ID CDN1B_HUMAN STANDARD; PRT; 198 AA. AC P46527; Q16307; Q9BUS6; DT 01-NOV-1995, integrated into UniProtKB/Swiss-Prot. DT 01-NOV-1995, sequence version 1. DT 07-FEB-2006, entry version 58. DE Cyclin-dependent kinase inhibitor 1B (Cyclin-dependent kinase DE inhibitor p27) (p27Kip1). GN Name=CDKN1B; Synonyms=KIP1; OS Homo sapiens (Human). OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; OC Mammalia; Eutheria; Euarchontoglires; Primates; Catarrhini; Hominidae; OC Homo. OX NCBI_TaxID=9606; RN [1] RP NUCLEOTIDE SEQUENCE, AND PROTEIN SEQUENCE OF 28-79 AND 104-152. RC TISSUE=Kidney; RX MEDLINE=94306518; PubMed=8033212; DOI=10.1016/0092-8674(94)90572-X; RA Polyak K., Lee M.-H., Erdjument-Bromage H., Koff A., Roberts J.M., RA Tempst P., Massague J.; RT "Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a RT potential mediator of extracellular antimitogenic signals."; RL Cell 78:59-66(1994). RN [2] RP NUCLEOTIDE SEQUENCE. RX MEDLINE=95188144; PubMed=7882309; RA Pietenpol J.A., Bohlander S.K., Sato Y., Papadopoulos N., Liu B., RA Friedman C., Trask B.J., Roberts J.M., Kinzler K.W., Rowley J.D.; RT "Assignment of the human p27Kip1 gene to 12p13 and its analysis in RT leukemias."; RL Cancer Res. 55:1206-1210(1995). RN [3] RP NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS TRP-15 AND GLY-109. RA Rieder M.J., Braun A.C., Montoya M.A., Chung M.-W., Nguyen C.P., RA Nguyen D.A., Livingston R.J., Poel C.L., Robertson P.D., RA Schackwitz W.S., Sherwood J.K., Witrak L.A., Nickerson D.A.; RT "NIEHS-SNPs, environmental genome project, NIEHS ES15478, Department RT of Genome Sciences, Seattle, WA (URL: http://egp.gs.washington.edu)."; RL Submitted (FEB-2002) to the EMBL/GenBank/DDBJ databases. RN [4] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANT GLY-109. RC TISSUE=Cervix; RX MEDLINE=22388257; PubMed=12477932; DOI=10.1073/pnas.242603899; RA Strausberg R.L., Feingold E.A., Grouse L.H., Derge J.G., RA Klausner R.D., Collins F.S., Wagner L., Shenmen C.M., Schuler G.D., RA Altschul S.F., Zeeberg B., Buetow K.H., Schaefer C.F., Bhat N.K., RA Hopkins R.F., Jordan H., Moore T., Max S.I., Wang J., Hsieh F., RA Diatchenko L., Marusina K., Farmer A.A., Rubin G.M., Hong L., RA Stapleton M., Soares M.B., Bonaldo M.F., Casavant T.L., Scheetz T.E., RA Brownstein M.J., Usdin T.B., Toshiyuki S., Carninci P., Prange C., RA Raha S.S., Loquellano N.A., Peters G.J., Abramson R.D., Mullahy S.J., RA Bosak S.A., McEwan P.J., McKernan K.J., Malek J.A., Gunaratne P.H., RA Richards S., Worley K.C., Hale S., Garcia A.M., Gay L.J., Hulyk S.W., RA Villalon D.K., Muzny D.M., Sodergren E.J., Lu X., Gibbs R.A., RA Fahey J., Helton E., Ketteman M., Madan A., Rodrigues S., Sanchez A., RA Whiting M., Madan A., Young A.C., Shevchenko Y., Bouffard G.G., RA Blakesley R.W., Touchman J.W., Green E.D., Dickson M.C., RA Rodriguez A.C., Grimwood J., Schmutz J., Myers R.M., RA Butterfield Y.S.N., Krzywinski M.I., Skalska U., Smailus D.E., RA Schnerch A., Schein J.E., Jones S.J.M., Marra M.A.; RT "Generation and initial analysis of more than 15,000 full-length human RT and mouse cDNA sequences."; RL Proc. Natl. Acad. Sci. U.S.A. 99:16899-16903(2002). RN [5] RP INTERACTION WITH UHMK1, PHOSPHORYLATION SITE SER-10, AND MUTAGENESIS RP OF SER-10 AND THR-187. RX PubMed=12093740; DOI=10.1093/emboj/cdf343; RA Boehm M., Yoshimoto T., Crook M.F., Nallamshetty S., True A., RA Nabel G.J., Nabel E.G.; RT "A growth factor-dependent nuclear kinase phosphorylates p27(Kip1) and RT regulates cell cycle progression."; RL EMBO J. 21:3390-3401(2002). RN [6] RP PHOSPHORYLATION SITE SER-10. RX PubMed=15302935; DOI=10.1073/pnas.0404720101; RA Beausoleil S.A., Jedrychowski M., Schwartz D., Elias J.E., Villen J., RA Li J., Cohn M.A., Cantley L.C., Gygi S.P.; RT "Large-scale characterization of HeLa cell nuclear phosphoproteins."; RL Proc. Natl. Acad. Sci. U.S.A. 101:12130-12135(2004). RN [7] RP X-RAY CRYSTALLOGRAPHY (2.3 ANGSTROMS) OF 23-106 OF COMPLEX WITH CDK2 RP AND CG2A. RX MEDLINE=96300318; PubMed=8684460; DOI=10.1038/382325a0; RA Russo A.A., Jeffrey P.D., Patten A.K., Massague J., Pavletich N.P.; RT "Crystal structure of the p27Kip1 cyclin-dependent-kinase inhibitor RT bound to the cyclin A-Cdk2 complex."; RL Nature 382:325-331(1996). CC -!