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Reviewed, UniProtKB/Swiss-Prot O60566 (BUB1B_HUMAN)

Last modified July 22, 2008. Version 82. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (7) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Binary interactions · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Mitotic checkpoint serine/threonine-protein kinase BUB1 beta
    EC=2.7.11.1
Alternative name(s):
    MAD3/BUB1-related protein kinase
      Short name(s)=hBUBR1
    Mitotic checkpoint kinase MAD3L
    SSK1
Gene names
Name: BUB1B
Synonyms: BUBR1, MAD3L
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length1050 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

Essential component of the mitotic checkpoint. Required for normal mitosis progression. The mitotic checkpoint delays anaphase until all chromosomes are properly attached to the mitotic spindle. One of its checkpoint functions is to inhibit the activity of the anaphase-promoting complex/cyclosome (APC/C) by blocking the binding of CDC20 to APC/C, independently of its kinase activity. The other is to monitor kinetochore activities that depend on the kinetochore motor CENPE. Also implicated in triggering apoptosis in polyploid cells that exit aberrantly from mitotic arrest. May play a role for tumor suppression.

Catalytic activity

ATP + a protein = ADP + a phosphoprotein.

Subunit structure

Interacts with CENPE, CENPF, mitosin and BUB3. Part of a complex containing BUB3, CDC20 and BUB1B. Interacts with anaphase-promoting complex/cyclosome (APC/C).

Subcellular location

Cytoplasm. Nucleus. Kinetochore. Note= Cytoplasmic in interphase cells. Associates with the kinetochores.

Tissue specificity

Highly expressed in thymus followed by spleen. Preferentially expressed in tissues with a high mitotic index.

Induction

Induced during mitosis.

Domain

The CD1 domain directs kinetochore localization and binding to BUB3.

The D-box targets the protein for rapid degradation by ubiquitin-dependent proteolysis during the transition from mitosis to interphase Potential.

Post-translational modification

Proteolytically cleaved by caspase-3 in a cell cycle specific manner. The cleavage might be involved in the durability of the cell cycle delay. Caspase-3 cleavage is associated with abrogation of the mitotic checkpoint. The major site of cleavage is at Asp-610.

Ubiquitinated Probable. Degradated by the proteasome.

Autophosphorylated in vitro. Phosphorylated during mitosis and hyperphosphorylated in mitotically arrested cells.

Involvement in disease

Defects in BUB1B are associated with tumor formation.

Defects in BUB1B are the cause of premature chromatid separation trait (PCS) [MIM:176430]. PCS consists of separate and splayed chromatids with discernible centromeres and involves all or most chromosomes of a metaphase. It is found in up to 2% of metaphases in cultured lymphocytes from approximately 40% of normal individuals. When PCS is present in 5% or more of cells, it is known as the heterozygous PCS trait and has no obvious phenotypic effect, although some have reported decreased fertility. Inheritance is autosomal dominant.

Defects in BUB1B are the cause of mosaic variegated aneuploidy syndrome (MVA) [MIM:257300]. MVA is a severe autosomal recessive developmental disorder characterized by mosaic aneuploidies, predominantly trisomies and monosomies, involving multiple different chromosomes and tissues. The proportion of aneuploid cells varies but is usually more than 25% and is substantially greater than in normal individuals. Affected individuals typically present with severe intrauterine growth retardation and microcephaly. Eye anomalies, mild dysmorphism, variable developmental delay, and a broad spectrum of additional congenital abnormalities and medical conditions may also occur. The risk of malignancy is high, with rhabdomyosarcoma, Wilms tumor and leukemia reported in several cases. MVA is caused by biallelic mutations in the BUB1B gene.

Sequence similarities

Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. BUB1 subfamily.

Contains 1 CD1 domain.

Contains 1 protein kinase domain.

