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PFKFB3

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PFKFB3
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesPFKFB3, IPFK2, PFK2, iPFK-2, 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3
External IDsOMIM: 605319; MGI: 2181202; HomoloGene: 88708; GeneCards: PFKFB3; OMA:PFKFB3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

5209

170768

Ensembl

ENSG00000170525

ENSMUSG00000026773

UniProt

Q16875
Q9BQU1

n/a

RefSeq (mRNA)
RefSeq (protein)

n/a

Location (UCSC)Chr 10: 6.14 – 6.25 MbChr 2: 11.48 – 11.56 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

PFKFB3 is a gene that encodes the 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 enzyme in humans.[5][6][7] It is one of 4 tissue-specific PFKFB isoenzymes identified currently (PFKFB1-4).[8]

Gene

The PFKFB3 gene is mapped to single locus on chromosome 10 (10p15-p14).[5][6] It spans a region of 32.5kb with an open reading frame that is 5,675bp long. It is estimated to consist of 19 exons, of which 15 are regularly expressed.[8] Alternative splicing of the variable, COOH-terminal domain has been observed, leading to 6 different isoforms termed UBI2K1 to UBI2K6 in humans.[9] Different nomenclature also recognizes two broad categories of PFKFB3 isoforms, termed ‘inducible’ and ‘ubiquitous’.[10] The inducible protein isoform, iPFK2, is named as such because its expression has been shown to be induced by hypoxic conditions.

The PFKFB3 promoter is predicted to contain multiple binding sites, including Sp-1 and AP-2 binding sites. It also contains motifs for the binding of E-box, nuclear factor-1 (NF-1), and progesterone response element. Expression of the promoter is shown to be induce by phorbol esters and cyclic-AMP-dependent protein kinase signaling.[10]

Structure

The four PFKFB isoforms share high (85%) ‘2-Kase/2-Pase core’ sequence homology, but have different properties based on variable N- and C- terminal regulatory domains and variation in residues surrounding the surrounding the active sites.[11] The PFKFB3 inducible isoform has higher ‘2-Kase’ (kinase) activity than other isoforms, due to phosphorylation of Ser-460 by PKA or AMP-dependent protein kinase.[11] The high ‘2-Kase’ activity of PFKFB3 is also due to the lack of a specific Ser that is phosphorylated in the other PFKFB isoforms to decrease kinase activity.[12]

The primary protein encoded by PFKFB3, iPFK2, consists of 590 amino acids. It has a predicted molecular weight of 66.9 kDa and an isoelectric point of 8.64.[8] The crystal structure was determined in 2006:[11]

  • Researcher found that iPFK2 has a beta-hairpin N-terminal structure that secures the binding of fructose-6-phosphate to the active site via interaction with the protein’s ‘2-Pase’ domain. There are two active pockets within iPFK2 for fructose-2,6-bisphosphatase and 6-phosphofructo-2-kinase which are structurally different. The F-2,6-BP active site structurally open, while the active pocket of 6-phosphofructo-2-kinase is more rigid. This rigidity permits the independent binding of F-6-P and ATP with increased affinity than other isoforms.

Function

iPFK2 converts fructose-6-phosphate to fructose-2,6-bisP (F2,6BP). F2,6BP is a ‘potent’ allosteric activator of 6-phosphofructokinase-1 (PFK-1), stimulating glycolysis. Click to see image of PFFKB3 function.

Cancer Connections

Warburg Effect

The Warburg effect, proposed by Otto Warbug in 1956,[13] describes the upregulation of glycolysis in most cancer cells, even in the presence of oxygen. The high rate of glycolysis is accompanied by increased lactic acid fermentation, providing additional nutrients for cancer cell growth and tumorigenesis.

