Entity Details

Primary name SYFB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NSD9
EntryNameSYFB_HUMAN
FullNamePhenylalanine--tRNA ligase beta subunit
TaxID9606
Evidenceevidence at protein level
Length589
SequenceStatuscomplete
DateCreated2000-12-08
DateModified2021-06-02

Ontological Relatives

GenesFARSB

GO terms

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GOName
GO:0000287 magnesium ion binding
GO:0003723 RNA binding
GO:0004826 phenylalanine-tRNA ligase activity
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006412 translation
GO:0006418 tRNA aminoacylation for protein translation
GO:0006432 phenylalanyl-tRNA aminoacylation
GO:0009328 phenylalanine-tRNA ligase complex
GO:0016020 membrane
GO:0051290 protein heterotetramerization

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR004531 Phenylalanyl-tRNA synthetase, class IIc, beta subunit, archael/eukaryotic typeFamilyFamily
IPR005146 B3/B4 tRNA-binding domainDomainDomain
IPR005147 tRNA synthetase, B5-domainDomainDomain
IPR009061 Putative DNA-binding domain superfamilyFamilyHomologous superfamily
IPR020825 Phenylalanyl-tRNA synthetase-like, B3/B4FamilyHomologous superfamily
IPR040659 Phenylalanine--tRNA ligase beta subunit, B1 domainDomainDomain
IPR041616 Phenylalanyl tRNA synthetase beta chain, core domainDomainDomain

Diseases

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Disease IDSourceNameDescription
613658 OMIMRajab interstitial lung disease with brain calcifications (RILDBC)An autosomal recessive, lethal neurodevelopmental disorder characterized by multiple clinical manifestations including intrauterine growth restriction, failure to thrive, developmental delay, hypotonia, interstitial lung disease, and liver dysfunction. Brain imaging shows abnormal periventricular white matter, basal ganglia echogenicity, cerebral volume loss, incomplete closure of the Sylvian fissures, and normal myelination. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00120 PhenylalanineDrugbanksmall molecule