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Signal Peptide Database - Drosophila melanogaster
Entry Details
ID
1196
Source Database
UniProtKB/Swiss-Prot
UniProtKB/Swiss-Prot Accession Number
P10040 (Created: 1989-07-01 Updated: 2009-01-20)
UniProtKB/Swiss-Prot Entry Name
CRB_DROME
Protein Name
Protein crumbs
Gene
crb
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]
2146
Protein Mass [Da]
233572
Features
Type
Description
Status
Start
End
signal peptide
1
88
chain
Protein crumbs
89
2146
disulfide bond
by similarity
269
280
disulfide bond
by similarity
274
289
disulfide bond
by similarity
291
300
disulfide bond
by similarity
308
319
disulfide bond
by similarity
313
329
disulfide bond
by similarity
331
340
disulfide bond
by similarity
350
361
disulfide bond
by similarity
355
372
disulfide bond
by similarity
374
383
disulfide bond
by similarity
390
401
disulfide bond
by similarity
395
410
disulfide bond
by similarity
412
422
disulfide bond
by similarity
429
440
disulfide bond
by similarity
434
449
disulfide bond
by similarity
451
460
disulfide bond
by similarity
466
477
disulfide bond
by similarity
471
486
disulfide bond
by similarity
488
497
disulfide bond
by similarity
503
513
disulfide bond
by similarity
507
518
disulfide bond
by similarity
520
529
disulfide bond
by similarity
547
560
disulfide bond
by similarity
554
567
disulfide bond
by similarity
569
578
disulfide bond
by similarity
584
595
disulfide bond
by similarity
589
600
disulfide bond
by similarity
602
608
disulfide bond
by similarity
611
622
disulfide bond
by similarity
616
632
disulfide bond
by similarity
634
643
disulfide bond
by similarity
650
662
disulfide bond
by similarity
657
671
disulfide bond
by similarity
673
682
disulfide bond
by similarity
689
700
disulfide bond
by similarity
694
709
disulfide bond
by similarity
711
720
disulfide bond
by similarity
727
738
disulfide bond
by similarity
732
747
disulfide bond
by similarity
749
758
disulfide bond
by similarity
765
776
disulfide bond
by similarity
770
785
disulfide bond
by similarity
787
797
disulfide bond
by similarity
804
815
disulfide bond
by similarity
809
824
disulfide bond
by similarity
826
835
disulfide bond
by similarity
842
853
disulfide bond
by similarity
847
888
disulfide bond
by similarity
890
899
disulfide bond
by similarity
906
917
disulfide bond
by similarity
911
926
disulfide bond
by similarity
928
937
disulfide bond
by similarity
944
955
disulfide bond
by similarity
950
964
disulfide bond
by similarity
966
975
disulfide bond
by similarity
982
993
disulfide bond
by similarity
987
1007
disulfide bond
by similarity
1009
1018
disulfide bond
by similarity
1171
1203
disulfide bond
by similarity
1209
1220
disulfide bond
by similarity
1214
1229
disulfide bond
by similarity
1231
1240
disulfide bond
by similarity
1483
1494
disulfide bond
by similarity
1488
1503
disulfide bond
by similarity
1505
1514
disulfide bond
by similarity
1713
1757
disulfide bond
by similarity
1760
1771
disulfide bond
by similarity
1765
1780
disulfide bond
by similarity
1782
1791
disulfide bond
by similarity
1798
1809
disulfide bond
by similarity
1803
1818
disulfide bond
by similarity
1820
1829
disulfide bond
by similarity
1836
1847
disulfide bond
by similarity
1841
1856
disulfide bond
by similarity
1858
1867
disulfide bond
by similarity
1875
1886
disulfide bond
by similarity