PFKFB3 is associated with the Warburg effect because its activity increases the rate of glycolysis. PFKFB3 has been found to be upregulated in numerous cancers, including colon, breast, ovarian, and thyroid.[14] Reduced methylation of PFKFB3 is also found in some cancers, triggering the shift to the glycolytic pathway that supports cancerous growth.[15]

Hypoxia Signaling Pathway

PFKFB3 expression is induced by hypoxia.[16] The promoter of PFKFB3 contains binding sites, called hypoxia response elements (HREs), that recruit the binding of hypoxia-inducible factor-1 (HIF-1).[17]

Hypoxia signaling via HIF-1α stabilization upregulates the transcription of genes that permit survival in low oxygen conditions. These genes include glycolysis enzymes, like PFKFB3, that permit ATP synthesis without oxygen, and vascular endothelial growth factor (VEGF), which promotes angiogenesis.

Cell Cycle & Apoptosis

It was more recently discovered that PFKFB3 promotes cell cycle progression (cell proliferation) and suppresses apoptosis by regulating cyclin-dependent kinase 1 (Cdk-1). PFKFB3’s synthesis of F2,6BP in the nucleus was found to regulate Cdk-1, whereas cytosolic PFKFB3 activates PFK-1. Nuclear PFKFB3 activates Cdk1 to phosphorylate the Thr-187 site of p27, causing decreased levels of p27.[18][19] (See summary figure). Reduced p27 causes protection against apoptosis and progression of cells through the G1/S phase checkpoint These findings established a significant link between PFKFB3 cancer cell survival and proliferation.

Circadian Clock

Circadian clocks dysregulation is associated with many types of cancer.[20] PFKFB3 expression exhibits circadian rhythmicity that is different between cancerous and non-cancerous cells.[21] It was specifically found that the circadian-driven transcription factor ‘CLOCK’ binds to the PFKFB3 promoter at a genuine ‘E-box’ site to increase transcription in cancer cells.

  • Inhibition of PFKFB3 using 3PO was successful in reducing cancer growth and increasing apoptosis, but only at certain time points within the circadian cycle. This finding highlights the need for time-based PFKFB3 inhibition in cancer treatment.

Additional Cancer Connections

  • PFKFB3 is activated by progestins in breast cancer cells[22]
  • PFKFB3 promotes angiogenesis
    • Silencing of PFKFB3 impairs angiogenesis. PFKFB3-driven glycolysis overrules the pro-stalk activity of Notch. PFKFB3 regulates tip and stalk cell behavior and compartmentalizes with F-actin.[23]

Anti-cancer Therapeutic Strategy

Inhibition of PFKFB3 is being analyzed as a potential anti-cancer therapy. Various small molecule inhibitors of PFKFB3 are currently in development. The most prominent inhibitor is 3PO, 3-(3-pyridinyl)-1-(4-pyridinyl)-2-propen-1-one. 3PO is a small molecule inhibitor that decreases glucose uptake and increases autophagy.[24] Research is currently exploring various 3PO derivatives (ie. PFKF15)[25] in an effort to increase their efficacy as anti-cancer therapies.

Other Pathways Involving PFKFB3

Autophagy

Enhanced activity of PFKFB3 accelerates ROS production as an end product of glycolysis, and thus increases autophagy. Likewise, inhibition of PFKFB3 has been found to induce autophagy.[26][27] See summary image.

Autophagy can prolong cellular survival during low energy conditions. This finding was discovered in relation to rheumatoid arthritis.[28] It was found that RA T cell fail to upregulate autophagy, and knockout experiments placed PFKFB3 as an upstream regulator of this process.

Insulin Signaling Pathway

PFKFB3 was identified in a kinome screen as a regulator of insulin/IGF-1. Suppression of PFKFB3 was found to decrease insulin-stimulated glucose uptake, GLUT4 translocation, and Akt signaling in 3T3-L1 adipocytes. Overexpression caused the insulin-dependent phosphorylation of Akt and Akt substrates.[29]

PFKFB3 expression increases in fat tissues during adipogenesis, but prolonged insulin exposure has been shown to decrease the expression of PFKFB3. This is thought to occur due to a negative feedback mechanism involving insulin.[30]

p38/MK2 Stress Sigaling Pathway

p38 MAPK have been found to increase PFKFB3 activity through (1) the transcriptional activation of PFKFB3 in response to stress stimuli and (2) the post-translational phosphorylation of iPFK2 at Ser-461.[31][32]

