Entity Details

Primary name TLK2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ86UE8
EntryNameTLK2_HUMAN
FullNameSerine/threonine-protein kinase tousled-like 2
TaxID9606
Evidenceevidence at protein level
Length772
SequenceStatuscomplete
DateCreated2003-08-22
DateModified2021-06-02

Ontological Relatives

GenesTLK2

GO terms

Show/Hide Table
GOName
GO:0001672 regulation of chromatin assembly or disassembly
GO:0004674 protein serine/threonine kinase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005882 intermediate filament
GO:0006325 chromatin organization
GO:0006468 protein phosphorylation
GO:0006974 cellular response to DNA damage stimulus
GO:0007049 cell cycle
GO:0007059 chromosome segregation
GO:0010507 negative regulation of autophagy
GO:0018105 peptidyl-serine phosphorylation
GO:0032435 negative regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0035556 intracellular signal transduction
GO:0042802 identical protein binding
GO:0048471 perinuclear region of cytoplasm
GO:0071480 cellular response to gamma radiation
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR000719 Protein kinase domainDomainDomain
IPR008271 Serine/threonine-protein kinase, active siteSiteActive site
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR017441 Protein kinase, ATP binding siteSiteBinding site
IPR027086 Serine/threonine-protein kinase TOUSLED-like 2FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
618050 OMIMMental retardation, autosomal dominant 57 (MRD57)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRD57 is characterized by delayed psychomotor development apparent in infancy or early childhood, and a variety of behavioral abnormalities. Affected individuals may have severe gastro-intestinal problems, and facial dysmorphism. MRD57 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry.

Drugs

Show/Hide Table
DrugNameSourceType
DB12010 FostamatinibDrugbanksmall molecule

Interactions

26 interactions

InteractorPartnerSourcesPublicationsLink
TLK2_HUMANASF1B_HUMANBioGRID, HPRD, IntAct, MINT11470414 17353931 17940067 20016786 24981860 28514442 details
TLK2_HUMANIRF4_HUMANBioGRID, IntAct21903422 details
TLK2_HUMANIRF7_HUMANBioGRID, IntAct21903422 details
TLK2_HUMANASF1A_HUMANBioGRID, HPRD, IntAct, MINT11470414 20016786 24981860 26496610 28514442 34079125 details
TLK2_HUMANPAX6_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANTLK2_HUMANBioGRID, HPRD, IntAct10523312 32296183 details
TLK2_HUMANCEP70_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANGMCL1_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANFRMD6_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANPAX5_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANDMAP1_HUMANBioGRID, IntAct32296183 details
TLK2_HUMANFEZ1_HUMANBioGRID, HPRD16484223 details
TLK2_HUMANFEZ2_HUMANBioGRID16484223 details
TLK2_HUMANAURKA_HUMANBioGRID17940067 details
TLK2_HUMANUBC9_HUMANBioGRID32296183 details
TLK2_HUMANDYL1_HUMANBioGRID, IntAct26496610 27173435 unassigned1312 details
TLK2_HUMANDYL2_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANIFFO1_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANCOBL1_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANAMOL1_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANCDAC1_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANSCML1_HUMANBioGRID, IntAct27173435 unassigned1312 details
TLK2_HUMANTLK1_HUMANBioGRID, HPRD, IntAct10523312 28514442 details
TLK2_HUMANTULP3_HUMANBioGRID33187986 details
TLK2_HUMAN1433Z_HUMANHPRD10455159 details
TLK2_HUMANMBP_HUMANHPRD10523312 details