| 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:0000315 | organellar large ribosomal subunit | 5 | 1 |
| GO:0005762 | mitochondrial large ribosomal subunit | 3 | 1 |
| GO:0015934 | large ribosomal subunit | 4 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0044391 | ribosomal subunit | 3 | 1 |
| GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
| GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HKN4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0001510 | RNA methylation | 4 | 12 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009987 | cellular process | 1 | 12 |
| GO:0016070 | RNA metabolic process | 5 | 12 |
| GO:0032259 | methylation | 2 | 12 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 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:0090304 | nucleic acid metabolic process | 4 | 12 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
| GO:0000154 | rRNA modification | 6 | 1 |
| GO:0006364 | rRNA processing | 8 | 1 |
| GO:0006396 | RNA processing | 6 | 1 |
| GO:0016072 | rRNA metabolic process | 7 | 1 |
| GO:0031167 | rRNA methylation | 5 | 1 |
| GO:0034470 | ncRNA processing | 7 | 1 |
| GO:0034660 | ncRNA metabolic process | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 12 |
| GO:0003723 | RNA binding | 4 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0008168 | methyltransferase activity | 4 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.453 |
| CLV_MEL_PAP_1 | 65 | 71 | PF00089 | 0.464 |
| CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.235 |
| CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.450 |
| CLV_PCSK_FUR_1 | 211 | 215 | PF00082 | 0.221 |
| CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.220 |
| CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.511 |
| CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.247 |
| CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.253 |
| CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.339 |
| CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.426 |
| CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.360 |
| DEG_SCF_FBW7_1 | 345 | 350 | PF00400 | 0.472 |
| DEG_SPOP_SBC_1 | 331 | 335 | PF00917 | 0.352 |
| DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.705 |
| DOC_CYCLIN_RxL_1 | 378 | 387 | PF00134 | 0.448 |
| DOC_MAPK_gen_1 | 323 | 330 | PF00069 | 0.416 |
| DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.421 |
| DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.477 |
| DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.292 |
| DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.623 |
| DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.478 |
| DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.477 |
| DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.648 |
| DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.741 |
| DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.508 |
| DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.579 |
| DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.653 |
| DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.635 |
| DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.477 |
| DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.421 |
| DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.675 |
| DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.562 |
| LIG_14-3-3_CanoR_1 | 300 | 310 | PF00244 | 0.448 |
| LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.434 |
| LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.505 |
| LIG_BIR_III_4 | 146 | 150 | PF00653 | 0.459 |
| LIG_FHA_1 | 20 | 26 | PF00498 | 0.598 |
| LIG_FHA_1 | 275 | 281 | PF00498 | 0.472 |
| LIG_FHA_1 | 292 | 298 | PF00498 | 0.406 |
| LIG_FHA_1 | 303 | 309 | PF00498 | 0.378 |
| LIG_FHA_1 | 367 | 373 | PF00498 | 0.658 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.505 |
| LIG_FHA_2 | 117 | 123 | PF00498 | 0.440 |
| LIG_FHA_2 | 172 | 178 | PF00498 | 0.464 |
| LIG_FHA_2 | 198 | 204 | PF00498 | 0.453 |
| LIG_FHA_2 | 228 | 234 | PF00498 | 0.440 |
| LIG_FHA_2 | 34 | 40 | PF00498 | 0.442 |
| LIG_FHA_2 | 409 | 415 | PF00498 | 0.580 |
| LIG_LIR_Apic_2 | 236 | 240 | PF02991 | 0.423 |
| LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.357 |
| LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.309 |
| LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.397 |
| LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.338 |
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.329 |
| LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.282 |
| LIG_Pex14_1 | 391 | 395 | PF04695 | 0.413 |
| LIG_Rb_LxCxE_1 | 194 | 207 | PF01857 | 0.512 |
| LIG_SH2_CRK | 379 | 383 | PF00017 | 0.438 |
| LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.433 |
| LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.433 |
| LIG_SH2_STAT3 | 238 | 241 | PF00017 | 0.559 |
| LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.310 |
| LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.456 |
| LIG_SH3_3 | 245 | 251 | PF00018 | 0.410 |
| LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.441 |
| MOD_CK1_1 | 273 | 279 | PF00069 | 0.480 |
| MOD_CK1_1 | 304 | 310 | PF00069 | 0.417 |
| MOD_CK1_1 | 335 | 341 | PF00069 | 0.455 |
| MOD_CK1_1 | 343 | 349 | PF00069 | 0.665 |
| MOD_CK1_1 | 357 | 363 | PF00069 | 0.560 |
| MOD_CK1_1 | 410 | 416 | PF00069 | 0.599 |
| MOD_CK2_1 | 116 | 122 | PF00069 | 0.441 |
| MOD_CK2_1 | 197 | 203 | PF00069 | 0.461 |
| MOD_CK2_1 | 265 | 271 | PF00069 | 0.479 |
| MOD_CK2_1 | 306 | 312 | PF00069 | 0.460 |
| MOD_CK2_1 | 33 | 39 | PF00069 | 0.512 |
| MOD_CK2_1 | 408 | 414 | PF00069 | 0.542 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.642 |
| MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.366 |
| MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.280 |
| MOD_GSK3_1 | 197 | 204 | PF00069 | 0.506 |
| MOD_GSK3_1 | 25 | 32 | PF00069 | 0.686 |
| MOD_GSK3_1 | 270 | 277 | PF00069 | 0.457 |
| MOD_GSK3_1 | 302 | 309 | PF00069 | 0.446 |
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.458 |
| MOD_GSK3_1 | 341 | 348 | PF00069 | 0.618 |
| MOD_GSK3_1 | 364 | 371 | PF00069 | 0.411 |
| MOD_GSK3_1 | 75 | 82 | PF00069 | 0.521 |
| MOD_GSK3_1 | 98 | 105 | PF00069 | 0.699 |
| MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.213 |
| MOD_NEK2_1 | 259 | 264 | PF00069 | 0.477 |
| MOD_NEK2_1 | 321 | 326 | PF00069 | 0.407 |
| MOD_NEK2_1 | 408 | 413 | PF00069 | 0.590 |
| MOD_PIKK_1 | 227 | 233 | PF00454 | 0.421 |
| MOD_PIKK_1 | 67 | 73 | PF00454 | 0.471 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.551 |
| MOD_PKA_2 | 67 | 73 | PF00069 | 0.414 |
| MOD_Plk_1 | 102 | 108 | PF00069 | 0.646 |
| MOD_Plk_1 | 116 | 122 | PF00069 | 0.441 |
| MOD_Plk_1 | 273 | 279 | PF00069 | 0.413 |
| MOD_Plk_1 | 341 | 347 | PF00069 | 0.464 |
| MOD_Plk_1 | 374 | 380 | PF00069 | 0.363 |
| MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.467 |
| MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.514 |
| MOD_Plk_4 | 171 | 177 | PF00069 | 0.391 |
| MOD_Plk_4 | 233 | 239 | PF00069 | 0.439 |
| MOD_Plk_4 | 368 | 374 | PF00069 | 0.493 |
| MOD_Plk_4 | 85 | 91 | PF00069 | 0.422 |
| MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.477 |
| MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.421 |
| MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.676 |
| MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.557 |
| MOD_SUMO_rev_2 | 400 | 408 | PF00179 | 0.453 |
| TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.451 |
| TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.317 |
| TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.336 |
| TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.367 |
| TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.436 |
| TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.213 |
| TRG_Pf-PMV_PEXEL_1 | 245 | 249 | PF00026 | 0.210 |
| TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.210 |
| TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.264 |
| TRG_Pf-PMV_PEXEL_1 | 381 | 386 | PF00026 | 0.404 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IK00 | Leptomonas seymouri | 65% | 100% |
| A0A0S4J448 | Bodo saltans | 40% | 100% |
| A0A1X0NRJ9 | Trypanosomatidae | 40% | 100% |
| A0A3Q8ID92 | Leishmania donovani | 80% | 100% |
| A0A3R7K4S3 | Trypanosoma rangeli | 46% | 100% |
| A4I865 | Leishmania infantum | 80% | 100% |
| D0AAD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
| E9B323 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
| Q0P5D8 | Bos taurus | 31% | 100% |
| Q0V8R7 | Bos taurus | 28% | 100% |
| Q4KMK0 | Danio rerio | 30% | 100% |
| Q4Q532 | Leishmania major | 80% | 99% |
| Q5M7E3 | Xenopus laevis | 29% | 100% |
| Q5SII2 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 27% | 93% |
| Q66KI9 | Xenopus tropicalis | 30% | 100% |
| Q8CCT7 | Mus musculus | 29% | 100% |
| Q96CB9 | Homo sapiens | 27% | 100% |
| Q9CZ57 | Mus musculus | 28% | 100% |
| Q9H649 | Homo sapiens | 29% | 100% |
| V5B8C1 | Trypanosoma cruzi | 44% | 100% |