See summary figure.[32]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000170525 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026773 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Nicholl J, Hamilton JA, Sutherland GR, Sutherland RL, Watts CK (April 1997). "The third human isoform of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB3) map position 10p14-p15". Chromosome Research. 5 (2): 150. PMID 9146922.
  6. ^ a b Manzano A, Rosa JL, Ventura F, Pérez JX, Nadal M, Estivill X, Ambrosio S, Gil J, Bartrons R (Mar 1999). "Molecular cloning, expression, and chromosomal localization of a ubiquitously expressed human 6-phosphofructo-2-kinase/ fructose-2, 6-bisphosphatase gene (PFKFB3)". Cytogenetics and Cell Genetics. 83 (3–4): 214–7. doi:10.1159/000015181. PMID 10072580.
  7. ^ "Entrez Gene: PFKFB3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3".
  8. ^ a b c Mahlknecht U, Chesney J, Hoelzer D, Bucala R (October 2003). "Cloning and chromosomal characterization of the 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-3 gene (PFKFB3, iPFK2)". International Journal of Oncology. 23 (4): 883–91. PMID 12963966.
  9. ^ Kessler R, Eschrich K (March 2001). "Splice isoforms of ubiquitous 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase in human brain". Brain Research. Molecular Brain Research. 87 (2): 190–5. doi:10.1016/s0169-328x(01)00014-6. PMID 11245921.
  10. ^ a b Navarro-Sabaté A, Manzano A, Riera L, Rosa JL, Ventura F, Bartrons R (February 2001). "The human ubiquitous 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase gene (PFKFB3): promoter characterization and genomic structure". Gene. 264 (1): 131–8. doi:10.1016/S0378-1119(00)00591-6. PMID 11245987.
  11. ^ a b c Kim, Song-Gun; Manes, Nathan P.; El-Maghrabi, M. Raafat; Lee, Yong-Hwan (2006-02-03). "Crystal Structure of the Hypoxia-inducible Form of 6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB3) A POSSIBLE NEW TARGET FOR CANCER THERAPY". Journal of Biological Chemistry. 281 (5): 2939–2944. doi:10.1074/jbc.M511019200. ISSN 0021-9258. PMID 16316985.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  12. ^ Sakakibara R, Kato M, Okamura N, Nakagawa T, Komada Y, Tominaga N, Shimojo M, Fukasawa M (July 1997). "Characterization of a human placental fructose-6-phosphate, 2-kinase/fructose-2,6-bisphosphatase". Journal of Biochemistry. 122 (1): 122–8. doi:10.1093/oxfordjournals.jbchem.a021719. PMID 9276680.
  13. ^ Warburg, Otto (1956-02-24). "On the Origin of Cancer Cells". Science. 123 (3191): 309–314. doi:10.1126/science.123.3191.309. ISSN 0036-8075. PMID 13298683.
  14. ^ Atsumi, Toshiya; Chesney, Jason; Metz, Christine; Leng, Lin; Donnelly, Seamas; Makita, Zenji; Mitchell, Robert; Bucala, Richard (2002-10-15). "High expression of inducible 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (iPFK-2; PFKFB3) in human cancers". Cancer Research. 62 (20): 5881–5887. ISSN 0008-5472. PMID 12384552.
  15. ^ Yamamoto, Takehiro; Takano, Naoharu; Ishiwata, Kyoko; Ohmura, Mitsuyo; Nagahata, Yoshiko; Matsuura, Tomomi; Kamata, Aki; Sakamoto, Kyoko; Nakanishi, Tsuyoshi (2014-03-17). "Reduced methylation of PFKFB3 in cancer cells shunts glucose towards the pentose phosphate pathway". Nature Communications. 5: 3480. doi:10.1038/ncomms4480. PMC 3959213. PMID 24633012.
