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Overview

Uniprot IDP07900
Protein NameHeat shock protein HSP 90-alpha
Gene NameHSP90AA1
OrganismHomo 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

10 MPEETQTQDQ 20 PMEEEEVETF 30 AFQAEIAQLM 40 SLIINTFYSN 50 KEIFLRELIS 60 NSSDALDKIR 70 YESLTDPSKL 80 DSGKELHINL 90 IPNKQDRTLT 100 IVDTGIGMTK 110 ADLINNLGTI 120 AKSGTKAFME 130 ALQAGADISM 140 IGQFGVGFYS 150 AYLVAEKVTV 160 ITKHNDDEQY 170 AWESSAGGSF 180 TVRTDTGEPM 190 GRGTKVILHL 200 KEDQTEYLEE 210 RRIKEIVKKH 220 SQFIGYPITL 230 FVEKERDKEV 240 SDDEAEEKED 250 KEEEKEKEEK 260 ESEDKPEIED 270 VGSDEEEEKK 280 DGDKKKKKKI 290 KEKYIDQEEL 300 NKTKPIWTRN 310 PDDITNEEYG 320 EFYKSLTNDW 330 EDHLAVKHFS 340 VEGQLEFRAL 350 LFVPRRAPFD 360 LFENRKKKNN 370 IKLYVRRVFI 380 MDNCEELIPE 390 YLNFIRGVVD 400 SEDLPLNISR 410 EMLQQSKILK 420 VIRKNLVKKC 430 LELFTELAED 440 KENYKKFYEQ 450 FSKNIKLGIH 460 EDSQNRKKLS 470 ELLRYYTSAS 480 GDEMVSLKDY 490 CTRMKENQKH 500 IYYITGETKD 510 QVANSAFVER 520 LRKHGLEVIY 530 MIEPIDEYCV 540 QQLKEFEGKT 550 LVSVTKEGLE 560 LPEDEEEKKK 570 QEEKKTKFEN 580 LCKIMKDILE 590 KKVEKVVVSN 600 RLVTSPCCIV 610 TSTYGWTANM 620 ERIMKAQALR 630 DNSTMGYMAA 640 KKHLEINPDH 650 SIIETLRQKA 660 EADKNDKSVK 670 DLVILLYETA 680 LLSSGFSLED 690 PQTHANRIYR 700 MIKLGLGIDE 710 DDPTADDTSA 720 AVTEEMPPLE 730 GDDDTSRMEE VD

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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[13] Wu Q, Li Z, Gong T, Zheng X, Zhou X et al.. Porphyromonas gingivalis infection induces lysine lactylation reprogramming in human umbilical vein endothelial cells.. Front Cell Infect Microbiol 16:1706727. 2026. PMID: 41696360.