Search Results
Overview
| Uniprot ID | P07900 |
|---|---|
| Protein Name | Heat shock protein HSP 90-alpha |
| Gene Name | HSP90AA1 |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position | Flanking peptide |
|---|---|
| 112 | NNLGTIAKSGTKAFM |
| 185 | EPMGRGTKVILHLKE |
| 191 | TKVILHLKEDQTEYL |
| 209 | RIKEIVKKHSQFIGY |
| 241 | EAEEKEDKEEEKEKE |
| 281 | KKKKKKIKEKYIDQE |
| 283 | KKKKIKEKYIDQEEL |
| 292 | IDQEELNKTKPIWTR |
| 294 | QEELNKTKPIWTRNP |
| 362 | RKKKNNIKLYVRRVF |
| 407 | REMLQQSKILKVIRK |
| 419 | IRKNLVKKCLELFTE |
| 436 | EDKENYKKFYEQFSK |
| 443 | KFYEQFSKNIKLGIH |
| 446 | EQFSKNIKLGIHEDS |
| 458 | EDSQNRKKLSELLRY |
| 478 | GDEMVSLKDYCTRMK |
| 489 | TRMKENQKHIYYITG |
| 499 | YYITGETKDQVANSA |
| 513 | AFVERLRKHGLEVIY |
| 539 | QLKEFEGKTLVSVTK |
| 546 | KTLVSVTKEGLELPE |
| 558 | LPEDEEEKKKQEEKK |
| 567 | KQEEKKTKFENLCKI |
| 576 | ENLCKIMKDILEKKV |
| 58 | NSSDALDKIRYESLT |
| 585 | ILEKKVEKVVVSNRL |
| 615 | ANMERIMKAQALRDN |
| 631 | TMGYMAAKKHLEINP |
| 632 | MGYMAAKKHLEINPD |
| 69 | ESLTDPSKLDSGKEL |
| 74 | PSKLDSGKELHINLI |
| 84 | HINLIPNKQDRTLTI |
Function
Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle that is linked to its ATPase activity which is essential for its chaperone activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:11274138, PubMed:12526792, PubMed:15577939, PubMed:15937123, PubMed:27353360, PubMed:29127155). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself (PubMed:29127155). Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:26991466, PubMed:27295069). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels (PubMed:25973397). In the first place, they alter the steady-state levels of certain transcription factors in response to various physiological cues (PubMed:25973397). Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment (PubMed:25973397). Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:11276205). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Mediates the association of TOMM70 with IRF3 or TBK1 in mitochondrial outer membrane which promotes host antiviral response (PubMed:20628368, PubMed:25609812)
Protein Sequence
Gene Ontology
| Classification | GO ID | Description |
|---|---|---|
| Cellular Component | GO:0044295 | axonal growth cone |
| Molecular Function | GO:0044325 | transmembrane transporter binding |
| Molecular Function | GO:0031625 | ubiquitin protein ligase binding |
| Molecular Function | GO:0051082 | unfolded protein binding |
| Molecular Function | GO:0002134 | UTP binding |
| Biological Process | GO:0002218 | activation of innate immune response |
| Biological Process | GO:0010659 | cardiac muscle cell apoptotic process |
| Biological Process | GO:0034605 | cellular response to heat |
| Biological Process | GO:0098586 | cellular response to virus |
| Biological Process | GO:0061684 | chaperone-mediated autophagy |
| Biological Process | GO:0051131 | chaperone-mediated protein complex assembly |
| Biological Process | GO:0006839 | mitochondrial transport |
| Biological Process | GO:1902988 | neurofibrillary tangle assembly |
| Biological Process | GO:0001764 | neuron migration |
| Biological Process | GO:0046209 | nitric oxide metabolic process |
| Biological Process | GO:0060452 | positive regulation of cardiac muscle contraction |
| Biological Process | GO:0045793 | positive regulation of cell size |
| Biological Process | GO:0002230 | positive regulation of defense response to virus by host |
| Biological Process | GO:0032728 | positive regulation of interferon-beta production |
| Biological Process | GO:0010592 | positive regulation of lamellipodium assembly |
| Biological Process | GO:0045429 | positive regulation of nitric oxide biosynthetic process |
| Biological Process | GO:0045732 | positive regulation of protein catabolic process |
| Biological Process | GO:0042307 | positive regulation of protein import into nucleus |
| Biological Process | GO:0032273 | positive regulation of protein polymerization |
| Biological Process | GO:0032212 | positive regulation of telomere maintenance via telomerase |
| Biological Process | GO:0006457 | protein folding |
| Biological Process | GO:0030150 | protein import into mitochondrial matrix |
| Biological Process | GO:0042026 | protein refolding |
