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Conserved domains on  [gi|47059108|ref|NP_034348|]
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four-jointed box protein 1 precursor [Mus musculus]

Protein Classification

Four-jointed-like_C domain-containing protein( domain architecture ID 10180060)

Four-jointed-like_C domain-containing protein

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
Four-jointed-like_C cd10468
C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; ...
146-430 5.31e-165

C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; Drosophila Fj is a Golgi type II transmembrane protein that is partially secreted, and is a kinase that phosphorylates Ser or Thr residues within extracellular cadherin domains of a transmembrane receptor Fat and its ligand, Dachsous (Ds). Mutation of three conserved Asp residues at the Drosophila Fj putative active site abolished its ability to phosphorylate Ft and Ds cadherin domains. The Fat signaling pathway regulates growth, gene expression, and planar cell polarity (PCP). Defects from mutation in Drosophila Fj include loss of the intermediate leg joint, and a PCP defect in the eye. The expression of the Drospophila fj gene is modulated by Notch, Unpaired (JAK/STAT), and Wingless signals. Mouse Fjx1, has been shown to be involved in both the Fat and Hippo signaling pathways; these two pathways intersect at multiple points. The Hippo pathway is important in organ size control and in cancer. The expression of the mouse fjx1 gene is also Notch dependent; fjx1 is expressed in the brain, the peripheral nervous system, in epithelial structures of different organs, and during limb development.


:

Pssm-ID: 198459  Cd Length: 286  Bit Score: 465.80  E-value: 5.31e-165
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 146 EVARGARVVaLDRGGCGRSSNRLARFADGTRACVRYGINPEQIQGEALSYYLARLLGLqRHVPPLALARVEARGAQWVQV 225
Cdd:cd10468   1 EFARQSRVV-RLEEGCGRMQNRLATFADGTRACVRYRINTDQIQGEIFSYYLARLLGL-RNLPPLALGLVEARGAQWVAV 78
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 226 QEELRTAHWTEGSVVSLTRWLPNLTDVVVPEPWRSEDGRLRPLRDAGGEL-TNLSQAELVDLVQWTDLILFDYLTANFDR 304
Cdd:cd10468  79 QSELRQAQWTERRPVVLTRWLPNLTPAVIPAPFRSEDRRLNPLDVAGGTLqNGLSQAELVELAQWSDLIVFDYLTANLDR 158
                       170       180       190       200       210       220       230       240
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 305 LVSNLFSLQWDPRVMHRATSNLHRGPG-GALVFLDNEAGLVHGYRVAGMWDKYNEPLLQSVCVFRERTARRVLELHRGQD 383
Cdd:cd10468 159 LVNNLYNLQWNPAVMDRPTHNLARTPHsGLLVFLDNESGLLHGYRLLDKYEKYHSPLLQSLCVFRKRTAERVRELHRGQD 238
                       250       260       270       280
                ....*....|....*....|....*....|....*....|....*...
gi 47059108 384 AAARLLRLYSRHEP-RFPELAELSEPHAQLLQRRLDFLAKHILHCKAK 430
Cdd:cd10468 239 AGARLLDLYRRHEPgVFDELPSLPDKSAQILQERIDQVYKHILKCKSK 286
 
Name Accession Description Interval E-value
Four-jointed-like_C cd10468
C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; ...
146-430 5.31e-165

C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; Drosophila Fj is a Golgi type II transmembrane protein that is partially secreted, and is a kinase that phosphorylates Ser or Thr residues within extracellular cadherin domains of a transmembrane receptor Fat and its ligand, Dachsous (Ds). Mutation of three conserved Asp residues at the Drosophila Fj putative active site abolished its ability to phosphorylate Ft and Ds cadherin domains. The Fat signaling pathway regulates growth, gene expression, and planar cell polarity (PCP). Defects from mutation in Drosophila Fj include loss of the intermediate leg joint, and a PCP defect in the eye. The expression of the Drospophila fj gene is modulated by Notch, Unpaired (JAK/STAT), and Wingless signals. Mouse Fjx1, has been shown to be involved in both the Fat and Hippo signaling pathways; these two pathways intersect at multiple points. The Hippo pathway is important in organ size control and in cancer. The expression of the mouse fjx1 gene is also Notch dependent; fjx1 is expressed in the brain, the peripheral nervous system, in epithelial structures of different organs, and during limb development.