1880
1900
disulfide bond
by similarity
1916
1927
disulfide bond
by similarity
1921
1936
disulfide bond
by similarity
1938
1947
disulfide bond
by similarity
1954
1965
disulfide bond
by similarity
1959
1974
disulfide bond
by similarity
1976
1986
disulfide bond
by similarity
1993
2006
disulfide bond
by similarity
2000
2015
disulfide bond
by similarity
2017
2026
disulfide bond
by similarity
2032
2044
disulfide bond
by similarity
2038
2056
disulfide bond
by similarity
2058
2067
transmembrane region
potential
2083
2109
topological domain
Extracellular
potential
89
2082
topological domain
Cytoplasmic
potential
2110
2146
domain
EGF-like 1
265
301
domain
EGF-like 2
304
341
domain
EGF-like 3
346
384
domain
EGF-like 4; calcium-binding
potential
386
423
domain
EGF-like 5
425
461
domain
EGF-like 6
462
498
domain
EGF-like 7
499
530
domain
EGF-like 8
543
579
domain
EGF-like 9
580
609
domain
EGF-like 10
607
644
domain
EGF-like 11; calcium-binding
potential
646
683
domain
EGF-like 12; calcium-binding
potential
685
721
domain
EGF-like 13; calcium-binding
potential
723
759
domain
EGF-like 14; calcium-binding
potential
761
798
domain
EGF-like 15; calcium-binding
potential
800
836
domain
EGF-like 16
838
900
domain
EGF-like 17; calcium-binding
potential
902
938
domain
EGF-like 18; calcium-binding
potential
940
976
domain
EGF-like 19
978
1019
domain
Laminin G-like 1
1021
1203
domain
EGF-like 20
1205
1241
domain
Laminin G-like 2
1248
1478
domain
EGF-like 21
1479
1515
domain
Laminin G-like 3
1555
1755
domain
EGF-like 22
1756
1792
domain
EGF-like 23; calcium-binding
potential
1794
1830
domain
EGF-like 24; calcium-binding
potential
1832
1868
domain
EGF-like 25
1871
1912
domain
EGF-like 26
1912
1948
domain
EGF-like 27; calcium-binding
potential
1950
1987
domain
EGF-like 28; calcium-binding
potential
1989
2027
domain
EGF-like 29
2028
2068
glycosylation site
N-linked (GlcNAc...)
potential
94
94
glycosylation site
N-linked (GlcNAc...)
potential
196
196
glycosylation site
N-linked (GlcNAc...)
potential
236
236
glycosylation site
N-linked (GlcNAc...)
potential
237
237
glycosylation site
N-linked (GlcNAc...)
potential
334
334
glycosylation site
N-linked (GlcNAc...)
potential
398
398
glycosylation site
N-linked (GlcNAc...)
potential
548
548
glycosylation site
N-linked (GlcNAc...)
potential
563
563
glycosylation site
N-linked (GlcNAc...)
potential
734
734
glycosylation site
N-linked (GlcNAc...)
potential
744
744
glycosylation site
N-linked (GlcNAc...)
potential
858
858
glycosylation site
N-linked (GlcNAc...)
potential
882
882
glycosylation site
N-linked (GlcNAc...)
potential
974
974
glycosylation site
N-linked (GlcNAc...)
potential
1006
1006
glycosylation site
N-linked (GlcNAc...)
1100
1100
glycosylation site
N-linked (GlcNAc...)
potential
1112
1112
glycosylation site
N-linked (GlcNAc...)
potential
1136
1136
glycosylation site
N-linked (GlcNAc...)
potential
1190
1190
glycosylation site
N-linked (GlcNAc...)
potential
1243
1243
glycosylation site
N-linked (GlcNAc...)
potential
1253
1253
glycosylation site
N-linked (GlcNAc...)
potential
1352
1352
glycosylation site
N-linked (GlcNAc...)
potential
1361
1361
glycosylation site
N-linked (GlcNAc...)
potential
1439
1439
glycosylation site
N-linked (GlcNAc...)
potential
1452
1452
glycosylation site
N-linked (GlcNAc...)
potential
1543
1543
glycosylation site
N-linked (GlcNAc...)