| Biological Process | GO:0050821 | protein stabilization |
| Biological Process | GO:0043335 | protein unfolding |
| Biological Process | GO:0042981 | regulation of apoptotic process |
| Biological Process | GO:0099072 | regulation of postsynaptic membrane neurotransmitter receptor levels |
| Biological Process | GO:0032880 | regulation of protein localization |
| Biological Process | GO:0031396 | regulation of protein ubiquitination |
| Biological Process | GO:0043254 | regulation of protein-containing complex assembly |
| Biological Process | GO:0046677 | response to antibiotic |
| Biological Process | GO:0042220 | response to cocaine |
| Biological Process | GO:0009409 | response to cold |
| Biological Process | GO:0043627 | response to estrogen |
| Biological Process | GO:0009408 | response to heat |
| Biological Process | GO:0009651 | response to salt stress |
| Biological Process | GO:0006986 | response to unfolded protein |
| Biological Process | GO:0009410 | response to xenobiotic stimulus |
| Biological Process | GO:0003009 | skeletal muscle contraction |
| Biological Process | GO:1905323 | telomerase holoenzyme complex assembly |
| Biological Process | GO:0007004 | telomere maintenance via telomerase |
| Cellular Component | GO:0016323 | basolateral plasma membrane |
| Cellular Component | GO:0031526 | brush border membrane |
| Cellular Component | GO:0009986 | cell surface |
| Cellular Component | GO:0005737 | cytoplasm |
| Cellular Component | GO:0005829 | cytosol |
| Cellular Component | GO:0044294 | dendritic growth cone |
| Cellular Component | GO:0071682 | endocytic vesicle lumen |
| Cellular Component | GO:0070062 | extracellular exosome |
| Cellular Component | GO:0031012 | extracellular matrix |
| Cellular Component | GO:0005576 | extracellular region |
| Cellular Component | GO:1904813 | ficolin-1-rich granule lumen |
| Cellular Component | GO:0043202 | lysosomal lumen |
| Cellular Component | GO:0042470 | melanosome |
| Cellular Component | GO:0016020 | membrane |
| Cellular Component | GO:0005739 | mitochondrion |
| Cellular Component | GO:0043209 | myelin sheath |
| Cellular Component | GO:0043025 | neuronal cell body |
| Cellular Component | GO:0005654 | nucleoplasm |
| Cellular Component | GO:0005634 | nucleus |
| Cellular Component | GO:0048471 | perinuclear region of cytoplasm |
| Cellular Component | GO:0005886 | plasma membrane |
| Cellular Component | GO:0101031 | protein folding chaperone complex |
| Cellular Component | GO:0032991 | protein-containing complex |
| Cellular Component | GO:0034774 | secretory granule lumen |
| Cellular Component | GO:0097226 | sperm mitochondrial sheath |
| Cellular Component | GO:0097524 | sperm plasma membrane |
| Molecular Function | GO:0005524 | ATP binding |
| Molecular Function | GO:0016887 | ATP hydrolysis activity |
| Molecular Function | GO:0140662 | ATP-dependent protein folding chaperone |
| Molecular Function | GO:0002135 | CTP binding |
| Molecular Function | GO:0032564 | dATP binding |
| Molecular Function | GO:0097718 | disordered domain specific binding |
| Molecular Function | GO:0070182 | DNA polymerase binding |
| Molecular Function | GO:0140767 | enzyme-substrate adaptor activity |
| Molecular Function | GO:0005525 | GTP binding |
| Molecular Function | GO:0051020 | GTPase binding |
| Molecular Function | GO:0042826 | histone deacetylase binding |
| Molecular Function | GO:0042802 | identical protein binding |
| Molecular Function | GO:0023026 | MHC class II protein complex binding |
| Molecular Function | GO:0003729 | mRNA binding |
| Molecular Function | GO:0030235 | nitric-oxide synthase regulator activity |
| Molecular Function | GO:0042803 | protein homodimerization activity |
| Molecular Function | GO:0019903 | protein phosphatase binding |
| Molecular Function | GO:1990782 | protein tyrosine kinase binding |
| Molecular Function | GO:0051022 | Rho GDP-dissociation inhibitor binding |
| Molecular Function | GO:0003723 | RNA binding |
| Molecular Function | GO:0097110 | scaffold protein binding |
| Molecular Function | GO:0017098 | sulfonylurea receptor binding |
| Molecular Function | GO:0048156 | tau protein binding |
| Molecular Function | GO:0030911 | TPR domain binding |
Reference
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