Binary interactions

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical view

Molecule processing

Chain1 – 10501050Mitotic checkpoint serine/threonine-protein kinase BUB1 beta

Regions

Domain62 – 213152CD1
Domain766 – 1050285Protein kinase
Nucleotide binding772 – 7809ATP By similarity
Motif111 – 1188Nuclear localization signal Potential
Motif224 – 2329D-box
Compositional bias209 – 2157Poly-Glu

Sites

Active site8821Proton acceptor By similarity
Binding site7951ATP By similarity
Site579 – 5802Cleavage; by caspase-3
Site610 – 6112Cleavage; by caspase-3

Amino acid modifications

Modified residue541Phosphothreonine

Natural variations

Natural variant151M → T in a colorectal cancer cell line.
Natural variant361R → Q in PCS.
Natural variant401T → M
Natural variant3491R → Q: dbSNP rs1801376.
Natural variant3901E → D: dbSNP rs1017842.
Natural variant5501R → Q in MVA; heterozygous compound with nonsense mutation. dbSNP rs28989187.
Natural variant6181V → A in colorectal cancer. dbSNP rs1801528.
Natural variant8141R → H in MVA; heterozygous compound with nonsense mutation. dbSNP rs28989182.
Natural variant8441L → F in MVA; associated with H-921; heterozygous compound with nonsense mutation. dbSNP rs28989181.
Natural variant9091I → T in MVA; heterozygous compound with nonsense mutation. dbSNP rs28989184.
Natural variant9211Q → H in MVA; associated with F-844; heterozygous compound with nonsense mutation. dbSNP rs28989183.
Natural variant10121L → P in MVA; heterozygous compound with nonsense mutation. dbSNP rs28989185.

Experimental info

Mutagenesis5791D → E: Abolishes the cleavage by caspase-3
Mutagenesis6101D → E: Abolishes the cleavage by caspase-3
Mutagenesis7951K → A: Does not abolish the capacity to inhibit APC/CDC20
Sequence conflict248 – 2492AL → VF in AAC23736. Ref.5
Sequence conflict7881S → F in AAC06260. Ref.1
Sequence conflict10181E → K in AAC33435. Ref.2

Sequences

Sequence LengthMass (Da)Tools
O60566-1 [UniParc].

Last modified April 3, 2007. Version 3.
Checksum: F7871103A56E6B46

FASTA1,050119,545
        10         20         30         40         50         60 
MAAVKKEGGA LSEAMSLEGD EWELSKENVQ PLRQGRIMST LQGALAQESA CNNTLQQQKR 

        70         80         90        100        110        120 
AFEYEIRFYT GNDPLDVWDR YISWTEQNYP QGGKESNMST LLERAVEALQ GEKRYYSDPR 

       130        140        150        160        170        180 
FLNLWLKLGR LCNEPLDMYS YLHNQGIGVS LAQFYISWAE EYEARENFRK ADAIFQEGIQ 

       190        200        210        220        230        240 
QKAEPLERLQ SQHRQFQARV SRQTLLALEK EEEEEVFESS VPQRSTLAEL KSKGKKTARA 

       250        260        270        280        290        300 
PIIRVGGALK APSQNRGLQN PFPQQMQNNS RITVFDENAD EASTAELSKP TVQPWIAPPM 

       310        320        330        340        350        360 
PRAKENELQA GPWNTGRSLE HRPRGNTASL IAVPAVLPSF TPYVEETARQ PVMTPCKIEP 

       370        380        390        400        410        420 
SINHILSTRK PGKEEGDPLQ RVQSHQQASE EKKEKMMYCK EKIYAGVGEF SFEEIRAEVF 

       430        440        450        460        470        480 
RKKLKEQREA ELLTSAEKRA EMQKQIEEME KKLKEIQTTQ QERTGDQQEE TMPTKETTKL 

       490        500        510        520        530        540 
QIASESQKIP GMTLSSSVCQ VNCCARETSL AENIWQEQPH SKGPSVPFSI FDEFLLSEKK 

