TTLL8
Protein monoglycylase TTLL8
Also known as: TTLL8_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- A6PVC2
- Gene
- TTLL8
- Canonical length
- 850 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
No narrative summary is available for TTLL8 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
850 residues, UniProt reviewed canonical sequence.
>A6PVC2|TTLL8
1 MEPERKGLSL ASSSDGDGRE ENKLKQGISQ DLASSSRLDR YKIARQLTEK AIKEKKIFSI
61 YGHYPVVRAA LRRKGWVEKK FHFLPKVIPD VEDEGARVND DTCAKVKENQ EMALEKTDNI
121 HDVMSRLVKN EMPYLLWTIK RDIIDYHSLT YDQMLNHYAK TASFTTKIGL CVNMRSLPWY
181 VPANPDSFFP RCYSLCTESE QQEFLEDFRR TMASSILKWV VSHQSCSRSS RSKPRDQREE
241 AGSSDLSSRQ DAENAEAKLR GLPGQLVDIA CKVCQAYLGQ LEHEDIDTSA DAVEDLTEAE
301 WEDLTQQYYS LVHGDAFISN SRNYFSQCQA LLNRITSVNP QTDIDGLRNI WIIKPAAKSR
361 GRDIVCMDRV EEILELAAAD HPLSRDNKWV VQKYIETPLL ICDTKFDIRQ WFLVTDWNPL
421 TIWFYKESYL RFSTQRFSLD KLDSAIHLCN NAVQKYLKND VGRSPLLPAH NMWTSTRFQE
481 YLQRQGRGAV WGSVIYPSMK KAIAHAMKVA QDHVEPRKNS FELYGADFVL GRDFRPWLIE
541 INSSPTMHPS TPVTAQLCAQ VQEDTIKVAV DRSCDIGNFE LLWRQPVVEP PPFSGSDLCV
601 AGVSVRRARR QVLPVCNLKA SASLLDAQPL KARGPSAMPD PAQGPPSPAL QRDLGLKEEK
661 GLPLALLAPL RGAAESGGAA QPTRTKAAGK VELPACPCRH VDSQAPNTGV PVAQPAKSWD
721 PNQLNAHPLE PVLRGLKTAE GALRPPPGGK GEGTVCSRLP HHGHHVAACQ TTGTTWDGGP
781 GVCFLRQLLA SELPMGPGLP RDPRAPPCLV CRGLLPPAGP CKRCRSFCAA VLQGASFVRL
841 GGRSCSPRTPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TTLL8 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 3.9 nTPM
Expression across tissuesHPA
Tissue
- testis: 3.9 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
- basal ganglia: 0 nTPM
Single-cell type
- early spermatids: 53 nCPM
- endometrial secretory cells: 27 nCPM
- late spermatids: 25 nCPM
- endometrial luminal cells: 24 nCPM
- late primary spermatocytes: 18 nCPM
- endometrial glandular cells: 15 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.2 nTPM
- medulla oblongata: 0.2 nTPM
- spinal cord: 0.2 nTPM
- basal ganglia: 0.1 nTPM
- hypothalamus: 0.1 nTPM
- midbrain: 0.1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- axoneme assembly
- flagellated sperm motility
- spermatogenesis
- protein polyglycylation
Molecular functions
- ATP binding
- metal ion binding
- protein-glycine ligase activity
- protein-glycine ligase activity, initiating
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TTLL8 as an antibody target. Whether an autoantibody or antibody against TTLL8 could matter depends on whether native TTLL8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TTLL8 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 TTLL8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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