FKBP1B
Peptidyl-prolyl cis-trans isomerase FKBP1B
Also known as: FKB1B_HUMAN, FKBP12.6, FKBP1L, FKBP9, OTK4, PPIase
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P68106
- Gene
- FKBP1B
- Ensembl
- ENSG00000119782
- Chromosome
- 2
- Canonical length
- 108 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Vesicles,Primary cilium,Basal body,Cytosol
OverviewNCBI Gene
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 and rapamycin. 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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
108 residues, UniProt reviewed canonical sequence.
>P68106|FKBP1B
1 MGVEIETISP GDGRTFPKKG QTCVVHYTGM LQNGKKFDSS RDRNKPFKFR IGKQEVIKGF
61 EEGAAQMSLG QRAKLTCTPD VAYGATGHPG VIPPNATLIF DVELLNLELocalizationUniProt · AlphaFold · HPA
Whether an antibody against FKBP1B can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 74 nTPM
- hippocampal formation: 69 nTPM
- cerebral cortex: 62 nTPM
- amygdala: 59 nTPM
- cerebellum: 37 nTPM
- hypothalamus: 32 nTPM
Single-cell type
- megakaryocytes: 383 nCPM
- platelets: 129 nCPM
- esophageal apical cells: 44 nCPM
- extravillous trophoblasts: 43 nCPM
- melanocytes: 40 nCPM
- hepatic stellate cells: 32 nCPM
Immune cell
- T-reg: 2.8 nTPM
- eosinophil: 2.2 nTPM
- naive B-cell: 1.2 nTPM
- myeloid DC: 1 nTPM
- total PBMC: 0.5 nTPM
- basophil: 0.4 nTPM
Brain region
- hippocampal formation: 40 nTPM
- basal ganglia: 33 nTPM
- cerebral cortex: 32 nTPM
- hypothalamus: 25 nTPM
- amygdala: 23 nTPM
- pons: 21 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.95
- gnomAD pLI
- 0.39
- gnomAD missense Z
- 1.21
- DepMap mean gene effect
- 0.19
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- 'de novo' protein folding
- calcium-mediated signaling
- insulin secretion involved in cellular response to glucose stimulus
- negative regulation of calcium-mediated signaling
- negative regulation of heart rate
- negative regulation of insulin secretion involved in cellular response to glucose stimulus
- negative regulation of release of sequestered calcium ion into cytosol
- neuronal action potential propagation
- positive regulation of cytosolic calcium ion concentration
- positive regulation of sequestering of calcium ion
- protein maturation
- protein refolding
- regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
- regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
- release of sequestered calcium ion into cytosol
- response to redox state
- smooth muscle contraction
- T cell proliferation
Molecular functions
- calcium channel inhibitor activity
- calcium channel regulator activity
- FK506 binding
- peptidyl-prolyl cis-trans isomerase activity
- signaling receptor binding
- transmembrane transporter binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FKBP1B in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FKBP1B as an antibody target. Whether an autoantibody or antibody against FKBP1B could matter depends on whether native FKBP1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FKBP1B is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label FKBP1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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