Structure of PDB 1aha Chain A Binding Site BS01
Receptor Information
>1aha Chain A (length=246) Species:
3673
(Momordica charantia) [
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DVSFRLSGADPRSYGMFIKDLRNALPFREKVYNIPLLLPSVSGAGRYLLM
HLFNYDGKTITVAVDVTNVYIMGYLADTTSYFFNEPAAELASQYVFRDAR
RKITLPYSGNYERLQIAAGKPREKIPIGLPALDSAISTLLHYDSTAAAGA
LLVLIQTTAEAARFKYIEQQIQERAYRDEVPSLATISLENSWSGLSKQIQ
LAQGNNGIFRTPIVLVDNKGNRVQITNVTSKVVTSNIQLLLNTRNI
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
1aha Chain A Residue 339 [
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Receptor-Ligand Complex Structure
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PDB
1aha
The N-glycosidase mechanism of ribosome-inactivating proteins implied by crystal structures of alpha-momorcharin.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Y70 I71 G109 Y111 I155 R163
Binding residue
(residue number reindexed from 1)
Y70 I71 G109 Y111 I155 R163
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
I71 E160 R163
Catalytic site (residue number reindexed from 1)
I71 E160 R163
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:0006952
defense response
GO:0017148
negative regulation of translation
GO:0035821
modulation of process of another organism
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Molecular Function
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Biological Process
External links
PDB
RCSB:1aha
,
PDBe:1aha
,
PDBj:1aha
PDBsum
1aha
PubMed
8075985
UniProt
P16094
|RIP1_MOMCH Ribosome-inactivating protein momordin I
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