Pssm-ID: 198459  Cd Length: 286  Bit Score: 465.80  E-value: 5.31e-165
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 146 EVARGARVVaLDRGGCGRSSNRLARFADGTRACVRYGINPEQIQGEALSYYLARLLGLqRHVPPLALARVEARGAQWVQV 225
Cdd:cd10468   1 EFARQSRVV-RLEEGCGRMQNRLATFADGTRACVRYRINTDQIQGEIFSYYLARLLGL-RNLPPLALGLVEARGAQWVAV 78
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 226 QEELRTAHWTEGSVVSLTRWLPNLTDVVVPEPWRSEDGRLRPLRDAGGEL-TNLSQAELVDLVQWTDLILFDYLTANFDR 304
Cdd:cd10468  79 QSELRQAQWTERRPVVLTRWLPNLTPAVIPAPFRSEDRRLNPLDVAGGTLqNGLSQAELVELAQWSDLIVFDYLTANLDR 158
                       170       180       190       200       210       220       230       240
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 305 LVSNLFSLQWDPRVMHRATSNLHRGPG-GALVFLDNEAGLVHGYRVAGMWDKYNEPLLQSVCVFRERTARRVLELHRGQD 383
Cdd:cd10468 159 LVNNLYNLQWNPAVMDRPTHNLARTPHsGLLVFLDNESGLLHGYRLLDKYEKYHSPLLQSLCVFRKRTAERVRELHRGQD 238
                       250       260       270       280
                ....*....|....*....|....*....|....*....|....*...
gi 47059108 384 AAARLLRLYSRHEP-RFPELAELSEPHAQLLQRRLDFLAKHILHCKAK 430
Cdd:cd10468 239 AGARLLDLYRRHEPgVFDELPSLPDKSAQILQERIDQVYKHILKCKSK 286
Fam20C pfam06702
Golgi casein kinase, C-terminal, Fam20; Fam20C represents the C-terminus of eukaryotic ...
240-434 2.26e-07

Golgi casein kinase, C-terminal, Fam20; Fam20C represents the C-terminus of eukaryotic secreted Golgi casein kinase proteins. Fam20C is the Golgi casein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs. Mutations in Fam20C cause Raine syndrome, an autosomal recessive osteosclerotic bone dysplasia.


Pssm-ID: 461992  Cd Length: 218  Bit Score: 51.44  E-value: 2.26e-07
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108   240 VSLTRWLPNLTDV---VVPEPWRsedgrlRPLRDAGGEL--------TNLSQAE-------LVDLVqwtDLILFDYLTAN 301
Cdd:pfam06702  34 GSLAAFLPDLSLAprkSWRHPWR------RSYSKRKKAEwevdpdycDKVKQTPpydsgrrLLDLI---DMAIFDFLIGN 104
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108   302 FDRlvsnlfslqwdprvmHRATSNLHRGPGGALVFLDNEAGLvhgyrvaGMWDKyNE-----PLLQSvCVFRERTARRVL 376
Cdd:pfam06702 105 MDR---------------HHYETFEKFGNETFLLHLDNGRGF-------GRPSH-DElsilaPLYQC-CIIRKSTLLRLL 160
                         170       180       190       200       210
                  ....*....|....*....|....*....|....*....|....*....|....*...
gi 47059108   377 ELHRGQDAAARLLRLYSRHEPRFPELAElsePHAQLLQRRLDFLAKHILHCKAKYGRR 434
Cdd:pfam06702 161 LLSGGPYRLSDLMRESLSSDPLAPILTE---PHLEALDRRLLIVLATVQKCIEKKGED 215
 
Name Accession Description Interval E-value
Four-jointed-like_C cd10468
C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; ...
146-430 5.31e-165

C-terminal kinase domain of Drosophila Four-jointed (Fj), mouse Fjx1, and related proteins; Drosophila Fj is a Golgi type II transmembrane protein that is partially secreted, and is a kinase that phosphorylates Ser or Thr residues within extracellular cadherin domains of a transmembrane receptor Fat and its ligand, Dachsous (Ds). Mutation of three conserved Asp residues at the Drosophila Fj putative active site abolished its ability to phosphorylate Ft and Ds cadherin domains. The Fat signaling pathway regulates growth, gene expression, and planar cell polarity (PCP). Defects from mutation in Drosophila Fj include loss of the intermediate leg joint, and a PCP defect in the eye. The expression of the Drospophila fj gene is modulated by Notch, Unpaired (JAK/STAT), and Wingless signals. Mouse Fjx1, has been shown to be involved in both the Fat and Hippo signaling pathways; these two pathways intersect at multiple points. The Hippo pathway is important in organ size control and in cancer. The expression of the mouse fjx1 gene is also Notch dependent; fjx1 is expressed in the brain, the peripheral nervous system, in epithelial structures of different organs, and during limb development.


