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6JSN

Crystal Structure of BACE1 in complex with N-{3-[(5R)-3-amino-5-methyl-9,9-dioxo-2,9lambda6-dithia-4-azaspiro[5.5]undec-3-en-5-yl]-4-fluorophenyl}-5-(fluoromethoxy)pyrazine-2-carboxamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004190molecular_functionaspartic-type endopeptidase activity
A0006508biological_processproteolysis
A0016020cellular_componentmembrane
Functional Information from PDB Data
site_idAC1
Number of Residues2
Detailsbinding site for residue IOD A 501
ChainResidue
AGLU128
ASER129

site_idAC2
Number of Residues2
Detailsbinding site for residue IOD A 502
ChainResidue
AGLN79
AARG373

site_idAC3
Number of Residues1
Detailsbinding site for residue IOD A 503
ChainResidue
ALYS131

site_idAC4
Number of Residues1
Detailsbinding site for residue IOD A 505
ChainResidue
AARG120

site_idAC5
Number of Residues4
Detailsbinding site for residue GOL A 507
ChainResidue
ASER211
AARG74
ATYR75
AGLN77

site_idAC6
Number of Residues16
Detailsbinding site for residue C7O A 508
ChainResidue
AGLY35
AGLN36
AGLY37
AASP56
AGLY58
ATYR95
APHE132
AILE134
AILE142
AASP252
ASER253
AGLY254
ATHR255
ATHR256
AARG331
AALA359

Functional Information from PROSITE/UniProt
site_idPS00141
Number of Residues12
DetailsASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ILVDTGSSNFAV
ChainResidueDetails
AILE53-VAL64

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10094","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues7
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"17425515","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19011241","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues3
DetailsGlycosylation: {"description":"N-linked (GlcNAc...) asparagine","evidences":[{"evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

246704

PDB entries from 2025-12-24

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