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CTSV
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  • CTSV
PROTEIN STRUCTURE
ANTIBODIES
AND
VALIDATION
Protein structures
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

CTSV
Synonyms CTSL2, CTSU
Gene descriptioni

Full gene name according to HGNC.

Cathepsin V
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Read more
Enzymes
Metabolic proteins
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Read more
Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 9
Cytoband q22.33
Chromosome location (bp) 97029677 - 97156556
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

7
Ensembl ENSG00000136943 (version 103.38)
Entrez gene 1515
HGNC HGNC:2538
UniProt O60911 (UniProt - Evidence at protein level)
neXtProt NX_O60911
Antibodypedia CTSV antibodies


PROTEIN STRUCTUREi

The Structure section provides predicted structures from the Alphafold protein structure database and available experimental structures from Protein Data Bank (PDB).

In the Structure drop-down menu all experimental structures from PDB are available for selection and display. The structures are displayed using the NGL Viewer and can be zoomed-in and rotated either manually or by checking the Autorotate box. The Color scheme can be selected to show the residue index, chain name or confidence score (as B-factors and pLDDT score for experimental and predicted structures, respectively). The positions for available antigen sequences in the structure are shown if Antigens is turned to ON, and the Variants slider can be used to show the positions of clinical and population variants.https://github.com/nglviewer/ngl

Read more

Predicted


Description: Structure prediction from Alphafold project. Structure version 2

# Chains: 1      # Clinical variants: 0      # Population variants: 206

Antigens:

Off
On

Variants:

Off
Clinical
Population

Color scheme:

Confidence
Residue index
Chain name

Autorotate:

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On



PROTEIN BROWSERi

The protein browser displays the antigen location on the target protein(s) and the features of the target protein. The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped.

At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.

Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).

The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).

If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are displayed.

Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.
CTSV-201
CTSV-203
CTSV-205
CTSV-208
CTSV-211
CTSV-215
CTSV-216


PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The ENSP identifier links to the Ensembl website protein summary, while the ENST identifier links to the Ensembl website transcript summary for the selected splice variant. The data in the UniProt column can be expanded to show links to all matching UniProt identifiers for this protein.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The Gene Ontology terms assigned to this protein are listed if expanding the Gene ontology column. The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide (according to a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius) and the number of predicted transmembrane region(s) (according to MDM) are also reported.
Splice variant UniProt Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
CTSV-201
ENSP00000259470
ENST00000259470
O60911 [Direct mapping]
Cathepsin L2
A0A024R141 [Target identity:100%; Query identity:100%]
Cathepsin L2, isoform CRA_a
Show all
Enzymes
   ENZYME proteins
   Hydrolases
   Peptidases
   Cysteine-type peptidases
Metabolic proteins
   MEMSAT3 predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004197 [cysteine-type endopeptidase activity]
GO:0005515 [protein binding]
GO:0005576 [extracellular region]
GO:0005615 [extracellular space]
GO:0005764 [lysosome]
GO:0006508 [proteolysis]
GO:0006955 [immune response]
GO:0008233 [peptidase activity]
GO:0008234 [cysteine-type peptidase activity]
GO:0016787 [hydrolase activity]
GO:0019886 [antigen processing and presentation of exogenous peptide antigen via MHC class II]
GO:0022617 [extracellular matrix disassembly]
GO:0043202 [lysosomal lumen]
GO:0045616 [regulation of keratinocyte differentiation]
GO:0051603 [proteolysis involved in cellular protein catabolic process]
Show all
334 aa
37.3 kDa
Yes 0
CTSV-203
ENSP00000445052
ENST00000538255
O60911 [Direct mapping]
Cathepsin L2
Show all
Enzymes
   ENZYME proteins
   Hydrolases
   Peptidases
   Cysteine-type peptidases
Metabolic proteins
   SPOCTOPUS predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004197 [cysteine-type endopeptidase activity]
GO:0005515 [protein binding]
GO:0005576 [extracellular region]
GO:0005615 [extracellular space]
GO:0005764 [lysosome]
GO:0006508 [proteolysis]
GO:0006955 [immune response]
GO:0008233 [peptidase activity]
GO:0008234 [cysteine-type peptidase activity]
GO:0016787 [hydrolase activity]
GO:0019886 [antigen processing and presentation of exogenous peptide antigen via MHC class II]
GO:0022617 [extracellular matrix disassembly]
GO:0043202 [lysosomal lumen]
GO:0045616 [regulation of keratinocyte differentiation]
GO:0051603 [proteolysis involved in cellular protein catabolic process]
Show all
285 aa
31.4 kDa
Yes 0
CTSV-205
ENSP00000506713
ENST00000679661
A0A024R141 [Target identity:100%; Query identity:100%]
Cathepsin L2, isoform CRA_a
Show all
Metabolic proteins
   MEMSAT3 predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0006508 [proteolysis]
GO:0008233 [peptidase activity]
GO:0008234 [cysteine-type peptidase activity]
GO:0016787 [hydrolase activity]
Show all
334 aa
37.3 kDa
Yes 0
CTSV-208
ENSP00000505001
ENST00000680221
Metabolic proteins
   MEMSAT3 predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0006508 [proteolysis]
GO:0008234 [cysteine-type peptidase activity]
Show all
332 aa
37.1 kDa
Yes 0
CTSV-211
ENSP00000505355
ENST00000680490
Metabolic proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0006508 [proteolysis]
GO:0008234 [cysteine-type peptidase activity]
Show all
210 aa
23.3 kDa
Yes 0
CTSV-215
ENSP00000505681
ENST00000681737
A0A024R141 [Target identity:100%; Query identity:100%]
Cathepsin L2, isoform CRA_a
Show all
Metabolic proteins
   MEMSAT3 predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0006508 [proteolysis]
GO:0008233 [peptidase activity]
GO:0008234 [cysteine-type peptidase activity]
GO:0016787 [hydrolase activity]
Show all
334 aa
37.3 kDa
Yes 0
CTSV-216
ENSP00000505141
ENST00000681927
A0A024R141 [Target identity:100%; Query identity:100%]
Cathepsin L2, isoform CRA_a
Show all
Metabolic proteins
   MEMSAT3 predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004177 [aminopeptidase activity]
GO:0004197 [cysteine-type endopeptidase activity]
GO:0005737 [cytoplasm]
GO:0005764 [lysosome]
GO:0005773 [vacuole]
GO:0005902 [microvillus]
GO:0006508 [proteolysis]
GO:0007154 [cell communication]
GO:0007283 [spermatogenesis]
GO:0008233 [peptidase activity]
GO:0008234 [cysteine-type peptidase activity]
GO:0008584 [male gonad development]
GO:0009267 [cellular response to starvation]
GO:0009749 [response to glucose]
GO:0009897 [external side of plasma membrane]
GO:0010259 [multicellular organism aging]
GO:0014070 [response to organic cyclic compound]
GO:0016787 [hydrolase activity]
GO:0021675 [nerve development]
GO:0030141 [secretory granule]
GO:0030984 [kininogen binding]
GO:0034698 [response to gonadotropin]
GO:0042277 [peptide binding]
GO:0043005 [neuron projection]
GO:0043204 [perikaryon]
GO:0044877 [protein-containing complex binding]
GO:0045177 [apical part of cell]
GO:0046697 [decidualization]
GO:0048102 [autophagic cell death]
GO:0051384 [response to glucocorticoid]
GO:0060008 [Sertoli cell differentiation]
GO:1990834 [response to odorant]
Show all
334 aa
37.3 kDa
Yes 0

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The Human Protein Atlas project is funded
by the Knut & Alice Wallenberg Foundation.