| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005730 | nucleolus | 5 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IPK7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006396 | RNA processing | 6 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016070 | RNA metabolic process | 5 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0090304 | nucleic acid metabolic process | 4 | 1 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 11 |
| GO:0003723 | RNA binding | 4 | 11 |
| GO:0005488 | binding | 1 | 11 |
| GO:0097159 | organic cyclic compound binding | 2 | 11 |
| GO:1901363 | heterocyclic compound binding | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.547 |
| CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.808 |
| CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.464 |
| CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.487 |
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.549 |
| CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.509 |
| CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.498 |
| CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.574 |
| CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.563 |
| CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.552 |
| CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.504 |
| CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.765 |
| CLV_PCSK_FUR_1 | 362 | 366 | PF00082 | 0.515 |
| CLV_PCSK_FUR_1 | 449 | 453 | PF00082 | 0.486 |
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.547 |
| CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.538 |
| CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.229 |
| CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.221 |
| CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.509 |
| CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.499 |
| CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.590 |
| CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.649 |
| CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.549 |
| CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.542 |
| CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.549 |
| CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.517 |
| CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.563 |
| CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.229 |
| CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.262 |
| CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.513 |
| CLV_PCSK_PC1ET2_1 | 380 | 382 | PF00082 | 0.590 |
| CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.549 |
| CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.549 |
| CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.644 |
| CLV_PCSK_PC7_1 | 138 | 144 | PF00082 | 0.480 |
| CLV_PCSK_PC7_1 | 361 | 367 | PF00082 | 0.562 |
| CLV_PCSK_PC7_1 | 444 | 450 | PF00082 | 0.539 |
| CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.625 |
| CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.577 |
| CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.305 |
| CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.221 |
| CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.603 |
| CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.575 |
| CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.569 |
| CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.523 |
| CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.579 |
| CLV_Separin_Metazoa | 91 | 95 | PF03568 | 0.575 |
| DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.656 |
| DOC_ANK_TNKS_1 | 428 | 435 | PF00023 | 0.551 |
| DOC_CYCLIN_RxL_1 | 111 | 121 | PF00134 | 0.514 |
| DOC_MAPK_gen_1 | 48 | 57 | PF00069 | 0.476 |
| DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.607 |
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.679 |
| DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.610 |
| DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.628 |
| DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.338 |
| DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.634 |
| DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.621 |
| DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.507 |
| DOC_USP7_UBL2_3 | 111 | 115 | PF12436 | 0.669 |
| DOC_USP7_UBL2_3 | 142 | 146 | PF12436 | 0.513 |
| DOC_USP7_UBL2_3 | 220 | 224 | PF12436 | 0.503 |
| DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.654 |
| DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.646 |
| DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.717 |
| LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.698 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
| LIG_BIR_III_4 | 387 | 391 | PF00653 | 0.512 |
| LIG_deltaCOP1_diTrp_1 | 284 | 291 | PF00928 | 0.421 |
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.483 |
| LIG_FHA_1 | 161 | 167 | PF00498 | 0.253 |
| LIG_FHA_1 | 226 | 232 | PF00498 | 0.405 |
| LIG_FHA_1 | 257 | 263 | PF00498 | 0.597 |
| LIG_FHA_2 | 119 | 125 | PF00498 | 0.572 |
| LIG_FHA_2 | 256 | 262 | PF00498 | 0.379 |
| LIG_FHA_2 | 280 | 286 | PF00498 | 0.431 |
| LIG_FHA_2 | 331 | 337 | PF00498 | 0.525 |
| LIG_FHA_2 | 404 | 410 | PF00498 | 0.515 |
| LIG_FHA_2 | 42 | 48 | PF00498 | 0.476 |
| LIG_Integrin_isoDGR_2 | 339 | 341 | PF01839 | 0.231 |
| LIG_Integrin_RGD_1 | 334 | 336 | PF01839 | 0.325 |
| LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.347 |
| LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.421 |
| LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.719 |
| LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.659 |
| LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.312 |
| LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.421 |
| LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.698 |
| LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.504 |
| LIG_Pex14_2 | 119 | 123 | PF04695 | 0.647 |
| LIG_PTB_Apo_2 | 274 | 281 | PF02174 | 0.421 |
| LIG_PTB_Phospho_1 | 274 | 280 | PF10480 | 0.421 |
| LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.320 |
| LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.310 |
| LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.421 |
| LIG_SH3_2 | 443 | 448 | PF14604 | 0.602 |
| LIG_SH3_3 | 398 | 404 | PF00018 | 0.536 |
| LIG_SH3_3 | 437 | 443 | PF00018 | 0.596 |
| LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.600 |
| LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.590 |
| LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.437 |
| LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.421 |
| LIG_UBA3_1 | 51 | 58 | PF00899 | 0.654 |
| LIG_WRC_WIRS_1 | 287 | 292 | PF05994 | 0.426 |
| MOD_CK1_1 | 13 | 19 | PF00069 | 0.680 |
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.525 |
| MOD_CK1_1 | 235 | 241 | PF00069 | 0.494 |
| MOD_CK1_1 | 392 | 398 | PF00069 | 0.589 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.606 |
| MOD_CK1_1 | 83 | 89 | PF00069 | 0.765 |
| MOD_CK1_1 | 95 | 101 | PF00069 | 0.641 |
| MOD_CK2_1 | 152 | 158 | PF00069 | 0.595 |
| MOD_CK2_1 | 238 | 244 | PF00069 | 0.505 |
| MOD_CK2_1 | 279 | 285 | PF00069 | 0.423 |
| MOD_CK2_1 | 357 | 363 | PF00069 | 0.534 |
| MOD_CK2_1 | 41 | 47 | PF00069 | 0.477 |
| MOD_Cter_Amidation | 74 | 77 | PF01082 | 0.785 |
| MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.628 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.452 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.348 |
| MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.440 |
| MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.757 |
| MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.568 |
| MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.699 |
| MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.716 |
| MOD_GSK3_1 | 1 | 8 | PF00069 | 0.522 |
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.533 |
| MOD_GSK3_1 | 392 | 399 | PF00069 | 0.704 |
| MOD_GSK3_1 | 405 | 412 | PF00069 | 0.565 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.668 |
| MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.330 |
| MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.605 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.645 |
| MOD_NEK2_1 | 118 | 123 | PF00069 | 0.650 |
| MOD_NEK2_1 | 232 | 237 | PF00069 | 0.507 |
| MOD_NEK2_1 | 255 | 260 | PF00069 | 0.393 |
| MOD_NEK2_1 | 26 | 31 | PF00069 | 0.644 |
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.483 |
| MOD_NEK2_1 | 33 | 38 | PF00069 | 0.654 |
| MOD_NEK2_2 | 269 | 274 | PF00069 | 0.338 |
| MOD_PKA_1 | 141 | 147 | PF00069 | 0.638 |
| MOD_PKA_1 | 364 | 370 | PF00069 | 0.495 |
| MOD_PKA_1 | 379 | 385 | PF00069 | 0.514 |
| MOD_PKA_1 | 41 | 47 | PF00069 | 0.487 |
| MOD_PKA_2 | 307 | 313 | PF00069 | 0.431 |
| MOD_PKA_2 | 364 | 370 | PF00069 | 0.489 |
| MOD_PKA_2 | 80 | 86 | PF00069 | 0.742 |
| MOD_PKB_1 | 139 | 147 | PF00069 | 0.631 |
| MOD_PKB_1 | 379 | 387 | PF00069 | 0.576 |
| MOD_Plk_1 | 2 | 8 | PF00069 | 0.451 |
| MOD_Plk_1 | 269 | 275 | PF00069 | 0.344 |
| MOD_Plk_1 | 396 | 402 | PF00069 | 0.686 |
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.520 |
| MOD_Plk_4 | 269 | 275 | PF00069 | 0.347 |
| MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.718 |
| MOD_SUMO_rev_2 | 120 | 128 | PF00179 | 0.601 |
| MOD_SUMO_rev_2 | 218 | 226 | PF00179 | 0.500 |
| MOD_SUMO_rev_2 | 293 | 302 | PF00179 | 0.487 |
| MOD_SUMO_rev_2 | 307 | 316 | PF00179 | 0.487 |
| MOD_SUMO_rev_2 | 351 | 357 | PF00179 | 0.660 |
| MOD_SUMO_rev_2 | 377 | 382 | PF00179 | 0.688 |
| MOD_SUMO_rev_2 | 427 | 436 | PF00179 | 0.571 |
| MOD_SUMO_rev_2 | 54 | 60 | PF00179 | 0.509 |
| TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.405 |
| TRG_DiLeu_BaEn_2 | 269 | 275 | PF01217 | 0.367 |
| TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.329 |
| TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.421 |
| TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.583 |
| TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.613 |
| TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.439 |
| TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.424 |
| TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.635 |
| TRG_NLS_Bipartite_1 | 364 | 384 | PF00514 | 0.652 |
| TRG_NLS_Bipartite_1 | 41 | 62 | PF00514 | 0.445 |
| TRG_NLS_MonoCore_2 | 401 | 406 | PF00514 | 0.702 |
| TRG_NLS_MonoCore_2 | 447 | 452 | PF00514 | 0.483 |
| TRG_NLS_MonoExtC_3 | 140 | 145 | PF00514 | 0.485 |
| TRG_NLS_MonoExtC_3 | 401 | 407 | PF00514 | 0.620 |
| TRG_NLS_MonoExtC_3 | 447 | 452 | PF00514 | 0.548 |
| TRG_NLS_MonoExtN_4 | 138 | 145 | PF00514 | 0.536 |
| TRG_NLS_MonoExtN_4 | 379 | 384 | PF00514 | 0.624 |
| TRG_NLS_MonoExtN_4 | 446 | 453 | PF00514 | 0.546 |
| TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.557 |
| TRG_Pf-PMV_PEXEL_1 | 213 | 218 | PF00026 | 0.432 |
| TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.535 |
| TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.504 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8R8 | Leptomonas seymouri | 72% | 100% |
| A0A0S4KJJ6 | Bodo saltans | 49% | 100% |
| A0A1X0P6L1 | Trypanosomatidae | 46% | 100% |
| A0A3R7LUT6 | Trypanosoma rangeli | 46% | 100% |
| A4HMS6 | Leishmania braziliensis | 84% | 100% |
| C9ZZA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
| E9AF78 | Leishmania major | 93% | 100% |
| E9B6D4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
| V5BNV3 | Trypanosoma cruzi | 49% | 100% |