PFKL
| Fosfofruktokinaza, jetra | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifikatori | |||||||||||
| Simboli | PFKL; ATP-PFK; PFK-B; PFK-L | ||||||||||
| Vanjski ID | OMIM: 171860 MGI: 97547 HomoloGene: 55668 GeneCards: PFKL Gene | ||||||||||
| EC broj | 2.7.1.11 | ||||||||||
| |||||||||||
| Pregled RNK izražavanja | |||||||||||
|
| |||||||||||
|
| |||||||||||
|
| |||||||||||
| podaci | |||||||||||
| Ortolozi | |||||||||||
| Vrsta | Čovek | Miš | |||||||||
| Entrez | 5211 | 18641 | |||||||||
| Ensembl | ENSG00000141959 | ENSMUSG00000020277 | |||||||||
| UniProt | P17858 | P12382 | |||||||||
| RefSeq (mRNA) | NM_001002021 | NM_008826 | |||||||||
| RefSeq (protein) | NP_001002021 | NP_032852 | |||||||||
| Lokacija (UCSC) |
Chr 21: 45.72 - 45.75 Mb |
Chr 10: 77.99 - 78.01 Mb | |||||||||
| PubMed pretraga | [1] | [2] | |||||||||
6-Fosfofruktokinaza, jetreni tip je enzim koji je kod ljudi kodiran PFKL genom.[1]
Fosfofruktokinaza (PFK) je tetramerni enzim koji katalizuje ključni korak u glikolizi, konverziju D-fruktoze 6-fosfata do D-fruktoze 1,6-bisfosfata. Zasebni genei kodiraju mišićnu podjedinicu (M) i jetrenu podjedinicu (L). PFK iz mišića je homotetramer M podjedinica, PFK iz jetre je homotetramer L-jedinica, dok se PFK iz trombocita može sastojati od bilo koje tetramerne kombinacije M i L podjedinica. Protein kodiran ovim genom je L podjedinica. Dve transkriptne varijante koje kodiraju različite izoforme su poznate.[1]
Reference
Literatura
- Kahn A; Meienhofer MC; Cottreau D; et al. (1979). „Phosphofructokinase (PFK) isozymes in man. I. Studies of adult human tissues”. Hum. Genet.. 48 (1): 93—108. PMID 156693. doi:10.1007/bf00273280.
- Kristensen T, Lopez R, Prydz H (1992). „An estimate of the sequencing error frequency in the DNA sequence databases”. DNA Seq.. 2 (6): 343—6. PMID 1446073. doi:10.3109/10425179209020815.
- Wang D, Fang H, Cantor CR, Smith CL (1992). „A contiguous Not I restriction map of band q22.3 of human chromosome 21”. Proc. Natl. Acad. Sci. U.S.A.. 89 (8): 3222—6. PMC 48838
. PMID 1565613. doi:10.1073/pnas.89.8.3222. - Elson A; Levanon D; Brandeis M; et al. (1990). „The structure of the human liver-type phosphofructokinase gene”. Genomics. 7 (1): 47—56. PMID 2139864. doi:10.1016/0888-7543(90)90517-X.
- Levanon D; Danciger E; Dafni N; et al. (1990). „The primary structure of human liver type phosphofructokinase and its comparison with other types of PFK”. DNA. 8 (10): 733—43. PMID 2533063. doi:10.1089/dna.1989.8.733.
- Van Keuren M; Drabkin H; Hart I; et al. (1986). „Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody”. Hum. Genet.. 74 (1): 34—40. PMID 2944814. doi:10.1007/bf00278782.
- Levanon D, Danciger E, Dafni N, Groner Y (1987). „Genomic clones of the human liver-type phosphofructokinase”. Biochem. Biophys. Res. Commun.. 141 (1): 374—80. PMID 2948503. doi:10.1016/S0006-291X(86)80379-5.
- Vora S; Davidson M; Seaman C; et al. (1984). „Heterogeneity of the molecular lesions in inherited phosphofructokinase deficiency”. J. Clin. Invest.. 72 (6): 1995—2006. PMC 437040
. PMID 6227635. doi:10.1172/JCI111164. - Vora S, Seaman C, Durham S, Piomelli S (1980). „Isozymes of human phosphofructokinase: identification and subunit structural characterization of a new system”. Proc. Natl. Acad. Sci. U.S.A.. 77 (1): 62—6. PMC 348208
. PMID 6444721. doi:10.1073/pnas.77.1.62. - Koster JF, Slee RG, Van Berkel TJ (1980). „Isoenzymes of human phosphofructokinase”. Clin. Chim. Acta. 103 (2): 169—73. PMID 6445244. doi:10.1016/0009-8981(80)90210-7.
- Vora S, Francke U (1981). „Assignment of the human gene for liver-type 6-phosphofructokinase isozyme (PFKL) to chromosome 21 by using somatic cell hybrids and monoclonal anti-L antibody”. Proc. Natl. Acad. Sci. U.S.A.. 78 (6): 3738—42. PMC 319647
. PMID 6455664. doi:10.1073/pnas.78.6.3738. - Zeitschel U, Bigl M, Eschrich K, Bigl V (1996). „Cellular distribution of 6-phosphofructo-1-kinase isoenzymes in rat brain”. J. Neurochem.. 67 (6): 2573—80. PMID 8931492. doi:10.1046/j.1471-4159.1996.67062573.x.
- Hattori M; Fujiyama A; Taylor TD; et al. (2000). „The DNA sequence of human chromosome 21”. Nature. 405 (6784): 311—9. PMID 10830953. doi:10.1038/35012518.
- Strausberg RL; Feingold EA; Grouse LH; et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A.. 99 (26): 16899—903. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899. - Gevaert K; Goethals M; Martens L; et al. (2004). „Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides”. Nat. Biotechnol.. 21 (5): 566—9. PMID 12665801. doi:10.1038/nbt810.
- Zhang C; Dowd DR; Staal A; et al. (2003). „Nuclear coactivator-62 kDa/Ski-interacting protein is a nuclear matrix-associated coactivator that may couple vitamin D receptor-mediated transcription and RNA splicing”. J. Biol. Chem.. 278 (37): 35325—36. PMID 12840015. doi:10.1074/jbc.M305191200.
- Ota T; Suzuki Y; Nishikawa T; et al. (2004). „Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet.. 36 (1): 40—5. PMID 14702039. doi:10.1038/ng1285.
- Colland F; Jacq X; Trouplin V; et al. (2004). „Functional proteomics mapping of a human signaling pathway”. Genome Res.. 14 (7): 1324—32. PMC 442148
. PMID 15231748. doi:10.1101/gr.2334104. - Gerhard DS; Wagner L; Feingold EA; et al. (2004). „The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)”. Genome Res.. 14 (10B): 2121—7. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504. - Rush J; Moritz A; Lee KA; et al. (2005). „Immunoaffinity profiling of tyrosine phosphorylation in cancer cells”. Nat. Biotechnol.. 23 (1): 94—101. PMID 15592455. doi:10.1038/nbt1046.
Content Disclaimer
Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.
- The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
- There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
- It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
- Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
- Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.