Structure of PDB 2i4o Chain B Binding Site BS01
Receptor Information
>2i4o Chain B (length=441) Species:
1076
(Rhodopseudomonas palustris) [
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GSHMRLSRFFLPILKENPKEAEIVSHRLMLRAGMLRQEAAGIYAWLPLGH
RVLKKIEQIVREEQNRAGAIELLMPTLQLADLWRESGRYDAYGPEMLRIA
DRHKRELLYGPTNEEMITEIFRAYIKSYKSLPLNLYHIQWKFRDEQRPRF
GVMRGREFLMKDAYSFDVDEAGARKSYNKMFVAYLRTFARMGLKAIPMRA
ETGPIGGDLSHEFIVLAETGESGVYIDRDVLNLPVPDENVDYDGDLTPII
KQWTSVYAATEDVHEPARYESEVPEANRLNTRGIEVGQIFYFGTKYSDSM
KANVTGPDGTDAPIHGGSYGVGVSRLLGAIIEACHDDNGIIWPEAVAPFR
VTILNLKQGDAATDAACDQLYRELSAKGVDVLYDDTDQRAGAKFATADLI
GIPWQIHVGPRGLAEGKVELKRRSDGARENLALADVVARLT
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
2i4o Chain B Residue 439 [
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Receptor-Ligand Complex Structure
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PDB
2i4o
Structures of Two Bacterial Prolyl-tRNA Synthetases with and without a cis-Editing Domain.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
E282 Q285
Binding residue
(residue number reindexed from 1)
E285 Q288
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E111 R140 M157 D159 Y161 I246 H312
Catalytic site (residue number reindexed from 1)
E114 R143 M160 D162 Y164 I249 H315
Enzyme Commision number
6.1.1.15
: proline--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004827
proline-tRNA ligase activity
GO:0005524
ATP binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006433
prolyl-tRNA aminoacylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2i4o
,
PDBe:2i4o
,
PDBj:2i4o
PDBsum
2i4o
PubMed
17027500
UniProt
Q6N5P6
|SYP_RHOPA Proline--tRNA ligase (Gene Name=proS)
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