Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

4FSE

crystal structure of beta-site app-cleaving enzyme 1 (bace-wt) complex with N-(N-(4-amino-3,5- dichlorobenzyl)carbamimidoyl)-3-(4-methoxyphenyl)-5- methyl-4-isothiazolecarboxamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004190molecular_functionaspartic-type endopeptidase activity
A0006508biological_processproteolysis
A0016020cellular_componentmembrane
B0004190molecular_functionaspartic-type endopeptidase activity
B0006508biological_processproteolysis
B0016020cellular_componentmembrane
D0004190molecular_functionaspartic-type endopeptidase activity
D0006508biological_processproteolysis
D0016020cellular_componentmembrane
E0004190molecular_functionaspartic-type endopeptidase activity
E0006508biological_processproteolysis
E0016020cellular_componentmembrane
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 0VA A 501
ChainResidue
ALEU78
AILE274
AASP276
AGLY278
ATHR279
AARG283
ATHR377
AHOH635
AASP80
ATYR119
AGLN121
AGLY122
ALYS155
APHE156
ATRP163
ATYR246

site_idAC2
Number of Residues1
DetailsBINDING SITE FOR RESIDUE IOD A 502
ChainResidue
AASN281

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE 0VA B 501
ChainResidue
BLEU78
BASP80
BTYR119
BTHR120
BGLN121
BGLY122
BLYS155
BPHE156
BTRP163
BTYR246
BILE274
BASP276
BGLY278
BTHR279
BARG283
BTHR377
BVAL380
BHOH730

site_idAC4
Number of Residues1
DetailsBINDING SITE FOR RESIDUE IOD B 502
ChainResidue
BASN281

site_idAC5
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 0VA D 501
ChainResidue
DASP80
DTYR119
DTHR120
DGLN121
DGLY122
DLYS155
DPHE156
DTRP163
DTYR246
DILE274
DASP276
DGLY278
DTHR279
DARG283
DTHR377
DHOH653

site_idAC6
Number of Residues1
DetailsBINDING SITE FOR RESIDUE IOD D 502
ChainResidue
DASN281

site_idAC7
Number of Residues19
DetailsBINDING SITE FOR RESIDUE 0VA E 501
ChainResidue
ELEU78
EASP80
EGLY82
ETYR119
ETHR120
EGLN121
EGLY122
ELYS155
EPHE156
ETRP163
ETYR246
EILE274
EASP276
EGLY278
ETHR279
EARG283
ETHR377
EHOH623
EHOH667

Functional Information from PROSITE/UniProt
site_idPS00141
Number of Residues12
DetailsASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ILVDTGSSNFAV
ChainResidueDetails
AILE77-VAL88

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1364
DetailsDomain: {"description":"Peptidase A1","evidences":[{"source":"PROSITE-ProRule","id":"PRU01103","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues8
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10094","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues28
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"17425515","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19011241","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues16
DetailsGlycosylation: {"description":"N-linked (GlcNAc...) asparagine","evidences":[{"evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

246704

PDB entries from 2025-12-24

PDB statisticsPDBj update infoContact PDBjnumon