Structure of PDB 4inu Chain Y Binding Site BS01
Receptor Information
>4inu Chain Y (length=212) Species:
4932
(Saccharomyces cerevisiae) [
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TTTLAFRFQGGIIVAVDSRATAGNWVASQTVKKVIEINPFLLGTMAGGAA
DCQFWETWLGSQCRLHELREKERISVAAASKILSNLVYQYKGAGLSMGTM
ICGYTRKEGPTIYYVDSDGTRLKGDIFCVGSGQTFAYGVLDSNYKWDLSV
EDALYLGKRSILAAAHRDAYSGGSVNLYHVTEDGWIYHGNHDVGELFWKV
KEEEGSFNNVIG
Ligand information
Ligand ID
1G6
InChI
InChI=1S/C37H50N8O5S/c1-25(2)19-32(35(46)41-31(17-18-51(3,49)50)20-27-9-13-29(23-38)14-10-27)42-36(47)33(21-28-11-15-30(24-39)16-12-28)43-37(48)34(44-45-40)22-26-7-5-4-6-8-26/h4-16,25,31-34H,17-24,38-39H2,1-3H3,(H,41,46)(H,42,47)(H,43,48)/t31-,32+,33-,34+/m1/s1
InChIKey
QRQMUCDZCOVIHS-ITHRCTNCSA-N
SMILES
Software
SMILES
ACDLabs 12.01
NCc1ccc(CC(CCS(C)(=O)=O)NC(=O)C(CC(C)C)NC(=O)C(Cc2ccc(CN)cc2)NC(=O)C(Cc2ccccc2)\N=[N+]=[N-])cc1
OpenEye OEToolkits 2.0.7
CC(C)C[C@@H](C(=O)N[C@H](CCS(=O)(=O)C)Cc1ccc(cc1)CN)NC(=O)[C@@H](Cc2ccc(cc2)CN)NC(=O)[C@H](Cc3ccccc3)N=[N+]=[N-]
CACTVS 3.385
CC(C)C[CH](NC(=O)[CH](Cc1ccc(CN)cc1)NC(=O)[CH](Cc2ccccc2)N=[N+]=[N-])C(=O)N[CH](CC[S](C)(=O)=O)Cc3ccc(CN)cc3
OpenEye OEToolkits 2.0.7
CC(C)CC(C(=O)NC(CCS(=O)(=O)C)Cc1ccc(cc1)CN)NC(=O)C(Cc2ccc(cc2)CN)NC(=O)C(Cc3ccccc3)N=[N+]=[N-]
CACTVS 3.385
CC(C)C[C@H](NC(=O)[C@@H](Cc1ccc(CN)cc1)NC(=O)[C@H](Cc2ccccc2)N=[N+]=[N-])C(=O)N[C@H](CC[S](C)(=O)=O)Cc3ccc(CN)cc3
Formula
C37 H50 N8 O5 S
Name
N3Phe-Phe(4-NH2CH2)-Leu-Phe(4-NH2CH2)-methyl vinyl sulfone, bound form
ChEMBL
DrugBank
ZINC
PDB chain
4inu Chain Y Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4inu
Incorporation of Non-natural Amino Acids Improves Cell Permeability and Potency of Specific Inhibitors of Proteasome Trypsin-like Sites.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
T1 A20 T21 V31 M45 G47 A49 S131
Binding residue
(residue number reindexed from 1)
T1 A20 T21 V31 M45 G47 A49 S131
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T1 D17 R19 K33 G47 S131 D168 S171
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
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4inu
,
PDBe:4inu
,
PDBj:4inu
PDBsum
4inu
PubMed
23320547
UniProt
P30656
|PSB5_YEAST Proteasome subunit beta type-5 (Gene Name=PRE2)
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