Pre Gene Modal
BGIBMGA000862
Annotation
PREDICTED:_centromere-associated_protein_E-like_isoform_X1_[Amyelois_transitella]
Full name
Centromere-associated protein E
+ More
Kinesin-like protein KIN-7L
Kinesin-like protein KIN-7I
Kinesin-like protein KIN-7O
Kinesin-related protein 4
Kinesin-like protein KIN-7N
Kinesin-like protein KIN-7L, chloroplastic
Kinesin-like protein KIN-7K, chloroplastic
Kinesin-like protein KIN-7E, chloroplastic
Kinesin-like protein KIN-7D, chloroplastic
Kinesin-like protein KIN-7D, mitochondrial
Kinesin-like protein KIN-7C, mitochondrial
Kinesin-like protein KIN-7M, chloroplastic
Kinesin-like protein KIN-7G
Kinesin-like protein KIF3B
Kinesin-II 95 kDa subunit
Kinesin-related protein 11
Kinesin-like protein KIF3A
Kinesin heavy chain
Kinesin-II 85 kDa subunit
Osmotic avoidance abnormal protein 3
Kinesin heavy chain isoform 5C
Kinesin-like protein FLA10
Kinesin-like protein KIN-7A
Kinesin-like protein KIF3C
Kinesin-like protein KIN-7J
Kinesin-like protein KIN-7E
Kinesin heavy chain isoform 5A
Kinesin-1 heavy chain
Kinesin-like protein KIN-7C
Kinesin-like protein NACK1
Kinesin-like protein KIN-7H
Kinesin-like protein KIF17
Kinesin-like protein KIN-7F
Kinesin-like protein KIF15
Kinesin-related protein 3
Kinesin-like protein KIN-7B
Kinesin-like protein KIN-4A
Kinesin-like protein Klp68D
Chromosome-associated kinesin KIF4
Kinesin-like protein NACK2
Chromosome-associated kinesin KIF4A
Chromosome-associated kinesin KIF4B
Kinesin-like protein KIF15-B
Kinesin-like protein KIN-4C
Kinesin-like protein 3
Kinesin-like protein KIN-5C
Kinesin-like protein klp-20
Kinesin-like protein KIF27
Kinesin-like protein Klp98A
Kinesin-like protein KIF15-A
Kinesin-like protein KIF11-B
Kinesin-like protein KIN-5A
Kinesin-like protein KIF11-A
Kinesin-like protein KIN-12G
Kinesin-like protein KIF11
Kinesin-like protein KIF18A
Kinesin-like protein KIN-12E
Alternative Name
Centromere protein E
Kinesin superfamily protein 10
Motor domain of KIF10
Kinesin-7
Kinesin-related protein CENPE
Kinesin family member 4
Mitochondria-targeted kinesin-related protein 2
Mitochondria-targeted kinesin-related protein 1
HH0048
Microtubule plus end-directed kinesin motor 3B
KRP-85/95 95 kDa subunit
Kinesin family member 11
Microtubule plus end-directed kinesin motor 3A
KRP-85/95 85 kDa subunit
Synkin
Kinesin-like protein osm-3
Kinesin heavy chain neuron-specific 2
Protein KHP1
NPK1-activating kinesin-like protein
Protein DWARF BAMBOO SHOOT 1
Kinesin heavy chain neuron-specific 1
Neuronal kinesin heavy chain
Conventional kinesin heavy chain
Ubiquitous kinesin heavy chain
Uncoordinated protein 116
NPK1-activating kinesin-1
KIF3-related motor protein
Kinesin-like protein 2
Kinesin-like protein 7
Serologically defined breast cancer antigen NY-BR-62
Kinesin family member 3
Kinesin-1
NPK1-activating kinesin-2
Protein STUD
Protein TETRASPORE
Protein HINKEL
AtKINESIN-4A
Protein FRAGILE FIBER 1
Chromokinesin
NPK1-activating kinesin 2
Chromokinesin-A
Chromokinesin-B
Kinesin-like protein 2-B
Kinesin-related protein KRP180
Chromosome-associated kinesin KLP1
AtKINESIN-4C
Kinesin-related protein 1
125 kDa kinesin-related protein
Kinesin-like protein 2-A
Kinesin-5
Kinesin-related motor protein Eg5-1
AtKRP125c
Protein LOOPHOLE
Protein RADIALLY SWOLLEN 7
AtKRP125b
Kinesin-related motor protein Eg5-2
Protein BRITTLE CULM 2
Protein GIBBERELLIN-DEFICIENT DWARF 1
Kinesin-like protein 1
Kinesin-like spindle protein HKSP
Kinesin-related motor protein Eg5
Thyroid receptor-interacting protein 5
Costal2
Location in the cell
Nuclear   Reliability : 3.6
Sequence
CDS
ATGAGTGATAATATCAAAGTGGTTGTCAAAGTTCGGCCTTTGATTACAAGGGAAATTGAAGAGAAACTCCCTTACCAGTGGCGCATTAAAAATAATTCCCTATATCAACTAGATCAGAATGGCAAAGAGTTCGGATCTTCATTTACATTTGACAAAGTTTATGATGAAAGTACAAAAACCAGTGAAGTTTACAATGATATTGCAAAGCCTATCGTTGAAGCAGCAGTTGCTGGATTCAATGGTACTATCTTTGCATACGGGCAGACCTCCTCCGGGAAGACTTACACTATGGCAGGAACTGAGAGCTCGCCGGGTATAATAACATTAGCTGTTTTAAACCTATTTGAAATTATCAAGAATATACCTGACCGTGACTTTTTAGTAAGAGTATCTTACATAGAAATCTATAATGAAACTGTAAAAGATCTTCTTAACATTGAAAAAGACAACATAAAGATCCATGACACTTTACAAGGTATTAAAGTGGATGCAACTGAGAAAGTCACTTCCTCGCCTGAAGAAGTACTGGAAATTATAAAACAGGGTGAAGCAAATCGGCAAACAGGGTCAACAAATATGAATGAGAAAAGTAGCAGATCACATTCTATCTTTCAAATAACTATTGAATCTAAAGAACATGTTGAAGGTAAAGAGGAGGTTGGTAGCGTTAACGTATCACAGCTGAATCTAGTTGATCTTGCGGGCTCTGAACGTGCAGGACAAACAGGTGCTAAGGGCTTACGTTTTAAAGAAGGAACCCATATTAATAAATCGCTGTCTGCCCTTGCTTTGGTCATCAAAAAACTTGCTGAGAATCCTGGGCAGTTCAACAACTACCGTGACAGCAAATTAACAAGAATACTACAGAACTCACTCGGTGGGAATGCTAAAACAAGTATCATATGTGCAGTTACACCAGCTGCTCTAGAAGAAACAATTTCTACCTTACAATTCGGAAACCGTGCGAAATTTATAAAGAACGAACCTATTTTGAATGAAGTACAGAGTAACGCTACAATGATCCAGCAGTTAACTAAGAAACTTGGGGCCCTCCAAACTGAACTTGAATGCAAGAAACATCTTGAGCAAGACAACTACAACCTCCAGAAACAGATAGCGGGATTACAGAGGCTAATATTAAGTGGCGTAACGCGACATTCTACTGAAGACATCATCAGCACCCGTCGCAAACATCCTCAACGCAGGATTACAATATCGGCTTTGCACTCGGTCGAAGAATCCACAACTAGCATCCCGAGGTTTTGTACTCCTGTCTTGAAATACAACCCGATGACGTTAGGCGGTTGTTCATCAGACTTAGCTCCGTTACAACGTCCGGGAACCTTATCCACTGTTCCTGAAGAAACTTCACGGATGGTCACCCCGCCCCCTGGTGACAAGAGAGTCAACTTTGAGGATGAAATCATCGAGCTCGATAGCGACGATGACGAAGTAGCAAATAATCAAACTTGTTCACCTATTCATGAATGCTATGACAAATCGAAGACGCCTCCTTGTGTACTGAGGAAGACAGCGAAACGAGCCGAGAAGAATCTCAAAGACATAGTCGAGTTAACTGAACGAGAGAAAATTTATCCTCCTAGAGTTGCGGAATTGTTGGAGAAATTGGAAGAAAAAACTTATGCTATTACGATGCTACAAGACGAGATGGAGACTTTCAATAAACAGAGTAAAGAAAAAGATCTACAGATGGAATATATGAAGAAGAAAATCCAAAAATTAGAAGACACAATTGTTAATGTCACTTCGGAAAAGGAAAAATTAGAAACCCGTTGCAAAGATGTTGACATCAAGCTAACGGACTGGGAAGTTAGCTACGACACTTTCAAGAAAAAAGCGAAACAAAGAGAAGAAGAATTGCTTTCGATAGTAGAAGAACTGAAAACTAAATCACATACAGGAGGTATATCCCTAAATCAAAGTCTCAAAGAGCAATCGATTTTAAAATGTCCAGAAATCAGTACAAATAAAGAAGATGAATCTTCAACCCCAAATTTAGTCTCAGACTTACAGTCACAACTGGTCGTCAAAAACCAAACTATCGTAGAATTACAGGCGGATATCTGTGCACAAAATCAAACGATCACGTTCTTAGAAAAATCTAGTCAAGAATTACAAGACATGATAAACAATTACAAGGAAAATCTAACAGATAAAGATGAAGAAATTGGATTGCTTAAATGTGCCATAGAAACATTAAATTCGACTATAAAAAGCCAAAAATCTTGTCTAGATACTGCAAACGACGACATTAAATCCTATAACAGTGTTATACAGGAGTTACAAATAAAACTCACCGGTAAAGAGACCCAATTAAATTTAAACATAGAAGACGATCTTTTGCAAAACATGATTGACAATGAAGCAACACTATTTGCCAACAACGAAAACATTAGAAACATAATACACGCTTTCAAAATTAGACTTGAAGAATGCTATAAGGAAATTGGCCAATTAAAATCTGGTTTACAACAAAATGTTGGCGTTGGAGACAAAACTGTAGCAGAACTAAAAAATGATGAAATTAATAGCATGATTCGTCAGTTGGAAGAAGAGATTGAGAAATGTAAAATAGTCGAGGAAGAACTCACCGAAAAATTAACAATAGCAGAAACTAAACATAATGATTTGAAAAAATTGTATGAGGATAGTGCATCAGAATTGGAAGCATTAAAAAGAGAAAACATACAAATGCATACAAGTGAGGGTGAATCAAAAAAAGTAGTCGAACAATTATTGGAAAAAAATATAATATTAACAGATGAAATAGATGCCATGACCAAGAAAATCACAACATTACAAGAGAACATTAGTTCAAAAGAAATAATAATAGAATCTTTACAAGAAAACAATAAAGACAGAATGGAATATTTAGATAAAGCTAAATTAATCATTAAAAAACTTCAAGATGTTTTCTTAATTTTATCAGGTGATGTCATGGTGGTTCCAGAAATTATTGATAGTTTAACAGAAGTAATCAATACGTTGACTAACGGTTTTGAGTCTTTAGAAGAAGTAGCACTAGAAATAGACTTAAAGAAAAATTCAATAACAAAAGATAATATATCCATAAAGACCTTGTTAGATAAATTAATAACCAAAAATGAAACAGACATTAATGAGTTAAGGAACTCTATAAAATATCTTGAAAGTGTAAAAAGTGAATACAATACTGCTAACGAAAAGCTTTTTGAACAGTTAAATAATGCAGTAGATAAACAAAATTGCATTCAGGAAGAAGTGGATTTATTAAAAATTGAAAATCAAAATCTATTACAAGAATTACTATCTCGTAAAACAGAACTAGAAAAATTGGAGTTAGAAATATTAGCCCGCGACAAATTTATTGCAAATTTAGAAGAAATGAAAACTATGCTCGTCGAGGAGAAGCTGTCAGAAATTAAAGAGAAGGACGAAAATTTCAAACAAGAAATTGATATGTTGAATGAAAAGTTAATCTGTGATCGACGTGAATTTAATGAAACTATGCAAGAGAAAAACATACTACTCTCTGATTTATCTAAGAAAGTCAACAAAACAGAACGCGAGTTAGAAGAGAAACAAGAACAACTTACCCATCTAATGGAGCAACTCAATGACACTGAGAATAACAGTTACAAGCTTATCGAAAATATGTTCAATAAAGTTTCTCAAATCGCATCAGATTTTAAAATTTCCAATCAGCTGTCCTGTGAACTTGATGATGAGAGTGAAAACACATACGAAAGAATTAGTCTAACTTTGGACAAGATAACTAATCACATAACGTATTTAAACACGCAAATAAATGAGACACAGAAGAATGATAATGCGCAGTTATTATGGGAAGCAAAGAAACAGATTGCAGATCTAACGGAACAAAATATCATTTTAAAAGAAAGATTATCACAATTAGAAACAGAAAATAAAGAACTTCTTATTGAAATTCAAACAGTTCGAGGTAGTAATGAAGAAGTAACACTAAATTTAAAAGACAGTAGCACATTGTTGAAACAACTCAAAGAAGAATTGAAACAAAAAAGTAACGAGATAGAAGATATGAAAACTAAAGTGATGGAATGGAAAAGCCAATTCGAGGATTTAGATGACGTGATGAAACAACAACAAAAAGAATTAAAACTGGAAAATAAAAAACTTCATGATAAAAGAACTGAAAAAAGTGCAGAAAGCTTAGATTCTGAAGAGGACGAAGAATGTGTAAACAATTTTTATGAAATAAGCGTGAACACAGACAGTGAAAATACATTAGAGCAATCAGCCTATTCTCCAAAAAGTCTTGTCACAATATGCTGTAGCAAGATTTTAGATAGCATTCAATCGAATGATACCAAAAAAGACATATCGACTTGTGACAAAGACGAGACGACGAAATGCAGCAACTGTGATGAGTTTTCCTCCCAATTGACTTCTGCACAAGATAAAAACGACAAATTGACGCAGAAGGTACAACAGCTACAAGCCTTTAACCTACAACTAATGGACGAACACGAATTAGTTCGTTTAGAACTACAAAAATTAATAGAACCAGCTCATGAATTACAAAAAAAGATTATCAATCATAAAACTAATTTGTCGATACTCACCGCGACAACGTATGCTGAGAATAAACTACTCAATTCTCAGGTTAAGAGTTTACAACATCACCACGGTCGCTTTCACTACGTATGTCAAAGAGATTTGCCAGCGTTTAAAAAGCAATTGTGTGATCTCTTAGCAATCCTAAAAAACTGTCCTACATTAGTCGAATCAGAAAATGGTAGTTTGAAAAGATTTTCCTTGCCAGATGTCTTAGAAAAAAATACAACGATTGCAAGAAACGAATCCGTTTTGGATGGTGATTTATTAATGCTGGATACAAATGTTAGTCTTACAACAGCTGACAGTACCTTGGTAGCCTGCGACCAAACATGTTTAGATTTGACCCAAAACCTAATCAATGAAATCTCTATACAAACTAATTTCAACCAAACTATAGAAGCAAGTGATGTCAATTCTCAAATCGAAATGTTAAATAATGATAACCGAATTATGTTTGAGAAATTAGAAATTTTGAAGGAGGAAAACGAAAAATTACGTAACCAATTAGATGGAGCTAAAAGTAAAAATGACAACATTATAGAAACACAAAGTAATCCAATAAAGTTACAGGATTCCGGAACCATAACAATTTCTTGTAAAATGTGTCAGAGTCTAAAAGAATCTTCAAACGAAATCAATCTAAAACTTGAAAAGCTATCCGGAGAGTTATTCGATATTAAAGAACAAAAGAGTGCTTTGGAGGGTAAATATCAAAATTTAATATTGGAAACACAAACGAGAGATCTACTGATGTCCCAAATTAAGTCCTTAGAAATGGAAAACCTCACTAAAGATAAAGAAATCAAGAACTTAACAGACTCTTTAAAAACTAAAAGTAAAAAAATTAATGAGCTGCAAGAAGAGAATGATACACTTTCCAATCTTATAATGGAAAACGTTACCGAAAGTGATAATTTGAATAAAGAAGTAGACGATCTAAAGAAAAATAATGAATGTCTTACACAAAAATGTATTGATTTGGAAAAACTTGTTAATGAATCCGAAAATAAAATTGGACCTAAAAATATATGTGCTCAATGTAAATTAAAAGAAAATTTAATACAATCTTTACATATCGGTTACGACAACACTCTATCAAAACTGAATCGAAGCATTAGTGACTCTAATACTTCAACACGATACAATAAAATTTGTACACTACAAAGCGAATTGGACGCGGGAAGAGAAGATTGTAAAGAACTCTGCGAAGATTTCACGTCAATAAAGAACCATTTAGAACTACACGAACCTAATATGACCATGGATTTAGATGAAAGTATTGAAAATGCAAACTTTTTACCACAATCAACAGCAAACCTGTCTAAAATCGCTGACGAAAAAAATCTTGACATGTCTTATGTAATGGATAAAACGATGTGCCTAAATTATTATACAGAAATTGTAGGAGTGGAAGATCACGATCTAAAAGAAAATATTAAAATAATTGATGTTATGAAAATGCTGCATAATCATTTGTTAACGAGTCACGGCAATGAAGTTGAAAATCTAGTGAATAAGCTTAAGGATTATGAAGAAACTAAAAATGACTTACTGAACCAGTTGGAGACTACTAGTGCTAAATGTTCAATAATAAACAAAGAACTTGGAGAAAACAATGAATTTGAAACTAAAGCCGTCAAGGTCATGTCCGAAATCAAAAGAAATTTAAATTCCCTTAGCGAACAATTAATAAATAATGAAAGTAAAAAAAGCAAAGATCACATAGACAGATACAAAGATAGCTTACTTGCTGTTCTGGATGCAGAATTCGGAACTACCAGCTTAGATGTATTTGAAATTCTAATGGATAACATAATAAACAAATATCAAATAGACTTAGATGAAATCTTGGAAAAATACACCAAAGTACAAGGAGATTTAAATGAGTGCACTTCGGAACTAAAATCAGTAAACGAAAAATTGGCATCCCTGAATAGTCAATTAATTGAAAAAGAAAACGCCTGTAATATTTTGAGAATACAGAAAGAAAGAATACATGAAATCAGCTCAGCGGTTACAATAGATATTGTTAAGAAAGAAAATGAATTAAAGGAAATACTGACCAAAGAATGTTTGAAACTTTCAAAATTAAAAATAGATATTCCACGCGACTTAGATCAGGACTTACCGGCGCATAAAAAAATTACTATTCTGTTTGATGCTCTCATAACACAGTATGAACTCTCGCGAACGGATTACGAAATCGAAAAGGAAAAACTTAGATTGGAAACTGGTACGGCGAAAGCAGTGTTAGAAGAAAAAGAAAAAGAATTATCTGAACTAAAATTAAAATTCGATACACTCGAAGAGGCGCACAACGAAGTAAAATCATTGCATGAAGAATTAACGAAACTGTACAAGAGTAAAGTAGACGAAAATAATGCGAACTTGAATTTAATAAAAATATTATCCGAAGAAATCGATGCACTTAAAATAGCGATAGCTAAAAACGAAGAAAAAATGCTGTCTCTATCTGAAAAAGACAATAAATTAACGGAGCTGGTCTCTACAATAAACGGCTTAAAAGAAGAAAATAACTCACTAAAGTCGCTCAATGATGTTATAACAAGAGAAAAAGAAACTCAAGCTTCAGAATTGGAAAGGTCGTGTCAAGTAATAAAACAAAACGGTTTCGAACTGGACAAGATGAAAGCAGATATATTGATGTTAAATGAAACTGTCAAAGAGAATACAGTAGTTGTTGAAACTTTAAAAGATGAAGCTAAATCACTGTTGGAGCAAAATCTAGCTTTGAAGGAACAGTGTGAGGAGAAAACGCGCGATTGCTCTCGTCTCGAAATTAACATCAAAACACACGAGAAAACTGCCGAAATCCAAAACAGAATGATCATGAGACTTCAAAAACAGAAACAGGAAGACGATAAACTATTCATAGAGAAAGAAACTAAATTGAACGAACTAACGAACAAATATGAAGCTCTGAAGAGAGATTATGATGCGGCGGTAAAGGATCTCGAGTCAAGCAGAGAAGCGGTGAACCAATTGACTACACAGAAAGATCTTGTTGAGGGTCGTATAGCCGAACTGGAATCTGATATACGAACGGAACAAACAGCAACAGTTTCGCTAGACGACGCGTCCAAGTCGTCCCGGAGCCGCCGCCGCAGTCTGCACGACTCGAAGAGGACGTTTGGCGACGAAAACCGTGACCTGGGAGAAAGCAATTTGGAAGCTGTTTTCGAGTCGCGTCGCCAACCCGACGATCTCTTCATGGATGTAGACGGACACGATTCAAACAGAAGCACACCTATTCGACTCAAAGGACGTGACAGTTTACTAAAATCAGATAATAGCGACGTAGGAGAGGAGCACTCGTCCCGGCCCGGCAGCGTGCAGGCTTCGCGACGGAGGCGACAGAGTATACACGACTTCCACCGGAGTATAATGCGGTCTAGCCGAGATACTTCCCACGAAAATCCAAAACTTGACGATTCCCCAAAGAGGTCAATATCAGTAATCAGTGACAGTGAAGTGTCTCAGCTTAAGGAGCGGCTATTGTCATGTCAACAAGAACTAGACGATCTAAAGGAGAGGTACAAAGAATTGGACGACGAGTGCGAAACCTGCGCAGAGTACTTGCAAGAAAGAGACGAGCAATGCGCTCGCTTGAAAAAGGAAAAATTGAGTTTAGAGCAACAAGTATCAAATTTGAAAGAACAAATACGTACGCAACAACCTGTTGAACGTCAAGCAAAATTCGCGGATGTCGCCGTCAACACAGACGAAGATTGGGCCAATCTACATTCGGTGGTCGTCGATCGAATGTCGTACGACGCGGAGGTCGAAAAGAACAAGAGGCTAATGAAAACCATTGAAGAACTGCGATACAAGAAGCAAGATCTGAAGAATACTGTCACAAAAATGCAAAAAGCAATGGAGAAATATACTAAAAAAGACAAAGAATTCGAAGCGAAAAGGAAAGAGCTGGAGGATTGTAAAGCAGAACTTGAAGAATTAAAACAAAGATATAAGGAGTTGGACGAAGAATGCGAGACATGTGCAGAGTACCTTAAACAAAGAGAAGAACAATGTAAGAGGCTTAAAGAGGCTAAAATCGCTCTAGAGATGAAATTACAAGAGTTCCAAACCGACGCTAGTATAGTACATCTGCAATCCGTACGTAAGAAACGAAGGAGCATACACGATCAGAACCGAGCTTCCAACGTCGATCTTGTGGATGCATCCACACAGATTGGTGACGATTTTCTAAATAATCAAGTTGAACGCGACCGCGGCTCCGGTAACGCAACCGACGAATCTCATGTCCGTGAAATGCAACGACTTCAGAAGATTGTGGACAAGTTAAGCAACCAGAAGGTCGCCTTGGAGAAGCAAATAGAATCTTTGAGTAATACGCCTGTATCGAATTCCACTATGTATGTAGCCACTGGCAGTGCGATAGTGCAGAACCAACAAATAACTGACGTGATGAAGGAAAATCAAAAACTAAAGAAGATGAATGCCAAACTGATTACGATATGCAAGAAACGAGGCAAGACAGGCGCCAACAGAGAGAATGAGGATCCGTCCGATGTTTGA
Protein
