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Signal Peptide Database - Drosophila melanogaster
Entry Details
ID
27025
Source Database
UniProtKB/Swiss-Prot
UniProtKB/Swiss-Prot Accession Number
P18168 (Created: 1990-11-01 Updated: 2008-12-16)
UniProtKB/Swiss-Prot Entry Name
SERR_DROME
Protein Name
Serrate protein
Gene
Ser
Organism Scientific
Drosophila melanogaster
Organism Common
Fruit fly
Lineage
Eukaryota
Metazoa
Arthropoda
Hexapoda
Insecta
Pterygota
Neoptera
Endopterygota
Diptera
Brachycera
Muscomorpha
Ephydroidea
Drosophilidae
Drosophila
Sophophora
Protein Length [aa]
1404
Protein Mass [Da]
150344
Features
Type
Description
Status
Start
End
signal peptide
potential
1
79
chain
Serrate protein
80
1404
disulfide bond
by similarity
284
295
disulfide bond
by similarity
288
301
disulfide bond
by similarity
303
312
disulfide bond
by similarity
315
326
disulfide bond
by similarity
321
333
disulfide bond
by similarity
335
344
disulfide bond
by similarity
351
363
disulfide bond
by similarity
357
373
disulfide bond
by similarity
375
384
disulfide bond
by similarity
391
402
disulfide bond
by similarity
396
473
disulfide bond
by similarity
475
484
disulfide bond
by similarity
491
502
disulfide bond
by similarity
496
511
disulfide bond
by similarity
513
522
disulfide bond
by similarity
529
584
disulfide bond
by similarity
578
593
disulfide bond
by similarity
595
604
disulfide bond
by similarity
611
621
disulfide bond
by similarity
615
630
disulfide bond
by similarity
632
641
disulfide bond
by similarity
648
659
disulfide bond
by similarity
653
668
disulfide bond
by similarity
670
679
disulfide bond
by similarity
686
696
disulfide bond
by similarity
691
705
disulfide bond
by similarity
707
716
disulfide bond
by similarity
766
781
disulfide bond
by similarity
783
792
disulfide bond
by similarity
799
810
disulfide bond
by similarity
804
819
disulfide bond
by similarity
821
830
disulfide bond
by similarity
837
848
disulfide bond
by similarity
842
861
disulfide bond
by similarity
863
872
disulfide bond
by similarity
879
890
disulfide bond
by similarity
884
899
disulfide bond
by similarity
901
910
disulfide bond
by similarity
917
928
disulfide bond
by similarity
922
937
disulfide bond
by similarity
939
948
transmembrane region
potential
1220
1245
topological domain
Extracellular
potential
80
1219
topological domain
Cytoplasmic
potential
1246
1404
domain
DSL
235
279
domain
EGF-like 1
280
313
domain
EGF-like 2
311
345
domain
EGF-like 3
347
385
domain
EGF-like 4
387
485
domain
EGF-like 5; calcium-binding
potential
487
523
domain
EGF-like 6; calcium-binding
potential
525
605
domain
EGF-like 7; calcium-binding
potential
607
642
domain
EGF-like 8; calcium-binding
potential
644
680
domain
EGF-like 9
682
717
domain
EGF-like 10
719
793
domain
EGF-like 11; calcium-binding
potential
795
831
domain
EGF-like 12
833
873
domain
EGF-like 13
875
911
domain
EGF-like 14; calcium-binding
potential
913
949
modified residue
Phosphoserine
1292
1292
glycosylation site
N-linked (GlcNAc...)
potential
148
148
glycosylation site
N-linked (GlcNAc...)
potential
192
192
glycosylation site
N-linked (GlcNAc...)
potential
243
243
glycosylation site
N-linked (GlcNAc...)
potential
327
327
glycosylation site
N-linked (GlcNAc...)
potential
408
408
glycosylation site
N-linked (GlcNAc...)
potential
448
448
glycosylation site
N-linked (GlcNAc...)
