Tag |
Content |
dbPAF ID |
dbPAF-0001546 |
Uniprot Accession |
O43463; SUV91_HUMAN; B2R6E8; B4DST0; Q53G60; Q6FHK6; |
Genbank Protein ID |
NP_001269095.1; NP_003164.1; |
Genbank Nucleotide ID |
NM_001282166.1; NM_003173.3; |
Protein Name |
Histone-lysine N-methyltransferase SUV39H1 |
Protein Synonyms/Alias |
Histone H3-K9 methyltransferase 1;H3-K9-HMTase 1;Lysine N-methyltransferase 1A;Position-effect variegation 3-9 homolog;Suppressor of variegation 3-9 homolog 1;Su(var)3-9 homolog 1; |
Gene Name |
SUV39H1 |
Gene Synonyms/Alias |
KMT1A;SUV39H; |
Organism |
Homo sapiens(Human) |
NCBI Taxa ID |
9606 |
Functional Description (View all) |
Histone methyltransferase that specifically trimethylates 'Lys-9' of histone H3 using monomethylated H3 'Lys-9' as substrate. Also weakly methylates histone H1 (in vitro). H3 'Lys-9' trimethylation represents a specific tag for epigenetic transcriptional repression by recruiting HP1 (CBX1, CBX3 and/or CBX5) proteins to methylated histones. Mainly functions in heterochromatin regions, thereby playing a central role in the establishment of constitutive heterochromatin at pericentric and telomere regions. H3 'Lys-9' trimethylation is also required to direct DNA methylation at pericentric repeats. SUV39H1 is targeted to histone H3 via its interaction with RB1 and is involved in many processes, such as repression of MYOD1-stimulated differentiation, regulation of the control switch for exiting the cell cycle and entering differentiation, repression by the PML-RARA fusion protein, BMP-induced repression, repression of switch recombination to IgA and regulation of telomere length. Component of the eNoSC (energy-dependent nucleolar silencing) complex, a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes. The eNoSC complex is able to sense the energy status of cell: upon glucose starvation, elevation of NAD(+)/NADP(+) ratio activates SIRT1, leading to histone H3 deacetylation followed by dimethylation of H3 at 'Lys-9' (H3K9me2) by SUV39H1 and the formation of silent chromatin in the rDNA locus. Recruited by the large PER complex to the E-box elements of the circadian target genes such as PER2 itself or PER1, contributes to the conversion of local chromatin to a heterochromatin-like repressive state through H3 'Lys-9' trimethylation.Functional Description
Histone methyltransferase that specifically trimethylates 'Lys-9' of histone H3 using monomethylated H3 'Lys-9' as substrate. Also weakly methylates histone H1 (in vitro). H3 'Lys-9' trimethylation represents a specific tag for epigenetic transcriptional repression by recruiting HP1 (CBX1, CBX3 and/or CBX5) proteins to methylated histones. Mainly functions in heterochromatin regions, thereby playing a central role in the establishment of constitutive heterochromatin at pericentric and telomere regions. H3 'Lys-9' trimethylation is also required to direct DNA methylation at pericentric repeats. SUV39H1 is targeted to histone H3 via its interaction with RB1 and is involved in many processes, such as repression of MYOD1-stimulated differentiation, regulation of the control switch for exiting the cell cycle and entering differentiation, repression by the PML-RARA fusion protein, BMP-induced repression, repression of switch recombination to IgA and regulation of telomere length. Component of the eNoSC (energy-dependent nucleolar silencing) complex, a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes. The eNoSC complex is able to sense the energy status of cell: upon glucose starvation, elevation of NAD(+)/NADP(+) ratio activates SIRT1, leading to histone H3 deacetylation followed by dimethylation of H3 at 'Lys-9' (H3K9me2) by SUV39H1 and the formation of silent chromatin in the rDNA locus. Recruited by the large PER complex to the E-box elements of the circadian target genes such as PER2 itself or PER1, contributes to the conversion of local chromatin to a heterochromatin-like repressive state through H3 'Lys-9' trimethylation.
