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Unless otherwise stated all data on this page refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).
Fatty acid-binding proteins are low molecular weight (100-130 aa) chaperones for long chain fatty acids, fatty acyl CoA esters, eicosanoids, retinols, retinoic acids and related metabolites and are usually regarded as being responsible for allowing the otherwise hydrophobic ligands to be mobile in aqueous media. These binding proteins may perform functions extracellularly (e.g. in plasma) or transport these agents; to the nucleus to interact with nuclear receptors (principally PPARs and retinoic acid receptors [13]) or for interaction with metabolic enzymes. Although sequence homology is limited, crystallographic studies suggest conserved 3D structures across the group of binding proteins.
fatty acid binding protein 1 C Show summary »« Hide summary
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fatty acid binding protein 2 C Show summary »« Hide summary
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fatty acid binding protein 3 C Show summary »« Hide summary More detailed page
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fatty acid binding protein 4 C Show summary »« Hide summary More detailed page
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fatty acid binding protein 5 C Show summary »« Hide summary
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fatty acid binding protein 6 C Show summary »« Hide summary
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fatty acid binding protein 7 C Show summary »« Hide summary
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peripheral myelin protein 2 C Show summary »« Hide summary
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fatty acid binding protein 9 C Show summary »« Hide summary
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fatty acid binding protein 12 C Show summary »« Hide summary
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retinol binding protein 1 C Show summary »« Hide summary
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retinol binding protein 2 C Show summary »« Hide summary
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retinol binding protein 3 C Show summary »« Hide summary
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retinol binding protein 4 C Show summary »« Hide summary More detailed page
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retinol binding protein 5 C Show summary »« Hide summary
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retinol binding protein 7 C Show summary »« Hide summary
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retinaldehyde binding protein 1 C Show summary »« Hide summary
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cellular retinoic acid binding protein 1 C Show summary »« Hide summary
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cellular retinoic acid binding protein 2 C Show summary »« Hide summary
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* Key recommended reading is highlighted with an asterisk
Chmurzyńska A. (2006) The multigene family of fatty acid-binding proteins (FABPs): function, structure and polymorphism. J Appl Genet, 47 (1): 39-48. [PMID:16424607]
Furuhashi M, Hotamisligil GS. (2008) Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discov, 7 (6): 489-503. [PMID:18511927]
* Gajda AM, Storch J. (2015) Enterocyte fatty acid-binding proteins (FABPs): different functions of liver and intestinal FABPs in the intestine. Prostaglandins Leukot Essent Fatty Acids, 93: 9-16. [PMID:25458898]
* Glatz JF. (2015) Lipids and lipid binding proteins: a perfect match. Prostaglandins Leukot Essent Fatty Acids, 93: 45-9. [PMID:25154384]
* Hotamisligil GS, Bernlohr DA. (2015) Metabolic functions of FABPs--mechanisms and therapeutic implications. Nat Rev Endocrinol, 11 (10): 592-605. [PMID:26260145]
Kralisch S, Fasshauer M. (2013) Adipocyte fatty acid binding protein: a novel adipokine involved in the pathogenesis of metabolic and vascular disease?. Diabetologia, 56 (1): 10-21. [PMID:23052058]
* Matsumata M, Inada H, Osumi N. (2016) Fatty acid binding proteins and the nervous system: Their impact on mental conditions. Neurosci Res, 102: 47-55. [PMID:25205626]
* Nguyen HC, Qadura M, Singh KK. (2020) Role of the Fatty Acid Binding Proteins in Cardiovascular Diseases: A Systematic Review. J Clin Med, 9 (11). DOI: 10.3390/jcm9113390 [PMID:33105856]
* Osumi T, Kuramoto K. (2016) Heart lipid droplets and lipid droplet-binding proteins: Biochemistry, physiology, and pathology. Exp Cell Res, 340 (2): 198-204. [PMID:26524506]
Schroeder F, Petrescu AD, Huang H, Atshaves BP, McIntosh AL, Martin GG, Hostetler HA, Vespa A, Landrock D, Landrock KK et al.. (2008) Role of fatty acid binding proteins and long chain fatty acids in modulating nuclear receptors and gene transcription. Lipids, 43 (1): 1-17. [PMID:17882463]
Storch J, Thumser AE. (2010) Tissue-specific functions in the fatty acid-binding protein family. J Biol Chem, 285 (43): 32679-83. [PMID:20716527]
Yamamoto T, Yamamoto A, Watanabe M, Matsuo T, Yamazaki N, Kataoka M, Terada H, Shinohara Y. (2009) Classification of FABP isoforms and tissues based on quantitative evaluation of transcript levels of these isoforms in various rat tissues. Biotechnol Lett, 31 (11): 1695-701. [PMID:19565192]