  16. ^ Minchenko, Alexander; Leshchinsky, Irene; Opentanova, Irina; Sang, Nianli; Srinivas, Vickram; Armstead, Valerie; Caro, Jaime (2002-02-22). "Hypoxia-inducible factor-1-mediated expression of the 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-3 (PFKFB3) gene. Its possible role in the Warburg effect". The Journal of Biological Chemistry. 277 (8): 6183–6187. doi:10.1074/jbc.M110978200. ISSN 0021-9258. PMC 4518871. PMID 11744734.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  17. ^ Obach, Mercè; Navarro-Sabaté, Aurea; Caro, Jaime; Kong, Xianguo; Duran, Joan; Gómez, Marta; Perales, Jose Carlos; Ventura, Francesc; Rosa, Jose Luis (2004-12-17). "6-Phosphofructo-2-kinase (pfkfb3) gene promoter contains hypoxia-inducible factor-1 binding sites necessary for transactivation in response to hypoxia". The Journal of Biological Chemistry. 279 (51): 53562–53570. doi:10.1074/jbc.M406096200. ISSN 0021-9258. PMID 15466858.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  18. ^ Yalcin, Abdullah; Clem, Brian F.; Simmons, Alan; Lane, Andrew; Nelson, Kristin; Clem, Amy L.; Brock, Erin; Siow, Deanna; Wattenberg, Binks (2009-09-04). "Nuclear Targeting of 6-Phosphofructo-2-kinase (PFKFB3) Increases Proliferation via Cyclin-dependent Kinases". Journal of Biological Chemistry. 284 (36): 24223–24232. doi:10.1074/jbc.M109.016816. ISSN 0021-9258. PMC 2782016. PMID 19473963.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  19. ^ Yalcin, A.; Clem, B. F.; Imbert-Fernandez, Y.; Ozcan, S. C.; Peker, S.; O'Neal, J.; Klarer, A. C.; Clem, A. L.; Telang, S. (2014-07-17). "6-Phosphofructo-2-kinase (PFKFB3) promotes cell cycle progression and suppresses apoptosis via Cdk1-mediated phosphorylation of p27". Cell Death & Disease. 5 (7): e1337. doi:10.1038/cddis.2014.292. PMC 4123086. PMID 25032860.
  20. ^ Savvidis, C; Michael, Koutsilieris (2012). "Circadian Rhythm Disruption in Cancer Biology". Molecular Medicine. 18 (1): 1249–1260. doi:10.2119/molmed.2012.00077. PMC 3521792.
  21. ^ Chen, Lili; Zhao, Jiajia; Tang, Qingming; Li, Honggui; Zhang, Chenguang; Yu, Ran; Zhao, Yan; Huo, Yuqing; Wu, Chaodong (2016-01-01). "PFKFB3 Control of Cancer Growth by Responding to Circadian Clock Outputs". Scientific Reports. 6: 24324. doi:10.1038/srep24324. ISSN 2045-2322. PMC 4832144. PMID 27079271.
  22. ^ Novellasdemunt, Laura; Obach, Mercè; Millán-Ariño, Lluís; Manzano, Anna; Ventura, Francesc; Rosa, Jose Luis; Jordan, Albert; Navarro-Sabate, Àurea; Bartrons, Ramon (2012-03-01). "Progestins activate 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) in breast cancer cells". Biochemical Journal. 442 (2): 345–356. doi:10.1042/BJ20111418. ISSN 0264-6021. PMID 22115192.
  23. ^ De Bock, Katrien; Georgiadou, Maria; Schoors, Sandra; Kuchnio, Anna; Wong, Brian W.; Cantelmo, Anna Rita; Quaegebeur, Annelies; Ghesquière, Bart; Cauwenberghs, Sandra (2013-08-01). "Role of PFKFB3-Driven Glycolysis in Vessel Sprouting". Cell. 154 (3): 651–663. doi:10.1016/j.cell.2013.06.037. ISSN 0092-8674. PMID 23911327.