potential
1737
1737
glycosylation site
N-linked (GlcNAc...)
potential
1749
1749
glycosylation site
N-linked (GlcNAc...)
potential
1806
1806
glycosylation site
N-linked (GlcNAc...)
potential
1846
1846
glycosylation site
N-linked (GlcNAc...)
potential
1882
1882
glycosylation site
N-linked (GlcNAc...)
potential
1891
1891
glycosylation site
N-linked (GlcNAc...)
potential
1897
1897
glycosylation site
N-linked (GlcNAc...)
potential
2027
2027
glycosylation site
N-linked (GlcNAc...)
potential
2033
2033
glycosylation site
N-linked (GlcNAc...)
potential
2066
2066
splice variant
(in isoform B)
0
0
SP Length
88
----+----1----+----2----+----3----+----4----+----5
Signal Peptide
MAKIANASLSQQQKQRQAETATTTTTTVAASVETATTTARSRDRTKSAAQ
ITSHLLKRAISVYSSPQWIPLFILIYLATDVASVAVPT
Sequence
MAKIANASLSQQQKQRQAETATTTTTTVAASVETATTTARSRDRTKSAAQ
ITSHLLKRAISVYSSPQWIPLFILIYLATDVASVAVPT
KEAYF
N
GSTYLR
LTTPMPIWDHSAISFRSCRGGEILAQQYNKNSIVISVLNDFLQISLAGPA
VHGPNNRLDVKLPYQLLDNRWHTLQFKYEYGNLYLHVDRAASIFA
N
STYN
SQFLTNQDIGYKDAILILGNSFSGCLLDGPGLQFV
N
N
STVQNVVFGHCPL
TPGPCSDHDLFTRL
PDNFCLNDPCMGHGTCSSSPEGYECRCTARYSGKNC
Q
KD
NGSPCAKNPCENGGSCLENSRGDYQCFCDP
N
HSGQHCE
TEVN
IHPLC
QTNPCLNNGACVVIGGSGALTCECPKGYAGARCE
V
DTDECASQPCQN
N
GS
CIDRINGFSCDCSGTGYTGAFCQ
T
NVDECDKNPCLNGGRCFDTYGWYTCQ
CLDGWGGEICD
RPMTCQTQQCLNGGTCLDKPIGFQCLCPPEYTGELCQ
IA
PSCAQQCPIDSECVGGKCVCKPGSSGYNCQ
TSTGDGASALAL
TPINC
N
AT
NGKCLNGGTCSM
N
GTHCYCAVGYSGDRCE
KAENCSPLNCQEPMVCVQNQC
LCPENK
VCNQCATQPCQNGGECVDLPNGDYECKCTRGWTGRTCG
N
DVDEC
TLHPKICGNGICKNEKGSYKCYCTPGFTGVHCD
S
DVDECLSFPCLNGATC
HNKINAYECVCQPGYEGENCE
V
DIDECGSNPCS
N
GSTCIDRIN
N
FTCNCI
PGMTGRICD
I
DIDDCVGDPCLNGGQCIDQLGGFRCDCSGTGYEGENCE
L
N
IDECLSNPCTNGAKCLDRVKDYFCDCHNGYKGKNCE
Q
DINECESNPCQYN
GNCLERS
N
ITLYQMSRITDLPKVFSQPFSFE
N
ASGYECVCVPGIIGKNCE
I
NINECDSNPCSKHGNCNDGIGTYTCECEPGFEGTHCE
I
NIDECDRYNPC