       550        560        570        580        590        600 
NKSPPADPPR VLAQRRPLAV LKTSESITSN EDVSPDVCDE FTGIEPLSED AIITGFRNVT 

       610        620        630        640        650        660 
ICPNPEDTCD FARAARFVST PFHEIMSLKD LPSDPERLLP EEDLDVKTSE DQQTACGTIY 

       670        680        690        700        710        720 
SQTLSIKKLS PIIEDSREAT HSSGFSGSSA SVASTSSIKC LQIPEKLELT NETSENPTQS 

       730        740        750        760        770        780 
PWCSQYRRQL LKSLPELSAS AELCIEDRPM PKLEIEKEIE LGNEDYCIKR EYLICEDYKL 

       790        800        810        820        830        840 
FWVAPRNSAE LTVIKVSSQP VPWDFYINLK LKERLNEDFD HFCSCYQYQD GCIVWHQYIN 

       850        860        870        880        890        900 
CFTLQDLLQH SEYITHEITV LIIYNLLTIV EMLHKAEIVH GDLSPRCLIL RNRIHDPYDC 

       910        920        930        940        950        960 
NKNNQALKIV DFSYSVDLRV QLDVFTLSGF RTVQILEGQK ILANCSSPYQ VDLFGIADLA 

       970        980        990       1000       1010       1020 
HLLLFKEHLQ VFWDGSFWKL SQNISELKDG ELWNKFFVRI LNANDEATVS VLGELAAEMN 