MSDNIKVVVKVRPLITREIEEKLPYQWRIKNNSLYQLDQNGKEFGSSFTFDKVYDESTKTSEVYNDIAKPIVEAAVAGFNGTIFAYGQTSSGKTYTMAGTESSPGIITLAVLNLFEIIKNIPDRDFLVRVSYIEIYNETVKDLLNIEKDNIKIHDTLQGIKVDATEKVTSSPEEVLEIIKQGEANRQTGSTNMNEKSSRSHSIFQITIESKEHVEGKEEVGSVNVSQLNLVDLAGSERAGQTGAKGLRFKEGTHINKSLSALALVIKKLAENPGQFNNYRDSKLTRILQNSLGGNAKTSIICAVTPAALEETISTLQFGNRAKFIKNEPILNEVQSNATMIQQLTKKLGALQTELECKKHLEQDNYNLQKQIAGLQRLILSGVTRHSTEDIISTRRKHPQRRITISALHSVEESTTSIPRFCTPVLKYNPMTLGGCSSDLAPLQRPGTLSTVPEETSRMVTPPPGDKRVNFEDEIIELDSDDDEVANNQTCSPIHECYDKSKTPPCVLRKTAKRAEKNLKDIVELTEREKIYPPRVAELLEKLEEKTYAITMLQDEMETFNKQSKEKDLQMEYMKKKIQKLEDTIVNVTSEKEKLETRCKDVDIKLTDWEVSYDTFKKKAKQREEELLSIVEELKTKSHTGGISLNQSLKEQSILKCPEISTNKEDESSTPNLVSDLQSQLVVKNQTIVELQADICAQNQTITFLEKSSQELQDMINNYKENLTDKDEEIGLLKCAIETLNSTIKSQKSCLDTANDDIKSYNSVIQELQIKLTGKETQLNLNIEDDLLQNMIDNEATLFANNENIRNIIHAFKIRLEECYKEIGQLKSGLQQNVGVGDKTVAELKNDEINSMIRQLEEEIEKCKIVEEELTEKLTIAETKHNDLKKLYEDSASELEALKRENIQMHTSEGESKKVVEQLLEKNIILTDEIDAMTKKITTLQENISSKEIIIESLQENNKDRMEYLDKAKLIIKKLQDVFLILSGDVMVVPEIIDSLTEVINTLTNGFESLEEVALEIDLKKNSITKDNISIKTLLDKLITKNETDINELRNSIKYLESVKSEYNTANEKLFEQLNNAVDKQNCIQEEVDLLKIENQNLLQELLSRKTELEKLELEILARDKFIANLEEMKTMLVEEKLSEIKEKDENFKQEIDMLNEKLICDRREFNETMQEKNILLSDLSKKVNKTERELEEKQEQLTHLMEQLNDTENNSYKLIENMFNKVSQIASDFKISNQLSCELDDESENTYERISLTLDKITNHITYLNTQINETQKNDNAQLLWEAKKQIADLTEQNIILKERLSQLETENKELLIEIQTVRGSNEEVTLNLKDSSTLLKQLKEELKQKSNEIEDMKTKVMEWKSQFEDLDDVMKQQQKELKLENKKLHDKRTEKSAESLDSEEDEECVNNFYEISVNTDSENTLEQSAYSPKSLVTICCSKILDSIQSNDTKKDISTCDKDETTKCSNCDEFSSQLTSAQDKNDKLTQKVQQLQAFNLQLMDEHELVRLELQKLIEPAHELQKKIINHKTNLSILTATTYAENKLLNSQVKSLQHHHGRFHYVCQRDLPAFKKQLCDLLAILKNCPTLVESENGSLKRFSLPDVLEKNTTIARNESVLDGDLLMLDTNVSLTTADSTLVACDQTCLDLTQNLINEISIQTNFNQTIEASDVNSQIEMLNNDNRIMFEKLEILKEENEKLRNQLDGAKSKNDNIIETQSNPIKLQDSGTITISCKMCQSLKESSNEINLKLEKLSGELFDIKEQKSALEGKYQNLILETQTRDLLMSQIKSLEMENLTKDKEIKNLTDSLKTKSKKINELQEENDTLSNLIMENVTESDNLNKEVDDLKKNNECLTQKCIDLEKLVNESENKIGPKNICAQCKLKENLIQSLHIGYDNTLSKLNRSISDSNTSTRYNKICTLQSELDAGREDCKELCEDFTSIKNHLELHEPNMTMDLDESIENANFLPQSTANLSKIADEKNLDMSYVMDKTMCLNYYTEIVGVEDHDLKENIKIIDVMKMLHNHLLTSHGNEVENLVNKLKDYEETKNDLLNQLETTSAKCSIINKELGENNEFETKAVKVMSEIKRNLNSLSEQLINNESKKSKDHIDRYKDSLLAVLDAEFGTTSLDVFEILMDNIINKYQIDLDEILEKYTKVQGDLNECTSELKSVNEKLASLNSQLIEKENACNILRIQKERIHEISSAVTIDIVKKENELKEILTKECLKLSKLKIDIPRDLDQDLPAHKKITILFDALITQYELSRTDYEIEKEKLRLETGTAKAVLEEKEKELSELKLKFDTLEEAHNEVKSLHEELTKLYKSKVDENNANLNLIKILSEEIDALKIAIAKNEEKMLSLSEKDNKLTELVSTINGLKEENNSLKSLNDVITREKETQASELERSCQVIKQNGFELDKMKADILMLNETVKENTVVVETLKDEAKSLLEQNLALKEQCEEKTRDCSRLEINIKTHEKTAEIQNRMIMRLQKQKQEDDKLFIEKETKLNELTNKYEALKRDYDAAVKDLESSREAVNQLTTQKDLVEGRIAELESDIRTEQTATVSLDDASKSSRSRRRSLHDSKRTFGDENRDLGESNLEAVFESRRQPDDLFMDVDGHDSNRSTPIRLKGRDSLLKSDNSDVGEEHSSRPGSVQASRRRRQSIHDFHRSIMRSSRDTSHENPKLDDSPKRSISVISDSEVSQLKERLLSCQQELDDLKERYKELDDECETCAEYLQERDEQCARLKKEKLSLEQQVSNLKEQIRTQQPVERQAKFADVAVNTDEDWANLHSVVVDRMSYDAEVEKNKRLMKTIEELRYKKQDLKNTVTKMQKAMEKYTKKDKEFEAKRKELEDCKAELEELKQRYKELDEECETCAEYLKQREEQCKRLKEAKIALEMKLQEFQTDASIVHLQSVRKKRRSIHDQNRASNVDLVDASTQIGDDFLNNQVERDRGSGNATDESHVREMQRLQKIVDKLSNQKVALEKQIESLSNTPVSNSTMYVATGSAIVQNQQITDVMKENQKLKKMNAKLITICKKRGKTGANRENEDPSDV
Summary
Description
Microtubule plus-end-directed kinetochore motor which plays an important role in chromosome congression, microtubule-kinetochore conjugation and spindle assembly checkpoint activation. Drives chromosome congression (alignment of chromosomes at the spindle equator resulting in the formation of the metaphase plate) by mediating the lateral sliding of polar chromosomes along spindle microtubules towards the spindle equator and by aiding the establishment and maintenance of connections between kinetochores and spindle microtubules. The transport of pole-proximal chromosomes towards the spindle equator is favored by microtubule tracks that are detyrosinated. Acts as a processive bi-directional tracker of dynamic microtubule tips; after chromosomes have congressed, continues to play an active role at kinetochores, enhancing their links with dynamic microtubule ends. Suppresses chromosome congression in NDC80-depleted cells and contributes positively to congression only when microtubules are stabilized (By similarity). Plays an important role in the formation of stable attachments between kinetochores and spindle microtubules (PubMed:12925705). The stabilization of kinetochore-microtubule attachment also requires CENPE-dependent localization of other proteins to the kinetochore including BUB1B, MAD1 and MAD2. Plays a role in spindle assembly checkpoint activation (SAC) via its interaction with BUB1B resulting in the activation of its kinase activity, which is important for activating SAC (PubMed:12361599). Necessary for the mitotic checkpoint signal at individual kinetochores to prevent aneuploidy due to single chromosome loss (PubMed:12925705).
