Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HC38
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006396 | RNA processing | 6 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0031123 | RNA 3'-end processing | 7 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071076 | RNA 3' uridylation | 8 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016779 | nucleotidyltransferase activity | 4 | 13 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 13 |
GO:0070566 | adenylyltransferase activity | 5 | 5 |
GO:0070569 | uridylyltransferase activity | 5 | 13 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.425 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.423 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.578 |
DOC_CKS1_1 | 283 | 288 | PF01111 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 333 | 339 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 110 | 120 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 135 | 143 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 364 | 370 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 113 | 122 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 156 | 163 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.382 |
DOC_MAPK_NFAT4_5 | 156 | 164 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 342 | 349 | PF00149 | 0.361 |
DOC_PP1_RVXF_1 | 47 | 54 | PF00149 | 0.332 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.467 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 27 | 34 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 303 | 310 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.289 |
LIG_Actin_WH2_2 | 154 | 169 | PF00022 | 0.390 |
LIG_AP2alpha_2 | 335 | 337 | PF02296 | 0.375 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.364 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.409 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.480 |
LIG_LIR_Gen_1 | 212 | 219 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 369 | 374 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.413 |
LIG_NRBOX | 43 | 49 | PF00104 | 0.423 |
LIG_PCNA_PIPBox_1 | 273 | 282 | PF02747 | 0.319 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.329 |
LIG_REV1ctd_RIR_1 | 346 | 354 | PF16727 | 0.379 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.499 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.392 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.449 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.390 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.386 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 268 | 273 | PF11976 | 0.520 |
LIG_SUMO_SIM_anti_2 | 329 | 335 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 329 | 335 | PF11976 | 0.349 |
LIG_TRAF2_2 | 263 | 268 | PF00917 | 0.416 |
LIG_TYR_ITIM | 69 | 74 | PF00017 | 0.456 |
LIG_UBA3_1 | 118 | 124 | PF00899 | 0.421 |
LIG_UBA3_1 | 213 | 220 | PF00899 | 0.365 |
LIG_UBA3_1 | 44 | 49 | PF00899 | 0.227 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.427 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.567 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.482 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.449 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.406 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.289 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.585 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.503 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.479 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.364 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.259 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.443 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.474 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.481 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.486 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.343 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.318 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.361 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.415 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.269 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.450 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.340 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.495 |
MOD_PK_1 | 359 | 365 | PF00069 | 0.416 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.516 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.261 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.519 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.451 |
MOD_PKB_1 | 301 | 309 | PF00069 | 0.442 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.480 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.429 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.467 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.319 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.295 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.405 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.452 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.465 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.362 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.304 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.346 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.410 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.520 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.373 |
TRG_DiLeu_BaEn_1 | 321 | 326 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.405 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA71 | Leptomonas seymouri | 61% | 100% |
A0A0S4IUE3 | Bodo saltans | 35% | 84% |
A0A0S4IXY7 | Bodo saltans | 21% | 100% |
A0A1X0NI50 | Trypanosomatidae | 45% | 100% |
A0A1X0NT04 | Trypanosomatidae | 23% | 100% |
A0A3R7M9K0 | Trypanosoma rangeli | 45% | 100% |
A0A3S7WWT5 | Leishmania donovani | 82% | 98% |
A4HZI0 | Leishmania infantum | 82% | 98% |
D0A0Y4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AVH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 98% |
Q4QC09 | Leishmania major | 80% | 100% |