potential
554
554
glycosylation site
N-linked (GlcNAc...)
potential
735
735
glycosylation site
N-linked (GlcNAc...)
potential
961
961
glycosylation site
N-linked (GlcNAc...)
potential
973
973
glycosylation site
N-linked (GlcNAc...)
potential
1000
1000
glycosylation site
N-linked (GlcNAc...)
potential
1026
1026
glycosylation site
N-linked (GlcNAc...)
potential
1146
1146
compositionally biased region
Ser-rich
403
472
compositionally biased region
Thr-rich
733
765
SP Length
79
----+----1----+----2----+----3----+----4----+----5
Signal Peptide
MFRKHFRRKPATSSSLESTIESADSLGMSKKTATKRQRPRHRVPKIATLP
STIRDCRSLKSACNLIALILILLVHKISA
Sequence
MFRKHFRRKPATSSSLESTIESADSLGMSKKTATKRQRPRHRVPKIATLP
STIRDCRSLKSACNLIALILILLVHKISA
AGNFELEILEISNTNSHLLNG
YCCGMPAELRATKTIGCSPCTTAFRLCLKEYQTTEQGASISTGCSFG
N
AT
TKILGGSSFVLSDPGVGAIVLPFTFRWTKSFTLILQALDMY
N
TSYPDAER
LIEETSYSGVILPSPEWKTLDHIGRNARITYRVR
VQCAVTYY
N
TTCTTFC
RPRDDQFGHYACGSEGQKLCLNGWQGVNC
EEAICKAGCDPVHGKCDRPGE
CECRPGWRGP
LCNECMVYPGCKHGSC
N
GSAWKCVCDTNWGGILCD
Q
DLNF
CGTHEPCKHGGTCENTAPDKYRCTCAEGLSGEQCE
I
VEHPCATRPCRNGG
TC
TLKTSNRTQAQVYRTSHGRSNMGRPVRRSSSMRSLDHLRPEGQALNGS
SSPGLVSLGSLQLQQQLAPDFT
CDCAAGWTGPTCE
I
NIDECAGGPCEHGG
TCIDLIGGFRCECPPEWHGDVCQ
V
DVNECEAPHSAGIAANALLTTTATAI
IGS
N
LSSTALLAALTSAVASTSLAIGPCINAKECRNQPGSFACICKEGWG
GVTCA
E
NLDDCVGQCRNGATCIDLVNDYRCACASGFKGRDCE
T
DIDECAT
SPCRNGGECVDMVGKFNCICPLGYSGSLCE
E
AKENCTPSPCLEGHCLNTP
EGYYCHCPPDRAGKHCE
Q
LRPLCSQPPCNEGC
FANVSLATSATTTTTTTT
TATTTRKMAKPSGLP
CSGHGSCEMSDVGTFCKCHVGHTGTFCE
H
NLNECS
PNPCRNGGICLDGDGDFTCECMSGWTGKRCS
E
RATGCYAGQCQNGGTCMP
GAPDKALQPHCRCAPGWTGLFCA
E
AIDQCRGQPCHNGGTCESGAGWFRCV
CAQGFSGPDCR
I
NVNECSPQPCQGGATCIDGIGGYSCICPPGRHGLRCE
I
LLSDPKSACQ
N
ASNTISPYTAL
N
RSQNWLDIALTGRTEDDENCNACVCE
N
GTSRCTNLWCGLPNCYKVDPLSKSS
N
LSGVCKQHEVCVPALSETCLSSPC
NVRGDCRALEPSRRVAPPRLPAKSSCWPNQAVVNENCARLTILLALERVG
KGASVEGLCSLVRVLLAAQLIKKPASTFGQDPGMLMVLCDLKTGT
N
DTVE
