Structure of PDB 4fba Chain B Binding Site BS01
Receptor Information
>4fba Chain B (length=278) Species:
4513
(Hordeum vulgare) [
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KMAKNVDKPLFTATFNVQASSADYATFIAGIRNKLRNPAHFSHNRPVLPP
VEPNVPPSRWFHVVLKASPTSAGLTLAIRADNIYLEGFKSSDGTWWELTP
GLIPGATYVGFGGTYRDLLGDTDKLTNVALGRQQLADAVTALHGRTKADK
PSGPKQQQAREAVTTLLLMVNEATRFQTVSGFVAGLLHPKAVAAASGKIG
NEMKAQVNGWQDLSAALLKTDVKPPPGKSPAKFAPIEKMGVRTAVQAANT
LGILLFVEVPGGLTVAKALELFHASGGK
Ligand information
Ligand ID
ADE
InChI
InChI=1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)
InChIKey
GFFGJBXGBJISGV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Nc1ncnc2[nH]cnc12
OpenEye OEToolkits 1.5.0
c1[nH]c2c(n1)c(ncn2)N
ACDLabs 10.04
n1c(c2ncnc2nc1)N
Formula
C5 H5 N5
Name
ADENINE
ChEMBL
CHEMBL226345
DrugBank
DB00173
ZINC
ZINC000000000882
PDB chain
4fba Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4fba
Structures of the ribosome-inactivating protein from barley seeds reveal a unique activation mechanism.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
Y87 L88 G116 Y118 L170 R178
Binding residue
(residue number reindexed from 1)
Y84 L85 G113 Y115 L167 R175
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.2.2.22
: rRNA N-glycosylase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0030598
rRNA N-glycosylase activity
GO:0090729
toxin activity
Biological Process
GO:0017148
negative regulation of translation
GO:0031640
killing of cells of another organism
GO:0035821
modulation of process of another organism
GO:0050832
defense response to fungus
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4fba
,
PDBe:4fba
,
PDBj:4fba
PDBsum
4fba
PubMed
23090398
UniProt
P22244
|RIP1_HORVU Protein synthesis inhibitor I (Gene Name=RIP30)
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