Pssm-ID: 198459  Cd Length: 286  Bit Score: 465.80  E-value: 5.31e-165
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 146 EVARGARVVaLDRGGCGRSSNRLARFADGTRACVRYGINPEQIQGEALSYYLARLLGLqRHVPPLALARVEARGAQWVQV 225
Cdd:cd10468   1 EFARQSRVV-RLEEGCGRMQNRLATFADGTRACVRYRINTDQIQGEIFSYYLARLLGL-RNLPPLALGLVEARGAQWVAV 78
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 226 QEELRTAHWTEGSVVSLTRWLPNLTDVVVPEPWRSEDGRLRPLRDAGGEL-TNLSQAELVDLVQWTDLILFDYLTANFDR 304
Cdd:cd10468  79 QSELRQAQWTERRPVVLTRWLPNLTPAVIPAPFRSEDRRLNPLDVAGGTLqNGLSQAELVELAQWSDLIVFDYLTANLDR 158
                       170       180       190       200       210       220       230       240
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 305 LVSNLFSLQWDPRVMHRATSNLHRGPG-GALVFLDNEAGLVHGYRVAGMWDKYNEPLLQSVCVFRERTARRVLELHRGQD 383
Cdd:cd10468 159 LVNNLYNLQWNPAVMDRPTHNLARTPHsGLLVFLDNESGLLHGYRLLDKYEKYHSPLLQSLCVFRKRTAERVRELHRGQD 238
                       250       260       270       280
                ....*....|....*....|....*....|....*....|....*...
gi 47059108 384 AAARLLRLYSRHEP-RFPELAELSEPHAQLLQRRLDFLAKHILHCKAK 430
Cdd:cd10468 239 AGARLLDLYRRHEPgVFDELPSLPDKSAQILQERIDQVYKHILKCKSK 286
FAM20_C_like cd10467
C-terminal putative kinase domain of FAM20 (family with sequence similarity 20), Drosophila ...
147-430 1.11e-60

C-terminal putative kinase domain of FAM20 (family with sequence similarity 20), Drosophila Four-jointed (Fj), and related proteins; Drosophila Fj is a Golgi kinase that phosphorylates Ser or Thr residues within extracellular cadherin domains of a transmembrane receptor Fat and its ligand, Dachsous (Ds). The Fat signaling pathway regulates growth, gene expression, and planar cell polarity (PCP). Defects from mutation in the Drosophila fj gene include loss of the intermediate leg joint, and a PCP defect in the eye. Fjx1, the murine homologue of Fj, has been shown to be involved in both the Fat and Hippo signaling pathways, these two pathways intersect at multiple points. The Hippo pathway is important in organ size control and in cancer. FAM20B is a xylose kinase that may regulate the number of glycosaminoglycan chains by phosphorylating the xylose residue in the glycosaminoglycan-protein linkage region of proteoglycans. This domain has homology to a kinase-active site, mutation of three conserved Asp residues at the Drosophila Fj putative active site abolished its ability to phosphorylate Ft and Ds cadherin domains. FAM20A may participate in enamel development and gingival homeostasis, FAM20B in proteoglycan production, and FAM20C in bone development. FAM20C, also called Dentin Matrix Protein 4, is abundant in the dentin matrix, and may participate in the differentiation of mesenchymal precursor cells into functional odontoblast-like cells. Mutations in FAM20C are associated with lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), and mutations in FAM20A with Amelogenesis imperfecta (AI) and Gingival Hyperplasia Syndrome. This model includes the FAM20_C domain family, previously known as DUF1193; FAM20_C appears to be homologous to the catalytic domain of the phosphoinositide 3-kinase (PI3K)-like family.


