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3BGC

HIV-1 protease in complex with a benzyl decorated oligoamine

Functional Information from GO Data
ChainGOidnamespacecontents
A0004190molecular_functionaspartic-type endopeptidase activity
A0006508biological_processproteolysis
B0004190molecular_functionaspartic-type endopeptidase activity
B0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 2602
ChainResidue
BTHR74
BASN88
BHOH3015

site_idAC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE LJH A 2501
ChainResidue
ATHR80
AILE84
AHOH3131
BASP25
BGLY27
BALA28
BASP30
BGLY48
BGLY49
BILE50
BTHR80
BILE84
BHOH3150
AASP25
AGLY27
AALA28
AASP30
AGLY48
AILE50

Functional Information from PROSITE/UniProt
site_idPS00141
Number of Residues12
DetailsASP_PROTEASE Eukaryotic and viral aspartyl proteases active site. ALLDTGADDTVL
ChainResidueDetails
AALA22-LEU33

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: For protease activity; shared with dimeric partner => ECO:0000255|PROSITE-ProRule:PRU10094
ChainResidueDetails
AASP25
BASP25

site_idSWS_FT_FI2
Number of Residues2
DetailsSITE: Cleavage; by viral protease => ECO:0000250
ChainResidueDetails
APHE99
BPHE99

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PDB entries from 2024-06-12

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