TRAP1
Heat shock protein 75 kDa, mitochondrial
Also known as: HSP75, HSP90L, TRAP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q12931
- Gene
- TRAP1
- Ensembl
- ENSG00000126602
- Chromosome
- 16
- Canonical length
- 704 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a mitochondrial chaperone protein that is member of the heat shock protein 90 (HSP90) family. The encoded protein has ATPase activity and interacts with tumor necrosis factor type I. This protein may function in regulating cellular stress responses. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]
Canonical amino-acid sequenceUniProt
704 residues, UniProt reviewed canonical sequence.
>Q12931|TRAP1
1 MARELRALLL WGRRLRPLLR APALAAVPGG KPILCPRRTT AQLGPRRNPA WSLQAGRLFS
61 TQTAEDKEEP LHSIISSTES VQGSTSKHEF QAETKKLLDI VARSLYSEKE VFIRELISNA
121 SDALEKLRHK LVSDGQALPE MEIHLQTNAE KGTITIQDTG IGMTQEELVS NLGTIARSGS
181 KAFLDALQNQ AEASSKIIGQ FGVGFYSAFM VADRVEVYSR SAAPGSLGYQ WLSDGSGVFE
241 IAEASGVRTG TKIIIHLKSD CKEFSSEARV RDVVTKYSNF VSFPLYLNGR RMNTLQAIWM
301 MDPKDVREWQ HEEFYRYVAQ AHDKPRYTLH YKTDAPLNIR SIFYVPDMKP SMFDVSRELG
361 SSVALYSRKV LIQTKATDIL PKWLRFIRGV VDSEDIPLNL SRELLQESAL IRKLRDVLQQ
421 RLIKFFIDQS KKDAEKYAKF FEDYGLFMRE GIVTATEQEV KEDIAKLLRY ESSALPSGQL
481 TSLSEYASRM RAGTRNIYYL CAPNRHLAEH SPYYEAMKKK DTEVLFCFEQ FDELTLLHLR
541 EFDKKKLISV ETDIVVDHYK EEKFEDRSPA AECLSEKETE ELMAWMRNVL GSRVTNVKVT
601 LRLDTHPAMV TVLEMGAARH FLRMQQLAKT QEERAQLLQP TLEINPRHAL IKKLNQLRAS
661 EPGLAQLLVD QIYENAMIAA GLVDDPRAMV GRLNELLVKA LERHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRAP1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 182 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 182 nTPM
- tongue: 130 nTPM
- liver: 117 nTPM
- heart muscle: 83 nTPM
- pancreas: 73 nTPM
- esophagus: 68 nTPM
Single-cell type
- oocytes: 189 nCPM
- esophageal basal cells: 177 nCPM
- cytotrophoblasts: 148 nCPM
- migrating cytotrophoblasts: 139 nCPM
- myonuclei: 116 nCPM
- esophageal suprabasal cells: 111 nCPM
Immune cell
- myeloid DC: 55 nTPM
- MAIT T-cell: 47 nTPM
- memory B-cell: 42 nTPM
- naive CD4 T-cell: 42 nTPM
- intermediate monocyte: 39 nTPM
- memory CD4 T-cell: 36 nTPM
Brain region
- thalamus: 74 nTPM
- cerebral cortex: 69 nTPM
- basal ganglia: 69 nTPM
- hippocampal formation: 68 nTPM
- hypothalamus: 68 nTPM
- pons: 66 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRAP1.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 522 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 1.41
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.72
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of cellular respiration
- negative regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide
- negative regulation of reactive oxygen species biosynthetic process
- protein folding
- translational attenuation
Molecular functions
- ATP binding
- ATP hydrolysis activity
- ATP-dependent protein folding chaperone
- protein kinase binding
- RNA binding
- tumor necrosis factor receptor binding
- unfolded protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRAP1 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 TRAP1 as an antibody target. Whether an autoantibody or antibody against TRAP1 could matter depends on whether native TRAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRAP1 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 TRAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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