Reviewed, UniProtKB/Swiss-Prot P06829 (L_SENDE)

Names and origin

Protein names

Recommended name:
    Large structural protein
      Short name=Protein L
Alternative name(s):
    Transcriptase
    Replicase
Including the following 3 domains:
    1- Recommended name:
            RNA-directed RNA polymerase
              EC=2.7.7.48
    2- Recommended name:
            mRNA (guanine-N(7)-)-methyltransferase
              EC=2.1.1.56
    3- Recommended name:
            mRNA guanylyltransferase
              EC=2.7.7.-

Gene names

Name:

L

Organism

Sendai virus (strain Enders) (SeV)

Taxonomic identifier

11194 [NCBI]

Taxonomic lineage

Viruses › ssRNA negative-strand viruses › Mononegavirales › Paramyxoviridae › Paramyxovirinae › Respirovirus

Virus host

Mus musculus (Mouse) [TaxID: 10090]
Rattus norvegicus (Rat) [TaxID: 10116]
Cavia cutleri (Guinea pig) [TaxID: 10144]
Cricetidae sp. (Hamster) [TaxID: 36483]

Protein attributes

Sequence length	2228 AA.
Sequence status	Complete.
Sequence processing	The displayed sequence is not processed.
Protein existence	Inferred from homology.

General annotation (Comments)

Function	Displays RNA-directed RNA polymerase, mRNA guanylyl transferase, mRNA (guanine-N(7)-)-methyltransferase and poly(A) synthetase activities. The viral mRNA guanylyl transferase displays a different biochemical reaction than the cellular enzyme. The template is composed of the viral RNA tightly encapsidated by the nucleoprotein (N). Functions either as transcriptase or as replicase. The transcriptase synthesizes subsequently six subgenomic RNAs, assuring their capping and polyadenylation by a stuttering mechanism. The transcriptase stutters on a specific sequence, resulting on a cotranscriptional editing of the phosphoprotein (P) mRNA. The replicase mode is dependent on intracellular N protein concentration. In this mode, the polymerase replicates the whole viral genome without recognizing the transcriptional signals. 5' GpppApGpG sequence is required for mRNA cap methylation by the enzyme By similarity.
Catalytic activity	Nucleoside triphosphate + RNA(n) = diphosphate + RNA(n+1). S-adenosyl-L-methionine + G(5')pppR-RNA = S-adenosyl-L-homocysteine + m7G(5')pppR-RNA.
Subunit structure	Homooligomer. Interacts with the P and C proteins. The L protein complexes with P protein to form the functional polymerase. C protein binding to L has an inhibitory effect By similarity.
Subcellular location	Virion Potential. Host cytoplasm By similarity.
Domain	The N-terminal part (about 1-400) seems to be involved in binding to the P protein By similarity.
Miscellaneous	Least abundant structural protein (approximately 50 copies per virion). Unstable in the absence of P protein By similarity.
Sequence similarities	Belongs to the paramyxoviruses L protein family. Contains 1 RdRp catalytic domain.
Sequence caution	The sequence AAA69579.1 differs from that shown. Reason: Frameshift at positions 1 and 194. The sequence BAA00036.1 differs from that shown. Reason: Frameshift at positions 1 and 194.

Ontologies

Keywords
Biological process	RNA replication mRNA capping mRNA processing
Cellular component	Cytoplasm Virion
Ligand	ATP-binding Nucleotide-binding S-adenosyl-L-methionine
Molecular function	Methyltransferase Nucleotidyltransferase RNA-directed RNA polymerase Transferase
Technical term	Multifunctional enzyme
Gene Ontology (GO)
Biological process	mRNA capping Inferred from electronic annotation. Source: UniProtKB-KW transcription, RNA-dependent Inferred from electronic annotation. Source: UniProtKB-KW
Cellular component	cytoplasm Inferred from electronic annotation. Source: UniProtKB-KW host cell cytoplasm Inferred from electronic annotation. Source: UniProtKB-SubCell virion Inferred from electronic annotation. Source: UniProtKB-SubCell
Molecular function	ATP binding Inferred from electronic annotation. Source: UniProtKB-KW RNA binding Inferred from electronic annotation. Source: InterPro RNA-directed RNA polymerase activity Inferred from electronic annotation. Source: UniProtKB-KW mRNA (guanine-N7-)-methyltransferase activity Inferred from electronic annotation. Source: EC
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Molecule processing
	Chain	1 – 2228	2228	Large structural protein		PRO_0000142737
Regions
	Domain	656 – 840	185	RdRp catalytic
	Nucleotide binding	1801 – 1810	10	ATP Potential
	Region	1 – 174	174	Oligomerization domain By similarity
	Region	1756 – 2228	473	Involved in mRNA cap methylation By similarity
	Compositional bias	2031 – 2034	4	Poly-Ser

