CTSL3P
Putative inactive cathepsin L-like protein CTSL3P
Also known as: CATL3_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for CTSL3P in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
218 residues, UniProt reviewed canonical sequence.
>Q5NE16|CTSL3P
1 MKMIEQHNQE YREGKHSFTM AMNAFGEMTS EEFRQVVNGF QNQKHRKGKV LQEPLLHDIR
61 KSVDWREKGY VTPVKDQCNW GSVRTDVRKT EKLVSLSVQT WWTALGFKAM LAAFLENHYF
121 ASSMLPTMEA WTLRKPFHMK KSSGDWKVQG HRGASGESLL ASGESQQSPE VAQYSGKHQV
181 QCHLIEEALQ MLSGGDEDHD EDKWPHDMRN HLAGEAQVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CTSL3P can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.56
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
Protein domainsUniProt · Pfam · InterPro
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CTSL3P as an antibody target. Whether an autoantibody or antibody against CTSL3P could matter depends on whether native CTSL3P is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CTSL3P is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CTSL3P as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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