Lipid Modification Database
Tag Content
LipidDB ID
LipidDB-9606-00356
Entry Name
UniProt Accession
Theoretical PI
6.18
Molecular Weight
124345.27
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
Regulator of nonsense transcripts 1
Protein Synonyms/Alias
3.6.4.-; ATP-dependent helicase RENT1; Nonsense mRNA reducing factor 1; NORF1; Up-frameshift suppressor 1 homolog; hUpf1;
Gene Name
UPF1
Gene Synonyms/Alias
KIAA0221; RENT1;
Created Date
18-OCT-2001
 Lipid Modification Sites 
 Position   Sequence Form   Peptide   References   Modification Type 
209
Canonical
DSVVVLLCRQPCASQ
[1]
S-Palmitoylation
Organism
Homo sapiens (Human)
NCBI Taxa ID
9606
Reference
[1] Predicted from GPS-Lipid
Functional Description
RNA-dependent helicase and ATPase required for nonsense- mediated decay (NMD) of mRNAs containing premature stop codons. Is recruited to mRNAs upon translation termination and undergoes a cycle of phosphorylation and dephosphorylation; its phosphorylation appears to be a key step in NMD. Recruited by release factors to stalled ribosomes together with the SMG1C protein kinase complex to form the transient SURF (SMG1-UPF1-eRF1- eRF3) complex. In EJC-dependent NMD, the SURF complex associates with the exon junction complex (EJC) (located 50-55 or more nucleotides downstream from the termination codon) through UPF2 and allows the formation of an UPF1-UPF2-UPF3 surveillance complex which is believed to activate NMD. Phosphorylated UPF1 is recognized by EST1B/SMG5, SMG6 and SMG7 which are thought to provide a link to the mRNA degradation machinery involving exonucleolytic and endonucleolytic pathways, and to serve as adapters to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation and allowing the recycling of NMD factors. UPF1 can also activate NMD without UPF2 or UPF3, and in the absence of the NMD-enhancing downstream EJC indicative for alternative NMD pathways. Plays a role in replication-dependent histone mRNA degradation at the end of phase S; the function is independent of UPF2. For the recognition of premature termination codons (PTC) and initiation of NMD a competitive interaction between UPF1 and PABPC1 with the ribosome-bound release factors is proposed. The ATPase activity of UPF1 is required for disassembly of mRNPs undergoing NMD. Essential for embryonic viability.
Sequence Annotation
Nucleotide-binding: 506 510 ATP.
Region: 1 415 Sufficient for interaction with RENT2.
Motif: 1089 1090 [ST]-Q motif 1.
Motif: 1107 1108 [ST]-Q motif 2.
Binding site: 486 486 ATP.
Binding site: 676 676 ATP.
Binding site: 713 713 ATP.
Binding site: 844 844 ATP.
Modified residue: 1089 1089 Phosphoserine.
Modified residue: 1107 1107 Phosphoserine.
Modified residue: 1110 1110 Phosphoserine.
Modified residue: 1127 1127 Phosphoserine.
Protein Length
1129 AA.
Protein Sequence
(Canonical)
MSVEAYGPSS QTLTFLDTEE AELLGADTQG SEFEFTDFTL PSQTQTPPGG PGGPGGGGAG  60
GPGGAGAGAA AGQLDAQVGP EGILQNGAVD DSVAKTSQLL AELNFEEDEE DTYYTKDLPI  120
HACSYCGIHD PACVVYCNTS KKWFCNGRGN TSGSHIVNHL VRAKCKEVTL HKDGPLGETV  180
LECYNCGCRN VFLLGFIPAK ADSVVVLLCR QPCASQSSLK DINWDSSQWQ PLIQDRCFLS  240
WLVKIPSEQE QLRARQITAQ QINKLEELWK ENPSATLEDL EKPGVDEEPQ HVLLRYEDAY  300
QYQNIFGPLV KLEADYDKKL KESQTQDNIT VRWDLGLNKK RIAYFTLPKT DSGNEDLVII  360
WLRDMRLMQG DEICLRYKGD LAPLWKGIGH VIKVPDNYGD EIAIELRSSV GAPVEVTHNF  420
QVDFVWKSTS FDRMQSALKT FAVDETSVSG YIYHKLLGHE VEDVIIKCQL PKRFTAQGLP  480
