Structure of PDB 1dpj Chain A Binding Site BS02
Receptor Information
>1dpj Chain A (length=329) Species:
4932
(Saccharomyces cerevisiae) [
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GGHDVPLTNYLNAQYYTDITLGTPPQNFKVILDTGSSNLWVPSNECGSLA
CFLHSKYDHEASSSYKANGTEFAIQYGTGSLEGYISQDTLSIGDLTIPKQ
DFAEATSEPGLTFAFGKFDGILGLGYDTISVDKVVPPFYNAIQQDLLDEK
RFAFYLGDTSKDTENGGEATFGGIDESKFKGDITWLPVRRKAYWEVKFEG
IGLGDEYAELESHGAAIDTGTSLITLPSGLAEMINAEIGAKKGWTGQYTL
DCNTRDNLPDLIFNFNGYNFTIGPYDYTLEVSGSCISAITPMDFPEPVGP
LAIVGDAFLRKYYSIYDLGNNAVGLAKAI
Ligand information
Ligand ID
MAN
InChI
InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6+/m1/s1
InChIKey
WQZGKKKJIJFFOK-PQMKYFCFSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C1C(C(C(C(O1)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@@H]([C@H](O1)O)O)O)O)O
ACDLabs 10.04
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
alpha-D-mannopyranose;
alpha-D-mannose;
D-mannose;
mannose
ChEMBL
CHEMBL365590
DrugBank
ZINC
ZINC000003860903
PDB chain
1dpj Chain C Residue 8 [
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Receptor-Ligand Complex Structure
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PDB
1dpj
The aspartic proteinase from Saccharomyces cerevisiae folds its own inhibitor into a helix.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
K98 V134
Binding residue
(residue number reindexed from 1)
K99 V135
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D32 S35 N37 W39 Y75 D215 T218
Catalytic site (residue number reindexed from 1)
D33 S36 N38 W40 Y76 D218 T221
Enzyme Commision number
3.4.23.25
: saccharopepsin.
Gene Ontology
Molecular Function
GO:0004190
aspartic-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0000324
fungal-type vacuole
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1dpj
,
PDBe:1dpj
,
PDBj:1dpj
PDBsum
1dpj
PubMed
10655612
UniProt
P07267
|CARP_YEAST Saccharopepsin (Gene Name=PEP4)
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