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Conserved domains on  [gi|24585240|ref|NP_609971|]
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uncharacterized protein Dmel_CG13084 [Drosophila melanogaster]

Protein Classification

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
PRK10263 super family cl35903
DNA translocase FtsK; Provisional
260-445 1.37e-05

DNA translocase FtsK; Provisional


The actual alignment was detected with superfamily member PRK10263:

Pssm-ID: 236669 [Multi-domain]  Cd Length: 1355  Bit Score: 47.77  E-value: 1.37e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   260 QQPYPQYGHHDESYLPTYGAEVPEPQHAHP--KPKQVDLEQVWSIKEEPKHGEHSGNHKATAYAQSPEPKKNYQSSSAVS 337
Cdd:PRK10263  367 QTGEPVIAPAPEGYPQQSQYAQPAVQYNEPlqQPVQPQQPYYAPAAEQPAQQPYYAPAPEQPAQQPYYAPAPEQPVAGNA 446
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   338 WrqtVPWEYGSPYQSAPVHHhqpwnpapahvptsvtkpkpcPKKEHPTPASYVPlPHDQPESYKLPVDYSPKPNHEQPhK 417
Cdd:PRK10263  447 W---QAEEQQSTFAPQSTYQ---------------------TEQTYQQPAAQEP-LYQQPQPVEQQPVVEPEPVVEET-K 500
                         170       180
                  ....*....|....*....|....*...
gi 24585240   418 PHHEPQSYNEEIYKPQPiQPGESFRIWY 445
Cdd:PRK10263  501 PARPPLYYFEEVEEKRA-REREQLAAWY 527
 
Name Accession Description Interval E-value
PRK10263 PRK10263
DNA translocase FtsK; Provisional
260-445 1.37e-05

DNA translocase FtsK; Provisional


Pssm-ID: 236669 [Multi-domain]  Cd Length: 1355  Bit Score: 47.77  E-value: 1.37e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   260 QQPYPQYGHHDESYLPTYGAEVPEPQHAHP--KPKQVDLEQVWSIKEEPKHGEHSGNHKATAYAQSPEPKKNYQSSSAVS 337
Cdd:PRK10263  367 QTGEPVIAPAPEGYPQQSQYAQPAVQYNEPlqQPVQPQQPYYAPAAEQPAQQPYYAPAPEQPAQQPYYAPAPEQPVAGNA 446
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   338 WrqtVPWEYGSPYQSAPVHHhqpwnpapahvptsvtkpkpcPKKEHPTPASYVPlPHDQPESYKLPVDYSPKPNHEQPhK 417
Cdd:PRK10263  447 W---QAEEQQSTFAPQSTYQ---------------------TEQTYQQPAAQEP-LYQQPQPVEQQPVVEPEPVVEET-K 500
                         170       180
                  ....*....|....*....|....*...
gi 24585240   418 PHHEPQSYNEEIYKPQPiQPGESFRIWY 445
Cdd:PRK10263  501 PARPPLYYFEEVEEKRA-REREQLAAWY 527
Atrophin-1 pfam03154
Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ...
322-451 1.88e-03

Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian atrophy (DRPLA) gene. DRPLA OMIM:125370 is a progressive neurodegenerative disorder. It is caused by the expansion of a CAG repeat in the DRPLA gene on chromosome 12p. This results in an extended polyglutamine region in atrophin-1, that is thought to confer toxicity to the protein, possibly through altering its interactions with other proteins. The expansion of a CAG repeat is also the underlying defect in six other neurodegenerative disorders, including Huntington's disease. One interaction of expanded polyglutamine repeats that is thought to be pathogenic is that with the short glutamine repeat in the transcriptional coactivator CREB binding protein, CBP. This interaction draws CBP away from its usual nuclear location to the expanded polyglutamine repeat protein aggregates that are characteriztic of the polyglutamine neurodegenerative disorders. This interferes with CBP-mediated transcription and causes cytotoxicity.