      1030       1040       1050 
GVFDTTFQSH LNKALWKVGK LTSPGALLFQ 

« Hide

References

« Hide 'large scale' references
[1]"The human homologue of Bub3 is required for kinetochore localization of Bub1 and a Mad3/Bub1-related protein kinase."
Taylor S.S., Ha E., McKeon F.
J. Cell Biol. 142:1-11(1998) [PubMed: 9660858] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLN-349.
[2]"Characterization of the kinetochore binding domain of CENP-E reveals interactions with the kinetochore proteins CENP-F and hBUBR1."
Chan G.K.T., Schaar B.T., Yen T.J.
J. Cell Biol. 143:49-63(1998) [PubMed: 9763420] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLN-349.
[3]"Mutations of mitotic checkpoint genes in human cancers."
Cahill D.P., Lengauer C., Yu J., Riggins G.J., Willson J.K.V., Markowitz S.D., Kinzler K.W., Vogelstein B.
Nature 392:300-303(1998) [PubMed: 9521327] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANTS THR-15 AND GLN-349.
[4]"The mouse mitotic checkpoint gene bub1b, a novel bub1 family member, is expressed in a cell cycle-dependent manner."
Davenport J.W., Fernandes E.R., Harris L.D., Neale G.A.M., Goorha R.
Genomics 55:113-117(1999) [PubMed: 9889005] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[5]"Identification of a novel gene -- SSK1 -- in human endothelial cells exposed to shear stress."
Donadelli R., Benatti L., Remuzzi A., Morigi M., Gullans S.R., Benigni A., Remuzzi G., Noris M.
Biochem. Biophys. Res. Commun. 246:881-887(1998) [PubMed: 9618306] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLN-349.
Tissue: Umbilical vein.
[6]"Human MAD3-like protein kinase (hmad3)."
Dai W., Ouyang B., Lan Z., Pan H.
Submitted (MAY-1998) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLN-349.
[7]Seike M., Gemma A., Hosoya Y., Kurimoto F., Yoshimura A., Kudoh S.
Submitted (OCT-2000) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[8]"BUBR1 phosphorylation is regulated during mitotic checkpoint activation."
Li W., Lan Z., Wu H., Wu S., Meadows J., Chen J., Zhu V., Dai W.
Cell Growth Differ. 10:769-775(1999) [PubMed: 10593653] [Abstract]
Cited for: PHOSPHORYLATION, TISSUE SPECIFICITY, INDUCTION.
[9]"Human BUBR1 is a mitotic checkpoint kinase that monitors CENP-E functions at kinetochores and binds the cyclosome/APC."
Chan G.K., Jablonski S.A., Sudakin V., Hittle J.C., Yen T.J.
J. Cell Biol. 146:941-954(1999) [PubMed: 10477750] [Abstract]
Cited for: FUNCTION, SUBCELLULAR LOCATION, INDUCTION, PHOSPHORYLATION, INTERACTION WITH APC/C.
[10]"Mad2-independent inhibition of APC/Cdc20 by the mitotic checkpoint protein BubR1."
Tang Z., Bharadwaj R., Li B., Yu H.
Dev. Cell 1:227-237(2001) [PubMed: 11702782] [Abstract]
Cited for: FUNCTION, IDENTIFICATION IN A COMPLEX WITH CDC20 AND BUB3, MUTAGENESIS OF LYS-795.
[11]"Dual roles of human BubR1, a mitotic checkpoint kinase, in the monitoring of chromosomal instability."
Shin H.J., Baek K.H., Jeon A.H., Park M.T., Lee S.J., Kang C.M., Lee H.S., Yoo S.H., Chung D.H., Sung Y.C., McKeon F., Lee C.W.
Cancer Cell 4:483-497(2003) [PubMed: 14706340] [Abstract]
Cited for: FUNCTION, SUBCELLULAR LOCATION, DEGRADATION BY THE PROTEASOME.
[12]"Caspase-mediated specific cleavage of BubR1 is a determinant of mitotic progression."
Kim M., Murphy K., Liu F., Parker S.E., Dowling M.L., Baff W., Kao G.D.
Mol. Cell. Biol. 25:9232-9248(2005) [PubMed: 16227576] [Abstract]
Cited for: CASPASE-3 CLEAVAGE AT ASP-579 AND ASP-610, INDUCTION, MUTAGENESIS OF ASP-579 AND ASP-610.
[13]"Automated phosphoproteome analysis for cultured cancer cells by two-dimensional nanoLC-MS using a calcined titania/C18 biphasic column."
Imami K., Sugiyama N., Kyono Y., Tomita M., Ishihama Y.
Anal. Sci. 24:161-166(2008) [PubMed: 18187866] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-54, MASS SPECTROMETRY.
[14]"Characterization of MAD2B and other mitotic spindle checkpoint genes."
Cahill D.P., da Costa L.T., Carson-Walter E.B., Kinzler K.W., Vogelstein B., Lengauer C.
Genomics 58:181-187(1999) [PubMed: 10366450] [Abstract]
Cited for: VARIANTS GLN-349 AND ALA-618.
[15]"Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B."
Hanks S., Coleman K., Reid S., Plaja A., Firth H., Fitzpatrick D., Kidd A., Mehes K., Nash R., Robin N., Shannon N., Tolmie J., Swansbury J., Irrthum A., Douglas J., Rahman N.
Nat. Genet. 36:1159-1161(2004) [PubMed: 15475955] [Abstract]
Cited for: VARIANTS MVA GLN-550; HIS-814; PHE-844; THR-909; HIS-921 AND PRO-1012.
[16]"Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome."
Matsuura S., Matsumoto Y., Morishima K., Izumi H., Matsumoto H., Ito E., Tsutsui K., Kobayashi J., Tauchi H., Kajiwara Y., Hama S., Kurisu K., Tahara H., Oshimura M., Komatsu K., Ikeuchi T., Kajii T.
Am. J. Med. Genet. A 140:358-367(2006) [PubMed: 16411201] [Abstract]
Cited for: VARIANT PCS GLN-36.
[17]"Patterns of somatic mutation in human cancer genomes."
Greenman C., Stephens P., Smith R., Dalgliesh G.L., Hunter C., Bignell G., Davies H., Teague J., Butler A., Stevens C., Edkins S., O'Meara S., Vastrik I., Schmidt E.E., Avis T., Barthorpe S., Bhamra G., Buck G. expand/collapse author list , Choudhury B., Clements J., Cole J., Dicks E., Forbes S., Gray K., Halliday K., Harrison R., Hills K., Hinton J., Jenkinson A., Jones D., Menzies A., Mironenko T., Perry J., Raine K., Richardson D., Shepherd R., Small A., Tofts C., Varian J., Webb T., West S., Widaa S., Yates A., Cahill D.P., Louis D.N., Goldstraw P., Nicholson A.G., Brasseur F., Looijenga L., Weber B.L., Chiew Y.-E., DeFazio A., Greaves M.F., Green A.R., Campbell P., Birney E., Easton D.F., Chenevix-Trench G., Tan M.-H., Khoo S.K., Teh B.T., Yuen S.T., Leung S.Y., Wooster R., Futreal P.A., Stratton M.R.
Nature 446:153-158(2007) [PubMed: 17344846] [Abstract]
Cited for: VARIANTS [LARGE SCALE ANALYSIS] MET-40; GLN-349; ASP-390 AND ALA-618.

