Sequence information
Variant position: 127 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 463 The length of the canonical sequence.
Location on the sequence:
YKEEGSKVTTYCNETMTGWV
H DVLGRNWACFTGKKVGTASE
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human YKEEGSKVTTYCNETMTGWVH DVLGRNWACFTGKKVGTASE
Mouse YEVRGHTAISYCHETMTGWVH DVLGRNWACFVGKKVESHIE
Rat YEVKGSRAISYCHETMTGWVH DVLGRNWACFVGKKMANHSE
Bovine YKEEGGKVTSYCHETMTGWVH DVLGRNRACFTGRKTGNTSE
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
Chain
25 – 134
Dipeptidyl peptidase 1 exclusion domain chain
Glycosylation
119 – 119
N-linked (GlcNAc...) asparagine
Disulfide bond
54 – 136
Alternative sequence
107 – 141
YKEEGSKVTTYCNETMTGWVHDVLGRNWACFTGKK -> DVTDFISHLFMQLGTVGIYDLPHLRNKLAMNRRWG. In isoform 3.
Alternative sequence
107 – 137
YKEEGSKVTTYCNETMTGWVHDVLGRNWACF -> DVTDFISHLFMQLGTVGIYDLPHLRNKLVIK. In isoform 2.
Beta strand
123 – 128
Literature citations
Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefevre syndrome.
Lefevre C.; Blanchet-Bardon C.; Jobard F.; Bouadjar B.; Stalder J.-F.; Cure S.; Hoffmann A.; Prud'Homme J.-F.; Fischer J.;
J. Invest. Dermatol. 117:1657-1661(2001)
Cited for: VARIANTS PLS PRO-127; PRO-272; CYS-339 AND CYS-429; VARIANTS THR-153 AND LYS-401;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.