| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005681 | spliceosomal complex | 3 | 8 |
| GO:0032991 | protein-containing complex | 1 | 8 |
| GO:0140513 | nuclear protein-containing complex | 2 | 8 |
| GO:1990904 | ribonucleoprotein complex | 2 | 8 |
Related structures:
AlphaFold database: E9AQA2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000375 | RNA splicing, via transesterification reactions | 8 | 8 |
| GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 8 |
| GO:0000398 | mRNA splicing, via spliceosome | 8 | 8 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
| GO:0006396 | RNA processing | 6 | 8 |
| GO:0006397 | mRNA processing | 7 | 8 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
| GO:0008152 | metabolic process | 1 | 8 |
| GO:0008380 | RNA splicing | 7 | 8 |
| GO:0009987 | cellular process | 1 | 8 |
| GO:0016070 | RNA metabolic process | 5 | 8 |
| GO:0016071 | mRNA metabolic process | 6 | 8 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
| GO:0043170 | macromolecule metabolic process | 3 | 8 |
| GO:0044237 | cellular metabolic process | 2 | 8 |
| GO:0044238 | primary metabolic process | 2 | 8 |
| GO:0046483 | heterocycle metabolic process | 3 | 8 |
| GO:0071704 | organic substance metabolic process | 2 | 8 |
| GO:0090304 | nucleic acid metabolic process | 4 | 8 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.775 |
| CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.790 |
| CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.412 |
| CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.311 |
| CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.409 |
| CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.598 |
| CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.676 |
| CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.409 |
| CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.662 |
| CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.706 |
| CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.706 |
| CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.497 |
| CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.590 |
| CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.565 |
| CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.680 |
| CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.708 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.777 |
| DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.674 |
| DOC_ANK_TNKS_1 | 169 | 176 | PF00023 | 0.296 |
| DOC_CYCLIN_RxL_1 | 223 | 230 | PF00134 | 0.375 |
| DOC_MAPK_gen_1 | 138 | 144 | PF00069 | 0.404 |
| DOC_MAPK_gen_1 | 152 | 159 | PF00069 | 0.314 |
| DOC_MAPK_gen_1 | 246 | 255 | PF00069 | 0.556 |
| DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.568 |
| DOC_MAPK_HePTP_8 | 272 | 284 | PF00069 | 0.566 |
| DOC_MAPK_MEF2A_6 | 152 | 159 | PF00069 | 0.379 |
| DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.567 |
| DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.375 |
| DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.515 |
| DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.550 |
| DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.773 |
| DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.607 |
| DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.790 |
| DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.700 |
| DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.751 |
| DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.626 |
| DOC_USP7_MATH_2 | 83 | 89 | PF00917 | 0.535 |
| DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.428 |
| DOC_USP7_UBL2_3 | 421 | 425 | PF12436 | 0.680 |
| DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.667 |
| LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.751 |
| LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.636 |
| LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.523 |
| LIG_14-3-3_CanoR_1 | 65 | 75 | PF00244 | 0.549 |
| LIG_Actin_WH2_2 | 280 | 297 | PF00022 | 0.513 |
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.677 |
| LIG_FHA_1 | 38 | 44 | PF00498 | 0.546 |
| LIG_FHA_1 | 74 | 80 | PF00498 | 0.664 |
| LIG_FHA_2 | 281 | 287 | PF00498 | 0.541 |
| LIG_FHA_2 | 49 | 55 | PF00498 | 0.763 |
| LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.539 |
| LIG_SH3_3 | 137 | 143 | PF00018 | 0.428 |
| LIG_SH3_3 | 61 | 67 | PF00018 | 0.665 |
| LIG_SH3_4 | 33 | 40 | PF00018 | 0.586 |
| LIG_SUMO_SIM_par_1 | 110 | 119 | PF11976 | 0.499 |
| LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.545 |
| LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.428 |
| LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.593 |
| MOD_CK1_1 | 110 | 116 | PF00069 | 0.706 |
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.674 |
| MOD_CK1_1 | 66 | 72 | PF00069 | 0.687 |
| MOD_CK1_1 | 73 | 79 | PF00069 | 0.644 |
| MOD_CK2_1 | 293 | 299 | PF00069 | 0.629 |
| MOD_CK2_1 | 318 | 324 | PF00069 | 0.744 |
| MOD_Cter_Amidation | 351 | 354 | PF01082 | 0.579 |
| MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.646 |
| MOD_GlcNHglycan | 123 | 127 | PF01048 | 0.661 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.599 |
| MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.766 |
| MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.649 |
| MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.605 |
| MOD_GlcNHglycan | 400 | 406 | PF01048 | 0.655 |
| MOD_GSK3_1 | 107 | 114 | PF00069 | 0.712 |
| MOD_GSK3_1 | 22 | 29 | PF00069 | 0.746 |
| MOD_GSK3_1 | 310 | 317 | PF00069 | 0.752 |
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.665 |
| MOD_GSK3_1 | 361 | 368 | PF00069 | 0.614 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.759 |
| MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.572 |
| MOD_NEK2_1 | 107 | 112 | PF00069 | 0.749 |
| MOD_NEK2_1 | 144 | 149 | PF00069 | 0.428 |
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.766 |
| MOD_NEK2_1 | 39 | 44 | PF00069 | 0.721 |
| MOD_PIKK_1 | 33 | 39 | PF00454 | 0.709 |
| MOD_PKA_1 | 242 | 248 | PF00069 | 0.590 |
| MOD_PKA_2 | 242 | 248 | PF00069 | 0.643 |
| MOD_PKA_2 | 85 | 91 | PF00069 | 0.736 |
| MOD_PKA_2 | 9 | 15 | PF00069 | 0.747 |
| MOD_PKB_1 | 26 | 34 | PF00069 | 0.775 |
| MOD_PKB_1 | 273 | 281 | PF00069 | 0.569 |
| MOD_Plk_1 | 280 | 286 | PF00069 | 0.573 |
| MOD_Plk_1 | 298 | 304 | PF00069 | 0.597 |
| MOD_Plk_4 | 111 | 117 | PF00069 | 0.757 |
| MOD_Plk_4 | 298 | 304 | PF00069 | 0.664 |
| MOD_Plk_4 | 70 | 76 | PF00069 | 0.664 |
| MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.662 |
| MOD_SUMO_for_1 | 205 | 208 | PF00179 | 0.428 |
| MOD_SUMO_rev_2 | 66 | 74 | PF00179 | 0.597 |
| TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.542 |
| TRG_ER_diArg_1 | 395 | 398 | PF00400 | 0.745 |
| TRG_ER_diLys_1 | 424 | 429 | PF00400 | 0.681 |
| TRG_NLS_Bipartite_1 | 138 | 156 | PF00514 | 0.428 |
| TRG_NLS_MonoExtC_3 | 423 | 428 | PF00514 | 0.679 |
| TRG_NLS_MonoExtN_4 | 421 | 428 | PF00514 | 0.691 |
| TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.532 |
| TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.535 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I0X6 | Leptomonas seymouri | 62% | 77% |
| A0A1X0NU15 | Trypanosomatidae | 45% | 93% |
| A0A3S7WTI8 | Leishmania donovani | 90% | 100% |
| A4H876 | Leishmania braziliensis | 84% | 98% |
| A4HWK1 | Leishmania infantum | 91% | 100% |
| Q4QF81 | Leishmania major | 91% | 99% |