Structure of PDB 1evl Chain A Binding Site BS01
Receptor Information
>1evl Chain A (length=401) Species:
562
(Escherichia coli) [
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RDHRKIGKQLDLYHMQEEAPGMVFWHNDGWTIFRELEVFVRSKLKEYQYQ
EVKGPFMMDRVLWEKTGHWDNYKDAMFTTSSENREYCIKPMNCPGHVQIF
NQGLKSYRDLPLRMAEFGSCHRNEPSGSLHGLMRVRGFTQDDAHIFCTEE
QIRDEVNGCIRLVYDMYSTFGFEKIVVKLSTRPEKRIGSDEMWDRAEADL
AVALEENNIPFEYQLGEGAFYGPKIEFTLYDCLDRAWQCGTVQLDFSLPS
RLSASYVGEDNERKVPVMIHRAILGSMERFIGILTEEFAGFFPTWLAPVQ
VVIMNITDSQSEYVNELTQKLSNAGIRVKADLRNEKIGFKIREHTLRRVP
YMLVCGDKEVESGKVAVRTRRGKDLGSMDVNEVIEKLQQEIRSRSLKQLE
E
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
1evl Chain A Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
1evl
Zinc ion mediated amino acid discrimination by threonyl-tRNA synthetase.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
C334 H385 H511
Binding residue
(residue number reindexed from 1)
C93 H144 H270
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C334 R363 Q381 D383 H385 K465 H511
Catalytic site (residue number reindexed from 1)
C93 R122 Q140 D142 H144 K224 H270
Enzyme Commision number
6.1.1.3
: threonine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004829
threonine-tRNA ligase activity
GO:0005524
ATP binding
Biological Process
GO:0006418
tRNA aminoacylation for protein translation
GO:0006435
threonyl-tRNA aminoacylation
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:1evl
,
PDBe:1evl
,
PDBj:1evl
PDBsum
1evl
PubMed
10881191
UniProt
P0A8M3
|SYT_ECOLI Threonine--tRNA ligase (Gene Name=thrS)
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