SGID Silkworm Genome Informatics Database
Gene
KWMTBOMO12664
Pre Gene Modal
BGIBMGA001403
Annotation
PREDICTED:_uncharacterized_protein_LOC106129089_isoform_X2_[Amyelois_transitella]
Full name
Centrosomal protein of 120 kDa      
Alternative Name
Coiled-coil domain-containing protein 100
Location in the cell
Cytoplasmic   Reliability : 1.887 Nuclear   Reliability : 2.268
 

Sequence

CDS
ATGTACTTACTGGAGCCCGTCGTTTTGGAGACGAGCAAAAGCGACACGTGCATCACAAGTCCTAAACGGGCCGCCCGTAAAGACAATCACACAGATTTGGTGAAAATGGCGCTATCGGAAGCCGACCGCGACAGCATCATGCGGAGGTTCGTGGACGAGCTGGAAGACTGGAAGGAGAAGCAGCAGGAGCTGCACAAACTGCAGTTGAAGCGCAAAGAAGAGTACCATTTAGAGCTATTGGCCAAGGAGTGGGCCAAGCAGCGCGTGGAGCTGGAGTGCCGGCTGGCGAGGGGCATCGAGCAGTGCCGCGCCCTCGCCGCCGACCTCGCCGCCGCCACAGACGACTTCAGGGCGAGGGGACACAGGAACTCCGAGAGGGAGAAGAAGTTATTGGAAGCGAAGAAAGCTTTAGAAGCGCATTACACAGCCAAGTACCAGGAGTTGAGAGAGGCCTCATTAAAAATGGAGGACGACATGAATCATCAGCTGAAAGTCAAGGACATGAGGATCGAAGAGCTGGAGCTTAAAATAATGCAGCTTGAGAAACAGGTGGACGTTTTGAAGAATACCATGAAGGACATTGAGAAAGAAGCCGAAACCCGATATTCTGGTCTAACTAAAGATCAAACTGCGAGTCTCATACAAGAATTGAGATGTTTAGAAGAAAAACTAGATAGTGCGGTCCAATCGAAAGCGTTCTTCAAAGAGCAGTGGGGCCGCGCTGTCAGGGAACTGCACCTGCTGAAGCTGGACACCAGGAAGCAAATGTTGTCGCAGCTGCAGCAGGACAGGAGGGAGCTGGGTGATGCTGGTTTAGACACAATAATAGATGACAACGAAAGTAAACGCAATCAAGATGCGATGGACATTAAAAAATTGAAAGACGATTTTTATGTTGACATTTTAGCGAGCACACCGGCACTGGAAATCGATTCGTTCATCACCACATCTGGTTCGGGTGTTGTAGAAATGTTTGACGATTTAAGAAGCGTCGTTAAGAACCCGATAAATGATAAACTAAACAAATTGATATCACAACGCGATCGGCTCATACAGGACGAGAATCCGAATGAAGAACTTCTGAAGCAATTGAACCAGGAAATTAGAAGTATCCTATTAAACTGTGGCTCCTGA
Protein
MYLLEPVVLETSKSDTCITSPKRAARKDNHTDLVKMALSEADRDSIMRRFVDELEDWKEKQQELHKLQLKRKEEYHLELLAKEWAKQRVELECRLARGIEQCRALAADLAAATDDFRARGHRNSEREKKLLEAKKALEAHYTAKYQELREASLKMEDDMNHQLKVKDMRIEELELKIMQLEKQVDVLKNTMKDIEKEAETRYSGLTKDQTASLIQELRCLEEKLDSAVQSKAFFKEQWGRAVRELHLLKLDTRKQMLSQLQQDRRELGDAGLDTIIDDNESKRNQDAMDIKKLKDDFYVDILASTPALEIDSFITTSGSGVVEMFDDLRSVVKNPINDKLNKLISQRDRLIQDENPNEELLKQLNQEIRSILLNCGS