QRGTCYDQIDDYDCDCDANYGGK
N
CS
V
LLKGCDQNPCLNGGACLPYLINE
VTHLY
N
CTCENGFQGDKCE
K
TTTLSMVATSLISVTTEREEGYDINLQFRT
TLPNGVLAFGTTGEKNEPVSYILELINGRLNLHSSLLNKWEGVFIGSKL
N
DSNWHKVFVAI
N
TSHLVLSANDEQAIFPVGSYETA
N
NSQPSFPRTYLGGT
IPNLKSYLRHLTHQPSAFVGCMQDIMVNGKWIFPDEQDA
N
ISYTKLENVQ
SGC
P
RTEQCKPNPCHSNGECTDLWHTFACHCPRPFFGHTCQ
H
N
MTAA
TFG
HE
N
TTHSAVIVETTDVARRAIRSILDISMFIRTREPTGQVFYLGTDPRKA
PTKNIGDSYVAAKLHGGELLVKMQFSGTPEAYTVGGQKLDNGYNHLIEVV
R
N
QTLVQVKL
N
GTEYFRKTLSTTGLLDAQVLYLGGPAPTRESLLGATTEP
GIIPVPGAGIPIEDTTVPKEADDSRDYFKGIIQDVKVS
N
GSLNLIVEMYS
L
N
VTDVQVNAKPLGAVTIDRASVLPGEV
SDDLCRKNPCLHNAECRNTWND
YTCKCPNGYKGKNCQ
EIEFCQHVTCPGQSLCQNLDDGYECVT
N
TTFTGQE
RSPL
AFFYFQEQQSDDIVSEASPKQTLKPVIDIAFRTRAGGTLLYIDNVD
GFFEIGVNGGRVTITWKLSALHFGESARFEKENTDGEWSRIYLRAHNSKL
EGGWKGWESMVDPTPAFSTDIDQAAFQSLIATSTQVYLGGMPESRQARGS
TLSAQQGSQFKGCVGEARVGDLLLPYFSMAELYSRT
N
VSVQQKAQFRL
N
A
TRPEE
GCILCFQSDCKNDGFCQSPSDEYACTCQPGFEGDDCG
T
DIDECLN
TECLN
N
GTCINQVAAFFCQCQPGFEGQHCE
Q
NIDECADQPCHNGG
N
CTDL
IASYVCDCPEDYMGPQCD
VL
KQMTCENEPCR
N
GSTCQNGF
N
ASTGN
N
FTC
TCVPGFEGPLC
DIPFCEITPCDNGGLCLTTGAVPMCKCSLGYTGRLCE
Q
D
INECESNPCQNGGQCKDLVGRYECDCQGTGFEGIRCE
N
DIDECNMEGDYC
GGLGRCFNKPGSFQCICQKPYCGAYC
N
FTDPC
N
ATDLCSNGGRCVESCGA
KPDYYCECPEGFAGK
N
CT
APITAKEDGPSTTD
IAIIVIPVVVVLLLIAGA
LLGTFLVMA
RNKRATRGTYSPSAQEYCNPRLEMDNVLKPPPEERLI
Original
MAKIANASLSQQQKQRQAETATTTTTTVAASVETATTTARSRDRTKSAAQ
ITSHLLKRAISVYSSPQWIPLFILIYLATDVASVAVPTKEAYFNGSTYLR
LTTPMPIWDHSAISFRSCRGGEILAQQYNKNSIVISVLNDFLQISLAGPA
VHGPNNRLDVKLPYQLLDNRWHTLQFKYEYGNLYLHVDRAASIFANSTYN
SQFLTNQDIGYKDAILILGNSFSGCLLDGPGLQFVNNSTVQNVVFGHCPL
TPGPCSDHDLFTRLPDNFCLNDPCMGHGTCSSSPEGYECRCTARYSGKNC
QKDNGSPCAKNPCENGGSCLENSRGDYQCFCDPNHSGQHCETEVNIHPLC
QTNPCLNNGACVVIGGSGALTCECPKGYAGARCEVDTDECASQPCQNNGS
CIDRINGFSCDCSGTGYTGAFCQTNVDECDKNPCLNGGRCFDTYGWYTCQ
CLDGWGGEICDRPMTCQTQQCLNGGTCLDKPIGFQCLCPPEYTGELCQIA
