Homo sapiens Protein: TTLL7
Summary
InnateDB Protein IDBP-99928.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TTLL7
Protein Name tubulin tyrosine ligase-like family, member 7
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000260505
InnateDB Gene IDBG-99920 (TTLL7)
Protein Structure
UniProt Annotation
Function Polyglutamylase which preferentially modifies beta- tubulin. Involved in the side-chain initiation step of the polyglutamylation reaction rather than in the elongation step. Required for neurite growth (By similarity). {ECO:0000250}.
Subcellular Localization Cell projection, cilium {ECO:0000250}. Cytoplasm, cytoskeleton, cilium basal body {ECO:0000250}. Cell projection, dendrite {ECO:0000250}. Perikaryon {ECO:0000250}. Note=In cells with primary cilia, found in both cilia and basal bodies. In neuronal cells, found in dendrites and perikaryon (By similarity). {ECO:0000250}.
Disease Associations
Tissue Specificity Highly expressed in the nervous system including spinal cord, thalamus, hippocampus, hypothalamus and cerebellum. {ECO:0000269PubMed:16901895}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0016874 ligase activity
Biological Process
GO:0006464 cellular protein modification process
GO:0007399 nervous system development
GO:0018095 protein polyglutamylation
GO:0030154 cell differentiation
Cellular Component
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0005929 cilium
GO:0030425 dendrite
GO:0043204 perikaryon
Protein Structure and Domains
PDB ID
InterPro IPR004344 Tubulin-tyrosine ligase/Tubulin polyglutamylase
PFAM PF03133
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q6ZT98
PhosphoSite PhosphoSite-Q6ZT98
TrEMBL
UniProt Splice Variant
Entrez Gene 79739
UniGene Hs.636192
RefSeq NP_078962
HUGO HGNC:26242
OMIM
CCDS CCDS690
HPRD 08013
IMGT
EMBL AC104454 AK026686 AK126792 AL138844 AY170843 BC060878
GenPept AAH60878 AAO37763 BAB15526 BAC86695 CAI22725