Pssm-ID: 460830 [Multi-domain]  Cd Length: 991  Bit Score: 40.91  E-value: 1.88e-03
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   322 QSPEPKKNYQSSSAVSWRQTVPweygSPYQSAPVHHHQpwnpAPAHVPTSVTKPKPCPKKEHPTPASYVPLPHDQ-PESY 400
Cdd:pfam03154 290 QHPVPPQPFPLTPQSSQSQVPP----GPSPAAPGQSQQ----RIHTPPSQSQLQSQQPPREQPLPPAPLSMPHIKpPPTT 361
                          90       100       110       120       130
                  ....*....|....*....|....*....|....*....|....*....|.
gi 24585240   401 KLPVDYSPKPNHEQPHKPHHEPQSYNEEIYKPQPIQPGESFRIWYGDSSLP 451
Cdd:pfam03154 362 PIPQLPNPQSHKHPPHLSGPSPFQMNSNLPPPPALKPLSSLSTHHPPSAHP 412
 
Name Accession Description Interval E-value
PRK10263 PRK10263
DNA translocase FtsK; Provisional
260-445 1.37e-05

DNA translocase FtsK; Provisional


Pssm-ID: 236669 [Multi-domain]  Cd Length: 1355  Bit Score: 47.77  E-value: 1.37e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   260 QQPYPQYGHHDESYLPTYGAEVPEPQHAHP--KPKQVDLEQVWSIKEEPKHGEHSGNHKATAYAQSPEPKKNYQSSSAVS 337
Cdd:PRK10263  367 QTGEPVIAPAPEGYPQQSQYAQPAVQYNEPlqQPVQPQQPYYAPAAEQPAQQPYYAPAPEQPAQQPYYAPAPEQPVAGNA 446
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   338 WrqtVPWEYGSPYQSAPVHHhqpwnpapahvptsvtkpkpcPKKEHPTPASYVPlPHDQPESYKLPVDYSPKPNHEQPhK 417
Cdd:PRK10263  447 W---QAEEQQSTFAPQSTYQ---------------------TEQTYQQPAAQEP-LYQQPQPVEQQPVVEPEPVVEET-K 500
                         170       180
                  ....*....|....*....|....*...
gi 24585240   418 PHHEPQSYNEEIYKPQPiQPGESFRIWY 445
Cdd:PRK10263  501 PARPPLYYFEEVEEKRA-REREQLAAWY 527
PTZ00449 PTZ00449
104 kDa microneme/rhoptry antigen; Provisional
246-430 6.54e-04

104 kDa microneme/rhoptry antigen; Provisional


Pssm-ID: 185628 [Multi-domain]  Cd Length: 943  Bit Score: 42.37  E-value: 6.54e-04
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240  246 SQKRIELGLEECSRQQPYPQYGHhDESYLPTYGAEVPEPQHAHPKPKQVdleqvwsiKEEPKHGEHSGNHKATAYAQSPE 325
Cdd:PTZ00449 492 SKKKLAPIEEEDSDKHDEPPEGP-EASGLPPKAPGDKEGEEGEHEDSKE--------SDEPKEGGKPGETKEGEVGKKPG 562
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240  326 PKKNYQSSS--AVSWRQTVPWEYGSPYQ-------SAPVHHHQPWNPAPAHVPTSVTKPKPCPKKEHPT-----PASYVP 391
Cdd:PTZ00449 563 PAKEHKPSKipTLSKKPEFPKDPKHPKDpeepkkpKRPRSAQRPTRPKSPKLPELLDIPKSPKRPESPKspkrpPPPQRP 642
                        170       180       190
                 ....*....|....*....|....*....|....*....
gi 24585240  392 LPHDQPESYKLPvdYSPKPnhEQPHKPHHEPqSYNEEIY 430
Cdd:PTZ00449 643 SSPERPEGPKII--KSPKP--PKSPKPPFDP-KFKEKFY 676
Atrophin-1 pfam03154
Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ...
322-451 1.88e-03

Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian atrophy (DRPLA) gene. DRPLA OMIM:125370 is a progressive neurodegenerative disorder. It is caused by the expansion of a CAG repeat in the DRPLA gene on chromosome 12p. This results in an extended polyglutamine region in atrophin-1, that is thought to confer toxicity to the protein, possibly through altering its interactions with other proteins. The expansion of a CAG repeat is also the underlying defect in six other neurodegenerative disorders, including Huntington's disease. One interaction of expanded polyglutamine repeats that is thought to be pathogenic is that with the short glutamine repeat in the transcriptional coactivator CREB binding protein, CBP. This interaction draws CBP away from its usual nuclear location to the expanded polyglutamine repeat protein aggregates that are characteriztic of the polyglutamine neurodegenerative disorders. This interferes with CBP-mediated transcription and causes cytotoxicity.