Microtubule plus-end-directed kinetochore motor which plays an important role in chromosome congression, microtubule-kinetochore conjugation and spindle assembly checkpoint activation. Drives chromosome congression (alignment of chromosomes at the spindle equator resulting in the formation of the metaphase plate) by mediating the lateral sliding of polar chromosomes along spindle microtubules towards the spindle equator and by aiding the establishment and maintenance of connections between kinetochores and spindle microtubules (PubMed:7889940, PubMed:23891108, PubMed:25395579). The transport of pole-proximal chromosomes towards the spindle equator is favored by microtubule tracks that are detyrosinated (PubMed:25908662). Acts as a processive bi-directional tracker of dynamic microtubule tips; after chromosomes have congressed, continues to play an active role at kinetochores, enhancing their links with dynamic microtubule ends (PubMed:23955301). Suppresses chromosome congression in NDC80-depleted cells and contributes positively to congression only when microtubules are stabilized (PubMed:25743205). Plays an important role in the formation of stable attachments between kinetochores and spindle microtubules (PubMed:17535814) The stabilization of kinetochore-microtubule attachment also requires CENPE-dependent localization of other proteins to the kinetochore including BUB1B, MAD1 and MAD2. Plays a role in spindle assembly checkpoint activation (SAC) via its interaction with BUB1B resulting in the activation of its kinase activity, which is important for activating SAC. Necessary for the mitotic checkpoint signal at individual kinetochores to prevent aneuploidy due to single chromosome loss (By similarity).
Microtubule-associated force-producing protein that plays a role in organelle transport. Its motor activity is directed toward the microtubule's plus end (By similarity). Cooperates with dynein in organizing spindle assembly during cell division.
Probable minus end-directed motor protein with a microtubule-enhanced ATPase activity. Binds ATP/ADP in vitro. Retains total enzymatic activity even after the removal of the ADP bound in the active site.
Involved in tethering the chromosomes to the spindle pole and in chromosome movement. Microtubule-based anterograde translocator for membranous organelles. Plus end-directed microtubule sliding activity in vitro (By similarity).
Microtubule-associated force-producing protein that plays a role in organelle transport. Its motor activity is directed toward the microtubule's plus end (By similarity).
Microtubule-based anterograde translocator for membranous organelles. Plus end-directed microtubule sliding activity in vitro. Plays a role in primary cilia formation. Plays a role in centriole cohesion and subdistal appendage organization and function. Regulates the formation of the subdistal appendage via recruitement of DCTN1 to the centriole. Also required for ciliary basal feet formation and microtubule anchoring to mother centriole.
Microtubule-based anterograde translocator for membranous organelles. Plus end-directed microtubule sliding activity in vitro. Plays a role in primary cilia formation (PubMed:21670265). Plays a role in centriole cohesion and subdistal appendage organization and function. Regulates the formation of the subdistal appendage via recruitement of DCTN1 to the centriole. Also required for ciliary basal feet formation and microtubule anchoring to mother centriole (PubMed:23386061).
Kinesin motor protein which is required for the anterograde intraflagellar transport (IFT) along the middle segment of the sensory neuron cilia together with the kinesin II motor complex (composed of klp-11, klp-20 and kap-1) and on its own, is required for IFT along the distal segment (PubMed:17000880, PubMed:17420466). In addition, regulates the length of cilia (PubMed:17420466). May have a role during neurogenesis and axonal transport (PubMed:7714894, PubMed:7690265).
Involved in synaptic transmission (PubMed:24812067). Mediates dendritic trafficking of mRNAs (By similarity). Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport. Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity).
Involved in synaptic transmission (By similarity). Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport. Mediates dendritic trafficking of mRNAs (PubMed:19608740). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity).
Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport. Milt and Miro form an essential protein complex that links Khc to mitochondria for light chain-independent, anterograde transport of mitochondria.
May be essential to promote the progression of cytokinesis during node-internode differentiation.
Microtubule-based anterograde translocator for membranous organelles.
