| 词条 | Coiled-coil domain containing 166 | |||||||||||||||||||||||||||||||||||||||||||||
| 释义 |
Coiled-coil domain containing 166 is a protein that in humans is encoded by the CCDC166 gene. Its function is currently unknown. It contains a coiled-coil domain, hence the current origin of its name. It is primarily expressed in the testes. [1]GeneThe gene currently is known to contain only two exons, and one isoform. This primary transcript consists of 1320 DNA base pairs. Its location is on chromosome 8q24.3, between positions 143706694-143708109, on the + strand. The gene is located near BREA2 and MAPK15.[2] TranscriptsThe gene has only a single transcript, due to only have two exons, both which are always transcribed. The coding portion of the mRNA is 1320 nucleotides.[2] In tissues found to express the transcript for this gene it is typically found in low levels.[3] ProteinCCDC166 has only one isoform in humans, which has a molecular weight of 48.7 kDa and is composed of 439 amino acids. The pI of the protein is 10.537.[4] The protein has several amino acid repeat structures including; EREA, VQSL and (T)QLLH, all of which are conserved in mammals.[5] The composition of the protein reveals that it is high in serine, lysine, and arginine.[4] The protein contains three conserved domains including a coiled-coil domain between amino acids 27-74, a domain of unknown function between amino acids 72-260, and a serine-rich domain between amino acids 288-410.[6] It is believed that the 26-115 AA region is a SH3 domain.[7] The structure is mainly composed of alpha-helices that form a larger coiled-coil. It also contains several coiled-coils. {{infobox| title = CCDC166 | image = | image_size = 30px | alt = | caption = Proposed structure of CCDC166[8] | }} Gene level regulationThe gene seems to be expressed heavily in the testes, and this may be conserved in evolution.[9] The promoter region contains several conserved transcription factor binding sites. Notably among them are the CREB family, KLFs, and perhaps the most telling of which is the presence of Testis-determining factor.[10] These transcription factors are all important during the process of development. Transcript level regulationIn situ hybridization (ISH) data has found the gene's mRNAs are mostly found in the nucleus of Sertoli cells, with low expression in Leydig cells.[9] The gene has also been found in other germ cell tumors.[3] In addition the gene's primary transcript contains several miRNA binding sites, including: hsa-miR-2278, hsa-miR-3178, and hsa-miR-4516.[11]Protein level regulationCCDC166 is predicted to be regulated by SUMO protein. It has a conserved IKAD sequence at amino acid 220-223.[12] This combined with a conserved nuclear localization signal of PKKKR starting at amino acid 3, supports that this protein is imported into the nucleus.[13] The gene also contains several predicted phosphorylation sites, most of which are predicted to be clustered into the serine-rich domain. The occurrences of highest probability occur at serine 10, serine 308, and serine 391.[14] Homology / evolutionWhile the current function of the gene is unknown, many mammals possess on ortholog of the gene. In various primate species studies, several species have been found to possess on orthologous gene that shares 90% sequence identity.[6] While the gene does not seem to have paralogs, it has homologs that have been conserved throughout its evolutionary history. Evidence that its function has been conserved comes from the promoter region, which has predicted SRY-transcription factors binding sites conserved from zebrafish all the way to humans.[10]
Function / biochemistryThe function of the protein is currently unknown. 10. ^1 Cartharius K, Frech K, Grote K, Klocke B, Haltmeier M, Klingenhoff A, Frisch M, Bayerlein M, Werner T (2005) MatInspector and beyond: promoter analysis based on transcription factor binding sites. Bioinformatics 21, 2933-42 11. ^MiRDB - MicroRNA Target Prediction And Functional Study Database. Retrieved April 02, 2018, from http://mirdb.org/ 12. ^Cheng TS, Chang LK, Howng SL, Lu PJ, Lee CI, Hong YR (February 2006). "SUMO-1 modification of centrosomal protein hNinein promotes hNinein nuclear localization". Life Sciences. 78 (10): 1114–20. 13. ^Kalderon, D., Roberts, B. L., Richardson, W. D., & Smith, A. E. (1984). A short amino acid sequence able to specify nuclear location. Cell,39(3), 499-509. doi:10.1016/0092-8674(84)90457-4 14. ^Prediction of post-translational glycosylation and phosphorylation of proteins from the amino acid sequence. Blom N, Sicheritz-Ponten T, Gupta R, Gammeltoft S, Brunak S. Proteomics: Jun;4(6):1633-49, review 2004. 15. ^Kumar S, Stecher G, Suleski M, Hedges SB (2017) TimeTree: A Resource for Timelines, Timetrees, and Divergence Times. Mol Biol Evol 34 (7): 1812-1819 16. ^Stephen F. Altschul, Thomas L. Madden, Alejandro A. Schäffer, Jinghui Zhang, Zheng Zhang, Webb Miller, and David J. Lipman (1997), "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs", Nucleic Acids Res. 25:3389-3402. 17. ^Gasteiger E., Hoogland C., Gattiker A., Duvaud S., Wilkins M.R., Appel R.D., Bairoch A.;Protein Identification and Analysis Tools on the ExPASy Server; (In) John M. Walker (ed): The Proteomics Protocols Handbook, Humana Press (2005). pp. 571-607 " 18. ^{{cite web | title = CCDC166 | url = https://string-db.org/ | accessdate = 2018-05-05}} 19. ^{{cite web | title = CCDC166 | url = https://hive.biochemistry.gwu.edu/biomuta/proteinview/P0CW27 | accessdate = 2018-05-05}} External links
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