Pssm-ID: 198458  Cd Length: 210  Bit Score: 196.71  E-value: 1.11e-60
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 147 VARGARVvaLDRGGCGrssnrlARFADGTRACVrygiNPEQIQGEALSYYLARLLGLqrhvpplalarveargaqwVQVQ 226
Cdd:cd10467   2 FSPANNT--CFYGGCG------YYCKTEEAACG----NPDQIEGSLTSFLPDLLLLL-------------------RKKW 50
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 227 EELRTAHWTEGSVvslTRWLPNLTDVvvpepwrSEDGRLRPLRDAggeltnlsqaelVDLVQWTDLILFDYLTANFDRLV 306
Cdd:cd10467  51 RHPWQRTYTERKK---AEWEVDLDYC-------DEVKKLPPYDSG------------RRLLDLIDMAIFDFLIGNMDRHH 108
                       170       180       190       200       210       220       230       240
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 307 SNLFSLQWDprvmhratsnlhrgpGGALVFLDNEAGLVhgyRVAGMWDKYNEPLLQsVCVFRERTARRVLELHRGQDAAA 386
Cdd:cd10467 109 YELFELQWN---------------EGFLIHLDNGKGFG---RPSHDELSILAPLYQ-CCVIRKSTWERLLLLHRGGGVLS 169
                       250       260       270       280
                ....*....|....*....|....*....|....*....|....
gi 47059108 387 RLLRLYSRHEprfPELAELSEPHAQLLQRRLDFLAKHILHCKAK 430
Cdd:cd10467 170 RLLRESLRHD---PLLPVLTEPHLQALDRRLDIVLATVEKCIEK 210
Fam20C pfam06702
Golgi casein kinase, C-terminal, Fam20; Fam20C represents the C-terminus of eukaryotic ...
240-434 2.26e-07

Golgi casein kinase, C-terminal, Fam20; Fam20C represents the C-terminus of eukaryotic secreted Golgi casein kinase proteins. Fam20C is the Golgi casein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs. Mutations in Fam20C cause Raine syndrome, an autosomal recessive osteosclerotic bone dysplasia.


Pssm-ID: 461992  Cd Length: 218  Bit Score: 51.44  E-value: 2.26e-07
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108   240 VSLTRWLPNLTDV---VVPEPWRsedgrlRPLRDAGGEL--------TNLSQAE-------LVDLVqwtDLILFDYLTAN 301
Cdd:pfam06702  34 GSLAAFLPDLSLAprkSWRHPWR------RSYSKRKKAEwevdpdycDKVKQTPpydsgrrLLDLI---DMAIFDFLIGN 104
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108   302 FDRlvsnlfslqwdprvmHRATSNLHRGPGGALVFLDNEAGLvhgyrvaGMWDKyNE-----PLLQSvCVFRERTARRVL 376
Cdd:pfam06702 105 MDR---------------HHYETFEKFGNETFLLHLDNGRGF-------GRPSH-DElsilaPLYQC-CIIRKSTLLRLL 160
                         170       180       190       200       210
                  ....*....|....*....|....*....|....*....|....*....|....*...
gi 47059108   377 ELHRGQDAAARLLRLYSRHEPRFPELAElsePHAQLLQRRLDFLAKHILHCKAKYGRR 434
Cdd:pfam06702 161 LLSGGPYRLSDLMRESLSSDPLAPILTE---PHLEALDRRLLIVLATVQKCIEKKGED 215
FAM20_C cd10314
C-terminal putative kinase domain of FAM20 (family with sequence similarity 20) proteins; This ...
236-432 1.10e-04

C-terminal putative kinase domain of FAM20 (family with sequence similarity 20) proteins; This family contains the C-terminal domain of FAM20A, -B, -C and related proteins. FAM20A may participate in enamel development and gingival homeostasis, FAM20B in proteoglycan production, and FAM20C in bone development. FAM20B is a xylose kinase that may regulate the number of glycosaminoglycan chains by phosphorylating the xylose residue in the glycosaminoglycan-protein linkage region of proteoglycans. FAM20C, also called Dentin Matrix Protein 4, is abundant in the dentin matrix, and may participate in the differentiation of mesenchymal precursor cells into functional odontoblast-like cells. Mutations in FAM20C are associated with lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), and mutations in FAM20A with Amelogenesis imperfecta (AI) and Gingival Hyperplasia Syndrome. The C-terminal domains of members of this family are putative kinase domains, based on mutagenesis of the C-terminal domain of Drosophila Four-Jointed, a related Golgi kinase. This domain family is also known as DUF1193.