Cross-references

Sequence databases

AF053306 mRNA. Translation: AAC06260.1.
AF046918 mRNA. Translation: AAC33435.1.
AF046079 mRNA. Translation: AAC12730.2.
AF107297 mRNA. Translation: AAD11941.1.
AF035933 mRNA. Translation: AAC23736.1.
AF068760 mRNA. Translation: AAC19118.1.
AF310214 expand/collapse EMBL AC list , AF310192, AF310193, AF310194, AF310195, AF310196, AF310197, AF310198, AF310199, AF310200, AF310201, AF310202, AF310203, AF310204, AF310205, AF310206, AF310207, AF310208, AF310209, AF310210, AF310211, AF310212, AF310213 Genomic DNA. Translation: AAL10712.1.
PIRJW0092.
RefSeqNP_001202.4.
UniGeneHs.631699

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

DIPDIP:24203N.
IntActO60566.

Genome annotation databases

EnsemblENSG00000156970. Homo sapiens. [Contig view]
GeneID701.
KEGGhsa:701.

Organism-specific databases

H-InvDBHIX0012121.
HGNCHGNC:1149. BUB1B.
HPAHPA008419.
MIM176430. phenotype.
257300. phenotype.
602860. gene.
Orphanet1052. Mosaic variegated aneuploidy syndrome.
PharmGKBPA82.
GenAtlasSearch...
GeneCardsSearch...
GeneLynxSearch...

Phylogenomic databases

HOVERGENO60566.

Enzyme and pathway databases

ReactomeREACT_152. Cell Cycle, Mitotic.
REACT_1538. Cell Cycle Checkpoints.
REACT_6850. Cdc20:Phospho-APC/C mediated degradation of Cyclin A.
REACT_8017. APC-Cdc20 mediated degradation of Nek2A.

Gene expression databases

ArrayExpressO60566.
CleanExHS_BUB1B.

Family and domain databases

InterProIPR015661. Bub1.
IPR013212. Mad3_BUB1_I.
IPR000719. Prot_kinase_core.
IPR017441. Protein_kinase_ATP_bd_CS.
IPR008271. Ser_thr_pkin_AS.
[Graphical view]
PANTHERPTHR14030. Bub1. 1 hit.
PfamPF08311. Mad3_BUB1_I. 1 hit.
[Graphical view]
ProDomPD000001. Prot_kinase. 1 hit.
[Graphical view] [Entries sharing at least one domain]
SMARTSM00777. Mad3_BUB1_I. 1 hit.
[Graphical view]
PROSITEPS00107. PROTEIN_KINASE_ATP. False negative.
PS50011. PROTEIN_KINASE_DOM. False negative.
PS00108. PROTEIN_KINASE_ST. False negative.
[Graphical view]
BLOCKSSearch...

Other Resources

SOURCESearch...
ProtoNetSearch...

Entry information