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3WB4

Crystal Structure of beta secetase in complex with 2-amino-3,6-dimethyl-6-(2-phenylethyl)-3,4,5,6-tetrahydropyrimidin-4-one

Functional Information from GO Data
ChainGOidnamespacecontents
A0004190molecular_functionaspartic-type endopeptidase activity
A0006508biological_processproteolysis
A0016020cellular_componentmembrane
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 501
ChainResidue
ASER10
AGLY11
AGLN12
AGLY13
AVAL170
ATHR232
AALA335
AGLU339

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 502
ChainResidue
AASN28
AARG50
AASN114
AGLU17

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 503
ChainResidue
ATYR51
AGLN53
ASER187
AHOH1072

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 504
ChainResidue
ALEU56
AHIS181
ATYR184
AGLY186

site_idAC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE IOD A 505
ChainResidue
AARG96

site_idAC6
Number of Residues1
DetailsBINDING SITE FOR RESIDUE IOD A 506
ChainResidue
ALYS75

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 0B3 A 507
ChainResidue
AASP32
ATYR71
APHE108
AILE118
AASP228
AGLY230
ATHR231

Functional Information from PROSITE/UniProt
site_idPS00141
Number of Residues12
DetailsASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ILVDTGSSNFAV
ChainResidueDetails
AILE29-VAL40

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: ACT_SITE => ECO:0000255|PROSITE-ProRule:PRU10094
ChainResidueDetails
AASP32
AASP228

site_idSWS_FT_FI2
Number of Residues7
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:17425515, ECO:0000269|PubMed:19011241
ChainResidueDetails
ALYS65
ALYS214
ALYS218
ALYS224
ALYS238
ALYS239
ALYS246

site_idSWS_FT_FI3
Number of Residues4
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
AASN92
AASN111
AASN162
AASN293

224004

PDB entries from 2024-08-21

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