Structure of PDB 3fhj Chain D Binding Site BS02
Receptor Information
>3fhj Chain D (length=286) Species:
1422
(Geobacillus stearothermophilus) [
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MKTIFSGIQPSGVITIGNYIGALRQFVELQHEYNCYFCIVDQHAITVWQD
PHELRQNIRRLAALYLAVGIDPTQATLFIQSEVPAHAQAAWMLQCIVYIG
ELERMTQVSAGLLTYPPLMAADILLYNTDIVPVGEDQKQHIELTRDLAER
FFTIPEARIPKVGARIMSLVDPTKKMSKSDPNPKAYITLLDDAKTIEKKI
KSAISNLLNIYSTLSGQSIEELERQYVFKADLAQVVIETLRPIQERYHHW
MESEELDRVLDEGAEKANRVASEMVRKMEQAMGLGR
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
3fhj Chain D Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
3fhj
Independent saturation of three TrpRS subsites generates a partially assembled state similar to those observed in molecular simulations.
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
K192 S194 K195
Binding residue
(residue number reindexed from 1)
K175 S177 K178
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K192 K195
Catalytic site (residue number reindexed from 1)
K175 K178
Enzyme Commision number
6.1.1.2
: tryptophan--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004830
tryptophan-tRNA ligase activity
GO:0005524
ATP binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006436
tryptophanyl-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:3fhj
,
PDBe:3fhj
,
PDBj:3fhj
PDBsum
3fhj
PubMed
19174517
UniProt
P00953
|SYW_GEOSE Tryptophan--tRNA ligase (Gene Name=trpS)
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