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Signal Peptide Database - Mammalia
Entry Details
ID
175
Source Database
UniProtKB/Swiss-Prot
UniProtKB/Swiss-Prot Accession Number
Q9NZV1 (Created: 2005-06-07 Updated: 2008-12-16)
UniProtKB/Swiss-Prot Entry Name
CRIM1_HUMAN
Protein Name
Cysteine-rich motor neuron 1 protein
Gene
CRIM1
Organism Scientific
Homo sapiens
Organism Common
Human
Lineage
Eukaryota
Metazoa
Chordata
Craniata
Vertebrata
Euteleostomi
Mammalia
Eutheria
Euarchontoglires
Primates
Haplorrhini
Catarrhini
Hominidae
Homo
Protein Length [aa]
1036
Protein Mass [Da]
113738
Features
Type
Description
Status
Start
End
signal peptide
1
34
chain
Processed cysteine-rich motor neuron 1 protein
0
1036
chain
Cysteine-rich motor neuron 1 protein
35
1036
transmembrane region
potential
940
960
topological domain
Extracellular
potential
35
939
topological domain
Cytoplasmic
potential
961
1036
domain
IGFBP N-terminal
35
112
domain
VWFC 1
334
391
domain
VWFC 2
401
457
domain
Antistasin-like 1
469
498
domain
Antistasin-like 2
505
532
domain
Antistasin-like 3
539
564
domain
Antistasin-like 4
567
592
domain
VWFC 3
606
663
domain
VWFC 4
677
735
domain
VWFC 5
751
809
domain
VWFC 6
817
874
modified residue
Phosphothreonine
1035
1035
glycosylation site
N-linked (GlcNAc...)
potential
71
71
glycosylation site
N-linked (GlcNAc...)
potential
113
113
glycosylation site
N-linked (GlcNAc...)
potential
330
330
glycosylation site
N-linked (GlcNAc...)
potential
474
474
glycosylation site
N-linked (GlcNAc...)
potential
746
746
sequence variant
(in dbSNP:rs12997487)
0
0
short sequence motif
Cell attachment site
potential
314
316
SP Length
34
----+----1----+----2----+----3----+----4----+----5
Signal Peptide
MYLVAGDRGLAGCGHLLVSLLGLLLLLARSGTRA
Sequence
MYLVAGDRGLAGCGHLLVSLLGLLLLLARSGTRA
LVCLPCDESKCEEPRN
CPGSIVQGVCGCCYTCASQR
N
ESCGGTFGIYGTCDRGLRCVIRPPLNGDS
LTEYEAGVCEDE
N
WTDDQLLGFKPCNENLIAGCNIINGKCECNTIRTCSN
PFEFPSQDMCLSALKRIEEEKPDCSKARCEVQFSPRCPEDSVLIEGYAPP
GECCPLPSRCVCNPAGCLRKVCQPGNLNILVSKASGKPGECCDLYECKPV
FGVDCRTVECPPVQQTACPPDSYETQVRLTADGCCTLPTRCECLSGLCGF
PVCEVGSTPRIVS
RGD
GTPGKCCDVFECV
N
DTK
PACVFNNVEYYDGDMFR
MDNCRFCRCQGGVAICFTAQCGEINCERYYVPEGECCPVCE
DPVYPFNNP
AGCYANGLILAHGDRWREDDCTFCQCVNGERHCVATVCGQTCTNPVKVPG
ECCPVCE
EPTIITVDPPA
CGELS
N
CTLTGKDCINGFKRDHNGCRTCQC
IN
TEEL
CSERKQGCTLNCPFGFLTDAQNCEICEC
RPRPKK
CRPIICDKYCPL
GLLKNKHGCDICRC
KK
CPELSCSKICPLGFQQDSHGCLICKC
REASASAG
PPILS
GTCLTVDGHHHKNEESWHDGCRECYCLNGREMCALITCPVPACGN
PTIHPGQCCPSCA
DDFVVQKPELSTP
SICHAPGGEYFVEGETWNIDSCTQ
CTCHSGRVLCETEVCPPLLCQNPSRTQDSCCPQCT
DQPFRPSLSR
N
NSVP
NYCKNDEGDIFLAAESWKPDVCTSCICIDSVISCFSESCPSVSCERPVLR
KGQCCPYCI
EDTIPKK
VVCHFSGKAYADEERWDLDSCTHCYCLQGQTLCS
TVSCPPLPCVEPINVEGSCCPMCP
EMYVPEPTNIPIEKTNHRGEVDLEVP
LWPTPSENDIVHLPRDMGHLQVDYRDNRLHPSEDSSLDS
IASVVVPIIIC
LSIIIAFLFI
NQKKQWIPLLCWYRTPTKPSSLNNQLVSVDCKKGTRVQVD
SSQRMLRIAEPDARFSGFYSMQKQNHLQADNFYQ
T
V
Original
MYLVAGDRGLAGCGHLLVSLLGLLLLLARSGTRALVCLPCDESKCEEPRN
CPGSIVQGVCGCCYTCASQRNESCGGTFGIYGTCDRGLRCVIRPPLNGDS
LTEYEAGVCEDENWTDDQLLGFKPCNENLIAGCNIINGKCECNTIRTCSN
PFEFPSQDMCLSALKRIEEEKPDCSKARCEVQFSPRCPEDSVLIEGYAPP
GECCPLPSRCVCNPAGCLRKVCQPGNLNILVSKASGKPGECCDLYECKPV
FGVDCRTVECPPVQQTACPPDSYETQVRLTADGCCTLPTRCECLSGLCGF
PVCEVGSTPRIVSRGDGTPGKCCDVFECVNDTKPACVFNNVEYYDGDMFR
MDNCRFCRCQGGVAICFTAQCGEINCERYYVPEGECCPVCEDPVYPFNNP
AGCYANGLILAHGDRWREDDCTFCQCVNGERHCVATVCGQTCTNPVKVPG
ECCPVCEEPTIITVDPPACGELSNCTLTGKDCINGFKRDHNGCRTCQCIN
TEELCSERKQGCTLNCPFGFLTDAQNCEICECRPRPKKCRPIICDKYCPL
GLLKNKHGCDICRCKKCPELSCSKICPLGFQQDSHGCLICKCREASASAG
PPILSGTCLTVDGHHHKNEESWHDGCRECYCLNGREMCALITCPVPACGN
PTIHPGQCCPSCADDFVVQKPELSTPSICHAPGGEYFVEGETWNIDSCTQ
CTCHSGRVLCETEVCPPLLCQNPSRTQDSCCPQCTDQPFRPSLSRNNSVP
NYCKNDEGDIFLAAESWKPDVCTSCICIDSVISCFSESCPSVSCERPVLR
KGQCCPYCIEDTIPKKVVCHFSGKAYADEERWDLDSCTHCYCLQGQTLCS
TVSCPPLPCVEPINVEGSCCPMCPEMYVPEPTNIPIEKTNHRGEVDLEVP
LWPTPSENDIVHLPRDMGHLQVDYRDNRLHPSEDSSLDSIASVVVPIIIC
LSIIIAFLFINQKKQWIPLLCWYRTPTKPSSLNNQLVSVDCKKGTRVQVD
SSQRMLRIAEPDARFSGFYSMQKQNHLQADNFYQTV
----+----1----+----2----+----3----+----4----+----5
Hydropathies
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Dr. Katja Kapp
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