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IID00461
UniprotQ00613
ProteinHeat shock factor protein 1
GeneHSF1
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
xml
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
529
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-120 Homo dimer :
 Evidence X-RAY 5d5v D Reference
       Region 5d5v D 1-12 disorder
       Region 5d5v D 13-88 order
       Region 5d5v D 89-89 disorder
       Region 5d5v D 90-120 order
 Evidence X-RAY 5d5v B Reference
       Region 5d5v B 1-13 disorder
       Region 5d5v B 14-83 order
       Region 5d5v B 84-94 disorder
       Region 5d5v B 95-120 order
Seq 1-120 Homo dimer :
 Evidence X-RAY 5hdn D Reference
       Region 5hdn D 15-84 order
       Region 5hdn D 85-95 disorder
       Region 5hdn D 96-118 order
       Region 5hdn D 119-120 disorder
 Evidence X-RAY 5hdn C Reference
       Region 5hdn C 15-118 order
       Region 5hdn C 119-120 disorder
 Evidence X-RAY 5hdn B Reference
       Region 5hdn B 15-86 order
       Region 5hdn B 87-93 disorder
       Region 5hdn B 94-118 order
       Region 5hdn B 119-120 disorder
 Evidence X-RAY 5hdn A Reference
       Region 5hdn A 15-85 order
       Region 5hdn A 86-89 disorder
       Region 5hdn A 90-118 order
       Region 5hdn A 119-120 disorder
 Evidence X-RAY 5d5u B Reference
       Region 5d5u B 1-12 disorder
       Region 5d5u B 13-85 order
       Region 5d5u B 86-92 disorder
       Region 5d5u B 93-119 order
       Region 5d5u B 120-120 disorder
Seq 10-123 Monomer :
 Evidence NMR 2ldu A Reference
       Region 2ldu A 10-123 order
       Region 2ldu A 10-12 high_rmsd
       Region 2ldu A 88-88 high_rmsd
       Region 2ldu A 119-123 high_rmsd
 Evidence X-RAY 5hdg A Reference
       Region 5hdg A 15-85 order
       Region 5hdg A 86-95 disorder
       Region 5hdg A 96-117 order
       Region 5hdg A 118-120 disorder
Seqdisorder 208-379,412-529
 Evidence CD Reference
       Region 208-379 disorder
       Region 412-529 disorder
Seqphosphorylation
    121-121 Phosphoserine; by MAPKAPK2
    142-142 Phosphothreonine; by CK2
    216-216 Phosphoserine; by PLK1
    230-230 Phosphoserine; by CAMK2A
    275-275 Phosphoserine
    292-292 Phosphoserine
    303-303 Phosphoserine; by GSK3-beta
    307-307 Phosphoserine; by MAPK3
    314-314 Phosphoserine
    319-319 Phosphoserine
    320-320 Phosphoserine; by PKA
    323-323 Phosphothreonine
    326-326 Phosphoserine; by MAPK12
    344-344 Phosphoserine
    363-363 Phosphoserine; by MAPK8
    419-419 Phosphoserine; by PLK1
    444-444 Phosphoserine
Seqacetylation
    1-1 N-acetylmethionine
    80-80 N6-acetyllysine
    91-91 N6-acetyllysine; alternate
    118-118 N6-acetyllysine
    150-150 N6-acetyllysine
    188-188 N6-acetyllysine
    208-208 N6-acetyllysine; alternate
    298-298 N6-acetyllysine; alternate
    524-524 N6-acetyllysine
 
Prediction
NeProc
Disorder 1-15,119-135,199-529
Order 16-118,136-198
ProS 199-215,225-230,240-244,249-255,261-269,289-299,304-309,325-335,373-411,416-430,460-479,488-517,525-529
AlphaFold
Disorder 1-13,85-93,120-134,199-332,334-379,404-529
Order 14-84,94-119,135-198,333-333,380-403
Pfam Hmmer
PF00447 16-211 1e-129
PF06546 246-529 1.5e-184
SEG 236-255 ,361-370
Function
Function in SwissProt
Functions as a stress-inducible and DNA-binding transcription factor that plays a central role in the transcriptional activation of the heat shock response (HSR), leading to the expression of a large class of molecular chaperones heat shock proteins (HSPs) that protect cells from cellular insults' damage (PubMed:1871105, PubMed:11447121, PubMed:1986252, PubMed:7760831, PubMed:7623826, PubMed:8946918, PubMed:8940068, PubMed:9341107, PubMed:9121459, PubMed:9727490, PubMed:9499401, PubMed:9535852, PubMed:12659875, PubMed:12917326, PubMed:15016915, PubMed:25963659, PubMed:26754925). In unstressed cells, is present in a HSP90-containing multichaperone complex that maintains it in a non-DNA-binding inactivated monomeric form (PubMed:9727490, PubMed:11583998, PubMed:16278218). Upon exposure to heat and other stress stimuli, undergoes homotrimerization and activates HSP gene transcription through binding to site-specific heat shock elements (HSEs) present in the promoter regions of HSP genes (PubMed:1871105, PubMed:1986252, PubMed:8455624, PubMed:7935471, PubMed:7623826, PubMed:8940068, PubMed:9727490, PubMed:9499401, PubMed:10359787, PubMed:11583998, PubMed:12659875, PubMed:16278218, PubMed:25963659, PubMed:26754925). Activation is reversible, and during the attenuation and recovery phase period of the HSR, returns to its unactivated form (PubMed:11583998, PubMed:16278218). Binds to inverted 5'-NGAAN-3' pentamer DNA sequences (PubMed:1986252, PubMed:26727489). Binds to chromatin at heat shock gene promoters (PubMed:25963659). Plays also several other functions independently of its transcriptional activity. Involved in the repression of Ras-induced transcriptional activation of the c-fos gene in heat-stressed cells (PubMed:9341107). Positively regulates pre-mRNA 3'-end processing and polyadenylation of HSP70 mRNA upon heat-stressed cells in a symplekin (SYMPK)-dependent manner (PubMed:14707147). Plays a role in nuclear export of stress-induced HSP70 mRNA (PubMed:17897941). Plays a role in the regulation of mitotic progression (PubMed:18794143). Plays also a role as a negative regulator of non-homologous end joining (NHEJ) repair activity in a DNA damage-dependent manner (PubMed:26359349). Involved in stress-induced cancer cell proliferation in a IER5-dependent manner (PubMed:26754925).
(Microbial infection) Plays a role in latent human immunodeficiency virus (HIV-1) transcriptional reactivation. Binds to the HIV-1 long terminal repeat promoter (LTR) to reactivate viral transcription by recruiting cellular transcriptional elongation factors, such as CDK9, CCNT1 and EP300.