Summary

Description
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. Required for centriole duplication and maturation during mitosis and subsequent ciliogenesis. Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (By similarity).
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. Required for centriole duplication and maturation during mitosis and subsequent ciliogenesis (By similarity). Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (PubMed:27185865).
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. May play a role in centriole duplication during mitosis (By similarity). Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (By similarity).
Subunit
Interacts with TACC2, TACC3, CCDC52, TALPID3.
Interacts with TACC2 and TACC3. Interacts with CCDC52.
Similarity
Belongs to the CEP120 family.
Keywords
3D-structure   Alternative splicing   Coiled coil   Complete proteome   Cytoplasm   Cytoskeleton   Phosphoprotein   Reference proteome   Ciliopathy   Disease mutation   Joubert syndrome   Polymorphism  
Feature
chain  Centrosomal protein of 120 kDa
splice variant  In isoform 4.
sequence variant  In JBTS31; unknown pathological significance.
EMBL
BABH01006497    BABH01006498    NWSH01006503    PCG63390.1    ODYU01003897    SOQ43231.1    + More
RSAL01000006    RVE54266.1    KQ460325    KPJ15798.1    AGBW02008777    OWR52569.1    LBMM01005028    KMQ91887.1    GL435863    EFN72551.1    ADTU01011323    KQ435850    KOX70862.1    GL888932    EGI57172.1    KQ978068    KYM97554.1    KQ979433    KYN21585.1    GBYB01001427    JAG71194.1    GBYB01001428    JAG71195.1    NNAY01000633    OXU27297.1    KK107459    EZA50369.1    KQ414929    KOC59380.1    QOIP01000004    RLU24249.1    KZ288192    PBC34330.1    KQ982373    KYQ57030.1    GL448504    EFN84539.1    KK853055    KDR11964.1    KQ976500    KYM83171.1    DS235478    EEB16032.1    GEDC01020745    JAS16553.1    JH817066    EKC26375.1    GEDC01010015    JAS27283.1    AK038916    AK044808    AK044952    AK047594    AK079319    BC046493    BC048590    BC053439    KB107782    ELK29721.1    PZQS01000013    PVD19694.1    NBAG03000288    PNI47689.1    AC010369    AC106792    BC040527    AK093409    AK095646    AL833929    BX648687    CR627324    AACZ04009925    GABC01006869    GABD01006534    GABE01010287    JAA04469.1    JAA26566.1    JAA34452.1    PNI47687.1    PNI47688.1    CABD030040669    CABD030040670    GABF01004588    JAA17557.1    NDHI03003367    PNJ80334.1    ABGA01000616    ABGA01000617    ABGA01000618    ABGA01000619    ABGA01000620    PNJ80332.1    PNJ80339.1    AQIB01044001    LWLT01000008    AMGL01092062    AMGL01092063    AMGL01092064    AMGL01092065    AMGL01092066    AMGL01092067    AMGL01092068    AMGL01092069    AMGL01092070    AMGL01092071    AAFC03099167    AAFC03125893    AAFC03125142    AAFC03099169    AAFC03131164    AAFC03126660    BC126531    GEBF01004354    JAN99278.1    JH174046    EHB18094.1    AJFE02093464    AABR07032133    GAMR01007903    JAB26029.1    GAMT01004054    GAMS01010370    GAMP01007073    JAB07807.1    JAB12766.1    JAB45682.1    GBZA01000124    JAG69644.1    AEMK02000012    DQIR01096726    DQIR01163681    DQIR01253284    DQIR01258638    DQIR01258639    DQIR01269033    DQIR01269034    DQIR01269035    DQIR01277159    DQIR01281463    DQIR01285038    DQIR01287666    HDA52202.1    HDB19158.1   
Pfam
PF12416   DUF3668        + More
PF00168   C2
Interpro
IPR039893   CEP120-like        + More
IPR022136   DUF3668       
IPR035892   C2_domain_sf       
IPR000008   C2_dom       
Gene 3D

Ontologies

Topology

Subcellular location
  
Length:
377
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
0.00093
Exp number, first 60 AAs:
0
Total prob of N-in:
0.00108
outside
1  -  377
 
 

Population Genetic Test Statistics

Pi
17.75547
Theta
19.190003
Tajima's D
-0.428496
CLR
0.266904
CSRT
0.262786860656967
Interpretation
Uncertain
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