  24. ^ Klarer, Alden C; O’Neal, Julie; Imbert-Fernandez, Yoannis; Clem, Amy; Ellis, Steve R; Clark, Jennifer; Clem, Brian; Chesney, Jason; Telang, Sucheta (2014-01-23). "Inhibition of 6-phosphofructo-2-kinase (PFKFB3) induces autophagy as a survival mechanism". Cancer & Metabolism. 2 (1). doi:10.1186/2049-3002-2-2. ISSN 2049-3002. PMC 3913946. PMID 24451478.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  25. ^ Clem, Brian F.; O'Neal, Julie; Tapolsky, Gilles; Clem, Amy L.; Imbert-Fernandez, Yoannis; Kerr, Daniel A.; Klarer, Alden C.; Redman, Rebecca; Miller, Donald M. (2013-08-01). "Targeting 6-Phosphofructo-2-Kinase (PFKFB3) as a Therapeutic Strategy against Cancer". Molecular Cancer Therapeutics. 12 (8): 1461–1470. doi:10.1158/1535-7163.MCT-13-0097. ISSN 1535-7163. PMC 3742633. PMID 23674815.
  26. ^ Klarer, Alden C.; O’Neal, Julie; Imbert-Fernandez, Yoannis; Clem, Amy; Ellis, Steve R.; Clark, Jennifer; Clem, Brian; Chesney, Jason; Telang, Sucheta (2014-01-01). "Inhibition of 6-phosphofructo-2-kinase (PFKFB3) induces autophagy as a survival mechanism". Cancer & Metabolism. 2: 2. doi:10.1186/2049-3002-2-2. ISSN 2049-3002. PMC 3913946. PMID 24451478.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  27. ^ Yang, Zhen; Goronzy, Jörg J.; Weyand, Cornelia M. (2014-02-26). "The glycolytic enzyme PFKFB3/phosphofructokinase regulates autophagy". Autophagy. 10 (2): 382–383. doi:10.4161/auto.27345. ISSN 1554-8627. PMID 24351650.
  28. ^ Yang, Zhen; Fujii, Hiroshi; Mohan, Shalini V.; Goronzy, Jorg J.; Weyand, Cornelia M. (2013-09-23). "Phosphofructokinase deficiency impairs ATP generation, autophagy, and redox balance in rheumatoid arthritis T cells". The Journal of Experimental Medicine. 210 (10): 2119–2134. doi:10.1084/jem.20130252. ISSN 1540-9538. PMC 3782046. PMID 24043759.
  29. ^ Trefely, Sophie; Khoo, Poh-Sim; Krycer, James R.; Chaudhuri, Rima; Fazakerley, Daniel J.; Parker, Benjamin L.; Sultani, Ghazal; Lee, James; Stephan, Jean-Philippe (2015-10-23). "Kinome Screen Identifies PFKFB3 and Glucose Metabolism as Important Regulators of the Insulin/Insulin-like Growth Factor (IGF)-1 Signaling Pathway". Journal of Biological Chemistry. 290 (43): 25834–25846. doi:10.1074/jbc.M115.658815. ISSN 0021-9258. PMC 4646237. PMID 26342081.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  30. ^ Atsumi, Toshiya; Nishio, Taro; Niwa, Hirokatsu; Takeuchi, Jun; Bando, Hidenori; Shimizu, Chikara; Yoshioka, Narihito; Bucala, Richard; Koike, Takao (2005-12-01). "Expression of inducible 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase/PFKFB3 isoforms in adipocytes and their potential role in glycolytic regulation". Diabetes. 54 (12): 3349–3357. doi:10.2337/diabetes.54.12.3349. ISSN 0012-1797. PMID 16306349.
  31. ^ Novellasdemunt, Laura; Bultot, Laurent; Manzano, Anna; Ventura, Francesc; Rosa, Jose Luis; Vertommen, Didier; Rider, Mark H.; Navarro-Sabate, Àurea; Bartrons, Ramon (2013-06-15). "PFKFB3 activation in cancer cells by the p38/MK2 pathway in response to stress stimuli". Biochemical Journal. 452 (3): 531–543. doi:10.1042/bj20121886. ISSN 0264-6021.
  32. ^ a b Bolaños, Juan P. (2013-06-15). "Adapting glycolysis to cancer cell proliferation: the MAPK pathway focuses on PFKFB3: Figure 1". Biochemical Journal. 452 (3): e7–e9. doi:10.1042/bj20130560. ISSN 0264-6021.

