium

Functional Information from GO Data
ChainGOidnamespacecontents
A0004190molecular_functionaspartic-type endopeptidase activity
A0006508biological_processproteolysis
A0016020cellular_componentmembrane
B0004190molecular_functionaspartic-type endopeptidase activity
B0006508biological_processproteolysis
B0016020cellular_componentmembrane
Functional Information from PDB Data
site_idAC1
Number of Residues12
DetailsBINDING SITE FOR RESIDUE 3KO A 501
ChainResidue
ASER71
ATHR293
AHOH976
AHOH1008
AASP93
AGLY95
AVAL130
ATYR132
AILE171
AASP289
AGLY291
ATHR292

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE TLA B 501
ChainResidue
BARG68
BASN89
BHIS110
BARG111
BASN175
BHOH796
BHOH797
BHOH820
BHOH922

site_idAC3
Number of Residues14
DetailsBINDING SITE FOR RESIDUE 3KO B 502
ChainResidue
BSER71
BASP93
BGLY95
BVAL130
BTYR132
BILE171
BASP289
BGLY291
BTHR292
BTHR293
BHOH873
BHOH1001
BHOH1002
BHOH1037

Functional Information from PROSITE/UniProt
site_idPS00141
Number of Residues12
DetailsASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ILVDTGSSNFAV
ChainResidueDetails
AILE90-VAL101

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: ACT_SITE => ECO:0000255|PROSITE-ProRule:PRU10094
ChainResidueDetails
AASP93
AASP289
BASP93
BASP289

site_idSWS_FT_FI2
Number of Residues14
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:17425515, ECO:0000269|PubMed:19011241
ChainResidueDetails
ALYS126
BLYS279
BLYS285
BLYS299
BLYS300
BLYS307
ALYS275
ALYS279
ALYS285
ALYS299
ALYS300
ALYS307
BLYS126
BLYS275

site_idSWS_FT_FI3
Number of Residues8
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
AASN153
AASN172
AASN223
AASN354
BASN153
BASN172
BASN223
BASN354

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PDB entries from 2024-10-30

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