Pssm-ID: 198457  Cd Length: 209  Bit Score: 43.41  E-value: 1.10e-04
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 236 EGSvvsLTRWLPNLTDVV-VPEPWR---SEDGRlrplrdAGGELTNL------------SQAELVDLVqwtDLILFDYLT 299
Cdd:cd10314  31 EGS---LTAFLPDLSLLKkWRHPWRrtyHKRKK------AEWEVDPDycdkvkktppydSGRRLLDLI---DMAIFDFLI 98
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 300 ANFDRlvsnlfslqwdprvmHRATSNLHRGPGGALVFLDNEAGLvhgyrvaGMWDKyNE-----PLLQsVCVFRERTARR 374
Cdd:cd10314  99 GNMDR---------------HHYETFEKFGNETFLIHLDNGKSF-------GNPSH-DElsilaPLYQ-CCLIRKSTWLR 154
                       170       180       190       200       210
                ....*....|....*....|....*....|....*....|....*....|....*...
gi 47059108 375 VLELHRGQDAAARLLRLYSRHEPRFPELAElsePHAQLLQRRLDFLAKHILHCKAKYG 432
Cdd:cd10314 155 LQLLAKGGGSLSDLLRESLSHDPLSPVLTE---PHLDALDRRLLIVLATVEDCIEKNG 209
FAM20A_C cd10469
C-terminal putative kinase domain of FAM20A; Human FAM20A may play a fundamental role in ...
233-433 2.00e-03

C-terminal putative kinase domain of FAM20A; Human FAM20A may play a fundamental role in enamel development and gingival homeostasis as mutations in FAM20A may underlie the pathogenesis of the autosomal recessive Amelogenesis imperfecta (AI) and Gingival Hyperplasia Syndrome. It is expressed in ameloblasts and gingivae. AI refers to a heterogeneous group of disorders of biomineralization caused by a lack of normal enamel formation. Mouse FAM20A is a secreted protein and the gene encoding it is differentially expressed in hematopoietic cells undergoing myeloid differentiation. This protein has also been associated with growth disorder in mice. The C-terminal domain of FAM20A is a putative kinase domain, based on mutagenesis of the C-terminal domain of Drosophila Four-Jointed, a related Golgi kinase. This subfamily belongs to the FAM20_C (also known as DUF1193) domain family.


Pssm-ID: 198460  Cd Length: 217  Bit Score: 39.55  E-value: 2.00e-03
                        10        20        30        40        50        60        70        80
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 233 HWTEGSvvsLTRWLPNLT---DVVVPEPW-RS------EDGRLRPLR-DAGGELTNLSQAElvDLVQWTDLILFDYLTAN 301
Cdd:cd10469  29 HLLEGS---LSAFLPSLNlapRLSIPNPWiRSytfagkEEWEVNPLYcDTVKEIYPYNSGN--RLLNIIDMAIFDFLIGN 103
                        90       100       110       120       130       140       150       160
                ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 47059108 302 FDRLVSNLFSlqwdprvmhratsnlHRGPGGALVFLDNEAGL-VHGYRVAGMWdkynEPLLQsVCVFRERTARRVLELHR 380
Cdd:cd10469 104 MDRHHYEMFT---------------KFGDDGFLLHLDNARGFgKHSHDEISIL----SPLSQ-CCIIKKSTLLRLQLLAQ 163
                       170       180       190       200       210
                ....*....|....*....|....*....|....*....|....*....|....*.
gi 47059108 381 GQDAAARLLR---LYSRHEPrfpelaELSEPHAQLLQRRLDFLAKHILHCKAKYGR 433
Cdd:cd10469 164 PDYRLSDVMReslEKDALQP------VLTEPHLLALDRRLQKILRTVERCIRALGK 213
 
Blast search parameters
Data Source: Precalculated data, version = cdd.v.3.21
Preset Options:Database: CDSEARCH/cdd   Low complexity filter: no  Composition Based Adjustment: yes   E-value threshold: 0.01

References:

  • Wang J et al. (2023), "The conserved domain database in 2023", Nucleic Acids Res.51(D)384-8.
  • Lu S et al. (2020), "The conserved domain database in 2020", Nucleic Acids Res.48(D)265-8.
  • Marchler-Bauer A et al. (2017), "CDD/SPARCLE: functional classification of proteins via subfamily domain architectures.", Nucleic Acids Res.45(D)200-3.
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