FKBP1B

FKBP1B
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1C9H, 3J8E, 4C02, 4IQ2, 4IQC
Identifiers
Aliases	FKBP1B, FKBP12.6, FKBP1L, OTK4, PKBP1L, PPIase, FK506 binding protein 1B, FKBP prolyl isomerase 1B
External IDs	OMIM: 600620; MGI: 1336205; HomoloGene: 68380; GeneCards: FKBP1B; OMA:FKBP1B - orthologs
Gene location (Human) Chr. Chromosome 2 (human) Band 2p23.3 Start 24,049,701 bp End 24,063,681 bp
Gene location (Mouse) Chr. Chromosome 12 (mouse) Band 12|12 A1.1 Start 4,883,174 bp End 4,891,591 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in nucleus accumbens caudate nucleus putamen hippocampus proper anterior cingulate cortex temporal lobe amygdala dorsolateral prefrontal cortex right frontal lobe superior frontal gyrus Top expressed in trigeminal ganglion barrel cortex spinal ganglia islet of Langerhans facial motor nucleus lumbar spinal ganglion motor neuron substantia nigra CA3 field medulla oblongata More reference expression data BioGPS More reference expression data
Gene ontology Molecular function ryanodine-sensitive calcium-release channel activity calcium channel inhibitor activity transmembrane transporter binding FK506 binding isomerase activity peptidyl-prolyl cis-trans isomerase activity protein binding signaling receptor binding cyclic nucleotide binding Cellular component cytoplasm calcium channel complex intracellular membrane-bounded organelle membrane sarcoplasmic reticulum Z discdkac sarcoplasmic reticulum membrane cytosol Biological process smooth muscle contraction regulation of ryanodine-sensitive calcium-release channel activity release of sequestered calcium ion into cytosol regulation of cardiac conduction release of sequestered calcium ion into cytosol by sarcoplasmic reticulum regulation of cytosolic calcium ion concentration regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion positive regulation of cytosolic calcium ion concentration cell communication by electrical coupling involved in cardiac conduction negative regulation of insulin secretion involved in cellular response to glucose stimulus insulin secretion response to glucose positive regulation of axon regeneration protein maturation by protein folding response to organic substance negative regulation of heart rate response to vitamin E regulation of heart rate negative regulation of ryanodine-sensitive calcium-release channel activity response to redox state T cell proliferation ion transmembrane transport positive regulation of sequestering of calcium ion neuronal action potential propagation protein refolding negative regulation of release of sequestered calcium ion into cytosol regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum 'de novo' protein folding calcium-mediated signaling using intracellular calcium source response to hydrogen peroxide chaperone-mediated protein folding protein peptidyl-prolyl isomerization negative regulation of phosphoprotein phosphatase activity Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 2281 14226 Ensembl ENSG00000119782 ENSMUSG00000020635 UniProt P68106 Q9Z2I2 RefSeq (mRNA) NM_004116 NM_054033 NM_001322963 NM_001322964 NM_016863 NM_001378816 NM_001378817 NM_001378818 RefSeq (protein) NP_001309892 NP_001309893 NP_004107 NP_473374 NP_058559 NP_001365745 NP_001365746 NP_001365747 Location (UCSC) Chr 2: 24.05 – 24.06 Mb Chr 12: 4.88 – 4.89 Mb PubMed search
Wikidata
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Peptidyl-prolyl cis-trans isomerase FKBP1B is an enzyme that in humans is encoded by the FKBP1B gene.

Function

The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 (tacrolimus) and rapamycin (sirolimus). It is highly similar to the FK506-binding protein 1A. Its physiological role is thought to be in excitation-contraction coupling in cardiac muscle. There are two alternatively spliced transcript variants of this gene encoding different isoforms.

Clinical significance

Defective interaction between FKB1B and the ryanodine receptor is thought to be a potential mechanism underlying the arrhythmias seen in those with the genetic condition catecholaminergic polymorphic ventricular tachycardia.