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Phosphorylation Sites
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dbPAF PTMs: 4 |
Sequence (Fasta) | MAENLKGCSV CCKSSWNQLQ DLCRLAKLSC PALGISKRNL YDFEVEYLCD YKKIREQEYY 60 LVKWRGYPDS ESTWEPRQNL KCVRILKQFH KDLERELLRR HHRSKTPRHL DPSLANYLVQ 120 KAKQRRALRR WEQELNAKRS HLGRITVENE VDLDGPPRAF VYINEYRVGE GITLNQVAVG 180 CECQDCLWAP TGGCCPGASL HKFAYNDQGQ VRLRAGLPIY ECNSRCRCGY DCPNRVVQKG 240 IRYDLCIFRT DDGRGWGVRT LEKIRKNSFV MEYVGEIITS EEAERRGQIY DRQGATYLFD 300 LDYVEDVYTV DAAYYGNISH FVNHSCDPNL QVYNVFIDNL DERLPRIAFF ATRTIRAGEE 360 LTFDYNMQVD PVDMESTRMD SNFGLAGLPG SPKKRVRIEC KCGTESCRKY LF
413Fasta Sequence
>O43463|SUV39H1|Homo sapiens(Human) MAENLKGCSVCCKSSWNQLQDLCRLAKLSCPALGISKRNLYDFEVEYLCDYKKIREQEYYLVKWRGYPDSESTWEPRQNLKCVRILKQFHKDLERELLRRHHRSKTPRHLDPSLANYLVQKAKQRRALRRWEQELNAKRSHLGRITVENEVDLDGPPRAFVYINEYRVGEGITLNQVAVGCECQDCLWAPTGGCCPGASLHKFAYNDQGQVRLRAGLPIYECNSRCRCGYDCPNRVVQKGIRYDLCIFRTDDGRGWGVRTLEKIRKNSFVMEYVGEIITSEEAERRGQIYDRQGATYLFDLDYVEDVYTVDAAYYGNISHFVNHSCDPNLQVYNVFIDNLDERLPRIAFFATRTIRAGEELTFDYNMQVDPVDMESTRMDSNFGLAGLPGSPKKRVRIECKCGTESCRKYLF
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Keyword |
KW-0002--3D-structure KW-0007--Acetylation KW-0025--Alternative splicing KW-0090--Biological rhythms KW-0131--Cell cycle KW-0137--Centromere KW-0156--Chromatin regulator KW-0158--Chromosome KW-0181--Complete proteome KW-0221--Differentiation KW-0945--Host-virus interaction KW-0479--Metal-binding KW-0489--Methyltransferase KW-0539--Nucleus KW-0597--Phosphoprotein KW-1185--Reference proteome KW-0678--Repressor KW-0698--rRNA processing KW-0949--S-adenosyl-L-methionine KW-0804--Transcription KW-0805--Transcription regulation KW-0808--Transferase KW-0862--Zinc
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Interpro |
IPR000953--Chromo/shadow_dom IPR023780--Chromo_domain IPR016197--Chromodomain-like IPR023779--Chromodomain_CS IPR011381--Histone_H3-K9_MeTrfase IPR003616--Post-SET_dom IPR007728--Pre-SET_dom IPR003606--Pre-SET_Zn-bd_sub IPR001214--SET_dom
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PROSITE |
PS00598--CHROMO_1 PS50013--CHROMO_2 PS50868--POST_SET PS50867--PRE_SET PS51579--SAM_MT43_SUVAR39_3 PS50280--SET
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Pfam |
PF00385--Chromo PF05033--Pre-SET PF00856--SET
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Gene Ontology |
GO:0005677--C:chromatin silencing complex GO:0000775--C:chromosome, centromeric region GO:0000794--C:condensed nuclear chromosome GO:0000792--C:heterochromatin GO:0005652--C:nuclear lamina GO:0005654--C:nucleoplasm GO:0005634--C:nucleus GO:0033553--C:rDNA heterochromatin GO:0003682--F:chromatin binding GO:0042054--F:histone methyltransferase activity GO:0046974--F:histone methyltransferase activity (H3-K9 specific) GO:0018024--F:histone-lysine N-methyltransferase activity GO:0047485--F:protein N-terminus binding GO:0000977--F:RNA polymerase II regulatory region sequence-specific DNA binding GO:0008757--F:S-adenosylmethionine-dependent methyltransferase activity GO:0000976--F:transcription regulatory region sequence-specific DNA binding GO:0008270--F:zinc ion binding GO:0007049--P:cell cycle GO:0030154--P:cell differentiation GO:0006974--P:cellular response to DNA damage stimulus GO:0071456--P:cellular response to hypoxia GO:0006325--P:chromatin organization GO:0000183--P:chromatin silencing at rDNA GO:0010467--P:gene expression GO:0036123--P:histone H3-K9 dimethylation GO:0036124--P:histone H3-K9 trimethylation GO:0042754--P:negative regulation of circadian rhythm GO:0045814--P:negative regulation of gene expression, epigenetic GO:0000122--P:negative regulation of transcription from RNA polymerase II promoter GO:0045892--P:negative regulation of transcription, DNA-templated GO:0040029--P:regulation of gene expression, epigenetic GO:0001975--P:response to amphetamine GO:0031667--P:response to nutrient levels GO:0048511--P:rhythmic process GO:0006364--P:rRNA processing GO:0006351--P:transcription, DNA-templated GO:0016032--P:viral process
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