PSCAQQCPIDSECVGGKCVCKPGSSGYNCQTSTGDGASALALTPINCNAT
NGKCLNGGTCSMNGTHCYCAVGYSGDRCEKAENCSPLNCQEPMVCVQNQC
LCPENKVCNQCATQPCQNGGECVDLPNGDYECKCTRGWTGRTCGNDVDEC
TLHPKICGNGICKNEKGSYKCYCTPGFTGVHCDSDVDECLSFPCLNGATC
HNKINAYECVCQPGYEGENCEVDIDECGSNPCSNGSTCIDRINNFTCNCI
PGMTGRICDIDIDDCVGDPCLNGGQCIDQLGGFRCDCSGTGYEGENCELN
IDECLSNPCTNGAKCLDRVKDYFCDCHNGYKGKNCEQDINECESNPCQYN
GNCLERSNITLYQMSRITDLPKVFSQPFSFENASGYECVCVPGIIGKNCE
ININECDSNPCSKHGNCNDGIGTYTCECEPGFEGTHCEINIDECDRYNPC
QRGTCYDQIDDYDCDCDANYGGKNCSVLLKGCDQNPCLNGGACLPYLINE
VTHLYNCTCENGFQGDKCEKTTTLSMVATSLISVTTEREEGYDINLQFRT
TLPNGVLAFGTTGEKNEPVSYILELINGRLNLHSSLLNKWEGVFIGSKLN
DSNWHKVFVAINTSHLVLSANDEQAIFPVGSYETANNSQPSFPRTYLGGT
IPNLKSYLRHLTHQPSAFVGCMQDIMVNGKWIFPDEQDANISYTKLENVQ
SGCPRTEQCKPNPCHSNGECTDLWHTFACHCPRPFFGHTCQHNMTAATFG
HENTTHSAVIVETTDVARRAIRSILDISMFIRTREPTGQVFYLGTDPRKA
PTKNIGDSYVAAKLHGGELLVKMQFSGTPEAYTVGGQKLDNGYNHLIEVV
RNQTLVQVKLNGTEYFRKTLSTTGLLDAQVLYLGGPAPTRESLLGATTEP
GIIPVPGAGIPIEDTTVPKEADDSRDYFKGIIQDVKVSNGSLNLIVEMYS
LNVTDVQVNAKPLGAVTIDRASVLPGEVSDDLCRKNPCLHNAECRNTWND
YTCKCPNGYKGKNCQEIEFCQHVTCPGQSLCQNLDDGYECVTNTTFTGQE
RSPLAFFYFQEQQSDDIVSEASPKQTLKPVIDIAFRTRAGGTLLYIDNVD
GFFEIGVNGGRVTITWKLSALHFGESARFEKENTDGEWSRIYLRAHNSKL
EGGWKGWESMVDPTPAFSTDIDQAAFQSLIATSTQVYLGGMPESRQARGS
TLSAQQGSQFKGCVGEARVGDLLLPYFSMAELYSRTNVSVQQKAQFRLNA
TRPEEGCILCFQSDCKNDGFCQSPSDEYACTCQPGFEGDDCGTDIDECLN
TECLNNGTCINQVAAFFCQCQPGFEGQHCEQNIDECADQPCHNGGNCTDL
IASYVCDCPEDYMGPQCDVLKQMTCENEPCRNGSTCQNGFNASTGNNFTC
TCVPGFEGPLCDIPFCEITPCDNGGLCLTTGAVPMCKCSLGYTGRLCEQD
INECESNPCQNGGQCKDLVGRYECDCQGTGFEGIRCENDIDECNMEGDYC
GGLGRCFNKPGSFQCICQKPYCGAYCNFTDPCNATDLCSNGGRCVESCGA
KPDYYCECPEGFAGKNCTAPITAKEDGPSTTDIAIIVIPVVVVLLLIAGA
LLGTFLVMARNKRATRGTYSPSAQEYCNPRLEMDNVLKPPPEERLI
----+----1----+----2----+----3----+----4----+----5
Hydropathies
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