| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 12 |
| GO:0043226 | organelle | 2 | 12 |
| GO:0043227 | membrane-bounded organelle | 3 | 12 |
| GO:0043229 | intracellular organelle | 3 | 12 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AUA2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0001510 | RNA methylation | 4 | 12 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
| GO:0006370 | 7-methylguanosine mRNA capping | 8 | 12 |
| GO:0006396 | RNA processing | 6 | 12 |
| GO:0006397 | mRNA processing | 7 | 12 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009451 | RNA modification | 5 | 12 |
| GO:0009452 | 7-methylguanosine RNA capping | 8 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0016070 | RNA metabolic process | 5 | 12 |
| GO:0016071 | mRNA metabolic process | 6 | 12 |
| GO:0016556 | mRNA modification | 6 | 12 |
| GO:0032259 | methylation | 2 | 12 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
| GO:0036260 | RNA capping | 7 | 12 |
| GO:0036451 | cap mRNA methylation | 6 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0043412 | macromolecule modification | 4 | 12 |
| GO:0043414 | macromolecule methylation | 3 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
| GO:0046483 | heterocycle metabolic process | 3 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:0080009 | mRNA methylation | 5 | 12 |
| GO:0090304 | nucleic acid metabolic process | 4 | 12 |
| GO:0097309 | cap1 mRNA methylation | 7 | 12 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 10 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004483 | mRNA (nucleoside-2'-O-)-methyltransferase activity | 6 | 12 |
| GO:0005488 | binding | 1 | 10 |
| GO:0008168 | methyltransferase activity | 4 | 12 |
| GO:0008171 | O-methyltransferase activity | 5 | 12 |
| GO:0008173 | RNA methyltransferase activity | 4 | 12 |
| GO:0008174 | mRNA methyltransferase activity | 5 | 12 |
| GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 10 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 10 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.272 |
| CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.478 |
| CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.313 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.246 |
| CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.310 |
| CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.266 |
| CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.479 |
| CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.322 |
| CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.497 |
| CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.310 |
| CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.497 |
| CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.161 |
| CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.217 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.407 |
| DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.475 |
| DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.395 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.506 |
| DOC_MAPK_DCC_7 | 72 | 80 | PF00069 | 0.400 |
| DOC_MAPK_gen_1 | 72 | 80 | PF00069 | 0.493 |
| DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.458 |
| DOC_MAPK_MEF2A_6 | 291 | 298 | PF00069 | 0.442 |
| DOC_PP1_RVXF_1 | 6 | 13 | PF00149 | 0.380 |
| DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.573 |
| DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.460 |
| DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.431 |
| DOC_USP7_MATH_2 | 302 | 308 | PF00917 | 0.448 |
| DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.513 |
| DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.627 |
| DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.535 |
| DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.431 |
| DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.762 |
| LIG_14-3-3_CanoR_1 | 113 | 118 | PF00244 | 0.445 |
| LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.464 |
| LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.457 |
| LIG_BIR_III_2 | 363 | 367 | PF00653 | 0.475 |
| LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.458 |
| LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.505 |
| LIG_Clathr_ClatBox_1 | 293 | 297 | PF01394 | 0.535 |
| LIG_deltaCOP1_diTrp_1 | 304 | 313 | PF00928 | 0.401 |
