Structure of PDB 2rhq Chain A Binding Site BS01
Receptor Information
>2rhq Chain A (length=270) Species:
1283
(Staphylococcus haemolyticus) [
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LMEKLNQQLAEETIDVTLPSRQISIGSKHPLTRTVEEIEDLFLGLGYEIV
DGYEVEQDYYNFEALNLPKSHPARDMQDSFYITDEILMRTHTSPVQARTM
EKRNGQGPVKIICPGKVYRRDSDDATHSHQFTQIEGLVVDKNIKMSDLKG
TLELVAKKLFGADREIRLRPSYFPFTEPSVEVDVSCFKCKGKGCNVCKHT
GWIEILGAGMVHPNVLEMAGFDSNEYSGFAFGMGPDRIAMLKYGIEDIRY
FYTNDVRFLEQFKAVEDRGE
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
2rhq Chain A Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
2rhq
Rational protein engineering in action: the first crystal structure of a phenylalanine tRNA synthetase from Staphylococcus haemolyticus.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
C267 C270 C275 C278
Binding residue
(residue number reindexed from 1)
C186 C189 C194 C197
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q158 H172 R200 Q214 T257 A311
Catalytic site (residue number reindexed from 1)
Q77 H91 R119 Q133 T176 A230
Enzyme Commision number
6.1.1.20
: phenylalanine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000049
tRNA binding
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004826
phenylalanine-tRNA ligase activity
GO:0005524
ATP binding
Biological Process
GO:0006432
phenylalanyl-tRNA aminoacylation
GO:0043039
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:2rhq
,
PDBe:2rhq
,
PDBj:2rhq
PDBsum
2rhq
PubMed
18086534
UniProt
Q4L5E3
|SYFA_STAHJ Phenylalanine--tRNA ligase alpha subunit (Gene Name=pheS)
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