Sequences

	Sequence		Length	Mass (Da)
	P06829-1 [UniParc]. Last modified February 1, 2005. Version 2. Checksum: 7164A3EBCCB17D8E	FASTA	2,228	252,890
	10 20 30 40 50 60 MDGQESSQNP SDILYPECHL NSPIVRGKIA QLHVLLDVNQ PYRLKDDSII NITKHKIRNG 70 80 90 100 110 120 GLSPRQIKIR SLGKALQRTI KDLDRYTFEP YPTYSQELLR LDIPEICDKI RSVFAVSDRL 130 140 150 160 170 180 TRELSSGFQD LWLNIFKQLG NIEGREGYDP LQDISTIPEI TDKYSRNRWY RPFLTWFSIK 190 200 210 220 230 240 YDMRWMQKTR PGGPIDTSNS HNLLECKSYT LVTYGDLVMI LNKLTLTGYI LTPELVLMYC 250 260 270 280 290 300 DVVEGRWNMS AAGHLDKRSI GITSKGEELW ELVDSLFSSL GEEIYNVIAL LEPLSLALIQ 310 320 330 340 350 360 LNDPVIPLRG AFMRHVLTEL QTVLTSRDVY TDAEADTIVE SLLAIFHGTS IDEKAEIFSF 370 380 390 400 410 420 FRTFGHPSLE AVTAADKVRA HMYAQKAIKL KTLYECHAVF CTIIINGYRE RHGGQWPPCD 430 440 450 460 470 480 FPDHVCLELR NAQGSNTAIS YECAVDNYTS FIGFKFRKFI EPQLDEDLTI YMKDKALSPR 490 500 510 520 530 540 KEAWDSVYPD SNLYYKAPES EETRRLIEVF INDENFNPEE IINYVESGDW LKDEKFNISY 550 560 570 580 590 600 SLKEKEIKQE GRLFAKMTYK MRAVQVLAET LLAKGIGELF SENGMVKGEI DLLKRLTTLS 610 620 630 640 650 660 VSGVPRTDSV YNNSKSSEKR NEGMKKKNSG GYWDEKKRSR HEFKATDSST DGYETLSCFL 670 680 690 700 710 720 TTDLKKYCLN WRFESTALFG QRCNEIFGFK TFFNWMHPIL ERCTIYVGDP YCPVADRMHR 730 740 750 760 770 780 QLQDHADSGI FIHNPRGGIE GYCQKLWTLI SISAIHLAAV RVGVRVSAMV QGDNQAIAVT 790 800 810 820 830 840 SRVPVAQTYK QKKNHVYEET TKYFGALRHV MFDVGHELKL NETIISSKMF VYSKRIYYDG 850 860 870 880 890 900 KILPQCLKAL TRCVFWSETL VDENRSACSN ISTSIAKAIE NGYSPILGYC IALYKTCQQV 910 920 930 940 950 960 CISLGMTINP TISPTVRDQY FKGKNWLRCA VLIPANVGGF NYMSTSRCFV RNIGDPAVAA 970 980 990 1000 1010 1020 LADLKRFIRA DLLDKQVLYR VMNQEPGDSS FLDWAPDPYS CNLPHSQSIT TIIKNITARS 1030 1040 1050 1060 1070 1080 VLQESPNPLL SGLFTETSGE EDLNLASFLM DRKVILPRVA HEILGNSLTG VREAIAGMLD 1090 1100 1110 1120 1130 1140 TTKSLVRASV RKGGLSYGIL RRLVNYDLLQ YETLTRTLRK PVKDNIEYEY MCSVELAVGL 1150 1160 1170 1180 1190 1200 RQKMWIHLTY GRPIHGLETP DPLELLRGTF IEGSEVCKLC RSEGADPIYT WFYLPDNIDL 1210 1220 1230 1240 1250 1260 DTLTNGSPAI RIPYFGSATD ERSEAQLGYV RNLSKPAKAA IRIAMVYTWA YGTDEISWME 1270 1280 1290 1300 1310 1320 AALIAQTRAN LSLENLKLLT PVSTPTNLSH RLKDTATQMK FSSATLVRAS RFITISNDNM 1330 1340 1350 1360 1370 1380 ALKEAGESKD TNLVYQQIML TGLSLFEFNM RYKKGSLGKP LILHLHLNNG CCIMESPQEA 1390 1400 1410 1420 1430 1440 NIPPRSTLDL EITQENNKLI YDPDPLKDVD LELFSKVRDV VHTVDMTYWS DDEVIRATSI 1450 1460 1470 1480 1490 1500 CTAMTIADTM SQLDRDNLKE MIALVNDDDV NSLITEFMVI DVPLFCSTFG GILVNQFAYS 1510 1520 1530 1540 1550 1560 LYGLNIRGRE EIWGHVVRIL KDTSHAVLKV LSNALSHPKI FKRFWNAGVV EPVYGPNLSN 1570 1580 1590 1600 1610 1620 QDKILLALSV CEYSVDLFMH DWQGGVPLEI FICDNDPDVA DMRRSSFLAR HLAYLCSLAE 1630 1640 1650 1660 1670 1680 ISRDGPRLES MNSLERLESL KSYLELTFLD DPVLRYSQLT GLVIKVFPST LTYIRKSSIK 1690 1700 1710 1720 1730 1740 VLRTRGIGVP EVLEDWDPEA DNALLDGIAA EIQQNIPLGH QTRAPFWGLR VSKSQVLRLR 1750 1760 1770 1780 1790 1800 GYKEITRGEI GRSGVGLTLP FDGRYLSHQL RLFGINSTSC LKALELTYLL SPLVDKDKDR 1810 1820 1830 1840 1850 1860 LYLGEGAGAM LSCYDATLGP CINYYNSGVY SCDVNGQREL NIYPAEVALV GKKLNNVTSL 1870 1880 1890 1900 1910 1920 GQRVKVLFNG NPGSTWIGND ECEALIWNEL QNSSIGLVHC DMEGGDHKDD QVVLHEHYSV 1930 1940 1950 1960 1970 1980 IRIAYLVGDR DVVLISKIAP RLGTDWTRQL SLYLRYWDEV NLIVLKTSNP ASTEMYLLSR 1990 2000 2010 2020 2030 2040 HPKSDIIEDS KTVLASLLPL SKEDSIKIEK WILIEKAKAH EWVTRELREG SSSSGMLRPY 2050 2060 2070 2080 2090 2100 HQALQTFGFE PNLYKLSRDF LSTMNIADTH NCMIAFNRVL KDTIFEWARI TESDKRLKLT 2110 2120 2130 2140 2150 2160 GKYDLYPVRD SGKLKTISRR LVLSWISLSM STRLVTGSFP DQKFEARLQL GIVSLSSREI 2170 2180 2190 2200 2210 2220 RNLRVITKTL LDRFEDIIHS ITYRFLTKEI KILMKILGAV KMFGARQNEY TTVIDDGSLG DIEPYDSS