Microtubule-dependent motor required for slow axonal transport of neurofilament proteins (NFH, NFM and NFL) (PubMed:12682084). Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner. The ZFYVE27-KIF5A complex contributes to the vesicular transport of VAPA, VAPB, SURF4, RAB11A, RAB11B and RTN3 proteins in neurons (PubMed:21976701). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity).
Microtubule-dependent motor required for normal distribution of mitochondria and lysosomes. May be involved in the mechanisms of growth arrest induced by exposure to DNA-damaging drugs or by cellular senescence (PubMed:9657148). Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner (PubMed:21976701). Regulates centrosome and nuclear positioning during mitotic entry. During the G2 phase of the cell cycle in a BICD2-dependent manner, antagonizes dynein function and drives the separation of nuclei and centrosomes. Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity).
Microtubule-dependent motor required for normal distribution of mitochondria and lysosomes. Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner. Regulates centrosome and nuclear positioning during mitotic entry. During the G2 phase of the cell cycle in a BICD2-dependent manner, antagonizes dynein function and drives the separation of nuclei and centrosomes (By similarity). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (PubMed:23576431).
Microtubule-dependent motor required for slow axonal transport of neurofilament proteins (NFH, NFM and NFL). Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner. The ZFYVE27-KIF5A complex contributes to the vesicular transport of VAPA, VAPB, SURF4, RAB11A, RAB11B and RTN3 proteins in neurons. Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation.
Microtubule-dependent motor required for normal distribution of mitochondria and lysosomes. Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner (By similarity). Regulates centrosome and nuclear positioning during mitotic entry. During the G2 phase of the cell cycle in a BICD2-dependent manner, antagonizes dynein function and drives the separation of nuclei and centrosomes (PubMed:20386726). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity).
Microtubule-dependent motor protein required for organelle transport (By similarity). Plays a role in endosome transport (PubMed:22634595). Involved in the nuclear migration of hyp7 hypodermal precursor cells (PubMed:19605495, PubMed:27697906). Required for the formation of dendritic branches of PVD sensory neurons (PubMed:21205795).
Microtubule-dependent motor required for slow axonal transport of neurofilament proteins (NFH, NFM and NFL). Can induce formation of neurite-like membrane protrusions in non-neuronal cells in a ZFYVE27-dependent manner. The ZFYVE27-KIF5A complex contributes to the vesicular transport of VAPA, VAPB, SURF4, RAB11A, RAB11B and RTN3 proteins in neurons (By similarity). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (PubMed:23576431).
Probable plus end-directed motor protein that functions in the NACK-PQR (NPK1-NQK1/MEK1-NRK1) MAP kinase signaling pathway, which is essential for somatic cell cytokinesis, especially for the cell-plate formation and its expansion. Regulates the activity and the localization of NPK1 by association through the non-catalytic region of the kinase.
Transports vesicles containing N-methyl-D-aspartate (NMDA) receptor 2B along microtubules.
Plus-end directed kinesin-like motor enzyme involved in mitotic spindle assembly.
Binds ATP/ADP in vitro. Possesses low ATPase activity but high affinity for microtubules.
Microtubule-associated force-producing protein that plays a role in organelle transport. Its motor activity is directed toward the microtubule's plus end. The maximal velocity in an inverted motility assay (moving microtubules on fixed motors) was 1.96 um/s.
Probable plus end-directed motor protein that functions in the NACK-PQR (ANP3-MKK6-MPK4) MAP kinase signaling pathway, which is essential for somatic cell cytokinesis, especially for the cell-plate formation and its expansion. May regulate the activity and the localization of ANP3, probably by association through the non-catalytic region of the kinase. Functionally redundant with NACK1 and essential to promote the progression of cytokinesis and for cellularization (formation of the cell plate) during microgametogenesis and megagametogenesis.
Probable plus end-directed motor protein that functions in the NACK-PQR (ANP1-MKK6-MPK4) MAP kinase signaling pathway, which is essential for somatic cell cytokinesis, especially for the cell-plate formation and its expansion. Regulates the activity and the localization of ANP1, probably by association through the non-catalytic region of the kinase. Functionally redundant with NACK2 and essential to promote the progression of cytokinesis and for cellularization (formation of the cell plate) during microgametogenesis and megagametogenesis.
Kinesin-like motor protein involved in the control of the oriented deposition of cellulose microfibrils (PubMed:12468730, Ref.6). Its motor activity is directed toward the microtubule's plus end. It possesses the potential to drive long-distance transport of cargo along cortical microtubules (PubMed:21914648, PubMed:25646318). Regulates cell wall mechanics during cell elongation, by the regulation of primary and secondary walls deposition (Ref.6, PubMed:25600279, PubMed:25646318). Contributes to cortical microtubule-mediated trafficking of cell wall components (PubMed:25646318).
Plus-end directed microtubule motor that may be used for anterograde axonal transport and could conceivably move cargos in fly neurons different than those moved by kinesin heavy chain or other plus-end directed motors.
Required for mitotic chromosomal positioning and bipolar spindle stabilization.
Probable plus end-directed motor protein that may function in the NACK-PQR (NPK1-NQK1/MEK1-NRK1) MAP kinase signaling pathway, which is essential for somatic cell cytokinesis, especially for the cell-plate formation and its expansion. May regulate the activity and the localization of NPK1, probably by association through the non-catalytic region of the kinase.
Motor protein that translocates PRC1 to the plus ends of interdigitating spindle microtubules during the metaphase to anaphase transition, an essential step for the formation of an organized central spindle midzone and midbody and for successful cytokinesis. May play a role in mitotic chromosomal positioning and bipolar spindle stabilization.
Motor protein that translocates PRC1 to the plus ends of interdigitating spindle microtubules during the metaphase to anaphase transition, an essential step for the formation of an organized central spindle midzone and midbody and for successful cytokinesis. May play a role in mitotic chromosomal positioning and bipolar spindle stabilization (By similarity).
Plus-end directed kinesin-like motor enzyme involved in mitotic spindle assembly. Required for centrosome separation and maintenance of spindle bipolarity during mitosis (By similarity).
Plus-end directed kinesin-like motor enzyme involved in mitotic spindle assembly. Plays a role in positioning spindle poles during mitosis, specifically at prometaphase.
Kinesin-like motor protein involved in the control of the oriented deposition of cellulose microfibrils.
Cytoplasmic motor that could play a role in Golgi membrane recycling.
Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (PubMed:7983184). Plays an essential role in stabilizing the mitotic spindle. Required during mitotic cytokinesis (By similarity).
Component of the kinesin II motor complex (composed of kap-1 and the heterodimeric motor proteins klp-11 and klp-20) which is required for intraflagellar transport (IFT) (PubMed:20833139, PubMed:20498083). Heterodimerizes with klp-11 to form a 'processive' molecular motor upon IFT cargo binding, which, within the kinesin II motor complex, binds to and moves along microtubules in a unidirectional manner (without dissociation of the heterodimer), and in turn, is responsible for the IFT of cargo (PubMed:20498083). Specifically, the kinesin II motor complex, together with the kinesin motor protein osm-3 moves along microtubules and is required for anterograde IFT along the middle segment of the sensory neuron cilia (PubMed:17000880, PubMed:20833139, PubMed:28479320). In particular, the kinesin II motor complex delivers specific ciliary cargo proteins such as che-3 which are related to motility to ciliary tips (PubMed:28479320). This is likely mediated by IFT complexes A and B (PubMed:28479320).