Further reading

• Schiene-Fischer C, Yu C (April 2001). "Receptor accessory folding helper enzymes: the functional role of peptidyl prolyl cis/trans isomerases". FEBS Letters. 495 (1–2): 1–6. doi:10.1016/S0014-5793(01)02326-2. PMID 11322937. S2CID 42263861.
• Lam E, Martin MM, Timerman AP, Sabers C, Fleischer S, Lukas T, Abraham RT, O'Keefe SJ, O'Neill EA, Wiederrecht GJ (November 1995). "A novel FK506 binding protein can mediate the immunosuppressive effects of FK506 and is associated with the cardiac ryanodine receptor". The Journal of Biological Chemistry. 270 (44): 26511–22. doi:10.1074/jbc.270.44.26511. PMID 7592869.
• Noguchi N, Takasawa S, Nata K, Tohgo A, Kato I, Ikehata F, Yonekura H, Okamoto H (February 1997). "Cyclic ADP-ribose binds to FK506-binding protein 12.6 to release Ca2+ from islet microsomes". The Journal of Biological Chemistry. 272 (6): 3133–6. doi:10.1074/jbc.272.6.3133. PMID 9013543.
• Deivanayagam CC, Carson M, Thotakura A, Narayana SV, Chodavarapu RS (March 2000). "Structure of FKBP12.6 in complex with rapamycin". Acta Crystallographica D. 56 (Pt 3): 266–71. doi:10.1107/S0907444999016571. PMID 10713512.
• Marx SO, Reiken S, Hisamatsu Y, Jayaraman T, Burkhoff D, Rosemblit N, Marks AR (May 2000). "PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts". Cell. 101 (4): 365–76. doi:10.1016/S0092-8674(00)80847-8. PMID 10830164. S2CID 6496567.
• Jeyakumar LH, Ballester L, Cheng DS, McIntyre JO, Chang P, Olivey HE, Rollins-Smith L, Barnett JV, Murray K, Xin HB, Fleischer S (March 2001). "FKBP binding characteristics of cardiac microsomes from diverse vertebrates". Biochemical and Biophysical Research Communications. 281 (4): 979–86. doi:10.1006/bbrc.2001.4444. PMID 11237759.
• George CH, Sorathia R, Bertrand BM, Lai FA (March 2003). "In situ modulation of the human cardiac ryanodine receptor (hRyR2) by FKBP12.6". The Biochemical Journal. 370 (Pt 2): 579–89. doi:10.1042/BJ20021433. PMC 1223191. PMID 12443530.
• Masumiya H, Wang R, Zhang J, Xiao B, Chen SR (February 2003). "Localization of the 12.6-kDa FK506-binding protein (FKBP12.6) binding site to the NH2-terminal domain of the cardiac Ca2+ release channel (ryanodine receptor)". The Journal of Biological Chemistry. 278 (6): 3786–92. doi:10.1074/jbc.M210962200. PMID 12446682.
• Tiso N, Salamon M, Bagattin A, Danieli GA, Argenton F, Bortolussi M (December 2002). "The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations". Biochemical and Biophysical Research Communications. 299 (4): 594–8. doi:10.1016/S0006-291X(02)02689-X. PMID 12459180.
• Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH, Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW, Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW, Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U, Smailus DE, Schnerch A, Schein JE, Jones SJ, Marra MA (December 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proceedings of the National Academy of Sciences of the United States of America. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• George CH, Higgs GV, Mackrill JJ, Lai FA (August 2003). "Dysregulated ryanodine receptors mediate cellular toxicity: restoration of normal phenotype by FKBP12.6". The Journal of Biological Chemistry. 278 (31): 28856–64. doi:10.1074/jbc.M212440200. PMID 12754204.
• Nishanian TG, Waldman T (October 2004). "Interaction of the BMPR-IA tumor suppressor with a developmentally relevant splicing factor". Biochemical and Biophysical Research Communications. 323 (1): 91–7. doi:10.1016/j.bbrc.2004.08.060. PMID 15351706.
• Maalej A, Mbarki F, Rebai A, Karray F, Jouida J, Abid M, Ayadi H (May 2004). "Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family". Autoimmunity. 37 (3): 237–9. doi:10.1080/08916930410001702478. PMID 15497458. S2CID 31963934.
• Zissimopoulos S, Lai FA (February 2005). "Interaction of FKBP12.6 with the cardiac ryanodine receptor C-terminal domain". The Journal of Biological Chemistry. 280 (7): 5475–85. doi:10.1074/jbc.M412954200. PMID 15591045.
• Aizawa Y, Ueda K, Komura S, Washizuka T, Chinushi M, Inagaki N, Matsumoto Y, Hayashi T, Takahashi M, Nakano N, Yasunami M, Kimura A, Hiraoka M, Aizawa Y (March 2005). "A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardia". International Journal of Cardiology. 99 (2): 343–5. doi:10.1016/j.ijcard.2003.11.050. PMID 15749201.
• Wehrens XH, Lehnart SE, Reiken S, van der Nagel R, Morales R, Sun J, Cheng Z, Deng SX, de Windt LJ, Landry DW, Marks AR (July 2005). "Enhancing calstabin binding to ryanodine receptors improves cardiac and skeletal muscle function in heart failure". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9607–12. Bibcode:2005PNAS..102.9607W. doi:10.1073/pnas.0500353102. PMC 1172237. PMID 15972811.