- FUNCTION: Involved in G1 arrest. May mediate TGF beta-induced G1 CC arrest. Binds to and inhibits complexes formed by cyclin E-CDK2, CC cyclin A-CDK2, and cyclin D1-CDK4. Interaction with nucleoporin CC NUP50 is required for nuclear import and for degradation of CC phosphorylated p27Kip1 after nuclear import (By similarity). CC -!- SUBUNIT: Interacts with NUP50 and with UHMK1. Interacts with COPS5 CC subunit of COP9 signalosome complex, leading to its subsequent CC degradation (By similarity). CC -!- INTERACTION: CC P14635:CCNB1; NbExp=1; IntAct=EBI-519280, EBI-495332; CC P24385:CCND1; NbExp=1; IntAct=EBI-519280, EBI-375001; CC P24864:CCNE1; NbExp=1; IntAct=EBI-519280, EBI-519526; CC P11802:CDK4; NbExp=1; IntAct=EBI-519280, EBI-295644; CC O00505:KPNA3; NbExp=1; IntAct=EBI-519280, EBI-358297; CC O15131:KPNA5; NbExp=3; IntAct=EBI-519280, EBI-540602; CC P31946:YWHAB; NbExp=1; IntAct=EBI-519280, EBI-359815; CC P62258:YWHAE; NbExp=1; IntAct=EBI-519280, EBI-356498; CC P61981:YWHAG; NbExp=1; IntAct=EBI-519280, EBI-359832; CC -!- SUBCELLULAR LOCATION: Nuclear and cytoplasmic in quiescent cells. CC Upon cell cycle progression, mostly cytoplasmic (By similarity). CC -!- TISSUE SPECIFICITY: Expressed in all tissues tested. Highest CC levels in skeletal muscle, lowest in liver and kidney. CC -!- DOMAIN: A peptide sequence containing only AA 28-79 retains CC substantial KIP1 cyclin A/CDK2 inhibitory activity. CC -!- PTM: Phosphorylation on Ser-10 leads to nuclear export to the CC cytoplasm and promotes cell cycle progression (By similarity). CC -!- SIMILARITY: Belongs to the CDI family. CC -!- DATABASE: NAME=Atlas Genet. Cytogenet. Oncol. Haematol.; CC WWW="http://www.infobiogen.fr/services/chromcancer/Genes/CDKN1BID116.html". CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; U10906; AAA20240.1; -; mRNA. DR EMBL; S76988; AAD14244.1; -; Genomic_DNA. DR EMBL; S76986; AAD14244.1; JOINED; Genomic_DNA. DR EMBL; AF480891; AAL78041.1; -; Genomic_DNA. DR EMBL; BC001971; AAH01971.1; -; mRNA. DR PDB; 1H27; X-ray; E=25-35. DR PDB; 1JSU; X-ray; C=23-106. DR IntAct; P46527; -. DR SWISS-2DPAGE; P46527; HUMAN. DR Ensembl; ENSG00000111276; Homo sapiens. DR H-InvDB; HIX0010441; -. DR HGNC; HGNC:1785; CDKN1B. DR MIM; 600778; gene. DR LinkHub; P46527; -. DR GO; GO:0005737; C:cytoplasm; IDA. DR GO; GO:0005634; C:nucleus; IDA. DR GO; GO:0004861; F:cyclin-dependent protein kinase inhibitor a...; TAS. DR GO; GO:0005515; F:protein binding; IPI. DR GO; GO:0005072; F:transforming growth factor beta receptor, c...; TAS. DR GO; GO:0007050; P:cell cycle arrest; IMP. DR GO; GO:0008285; P:negative regulation of cell proliferation; TAS. DR GO; GO:0000079; P:regulation of cyclin dependent protein kina...; TAS. DR InterPro; IPR003175; CDI. DR Pfam; PF02234; CDI; 1. KW 3D-structure; Cell cycle; Direct protein sequencing; Nuclear protein; KW Phosphorylation; Polymorphism; Protein kinase inhibitor. FT CHAIN 1 198 Cyclin-dependent kinase inhibitor 1B. FT /FTId=PRO_0000190084. FT MOTIF 153 169 Nuclear localization signal (Potential). FT MOD_RES 10 10 Phosphoserine (by UHMK1). FT VARIANT 15 15 R -> W (in dbSNP:2066828). FT /FTId=VAR_011871. FT VARIANT 109 109 V -> G (in dbSNP:2066827). FT /FTId=VAR_011872. FT MUTAGEN 10 10 S->A: Loss of phosphorylation by UHMK1; FT causes cell cycle arrest. FT MUTAGEN 187 187 T->A: No effect on phosphorylation by FT UHMK1. FT CONFLICT 22 22 E -> D (in Ref. 2). FT STRAND 33 33 FT HELIX 38 49 FT TURN 50 53 FT HELIX 54 60 FT TURN 61 61 FT STRAND 62 63 FT TURN 64 67 FT STRAND 68 69 FT STRAND 71 74 FT STRAND 77 80 FT TURN 81 82 FT STRAND 83 84 FT HELIX 86 89 SQ SEQUENCE 198 AA; 22073 MW; 1118D58901CDF3FC CRC64; MSNVRVSNGS PSLERMDARQ AEHPKPSACR NLFGPVDHEE LTRDLEKHCR DMEEASQRKW NFDFQNHKPL EGKYEWQEVE KGSLPEFYYR PPRPPKGACK VPAQESQDVS GSRPAAPLIG APANSEDTHL VDPKTDPSDS QTGLAEQCAG IRKRPATDDS STQNKRANRT EENVSDGSPN AGSVEQTPKK PGLRRRQT //