Plays an essential role in motile ciliogenesis.
Plus end-directed motor protein involved in asymmetric cell division of sensory organ precursor (SOP) cells by playing a role in the asymmetric localization of Sara-expressing endosomes to the pIIa daughter cell but not to the pIIb cell. Targets Sara-expressing endosomes to the central spindle which is symmetrically arranged in early cell division. During late cytokinesis, central spindle asymmetry is generated by enrichment of Patronin on the pIIb side which protects microtubules from depolymerization by Klp10A while unprotected microtubules on the pIIa side are disassembled by Klp10A, leading to the asymmetric delivery of Sara-expressing endosomes to the pIIa daughter cell (PubMed:26659188). Also plays a role in regulation of autophagosome formation, fusion and positioning and is required for normal localization of Rab14 (PubMed:26763909).
Plus-end directed kinesin-like motor enzyme involved in mitotic spindle assembly. Required for centrosome separation and maintenance of spindle bipolarity during mitosis.
Plus end-directed motor protein required for establishing a bipolar spindle (PubMed:15583027). Associates with both interphase and spindle microtubules (PubMed:15583027). May be involved in nuclear divisions taking place during the development of unfertilized eggs (PubMed:15583027). Required in non-mitotic cells for transport of secretory proteins from the Golgi complex to the cell surface (By similarity).
Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (By similarity). Plays an essential role in stabilizing the mitotic spindle (PubMed:17652157). Required during mitotic cytokinesis (PubMed:26745275).
Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (By similarity). Plays an essential role in stabilizing the mitotic spindle. Required during mitotic cytokinesis (By similarity).
Microtubule-dependent motor protein involved in the control of the oriented deposition of cellulose microfibrils (PubMed:20444225, PubMed:21325138). Involved in wall biogenesis and modification, and contributes to cell-cycle progression and cell division (PubMed:20444225). Acts as a transcriptional activator in gibberellic acid (GA) biosynthesis pathway. Binds specifically to the DNA sequence 5'-ACCAACTTGAA-3' of the ent-kaurene oxidase 2 (CYP701A6 or OsKO2) promoter. May regulate CYP701A6 gene expression and mediates cell elongation by regulating the GA biosynthesis pathway (PubMed:21325138).
Motor protein required for establishing a bipolar spindle during mitosis (PubMed:19001501). Required in non-mitotic cells for transport of secretory proteins from the Golgi complex to the cell surface (PubMed:23857769).
Plus end-directed motor protein required for establishing a bipolar spindle. Associates with both interphase and mitotic spindle microtubules. May be involved in nuclear divisions taking place during the development of unfertilized eggs. Required in non-mitotic cells for transport of secretory proteins from the Golgi complex to the cell surface.
Microtubule-depolymerizing kinesin which plays a role in chromosome congression by reducing the amplitude of preanaphase oscillations and slowing poleward movement during anaphase, thus suppressing chromosome movements. May stabilize the CENPE-BUB1B complex at the kinetochores during early mitosis and maintains CENPE levels at kinetochores during chromosome congression (By similarity).
Motor protein required for establishing a bipolar spindle during mitosis. Required in non-mitotic cells for transport of secretory proteins from the Golgi complex to the cell surface.
Microtubule-dependent motor protein involved in the control of the oriented deposition of cellulose microfibrils.
Subunit
Monomer. Interacts with CENPF, SEPT7 KIF18A and PRC1 (By similarity). Interacts with BUB1B (PubMed:12925705). Interacts with SKAP; this interaction greatly favors SKAP binding to microtubules. Interacts with TRAPPC12 and CTCF (By similarity).
Monomer (PubMed:15236970). Interacts with CENPF (PubMed:9763420). Interacts with BUB1B (PubMed:9763420, PubMed:19625775). Interacts with SEPT7 (PubMed:18460473). Interacts with KIF18A (PubMed:19625775). Interacts with PRC1 (PubMed:15297875). Interacts with NUF2; this interaction determines kinetochore localization (PubMed:17535814). Interacts with SKAP; this interaction greatly favors SKAP binding to microtubules (PubMed:22110139). Interacts with TRAPPC12 (PubMed:25918224). Interacts with CTCF (PubMed:25395579).
Binds microtubules (PubMed:16672264). Homodimer (PubMed:16751590).
Heterodimer of KIF3A and KIF3B. Interacts directly with IFT20 (By similarity). Interacts with the SMC3 subunit of the cohesin complex.
Interacts with the SMC3 subunit of the cohesin complex (By similarity). Heterodimer of KIF3A and KIF3B (PubMed:7559760). Interacts directly with IFT20 (PubMed:12821668).
Heterotrimer of a 115 kDa subunit (KAP115) and two kinesin-like subunits of 95 kDa (KRP95) and 85 kDa (KRP85).
Heterodimer of KIF3A and KIF3B. Interacts with PIFO. Interacts with CLN3. Interacts with DCTN1.
Heterodimer of KIF3A and KIF3B (By similarity). Interacts with PIFO (PubMed:20643351). Interacts with CLN3 (PubMed:22261744). Interacts with DCTN1 (By similarity).
Heterodimer of KIF3A and KIF3B (PubMed:7559760). Interacts with PIFO (PubMed:20643351). Interacts with CLN3 (By similarity). Interacts with DCTN1 (PubMed:23386061).
Oligomer composed of two heavy chains and two light chains.
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 and KLC3 (By similarity). Interacts with TRAK1 (PubMed:15644324). Interacts with ZFYVE27 (By similarity).
Oligomer composed of two heavy chains and two light chains (PubMed:15286375). Interacts with GRIP1 (PubMed:11986669). Interacts with KLC3 and TRAK1 (By similarity). Interacts with ZFYVE27 (PubMed:21976701).
Interacts with D1BLIC, DHC1B and DAW1.
Heterodimer of KIF3A and KIF3C.
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 (PubMed:11986669). Interacts with FMR1 (via C-terminus); this interaction is increased in a mGluR-dependent manner (PubMed:18539120). Interacts with BORCS5 (By similarity). Interacts with ZFYVE27 (PubMed:21976701, PubMed:24251978). Interacts with VAPA, VAPB, SURF4, RAB11A (GDP-bound form), RAB11B (GDP-bound form) and RTN3 in a ZFYVE27-dependent manner (PubMed:21976701). Interacts with BICD2 (By similarity).
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 and PPP1R42 (PubMed:11986669, PubMed:19886865). Interacts with SYBU (By similarity). Interacts with JAKMIP1 (PubMed:17532644). Interacts with PLEKHM2. Interacts with ECPAS (By similarity). Interacts with ZFYVE27 (PubMed:21976701). Found in a complex with OGT, RHOT1, RHOT2 and TRAK1 (By similarity).
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 and PPP1R42 (By similarity). Interacts with SYBU. Interacts with JAKMIP1. Interacts with PLEKHM2. Interacts with ECPAS (By similarity). Interacts with ZFYVE27 (By similarity). Found in a complex with OGT, RHOT1, RHOT2 and TRAK1 (PubMed:24995978).
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1. Interacts with FMR1 (via C-terminus); this interaction is increased in a mGluR-dependent manner. Interacts with ZFYVE27. Interacts with VAPA, VAPB, SURF4, RAB11A (GDP-bound form), RAB11B (GDP-bound form) and RTN3 in a ZFYVE27-dependent manner (By similarity). Interacts with BORCS5 (PubMed:25898167). Interacts with BICD2 (PubMed:20386726).
