Structure of PDB 3sdi Chain Y Binding Site BS01
Receptor Information
>3sdi Chain Y (length=212) Species:
559292
(Saccharomyces cerevisiae S288C) [
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TTTLAFRFQGGIIVAVDSRATAGNWVASQTVKKVIEINPFLLGTMAGGAA
DCQFWETWLGSQCRLHELREKERISVAAASKILSNLVYQYKGAGLSMGTM
ICGYTRKEGPTIYYVDSDGTRLKGDIFCVGSGQTFAYGVLDSNYKWDLSV
EDALYLGKRSILAAAHRDAYSGGSVNLYHVTEDGWIYHGNHDVGELFWKV
KEEEGSFNNVIG
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3sdi Chain Y Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
3sdi
Optimization of a series of dipeptides with a P3 threonine residue as non-covalent inhibitors of the chymotrypsin-like activity of the human 20S proteasome.
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
A163 D166 A167 S169
Binding residue
(residue number reindexed from 1)
A165 D168 A169 S171
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T1 D17 R19 K33 G47 S129 D166 S169
Catalytic site (residue number reindexed from 1)
T1 D17 R19 K33 G47 S131 D168 S171
Enzyme Commision number
3.4.25.1
: proteasome endopeptidase complex.
Gene Ontology
Molecular Function
GO:0004298
threonine-type endopeptidase activity
Biological Process
GO:0051603
proteolysis involved in protein catabolic process
Cellular Component
GO:0005839
proteasome core complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3sdi
,
PDBe:3sdi
,
PDBj:3sdi
PDBsum
3sdi
PubMed
20875739
UniProt
P30656
|PSB5_YEAST Proteasome subunit beta type-5 (Gene Name=PRE2)
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