1. Balendiran GK, Schnutgen F, Scapin G, Borchers T, Xhong N, Lim K, Godbout R, Spener F, Sacchettini JC. (2000) Crystal structure and thermodynamic analysis of human brain fatty acid-binding protein. J Biol Chem, 275 (35): 27045-54. [PMID:10854433]
2. Chuang S, Velkov T, Horne J, Porter CJ, Scanlon MJ. (2008) Characterization of the drug binding specificity of rat liver fatty acid binding protein. J Med Chem, 51 (13): 3755-64. [PMID:18533710]
3. Crabb JW, Carlson A, Chen Y, Goldflam S, Intres R, West KA, Hulmes JD, Kapron JT, Luck LA, Horwitz J et al.. (1998) Structural and functional characterization of recombinant human cellular retinaldehyde-binding protein. Protein Sci, 7 (3): 746-57. [PMID:9541407]
4. Furuhashi M, Tuncman G, Görgün CZ, Makowski L, Atsumi G, Vaillancourt E, Kono K, Babaev VR, Fazio S, Linton MF et al.. (2007) Treatment of diabetes and atherosclerosis by inhibiting fatty-acid-binding protein aP2. Nature, 447 (7147): 959-65. [PMID:17554340]
5. Hertzel AV, Hellberg K, Reynolds JM, Kruse AC, Juhlmann BE, Smith AJ, Sanders MA, Ohlendorf DH, Suttles J, Bernlohr DA. (2009) Identification and characterization of a small molecule inhibitor of Fatty Acid binding proteins. J Med Chem, 52 (19): 6024-31. [PMID:19754198]
6. Hohoff C, Börchers T, Rüstow B, Spener F, van Tilbeurgh H. (1999) Expression, purification, and crystal structure determination of recombinant human epidermal-type fatty acid binding protein. Biochemistry, 38 (38): 12229-39. [PMID:10493790]
7. Liu X, Huang X, Lin W, Wang D, Diao Y, Li H, Hui X, Wang Y, Xu A, Wu D et al.. (2011) New aromatic substituted pyrazoles as selective inhibitors of human adipocyte fatty acid-binding protein. Bioorg Med Chem Lett, 21 (10): 2949-52. [PMID:21481589]
8. Machbub B, Ludwig HF, Gunaratnam D. (1988) Environmental impact from agrochemicals in Bali (Indonesia). Environ Monit Assess, 11 (1): 1-23. [PMID:24248795]
9. Majava V, Polverini E, Mazzini A, Nanekar R, Knoll W, Peters J, Natali F, Baumgärtel P, Kursula I, Kursula P. (2010) Structural and functional characterization of human peripheral nervous system myelin protein P2. PLoS ONE, 5 (4): e10300. [PMID:20421974]
10. Richieri GV, Ogata RT, Kleinfeld AM. (1994) Equilibrium constants for the binding of fatty acids with fatty acid-binding proteins from adipocyte, intestine, heart, and liver measured with the fluorescent probe ADIFAB. J Biol Chem, 269 (39): 23918-30. [PMID:7929039]
11. Richieri GV, Ogata RT, Zimmerman AW, Veerkamp JH, Kleinfeld AM. (2000) Fatty acid binding proteins from different tissues show distinct patterns of fatty acid interactions. Biochemistry, 39 (24): 7197-204. [PMID:10852718]
12. Sacchettini JC, Gordon JI, Banaszak LJ. (1989) Crystal structure of rat intestinal fatty-acid-binding protein. Refinement and analysis of the Escherichia coli-derived protein with bound palmitate. J Mol Biol, 208 (2): 327-39. [PMID:2671390]
13. Schroeder F, Petrescu AD, Huang H, Atshaves BP, McIntosh AL, Martin GG, Hostetler HA, Vespa A, Landrock D, Landrock KK et al.. (2008) Role of fatty acid binding proteins and long chain fatty acids in modulating nuclear receptors and gene transcription. Lipids, 43 (1): 1-17. [PMID:17882463]
14. Sulsky R, Magnin DR, Huang Y, Simpkins L, Taunk P, Patel M, Zhu Y, Stouch TR, Bassolino-Klimas D, Parker R et al.. (2007) Potent and selective biphenyl azole inhibitors of adipocyte fatty acid binding protein (aFABP). Bioorg Med Chem Lett, 17 (12): 3511-5. [PMID:17502136]
15. Thompson J, Winter N, Terwey D, Bratt J, Banaszak L. (1997) The crystal structure of the liver fatty acid-binding protein. A complex with two bound oleates. J Biol Chem, 272 (11): 7140-50. [PMID:9054409]
16. Wang Y, Connors R, Fan P, Wang X, Wang Z, Liu J, Kayser F, Medina JC, Johnstone S, Xu H et al.. (2014) Structure-assisted discovery of the first non-retinoid ligands for Retinol-Binding Protein 4. Bioorg Med Chem Lett, 24 (13): 2885-91. [PMID:24835984]
17. Young AC, Scapin G, Kromminga A, Patel SB, Veerkamp JH, Sacchettini JC. (1994) Structural studies on human muscle fatty acid binding protein at 1.4 A resolution: binding interactions with three C18 fatty acids. Structure, 2 (6): 523-34. [PMID:7922029]
18. Zwicker BL, Agellon LB. (2013) Transport and biological activities of bile acids. Int J Biochem Cell Biol, 45 (7): 1389-98. [PMID:23603607]
Database page citation:
Fatty acid-binding proteins. Accessed on 03/12/2024. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=783.
Concise Guide to PHARMACOLOGY citation:
Alexander SPH, Kelly E, Mathie AA, Peters JA, Veale EL, Armstrong JF, Buneman OP, Faccenda E, Harding SD, Spedding M, Cidlowski JA, Fabbro D, Davenport AP, Striessnig J, Davies JA et al. (2023) The Concise Guide to PHARMACOLOGY 2023/24: Introduction and Other Protein Targets. Br J Pharmacol. 180 Suppl 2:S1-22.
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Although not tested at all FABPs, BMS309403 exhibits high affinity for FABP4 (pIC50 ~8.8) compared to FABP3 or FABP5 (pIC50 <6.6) [4,14]. HTS01037 is reported to interfere with FABP4 action [5]. Ibuprofen displays some selectivity for FABP4 (pIC50 5.5) relative to FABP3 (pIC50 3.5) and FABP5 (pIC50 3.8) [8]. Fenofibric acid displays some selectivity for FABP5 (pIC50 5.5) relative to FABP3 (pIC50 4.5) and FABP4 (pIC50 4.6) [8]. Multiple pseudogenes for the FABPs have been identified in the human genome.