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1 and PPP1R42 (By similarity). Interacts with SYBU (PubMed:15459722). Interacts with JAKMIP1 (PubMed:17532644). Interacts with PLEKHM2 (PubMed:15905402). Interacts with ECPAS (PubMed:20682791). Interacts with ZFYVE27 (By similarity). Found in a complex with OGT, RHOT1, RHOT2 and TRAK1 (PubMed:24995978).
Oligomer composed of two heavy chains and two light chains. Interacts with GRIP1. Interacts with FMR1 (via C-terminus); this interaction is increased in a mGluR-dependent manner. Interacts with BORCS5. Interacts with ZFYVE27. Interacts with VAPA, VAPB, SURF4, RAB11A (GDP-bound form), RAB11B (GDP-bound form) and RTN3 in a ZFYVE27-dependent manner. Interacts with BICD2.
Interacts (via C-terminus) with NPK1 (via C-terminus).
Interacts with LIN-10 PDZ domain. Interacts with PIWIL1 (By similarity). Interacts with TBATA (By similarity).
Interacts with MKI67 and TPX2.
Binds microtubules.
Interacts with LIN-10 PDZ domain. Interacts with PIWIL1. Interacts with TBATA.
Dimer.
Interacts with ANP3 (PubMed:21575092). Interacts with TIO/FU (PubMed:24146312).
Homodimer.
Interacts with unphosphorylated PRC1 during late mitosis.
Homodimer. Dimerization is required for targeting to microtubule minus ends. Found in a complex with tpx2 and microtubules. Its association with microtubules and targeting to microtubule minus ends requires tpx2 (By similarity).
Component of the kinesin II motor complex, a heterotrimeric complex composed of kap-1, klp-11 and klp-20 (PubMed:17000880, PubMed:20833139, PubMed:20498083, PubMed:28479320). Interacts (via C-terminus) with klp-11 (via C-terminus) to form a heterodimer (PubMed:20498083, PubMed:21917588). Furthermore, within the heterodimer, the C-termini of klp-20 and klp-11 interact to form a coiled coil (stalk) or tail domain, and this is necessary for association with kap-1, and kinesin II motor complex activity upon IFT cargo binding (PubMed:20498083, PubMed:21917588). Prior to cargo binding, the klp-11/klp-20 heterodimer is autoinhibited by the tail domain of the heterodimer, which folds onto the kinesin motor domain (PubMed:20498083). Cargo binding to the heterodimer relieves the autoinhibition, and allows for an extended conformation of the tail domain, and function of the heterodimer (PubMed:20498083).
Interacts with STK36.
Interacts with Atg8a and Rab14.
Homodimer. Dimerization is required for targeting to microtubule minus ends. Found in a complex with tpx2 and microtubules. Its association with microtubules and targeting to microtubule minus ends requires tpx2.
Heterotetramer of two heavy and two light chains. Interacts with aurka.
Heterotetramer of two heavy and two light chains. Interacts with aurka (By similarity).
Interacts with the thyroid hormone receptor in the presence of thyroid hormone. Component of a large chromatin remodeling complex, at least composed of MYSM1, PCAF, RBM10 and KIF11/TRIP5. Interacts (via C-terminus) with the kinase NEK6 in both interphase and mitosis.
Interacts with CENPE and ESR1.
Interacts with the thyroid hormone receptor in the presence of thyroid hormone. Component of a large chromatin remodeling complex, at least composed of MYSM1, PCAF, RBM10 and KIF11/TRIP5.
Miscellaneous
Expression of a truncated protein lacking the motor domain causes inhibition of phragmoplast expansion and multinucleate cells.
Overexpression of KIN4A/FRA1 caused a severe reduction in the thickness of secondary walls in interfascicular fibers and deformation of vessels, an increase in the number of secondary wall layers, which are accompanied with a marked decrease in stem strength.
Similarity
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KIN-7 subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. Kinesin II subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. Kinesin subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KLP2 subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KIN-4 subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. Chromokinesin subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KIN-5/BimC subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KIF27 subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. BimC subfamily.
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. KIN-12 subfamily.
Keywords
ATP-binding
Cell cycle
Cell division
Centromere
Chromosome
Coiled coil
Complete proteome
Cytoplasm
Cytoskeleton
Developmental protein
Kinetochore
Lipoprotein
Methylation
Mitosis
Motor protein
Nucleotide-binding
Phosphoprotein
Prenylation
Reference proteome
Ubl conjugation
3D-structure
Alternative splicing
Direct protein sequencing
Disease mutation
Microtubule
Polymorphism
Primary microcephaly
Transport
Chloroplast
Plastid
Transit peptide
Metal-binding
Zinc
Zinc-finger
Alternative initiation
Mitochondrion
Acetylation
Cell projection
Cilium
Isopeptide bond
Amyotrophic lateral sclerosis
Epilepsy
Hereditary spastic paraplegia
Neurodegeneration
Nucleus
Protein transport
DNA-binding
Mental retardation
Autophagy
Endosome
Activator
Growth regulation
Transcription
Transcription regulation
Glycoprotein
Feature
chain Centromere-associated protein E
propeptide Removed in mature form
splice variant In isoform 3.
sequence variant In MCPH13; results in defective mitotic spindle formation and chromosome segregation; results in delayed mitotic progression; dbSNP:rs144716013.
PDB
1T5C
E-value=4.75883e-85,
Score=810
Ontologies
Topology
Subcellular location
Cytoplasm
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Cytoskeleton
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Spindle
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Chromosome
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Centromere
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Kinetochore
Associates with kinetochores during congression (as early as prometaphase), relocates to the spindle midzone at anaphase, and is quantitatively discarded at the end of the cell division (PubMed:12361599, PubMed:12925705). Recruited to the kinetochore in a SEPT7, CENPQ and TRAPPC12-dependent manner. Recruited to the pericentromeric/centromeric regions of the chromosome in a CTCF-dependent manner (By similarity). With evidence from 2 publications.
Mitochondrion
Cell projection
Cilium
Microtubule organizing center
Localizes to the subdistal appendage region of the centriole. With evidence from 1 publications.
Centrosome
Localizes to the subdistal appendage region of the centriole. With evidence from 1 publications.
Centriole
Localizes to the subdistal appendage region of the centriole. With evidence from 1 publications.
Cilium axoneme
Localizes along the full cilium length. With evidence from 4 publications.
Cilium basal body
Localizes along the full cilium length. With evidence from 4 publications.
Dendrite
Abundant in distal regions of dendrites. With evidence from 7 publications.
Perinuclear region
Nucleus
Phragmoplast
Nucleus matrix
Midbody
Spindle pole
Localizes during metaphase on spindle microtubules, with a strong enrichment at spindle poles. Localizes to the minus ends of spindle pole and aster microtubules in a dynein- and dynactin-dependent manner. Detected diffusively in the cytoplasm. Localized at the centrosome during the interphase and throughout mitosis (By similarity). With evidence from 1 publications.
Early endosome
Ruffle
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
0.21867
Exp number, first 60 AAs:
0
Total prob of N-in:
0.01037
Population Genetic Test Statistics