Recombinant Human Centromere protein J (CENPJ), partial

1. CPAP regulates delivery of its bound beta-tubulin to define the size of microtubule-based cellular structures using a "clutch-like" mechanism. PMID: 27306797
2. Data suggest that alcohol/ethanol exposure diminishes pool of proliferative neurons (Neuro2a cell line) through disordering of spindle orientation and promotion of asymmetric cell division; these neuronal abnormalities appear to be due to reduced CENPJ protein expression level. PMID: 29778912
3. CPAP-S467D protein has a low affinity for microtubule binding but a high affinity for pericentriolar material proteins. PMID: 26997271
4. CPAP promotes timely cilium disassembly to maintain neural progenitor pool. CPAP mutation causes Seckel syndrome with microcephaly. PMID: 26929011
5. Data suggest that the single G-box domain (that appears to fold into 14-20 antiparallel beta-strands) of CENPJ has stable but dynamic structure; CRAP forms multimers (in solution and in crystals) of elongated fibrils similar to amyloid fibrils. [REVIEW] PMID: 26517891
6. Centrobin plays a role in the stability and centriole elongation function of CPAP and limits the centriole length. PMID: 25616662
7. studies provide the first structural insight into how the malfunction of centriole proteins results in human disease and also reveal that the CPAP-STIL interaction constitutes a conserved key step in centriole biogenesis PMID: 24052813
8. The results showed a human-specific hypomethylation in the 5' UTR of CENPJ in the brain, where methylation levels among humans are only about one-third of those found among nonhuman primates. PMID: 24288161
9. Centrobin-CPAP interaction is critical for the recruitment of CPAP to procentrioles to promote the elongation of daughter centrioles and for the persistence of CPAP on preexisting mother centrioles. PMID: 24700465
10. CPAP depletion results in asymmetric spindle poles with uneven distribution of pericentriolar material. PMID: 24491538
11. Sas-4 acts as a vehicle to tether PCM complexes to centrioles independent of its well-known role in centriole duplication PMID: 24385583
12. CEP120 associates with SPICE1 and CPAP, and depletion of any of these proteins results in short procentrioles. Furthermore, CEP120 or CPAP overexpression results in excessive centriole elongation, a process dependent on CEP120, SPICE1, and CPAP. PMID: 23810536
13. SUMOylated CPAP could synergistically increase the HBx-induced NF-kappaB activity PMID: 23369793
14. CEP120 is a CPAP-interacting protein that positively regulates centriole elongation. PMID: 23857771
15. Authors propose that CEP135 directly connects the central hub protein, hSAS-6, to the outer microtubules, and suggest that this interaction stabilizes the proper cartwheel structure for further CPAP-mediated centriole elongation. PMID: 23511974
16. CPAP degradation and function is controlled by the poly(ADP-ribose) polymerase tankyrase 1. PMID: 22699936
17. STIL and CPAP are essential for centriole formation and for proper spindle position. PMID: 22100914
18. Results suggest that Cep152 recruits Plk4 and CPAP to the centrosome to ensure a faithful centrosome duplication process. PMID: 21059844
19. Data establishes that mutation of CENPJ can lead to Seckel syndrome and calls for further investigation of the role played by other microcephaly related genes in the pathogenesis of PD. PMID: 20522431
20. Results identify centrosomal P4.1-associated protein (CPAP), a human homologue of SAS-4, as a substrate of PLK2 whose activity oscillates during the cell cycle. PMID: 20531387
21. cell cycle-regulated phosphorylation orchestrates the dynamics of CPAP molecular interaction and centrosome splitting to ensure genomic stability in cell division PMID: 19889632
22. CPAP was found to augment Stat5-mediated transcription PMID: 12198240
23. CPAP carries a novel microtubule-destabilizing motif that not only inhibits microtubule nucleation from the centrosome but also depolymerizes taxol-stabilized microtubules. PMID: 15047868
24. CPAP functions as a coactivator of NF-kappaB-mediated transcription PMID: 15687488
25. Mutations in CENPJ gene is associated with autosomal recessive primary microcephaly PMID: 15793586
26. Together, our results reveal a structural role for CPAP to maintain centrosome integrity and normal spindle morphology during cell division. PMID: 16316625
27. In summary, our results show a direct interaction between CPAP and 14-3-3, and this interaction appears to be phosphorylation and cell cycle dependent. PMID: 16516142
28. discuss CENPJ, which similarly exhibits higher rate of protein evolution in primates as compared to rodents and carnivores PMID: 16631324
29. High levels of LIP1 were found in serum and synovial fluid of rheumatoid arthritis patients, providing evidence for a cytokine-like role. PMID: 18162190
30. Mutations in this conserved sequence also eliminate d-SAS-4's microtubule-destabilizing activity, suggesting that d-SAS-4 and CPAP may play similar roles within cells. PMID: 18586240
31. the PN2-3 fragment of CPAP as a protein with an unprecedented tubulin sequestering mechanism distinct from that of stathmin family proteins. PMID: 19131341
32. Results suggest that CPAP and CP110 play antagonistic roles in determining the extent of tubulin addition during centriole elongation, thereby controlling the length of newly formed centrioles. PMID: 19481458
33. Data show that the CPAP is required for centrosome duplication in cycling human cells, and that CPAP overexpression results in the formation of abnormally long centrioles. PMID: 19481460
34. Results suggest that CPAP is a new regulator of centriole length and its intrinsic tubulin-dimer binding activity is required for procentriole elongation. PMID: 19503075
35. Identifies CENPJ as LYST-interacting proteins LIP1 and LIP7, which interact with the lysosomal trafficking regulator (LYST) protein. PMID: 11984006

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HGNC: 17272

OMIM: 608393

KEGG: hsa:55835

STRING: 9606.ENSP00000371308

UniGene: Hs.513379