Further reading

  • Sakai A, Kato M, Fukasawa M, Ishiguro M, Furuya E, Sakakibara R (March 1996). "Cloning of cDNA encoding for a novel isozyme of fructose 6-phosphate, 2-kinase/fructose 2,6-bisphosphatase from human placenta". Journal of Biochemistry. 119 (3): 506–11. doi:10.1093/oxfordjournals.jbchem.a021270. PMID 8830046.
  • Hamilton JA, Callaghan MJ, Sutherland RL, Watts CK (April 1997). "Identification of PRG1, a novel progestin-responsive gene with sequence homology to 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase". Molecular Endocrinology. 11 (4): 490–502. doi:10.1210/me.11.4.490. PMID 9092801.
  • Sakakibara R, Kato M, Okamura N, Nakagawa T, Komada Y, Tominaga N, Shimojo M, Fukasawa M (July 1997). "Characterization of a human placental fructose-6-phosphate, 2-kinase/fructose-2,6-bisphosphatase". Journal of Biochemistry. 122 (1): 122–8. doi:10.1093/oxfordjournals.jbchem.a021719. PMID 9276680.
  • Scanlan MJ, Gordan JD, Williamson B, Stockert E, Bander NH, Jongeneel V, Gure AO, Jäger D, Jäger E, Knuth A, Chen YT, Old LJ (November 1999). "Antigens recognized by autologous antibody in patients with renal-cell carcinoma". International Journal of Cancer. 83 (4): 456–64. doi:10.1002/(SICI)1097-0215(19991112)83:4<456::AID-IJC4>3.0.CO;2-5. PMID 10508479.
  • Fukasawa M, Takayama E, Shinomiya N, Okumura A, Rokutanda M, Yamamoto N, Sakakibara R (January 2000). "Identification of the promoter region of human placental 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase gene". Biochemical and Biophysical Research Communications. 267 (3): 703–8. doi:10.1006/bbrc.1999.2022. PMID 10673355.
  • Kessler R, Eschrich K (March 2001). "Splice isoforms of ubiquitous 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase in human brain". Brain Research. Molecular Brain Research. 87 (2): 190–5. doi:10.1016/S0169-328X(01)00014-6. PMID 11245921.
  • Riera L, Obach M, Navarro-Sabaté A, Duran J, Perales JC, Viñals F, Rosa JL, Ventura F, Bartrons R (August 2003). "Regulation of ubiquitous 6-phosphofructo-2-kinase by the ubiquitin-proteasome proteolytic pathway during myogenic C2C12 cell differentiation". FEBS Letters. 550 (1–3): 23–9. doi:10.1016/S0014-5793(03)00808-1. PMID 12935880.
  • Obach M, Navarro-Sabaté A, Caro J, Kong X, Duran J, Gómez M, Perales JC, Ventura F, Rosa JL, Bartrons R (December 2004). "6-Phosphofructo-2-kinase (pfkfb3) gene promoter contains hypoxia-inducible factor-1 binding sites necessary for transactivation in response to hypoxia". The Journal of Biological Chemistry. 279 (51): 53562–70. doi:10.1074/jbc.M406096200. PMID 15466858.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  • Manes NP, El-Maghrabi MR (June 2005). "The kinase activity of human brain 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase is regulated via inhibition by phosphoenolpyruvate". Archives of Biochemistry and Biophysics. 438 (2): 125–36. doi:10.1016/j.abb.2005.04.011. PMID 15896703.
  • Minchenko OH, Ogura T, Opentanova IL, Minchenko DO, Esumi H (December 2005). "Splice isoform of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-4: expression and hypoxic regulation". Molecular and Cellular Biochemistry. 280 (1–2): 227–34. doi:10.1007/s11010-005-8009-6. PMID 16311927.
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