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

Chain	GOid	namespace	contents
A	0004190	molecular_function	aspartic-type endopeptidase activity
A	0006508	biological_process	proteolysis
A	0016020	cellular_component	membrane

Functional Information from PDB Data

site_id	AC1
Number of Residues	8
Details	BINDING SITE FOR RESIDUE GOL A 501

Chain	Residue
A	SER10
A	GLY11
A	GLN12
A	GLY13
A	VAL170
A	THR232
A	ALA335
A	GLU339

---

site_id	AC2
Number of Residues	4
Details	BINDING SITE FOR RESIDUE GOL A 502

Chain	Residue
A	ASN28
A	ARG50
A	ASN114
A	GLU17

---

site_id	AC3
Number of Residues	4
Details	BINDING SITE FOR RESIDUE GOL A 503

Chain	Residue
A	TYR51
A	GLN53
A	SER187
A	HOH1072

---

site_id	AC4
Number of Residues	4
Details	BINDING SITE FOR RESIDUE GOL A 504

Chain	Residue
A	LEU56
A	HIS181
A	TYR184
A	GLY186

---

site_id	AC5
Number of Residues	1
Details	BINDING SITE FOR RESIDUE IOD A 505

Chain	Residue
A	ARG96

---

site_id	AC6
Number of Residues	1
Details	BINDING SITE FOR RESIDUE IOD A 506

Chain	Residue
A	LYS75

---

site_id	AC7
Number of Residues	7
Details	BINDING SITE FOR RESIDUE 0B3 A 507

Chain	Residue
A	ASP32
A	TYR71
A	PHE108
A	ILE118
A	ASP228
A	GLY230
A	THR231

---

Functional Information from PROSITE/UniProt

site_id	PS00141
Number of Residues	12
Details	ASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ILVDTGSSNFAV

Chain	Residue	Details
A	ILE29-VAL40

---

Functional Information from SwissProt/UniProt

site_id	SWS_FT_FI1
Number of Residues	2
Details	Active site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10094","evidenceCode":"ECO:0000255"}]}

Chain

Residue

Details

---

site_id	SWS_FT_FI2
Number of Residues	7
Details	Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"17425515","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19011241","evidenceCode":"ECO:0000269"}]}

Chain

Residue

Details

---

site_id	SWS_FT_FI3
Number of Residues	3
Details	Glycosylation: {"description":"N-linked (GlcNAc...) asparagine","evidences":[{"evidenceCode":"ECO:0000255"}]}

Chain

Residue

Details

---