blastp_kegg |
lcl|cic:CICLE_v10007418mg
|
7 |
878 |
+ |
872 |
Gaps:6 |
99.66 |
871 |
77.53 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100242318
|
7 |
878 |
+ |
872 |
Gaps:11 |
99.88 |
866 |
77.57 |
0.0 |
tubulin--tyrosine ligase-like protein 12-like
|
blastp_kegg |
lcl|tcc:TCM_037527
|
10 |
878 |
+ |
869 |
Gaps:14 |
98.85 |
869 |
77.30 |
0.0 |
Tubulin-tyrosine ligases tubulin-tyrosine ligases isoform 1
|
blastp_kegg |
lcl|cit:102615710
|
7 |
878 |
+ |
872 |
Gaps:6 |
99.66 |
871 |
76.38 |
0.0 |
tubulin--tyrosine ligase-like protein 12-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa001302mg
|
10 |
878 |
+ |
869 |
Gaps:16 |
99.77 |
859 |
77.25 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0006s14420g
|
10 |
878 |
+ |
869 |
Gaps:7 |
99.77 |
868 |
77.14 |
0.0 |
tubulin-tyrosine ligase family protein
|
blastp_kegg |
lcl|cmo:103492368
|
8 |
878 |
+ |
871 |
Gaps:7 |
99.66 |
871 |
76.15 |
0.0 |
tubulin--tyrosine ligase-like protein 12
|
blastp_kegg |
lcl|csv:101208562
|
8 |
878 |
+ |
871 |
Gaps:11 |
99.66 |
875 |
75.80 |
0.0 |
tubulin--tyrosine ligase-like protein 12-like
|
blastp_kegg |
lcl|csv:101230272
|
8 |
878 |
+ |
871 |
Gaps:11 |
99.66 |
875 |
75.69 |
0.0 |
tubulin--tyrosine ligase-like protein 12-like
|
blastp_kegg |
lcl|pmum:103340588
|
10 |
878 |
+ |
869 |
Gaps:16 |
99.77 |
859 |
76.66 |
0.0 |
tubulin--tyrosine ligase-like protein 12
|
blastp_uniprot_sprot |
sp|Q3UDE2|TTL12_MOUSE
|
16 |
872 |
+ |
857 |
Gaps:86 |
93.58 |
639 |
39.13 |
5e-94 |
Tubulin--tyrosine ligase-like protein 12 OS Mus musculus GN Ttll12 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q14166|TTL12_HUMAN
|
15 |
871 |
+ |
857 |
Gaps:89 |
94.10 |
644 |
38.28 |
3e-91 |
Tubulin--tyrosine ligase-like protein 12 OS Homo sapiens GN TTLL12 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q09512|TTL12_CAEEL
|
14 |
878 |
+ |
865 |
Gaps:77 |
94.11 |
662 |
34.51 |
2e-74 |
Tubulin--tyrosine ligase-like protein 12 OS Caenorhabditis elegans GN ttll-12 PE 4 SV 1
|
blastp_uniprot_sprot |
sp|A8XXC0|TTL12_CAEBR
|
14 |
878 |
+ |
865 |
Gaps:76 |
91.67 |
672 |
33.44 |
5e-73 |
Tubulin--tyrosine ligase-like protein 12 OS Caenorhabditis briggsae GN ttll-12 PE 4 SV 2
|
blastp_uniprot_sprot |
sp|Q23K29|TTL3D_TETTS
|
651 |
847 |
+ |
197 |
Gaps:24 |
20.20 |
1015 |
32.20 |
2e-15 |
Tubulin glycylase 3D OS Tetrahymena thermophila (strain SB210) GN TTLL3D PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q23AS2|TTL3E_TETTS
|
629 |
849 |
+ |
221 |
Gaps:30 |
17.14 |
1394 |
27.62 |
6e-14 |
Tubulin glycylase 3E OS Tetrahymena thermophila (strain SB210) GN TTLL3E PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A4Q9F0|TTLL7_MOUSE
|
572 |
861 |
+ |
290 |
Gaps:42 |
34.21 |
912 |
27.24 |
4e-13 |
Tubulin polyglutamylase TTLL7 OS Mus musculus GN Ttll7 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6ZT98|TTLL7_HUMAN
|
572 |
851 |
+ |
280 |
Gaps:42 |
34.05 |
887 |
27.48 |
4e-12 |
Tubulin polyglutamylase TTLL7 OS Homo sapiens GN TTLL7 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P0CAZ1|TTL3F_TETTS
|
657 |
840 |
+ |
184 |
Gaps:27 |
21.89 |
909 |
27.64 |
4e-12 |
Tubulin glycylase 3F OS Tetrahymena thermophila (strain SB210) GN TTLL3F PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q23FE2|TTL3C_TETTS
|
654 |
836 |
+ |
183 |
Gaps:20 |
18.66 |
1088 |
25.12 |
4e-11 |
Tubulin glycylase 3C OS Tetrahymena thermophila (strain SB210) GN TTLL3C PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|202548
|
599 |
847 |
+ |
249 |
Gaps:20 |
89.69 |
291 |
27.97 |
3e-47 |
pfam03133 TTL Tubulin-tyrosine ligase family. Tubulins and microtubules are subjected to several post-translational modifications of which the reversible detyrosination/tyrosination of the carboxy-terminal end of most alpha-tubulins has been extensively analysed. This modification cycle involves a specific carboxypeptidase and the activity of the tubulin-tyrosine ligase (TTL). The true physiological function of TTL has so far not been established. Tubulin-tyrosine ligase (TTL) catalyzes the ATP-dependent post-translational addition of a tyrosine to the carboxy terminal end of detyrosinated alpha-tubulin. In normally cycling cells the tyrosinated form of tubulin predominates. However in breast cancer cells the detyrosinated form frequently predominates with a correlation to tumour aggressiveness. On the other hand 3-nitrotyrosine has been shown to be incorporated by TTL into the carboxy terminal end of detyrosinated alpha-tubulin. This reaction is not reversible by the carboxypeptidase enzyme. Cells cultured in 3-nitrotyrosine rich medium showed evidence of altered microtubule structure and function including altered cell morphology epithelial barrier dysfunction and apoptosis. Bacterial homologs of TTL are predicted to form peptide tags. Some of these are fused to a 2-oxoglutarate Fe(II)-dependent dioxygenase domain.
|
rpsblast_kog |
gnl|CDD|37366
|
14 |
878 |
+ |
865 |
Gaps:51 |
99.05 |
631 |
41.76 |
0.0 |
KOG2155 KOG2155 KOG2155 Tubulin-tyrosine ligase-related protein [Posttranslational modification protein turnover chaperones].
|
rpsblast_kog |
gnl|CDD|37368
|
552 |
846 |
+ |
295 |
Gaps:47 |
66.40 |
497 |
20.91 |
3e-17 |
KOG2157 KOG2157 KOG2157 Predicted tubulin-tyrosine ligase [Posttranslational modification protein turnover chaperones].
|
rpsblast_kog |
gnl|CDD|37367
|
558 |
845 |
+ |
288 |
Gaps:49 |
45.47 |
662 |
27.24 |
1e-15 |
KOG2156 KOG2156 KOG2156 Tubulin-tyrosine ligase-related protein [Posttranslational modification protein turnover chaperones].
|
rpsblast_kog |
gnl|CDD|37369
|
690 |
836 |
+ |
147 |
Gaps:29 |
30.09 |
565 |
24.12 |
3e-08 |
KOG2158 KOG2158 KOG2158 Tubulin-tyrosine ligase-related protein [Posttranslational modification protein turnover chaperones].
|