| LIG_deltaCOP1_diTrp_1 | 331 | 339 | PF00928 | 0.463 |
| LIG_FHA_1 | 177 | 183 | PF00498 | 0.438 |
| LIG_FHA_1 | 350 | 356 | PF00498 | 0.426 |
| LIG_FHA_1 | 367 | 373 | PF00498 | 0.376 |
| LIG_FHA_1 | 388 | 394 | PF00498 | 0.488 |
| LIG_FHA_2 | 2 | 8 | PF00498 | 0.515 |
| LIG_FHA_2 | 56 | 62 | PF00498 | 0.407 |
| LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.456 |
| LIG_LIR_Gen_1 | 124 | 132 | PF02991 | 0.474 |
| LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.472 |
| LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.474 |
| LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.449 |
| LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.548 |
| LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.456 |
| LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.426 |
| LIG_MYND_1 | 325 | 329 | PF01753 | 0.364 |
| LIG_NRBOX | 107 | 113 | PF00104 | 0.579 |
| LIG_Pex14_1 | 38 | 42 | PF04695 | 0.332 |
| LIG_Pex14_2 | 215 | 219 | PF04695 | 0.442 |
| LIG_Rb_pABgroove_1 | 249 | 257 | PF01858 | 0.431 |
| LIG_SH2_CRK | 273 | 277 | PF00017 | 0.442 |
| LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.482 |
| LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.445 |
| LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.466 |
| LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.376 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.395 |
| LIG_SH3_3 | 275 | 281 | PF00018 | 0.460 |
| LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.387 |
| LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.421 |
| LIG_SUMO_SIM_par_1 | 76 | 81 | PF11976 | 0.422 |
| LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.442 |
| MOD_CDK_SPxxK_3 | 256 | 263 | PF00069 | 0.431 |
| MOD_CK1_1 | 259 | 265 | PF00069 | 0.474 |
| MOD_CK1_1 | 98 | 104 | PF00069 | 0.535 |
| MOD_Cter_Amidation | 142 | 145 | PF01082 | 0.278 |
| MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.340 |
| MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.469 |
| MOD_GSK3_1 | 170 | 177 | PF00069 | 0.466 |
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.333 |
| MOD_GSK3_1 | 345 | 352 | PF00069 | 0.435 |
| MOD_GSK3_1 | 64 | 71 | PF00069 | 0.479 |
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.494 |
| MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.160 |
| MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.438 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.463 |
| MOD_NEK2_1 | 176 | 181 | PF00069 | 0.498 |
| MOD_NEK2_1 | 254 | 259 | PF00069 | 0.438 |
| MOD_NEK2_1 | 266 | 271 | PF00069 | 0.419 |
| MOD_NEK2_1 | 99 | 104 | PF00069 | 0.464 |
| MOD_NEK2_2 | 26 | 31 | PF00069 | 0.529 |
| MOD_PIKK_1 | 133 | 139 | PF00454 | 0.431 |
| MOD_PIKK_1 | 55 | 61 | PF00454 | 0.412 |
| MOD_PKA_2 | 281 | 287 | PF00069 | 0.442 |
| MOD_PKB_1 | 119 | 127 | PF00069 | 0.360 |
| MOD_Plk_1 | 121 | 127 | PF00069 | 0.360 |
| MOD_Plk_1 | 217 | 223 | PF00069 | 0.478 |
| MOD_Plk_1 | 6 | 12 | PF00069 | 0.365 |
| MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.504 |
| MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.535 |
| MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.431 |
| MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.766 |
| MOD_SUMO_rev_2 | 370 | 374 | PF00179 | 0.539 |
| TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.478 |
| TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.431 |
| TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.451 |
| TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.474 |
| TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.538 |
| TRG_NES_CRM1_1 | 51 | 66 | PF08389 | 0.378 |
| TRG_NLS_MonoCore_2 | 117 | 122 | PF00514 | 0.360 |
| TRG_NLS_MonoExtN_4 | 115 | 122 | PF00514 | 0.518 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P800 | Leptomonas seymouri | 77% | 99% |
| A0A0S4IIT9 | Bodo saltans | 49% | 98% |
| A0A1X0NL91 | Trypanosomatidae | 55% | 100% |
| A0A3S5IS12 | Trypanosoma rangeli | 54% | 100% |
| A0A3S7XCC2 | Leishmania donovani | 94% | 100% |
| A4HQI9 | Leishmania braziliensis | 83% | 100% |
| D0A3N7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
| E9AHZ8 | Leishmania infantum | 94% | 100% |
| Q38AH0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 50% | 100% |
| Q4E123 | Trypanosoma cruzi (strain CL Brener) | 55% | 100% |
| Q4Q089 | Leishmania major | 94% | 100% |
| V5BD10 | Trypanosoma cruzi | 54% | 100% |