Pssm-ID: 460830 [Multi-domain]  Cd Length: 991  Bit Score: 40.91  E-value: 1.88e-03
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   322 QSPEPKKNYQSSSAVSWRQTVPweygSPYQSAPVHHHQpwnpAPAHVPTSVTKPKPCPKKEHPTPASYVPLPHDQ-PESY 400
Cdd:pfam03154 290 QHPVPPQPFPLTPQSSQSQVPP----GPSPAAPGQSQQ----RIHTPPSQSQLQSQQPPREQPLPPAPLSMPHIKpPPTT 361
                          90       100       110       120       130
                  ....*....|....*....|....*....|....*....|....*....|.
gi 24585240   401 KLPVDYSPKPNHEQPHKPHHEPQSYNEEIYKPQPIQPGESFRIWYGDSSLP 451
Cdd:pfam03154 362 PIPQLPNPQSHKHPPHLSGPSPFQMNSNLPPPPALKPLSSLSTHHPPSAHP 412
PRK14951 PRK14951
DNA polymerase III subunits gamma and tau; Provisional
316-446 3.75e-03

DNA polymerase III subunits gamma and tau; Provisional


Pssm-ID: 237865 [Multi-domain]  Cd Length: 618  Bit Score: 39.70  E-value: 3.75e-03
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240  316 KATAYAQSPEPKKNYQSSSAVSwrqTVPWEYGSPYQSAPVHHHQPWNPAPAHVPTSVTKPKPCPKKEHPTPASYVPLPHD 395
Cdd:PRK14951 379 KTPARPEAAAPAAAPVAQAAAA---PAPAAAPAAAASAPAAPPAAAPPAPVAAPAAAAPAAAPAAAPAAVALAPAPPAQA 455
                         90       100       110       120       130
                 ....*....|....*....|....*....|....*....|....*....|.
gi 24585240  396 QPESYKLPVDYSPKPNHEQPHkPHHEPQSyneeiyKPQPIQPGESFRIWYG 446
Cdd:PRK14951 456 APETVAIPVRVAPEPAVASAA-PAPAAAP------AAARLTPTEEGDVWHA 499
PRK10263 PRK10263
DNA translocase FtsK; Provisional
267-441 4.28e-03

DNA translocase FtsK; Provisional


Pssm-ID: 236669 [Multi-domain]  Cd Length: 1355  Bit Score: 39.68  E-value: 4.28e-03
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   267 GHHDEsYLPTY-GAEVPEPQHAHPKPKQVdlEQVWSIKEEPKHGEHSgnhKATAYAQSPEPKKNYQSSSAVSWRQTV--- 342
Cdd:PRK10263  302 PEYDE-YDPLLnGAPITEPVAVAAAATTA--TQSWAAPVEPVTQTPP---VASVDVPPAQPTVAWQPVPGPQTGEPViap 375
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 24585240   343 -PWEYG--SPYQSAPVHHHQPWN-PAPAHVPTSVTKPKPCPKKEHPTPASYVPLPHDQPESyKLPVDYSPKPNHEQPHKP 418
Cdd:PRK10263  376 aPEGYPqqSQYAQPAVQYNEPLQqPVQPQQPYYAPAAEQPAQQPYYAPAPEQPAQQPYYAP-APEQPVAGNAWQAEEQQS 454
                         170       180
                  ....*....|....*....|....
gi 24585240   419 HHEPQSYNE-EIYKPQPIQPGESF 441
Cdd:PRK10263  455 TFAPQSTYQtEQTYQQPAAQEPLY 478
 
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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