LTVSSSKLNDPQLPVAVGLLGELLSFRQLNGIQRRKELELQHAKLAALTS
IVEVKLETARVADGSGHSL
LIGVLCGVFIVLVGFSVFISLYWKQR
LAYRT
SSGMNLTPSLDALRHEEEKSNNLQNEENLRRYTNPLKGSTS
S
LRAATGME
LSLNPAPELAASAASSSALHRSQPLFPPCDFERELDSSTGLKQAHKRSSQ
ILLHKTQNSDMRKNTVGSLDSPRKDFGKRSINCKSMPPSSGDEGSDVLAT
TVMV
Original
MFRKHFRRKPATSSSLESTIESADSLGMSKKTATKRQRPRHRVPKIATLP
STIRDCRSLKSACNLIALILILLVHKISAAGNFELEILEISNTNSHLLNG
YCCGMPAELRATKTIGCSPCTTAFRLCLKEYQTTEQGASISTGCSFGNAT
TKILGGSSFVLSDPGVGAIVLPFTFRWTKSFTLILQALDMYNTSYPDAER
LIEETSYSGVILPSPEWKTLDHIGRNARITYRVRVQCAVTYYNTTCTTFC
RPRDDQFGHYACGSEGQKLCLNGWQGVNCEEAICKAGCDPVHGKCDRPGE
CECRPGWRGPLCNECMVYPGCKHGSCNGSAWKCVCDTNWGGILCDQDLNF
CGTHEPCKHGGTCENTAPDKYRCTCAEGLSGEQCEIVEHPCATRPCRNGG
TCTLKTSNRTQAQVYRTSHGRSNMGRPVRRSSSMRSLDHLRPEGQALNGS
SSPGLVSLGSLQLQQQLAPDFTCDCAAGWTGPTCEINIDECAGGPCEHGG
TCIDLIGGFRCECPPEWHGDVCQVDVNECEAPHSAGIAANALLTTTATAI
IGSNLSSTALLAALTSAVASTSLAIGPCINAKECRNQPGSFACICKEGWG
GVTCAENLDDCVGQCRNGATCIDLVNDYRCACASGFKGRDCETDIDECAT
SPCRNGGECVDMVGKFNCICPLGYSGSLCEEAKENCTPSPCLEGHCLNTP
EGYYCHCPPDRAGKHCEQLRPLCSQPPCNEGCFANVSLATSATTTTTTTT
TATTTRKMAKPSGLPCSGHGSCEMSDVGTFCKCHVGHTGTFCEHNLNECS
PNPCRNGGICLDGDGDFTCECMSGWTGKRCSERATGCYAGQCQNGGTCMP
GAPDKALQPHCRCAPGWTGLFCAEAIDQCRGQPCHNGGTCESGAGWFRCV
CAQGFSGPDCRINVNECSPQPCQGGATCIDGIGGYSCICPPGRHGLRCEI
LLSDPKSACQNASNTISPYTALNRSQNWLDIALTGRTEDDENCNACVCEN
GTSRCTNLWCGLPNCYKVDPLSKSSNLSGVCKQHEVCVPALSETCLSSPC
NVRGDCRALEPSRRVAPPRLPAKSSCWPNQAVVNENCARLTILLALERVG
KGASVEGLCSLVRVLLAAQLIKKPASTFGQDPGMLMVLCDLKTGTNDTVE
LTVSSSKLNDPQLPVAVGLLGELLSFRQLNGIQRRKELELQHAKLAALTS
IVEVKLETARVADGSGHSLLIGVLCGVFIVLVGFSVFISLYWKQRLAYRT
SSGMNLTPSLDALRHEEEKSNNLQNEENLRRYTNPLKGSTSSLRAATGME
LSLNPAPELAASAASSSALHRSQPLFPPCDFERELDSSTGLKQAHKRSSQ
ILLHKTQNSDMRKNTVGSLDSPRKDFGKRSINCKSMPPSSGDEGSDVLAT
TVMV
----+----1----+----2----+----3----+----4----+----5
Hydropathies
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Dr. Katja Kapp
, Kassel &
thpr.net e. K.
, Dresden, Germany, last update 2010-06-11