DLNHSQVYAV KTVLQRPLSL IQGPPGTGKT VTSATIVYHL ARQGNGPVLV CAPSNIAVDQ  540
LTEKIHQTGL KVVRLCAKSR EAIDSPVSFL ALHNQIRNMD SMPELQKLQQ LKDETGELSS  600
ADEKRYRALK RTAERELLMN ADVICCTCVG AGDPRLAKMQ FRSILIDEST QATEPECMVP  660
VVLGAKQLIL VGDHCQLGPV VMCKKAAKAG LSQSLFERLV VLGIRPIRLQ VQYRMHPALS  720
AFPSNIFYEG SLQNGVTAAD RVKKGFDFQW PQPDKPMFFY VTQGQEEIAS SGTSYLNRTE  780
AANVEKITTK LLKAGAKPDQ IGIITPYEGQ RSYLVQYMQF SGSLHTKLYQ EVEIASVDAF  840
QGREKDFIIL SCVRANEHQG IGFLNDPRRL NVALTRARYG VIIVGNPKAL SKQPLWNHLL  900
NYYKEQKVLV EGPLNNLRES LMQFSKPRKL VNTINPGARF MTTAMYDARE AIIPGSVYDR  960
SSQGRPSSMY FQTHDQIGMI SAGPSHVAAM NIPIPFNLVM PPMPPPGYFG QANGPAAGRG  1020
TPKGKTGRGG RQKNRFGLPG PSQTNLPNSQ ASQDVASQPF SQGALTQGYI SMSQPSQMSQ  1080
PGLSQPELSQ DSYLGDEFKS QIDVALSQDS TYQGERAYQH GGVTGLSQY              1129
FASTA
(Canonical)
>LipidDB-9606-00356|Q92900
MSVEAYGPSSQTLTFLDTEEAELLGADTQGSEFEFTDFTLPSQTQTPPGGPGGPGGGGAG
GPGGAGAGAAAGQLDAQVGPEGILQNGAVDDSVAKTSQLLAELNFEEDEEDTYYTKDLPI
HACSYCGIHDPACVVYCNTSKKWFCNGRGNTSGSHIVNHLVRAKCKEVTLHKDGPLGETV
LECYNCGCRNVFLLGFIPAKADSVVVLLCRQPCASQSSLKDINWDSSQWQPLIQDRCFLS
WLVKIPSEQEQLRARQITAQQINKLEELWKENPSATLEDLEKPGVDEEPQHVLLRYEDAY
QYQNIFGPLVKLEADYDKKLKESQTQDNITVRWDLGLNKKRIAYFTLPKTDSGNEDLVII
WLRDMRLMQGDEICLRYKGDLAPLWKGIGHVIKVPDNYGDEIAIELRSSVGAPVEVTHNF
QVDFVWKSTSFDRMQSALKTFAVDETSVSGYIYHKLLGHEVEDVIIKCQLPKRFTAQGLP
DLNHSQVYAVKTVLQRPLSLIQGPPGTGKTVTSATIVYHLARQGNGPVLVCAPSNIAVDQ
LTEKIHQTGLKVVRLCAKSREAIDSPVSFLALHNQIRNMDSMPELQKLQQLKDETGELSS
ADEKRYRALKRTAERELLMNADVICCTCVGAGDPRLAKMQFRSILIDESTQATEPECMVP
VVLGAKQLILVGDHCQLGPVVMCKKAAKAGLSQSLFERLVVLGIRPIRLQVQYRMHPALS
AFPSNIFYEGSLQNGVTAADRVKKGFDFQWPQPDKPMFFYVTQGQEEIASSGTSYLNRTE
AANVEKITTKLLKAGAKPDQIGIITPYEGQRSYLVQYMQFSGSLHTKLYQEVEIASVDAF
QGREKDFIILSCVRANEHQGIGFLNDPRRLNVALTRARYGVIIVGNPKALSKQPLWNHLL
NYYKEQKVLVEGPLNNLRESLMQFSKPRKLVNTINPGARFMTTAMYDAREAIIPGSVYDR
SSQGRPSSMYFQTHDQIGMISAGPSHVAAMNIPIPFNLVMPPMPPPGYFGQANGPAAGRG
TPKGKTGRGGRQKNRFGLPGPSQTNLPNSQASQDVASQPFSQGALTQGYISMSQPSQMSQ
PGLSQPELSQDSYLGDEFKSQIDVALSQDSTYQGERAYQHGGVTGLSQY
Gene Ontology
GO:0000785; C:chromatin; IDA:HGNC
GO:0005737; C:cytoplasm; NAS:UniProtKB
GO:0005829; C:cytosol; TAS:Reactome
GO:0035145; C:exon-exon junction complex; IDA:UniProtKB
GO:0005634; C:nucleus; IDA:UniProtKB
GO:0044530; C:supraspliceosomal complex; IDA:UniProtKB
GO:0005524; F:ATP binding; IEA:UniProtKB-KW
GO:0004004; F:ATP-dependent RNA helicase activity; IDA:UniProtKB
GO:0003682; F:chromatin binding; IDA:HGNC
GO:0003677; F:DNA binding; IEA:InterPro
GO:0004386; F:helicase activity; NAS:UniProtKB
GO:0044822; F:poly(A) RNA binding; IDA:UniProtKB
GO:0003723; F:RNA binding; NAS:UniProtKB
GO:0008270; F:zinc ion binding; IEA:InterPro
GO:0006200; P:ATP catabolic process; IDA:GOC
GO:0006281; P:DNA repair; IDA:HGNC
GO:0006260; P:DNA replication; IMP:HGNC
GO:0009048; P:dosage compensation by inactivation of X chromosome; IEA:Ensembl
GO:0010467; P:gene expression; TAS:Reactome
GO:0071044; P:histone mRNA catabolic process; IMP:UniProtKB
GO:0006406; P:mRNA export from nucleus; TAS:HGNC
GO:0016071; P:mRNA metabolic process; TAS:Reactome
GO:0000956; P:nuclear-transcribed mRNA catabolic process; IMP:UniProt
GO:0000184; P:nuclear-transcribed mRNA catabolic process, nonsense-mediated decay; IDA:UniProtKB
GO:0006449; P:regulation of translational termination; IMP:UniProtKB
GO:0016070; P:RNA metabolic process; TAS:Reactome
Interpro
InterPro; IPR027417; P-loop_NTPase
InterPro; IPR018999; RNA-helicase_UPF1_UPF2-interct
Pfam
Pfam; PF09416; UPF1_Zn_bind;
SMART
PROSITE
PRINTS