References

[1]	"Sequence of the Sendai virus L gene: open reading frames upstream of the main coding region suggest that the gene may be polycistronic." Morgan E.M., Rakestraw K.M. Virology 154:31-40(1986) [PubMed: 3019006] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA].

Cross-references

Sequence databases
EMBLGenBankDDBJ	M14887 Genomic RNA. Translation: AAA69579.1. Frameshift. D00053 Genomic RNA. Translation: BAA00036.1. Frameshift.
PIR	ZLNZSE. A24293.
3D structure databases
ModBase	Search...
Family and domain databases
InterPro	IPR016269. RNA-dir_RNA_pol_paramyxovir. IPR014023. RNA_pol_cat. IPR001016. RNA_pol_L_viral. [Graphical view]
Pfam	PF00946. Paramyx_RNA_pol. 1 hit. [Graphical view]
PIRSF	PIRSF000830. RNA_pol_ParamyxoV. 1 hit.
PROSITE	PS50526. RDRP_SSRNA_NEG_NONSEG. 1 hit. [Graphical view]
ProtoNet	Search...

Entry information

Entry name

L_SENDE

Accession

Primary (citable) accession number: P06829

Entry history

Integrated into UniProtKB/Swiss-Prot:	January 1, 1988
Last sequence update:	February 1, 2005
Last modified:	June 16, 2009
This is version 62 of the entry and version 2 of the sequence. [Complete history]

Entry status

Reviewed (UniProtKB/Swiss-Prot)

Annotation project

Virus (Virus annotation project)