Structure of PDB 1li7 Chain B Binding Site BS01
Receptor Information
>1li7 Chain B (length=375) Species:
562
(Escherichia coli) [
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MLKIFNTLTRQKEEFKPIHAGEVGMYVCGITVYDLCHIGHGRTFVAFDVV
ARYLRFLGYKLKYVRNITDIDDKIIKRESFVAMVDRMIAEMHKDFDALNI
LRPDMEPRATHHIAEIIELTEQLIAKGHAYVADNGDVMFDVPTDPTYGVL
SRQRNPMDFVLWKMSKEGEPSWPSPWGAGRPGWHIECSAMNCKQLGNHFD
IHGGGSDLMFPHHENEIAQSTCAHDGQYVNYWMHSGMVMVDREKMNFFTV
RDVLKYYDAETVRYFLMSGHYRSQLNYSEENLKQARAALERLYTALRGTD
KTVAPAGGEAFEARFIEAMDDDFNTPEAYSVLFDMAREVNRLKAEDMAAA
NAMASHLRKLSAVLGLLEQEPEAFL
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1li7 Chain B Residue 964 [
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Receptor-Ligand Complex Structure
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PDB
1li7
Structural origins of amino acid selection without editing by cysteinyl-tRNA synthetase
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
C209 H234
Binding residue
(residue number reindexed from 1)
C187 H212
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H37 H40
Catalytic site (residue number reindexed from 1)
H37 H40
Enzyme Commision number
6.1.1.16
: cysteine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004817
cysteine-tRNA ligase activity
GO:0005524
ATP binding
GO:0008270
zinc ion binding
GO:0016874
ligase activity
GO:0046872
metal ion binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006423
cysteinyl-tRNA aminoacylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1li7
,
PDBe:1li7
,
PDBj:1li7
PDBsum
1li7
PubMed
12032090
UniProt
P21888
|SYC_ECOLI Cysteine--tRNA ligase (Gene Name=cysS)
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