| 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:0005840 | ribosome | 5 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0043226 | organelle | 2 | 12 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
| GO:0043229 | intracellular organelle | 3 | 12 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:1990904 | ribonucleoprotein complex | 2 | 12 |
| GO:0000974 | Prp19 complex | 2 | 1 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005681 | spliceosomal complex | 3 | 1 |
| GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
| GO:0140513 | nuclear protein-containing complex | 2 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7XBP3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000375 | RNA splicing, via transesterification reactions | 8 | 11 |
| GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 11 |
| GO:0000398 | mRNA splicing, via spliceosome | 8 | 11 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
| GO:0006396 | RNA processing | 6 | 11 |
| GO:0006397 | mRNA processing | 7 | 11 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0008380 | RNA splicing | 7 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016070 | RNA metabolic process | 5 | 11 |
| GO:0016071 | mRNA metabolic process | 6 | 11 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0046483 | heterocycle metabolic process | 3 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0090304 | nucleic acid metabolic process | 4 | 11 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.516 |
| CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.554 |
| CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.491 |
| CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.520 |
| CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.536 |
| CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.621 |
| CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.520 |
| CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.500 |
| CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.397 |
| CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.576 |
| CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.356 |
| CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.224 |
| CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.217 |
| CLV_Separin_Metazoa | 261 | 265 | PF03568 | 0.397 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.539 |
| DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.542 |
| DOC_CYCLIN_RxL_1 | 352 | 363 | PF00134 | 0.519 |
| DOC_MAPK_gen_1 | 150 | 157 | PF00069 | 0.597 |
| DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.397 |
| DOC_MAPK_gen_1 | 352 | 362 | PF00069 | 0.417 |
| DOC_PP1_RVXF_1 | 356 | 363 | PF00149 | 0.519 |
| DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.581 |
| DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.664 |
| DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.442 |
| DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.519 |
| DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.466 |
| DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.528 |
| DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.647 |
| DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.339 |
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.671 |
| DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.686 |
| DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.544 |
| DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.417 |
| DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.335 |
| LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.442 |
| LIG_14-3-3_CanoR_1 | 421 | 429 | PF00244 | 0.268 |
| LIG_14-3-3_CanoR_1 | 44 | 51 | PF00244 | 0.723 |
| LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.519 |
| LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.506 |
| LIG_EVH1_2 | 36 | 40 | PF00568 | 0.510 |
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.355 |
| LIG_FHA_1 | 291 | 297 | PF00498 | 0.435 |
| LIG_FHA_1 | 310 | 316 | PF00498 | 0.356 |
| LIG_FHA_1 | 391 | 397 | PF00498 | 0.533 |
| LIG_FHA_1 | 466 | 472 | PF00498 | 0.374 |
| LIG_FHA_1 | 483 | 489 | PF00498 | 0.417 |
| LIG_FHA_1 | 73 | 79 | PF00498 | 0.707 |
| LIG_FHA_2 | 111 | 117 | PF00498 | 0.582 |
| LIG_FHA_2 | 190 | 196 | PF00498 | 0.507 |
| LIG_FHA_2 | 2 | 8 | PF00498 | 0.669 |
| LIG_FHA_2 | 90 | 96 | PF00498 | 0.737 |
| LIG_LIR_Apic_2 | 446 | 450 | PF02991 | 0.425 |
| LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.519 |
| LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.519 |
| LIG_LIR_LC3C_4 | 153 | 157 | PF02991 | 0.594 |
| LIG_LIR_LC3C_4 | 317 | 320 | PF02991 | 0.484 |
| LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.519 |
| LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.519 |
| LIG_PCNA_yPIPBox_3 | 253 | 267 | PF02747 | 0.519 |
| LIG_Pex14_1 | 63 | 67 | PF04695 | 0.621 |
| LIG_Pex14_2 | 335 | 339 | PF04695 | 0.519 |
| LIG_REV1ctd_RIR_1 | 264 | 274 | PF16727 | 0.519 |
| LIG_RPA_C_Fungi | 53 | 65 | PF08784 | 0.510 |
| LIG_SH2_CRK | 170 | 174 | PF00017 | 0.545 |
| LIG_SH2_NCK_1 | 170 | 174 | PF00017 | 0.561 |
| LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.456 |
| LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.391 |
| LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.269 |
| LIG_SH3_2 | 33 | 38 | PF14604 | 0.616 |
| LIG_SH3_3 | 30 | 36 | PF00018 | 0.596 |
| LIG_SUMO_SIM_anti_2 | 281 | 287 | PF11976 | 0.254 |
| LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.676 |
| LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.318 |
| LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.430 |
| LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.609 |
| LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.524 |
| LIG_WW_3 | 35 | 39 | PF00397 | 0.543 |
| MOD_CDK_SPK_2 | 425 | 430 | PF00069 | 0.355 |
| MOD_CDK_SPxxK_3 | 168 | 175 | PF00069 | 0.511 |
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.657 |
| MOD_CK1_1 | 119 | 125 | PF00069 | 0.504 |
| MOD_CK1_1 | 237 | 243 | PF00069 | 0.284 |
| MOD_CK1_1 | 314 | 320 | PF00069 | 0.256 |
| MOD_CK1_1 | 329 | 335 | PF00069 | 0.246 |
| MOD_CK1_1 | 42 | 48 | PF00069 | 0.722 |
| MOD_CK1_1 | 498 | 504 | PF00069 | 0.269 |
| MOD_CK2_1 | 1 | 7 | PF00069 | 0.573 |
| MOD_CK2_1 | 110 | 116 | PF00069 | 0.581 |
| MOD_CK2_1 | 189 | 195 | PF00069 | 0.380 |
| MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.599 |
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.290 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.354 |
| MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.206 |
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.254 |
| MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.345 |
| MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.460 |
| MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.700 |
| MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.610 |
| MOD_GlcNHglycan | 487 | 491 | PF01048 | 0.254 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.637 |
| MOD_GSK3_1 | 119 | 126 | PF00069 | 0.576 |
| MOD_GSK3_1 | 230 | 237 | PF00069 | 0.397 |
| MOD_GSK3_1 | 244 | 251 | PF00069 | 0.301 |
| MOD_GSK3_1 | 386 | 393 | PF00069 | 0.471 |
| MOD_GSK3_1 | 39 | 46 | PF00069 | 0.691 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.609 |
| MOD_GSK3_1 | 416 | 423 | PF00069 | 0.359 |
| MOD_GSK3_1 | 467 | 474 | PF00069 | 0.401 |
| MOD_GSK3_1 | 482 | 489 | PF00069 | 0.219 |
| MOD_GSK3_1 | 67 | 74 | PF00069 | 0.673 |
| MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.473 |
| MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.631 |
| MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.269 |
| MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.408 |
| MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.625 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.600 |
| MOD_NEK2_1 | 155 | 160 | PF00069 | 0.541 |
| MOD_NEK2_1 | 222 | 227 | PF00069 | 0.281 |
| MOD_NEK2_1 | 360 | 365 | PF00069 | 0.314 |
| MOD_PIKK_1 | 434 | 440 | PF00454 | 0.328 |
| MOD_PIKK_1 | 89 | 95 | PF00454 | 0.744 |
| MOD_PKA_2 | 348 | 354 | PF00069 | 0.254 |
| MOD_PKA_2 | 420 | 426 | PF00069 | 0.303 |
| MOD_PKA_2 | 43 | 49 | PF00069 | 0.518 |
| MOD_Plk_1 | 1 | 7 | PF00069 | 0.470 |
| MOD_Plk_1 | 248 | 254 | PF00069 | 0.308 |
| MOD_Plk_1 | 290 | 296 | PF00069 | 0.269 |
| MOD_Plk_1 | 416 | 422 | PF00069 | 0.484 |
| MOD_Plk_1 | 498 | 504 | PF00069 | 0.288 |
| MOD_Plk_4 | 105 | 111 | PF00069 | 0.681 |
| MOD_Plk_4 | 304 | 310 | PF00069 | 0.307 |
| MOD_Plk_4 | 311 | 317 | PF00069 | 0.234 |
| MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.534 |
| MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.254 |
| MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.338 |
| TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.288 |
| TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.355 |
| TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.531 |
| TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.479 |
| TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.582 |
| TRG_NES_CRM1_1 | 18 | 32 | PF08389 | 0.586 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7N2 | Leptomonas seymouri | 68% | 99% |
| A0A0N1I6C2 | Leptomonas seymouri | 23% | 100% |
| A0A0N1IHN2 | Leptomonas seymouri | 22% | 98% |
| A0A0N1PBF5 | Leptomonas seymouri | 25% | 74% |
| A0A0S4IWG1 | Bodo saltans | 42% | 100% |
| A0A0S4JE21 | Bodo saltans | 27% | 100% |
| A0A0S4JL38 | Bodo saltans | 26% | 95% |
| A0A0S4KJ87 | Bodo saltans | 25% | 85% |
| A0A1X0NQ96 | Trypanosomatidae | 25% | 100% |
| A0A1X0P0F0 | Trypanosomatidae | 52% | 100% |
| A0A3Q8IBR2 | Leishmania donovani | 22% | 100% |
| A0A3R7KUH0 | Trypanosoma rangeli | 27% | 100% |
| A0A3R7MCP0 | Trypanosoma rangeli | 54% | 100% |
| A0A3R7N6M9 | Trypanosoma rangeli | 22% | 98% |
| A0A3S5H5M7 | Leishmania donovani | 26% | 75% |
| A0A3S7WR72 | Leishmania donovani | 24% | 100% |
| A0A3S7X9Q7 | Leishmania donovani | 24% | 100% |
| A4H4H1 | Leishmania braziliensis | 27% | 77% |
| A4H666 | Leishmania braziliensis | 24% | 100% |
| A4HBK3 | Leishmania braziliensis | 21% | 100% |
| A4HPZ9 | Leishmania braziliensis | 86% | 100% |
| A4HSP6 | Leishmania infantum | 26% | 75% |
| A4HUJ0 | Leishmania infantum | 24% | 100% |
| A4HZL2 | Leishmania infantum | 22% | 100% |
| A4IDR0 | Leishmania infantum | 100% | 100% |
| B8N9H4 | Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / IAM 13836 / NRRL 3357 / JCM 12722 / SRRC 167) | 24% | 100% |
| C4JPW9 | Uncinocarpus reesii (strain UAMH 1704) | 23% | 100% |
| C9ZVL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
| C9ZW72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 83% |
| D0A4F2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
| D3Z902 | Rattus norvegicus | 27% | 71% |
| E9AKN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 76% |
| E9AN88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| E9ATR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| E9AUX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
| E9B3I3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| E9B4L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 71% |
| F1MNN4 | Bos taurus | 27% | 72% |
| G0SC29 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 24% | 98% |
| O13615 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 100% |
| O14170 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 72% |
| O74855 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
| P0CS48 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 40% | 100% |
| P0CS49 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 40% | 100% |
| P25382 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 99% |
| P49846 | Drosophila melanogaster | 22% | 72% |
| Q0D0X6 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 22% | 100% |
| Q12417 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
| Q2UGU1 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 24% | 100% |
| Q4Q0T1 | Leishmania major | 93% | 100% |
| Q4QHD6 | Leishmania major | 24% | 100% |
| Q4QJ76 | Leishmania major | 26% | 75% |
| Q4WT34 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 38% | 100% |
| Q58D20 | Bos taurus | 23% | 100% |
| Q5A7Q3 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 100% |
| Q5BE22 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 38% | 100% |
| Q5RFF8 | Pongo abelii | 22% | 100% |
| Q6BU94 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 33% | 100% |
| Q6CKE8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 38% | 100% |
| Q6GPC6 | Xenopus laevis | 22% | 98% |
| Q75BY3 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 41% | 100% |
| Q7ZXK9 | Xenopus laevis | 25% | 100% |
| Q8BHJ5 | Mus musculus | 20% | 99% |
| Q8K450 | Mus musculus | 23% | 80% |
| Q8VBV4 | Mus musculus | 27% | 72% |
| Q8VEJ4 | Mus musculus | 23% | 100% |
| Q969H0 | Homo sapiens | 27% | 72% |
| Q9FN19 | Arabidopsis thaliana | 21% | 83% |
| Q9NVX2 | Homo sapiens | 22% | 100% |
| Q9QXE7 | Mus musculus | 21% | 97% |
| V5B4Z8 | Trypanosoma cruzi | 53% | 100% |
| V5BP59 | Trypanosoma cruzi | 26% | 100% |