| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 1 |
| Forrest at al. (metacyclic) | no | yes: 3 |
| Forrest at al. (procyclic) | no | yes: 3 |
| Silverman et al. | yes | yes: 2 |
| Pissara et al. | yes | yes: 12 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | yes | yes: 9 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 6 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 24 |
| NetGPI | no | yes: 0, no: 24 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0005829 | cytosol | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QGE5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 25 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 25 |
| GO:0008152 | metabolic process | 1 | 25 |
| GO:0019538 | protein metabolic process | 3 | 25 |
| GO:0043170 | macromolecule metabolic process | 3 | 25 |
| GO:0044238 | primary metabolic process | 2 | 25 |
| GO:0071704 | organic substance metabolic process | 2 | 25 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 25 |
| GO:0006518 | peptide metabolic process | 4 | 1 |
| GO:0043603 | amide metabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 25 |
| GO:0004180 | carboxypeptidase activity | 5 | 25 |
| GO:0004181 | metallocarboxypeptidase activity | 6 | 25 |
| GO:0008233 | peptidase activity | 3 | 25 |
| GO:0008235 | metalloexopeptidase activity | 5 | 25 |
| GO:0008237 | metallopeptidase activity | 4 | 25 |
| GO:0008238 | exopeptidase activity | 4 | 25 |
| GO:0016787 | hydrolase activity | 2 | 25 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 25 |
| GO:0016853 | isomerase activity | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.329 |
| CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.428 |
| CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.396 |
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.306 |
| CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.400 |
| CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.412 |
| CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.329 |
| CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.552 |
| CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.453 |
| CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.306 |
| CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.469 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.602 |
| DOC_CKS1_1 | 315 | 320 | PF01111 | 0.436 |
| DOC_CYCLIN_RxL_1 | 168 | 178 | PF00134 | 0.311 |
| DOC_CYCLIN_RxL_1 | 255 | 263 | PF00134 | 0.447 |
| DOC_MAPK_gen_1 | 13 | 23 | PF00069 | 0.378 |
| DOC_MAPK_gen_1 | 387 | 394 | PF00069 | 0.406 |
| DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.348 |
| DOC_USP7_UBL2_3 | 459 | 463 | PF12436 | 0.379 |
| DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.348 |
| DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.310 |
| DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.435 |
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.399 |
| LIG_14-3-3_CanoR_1 | 16 | 23 | PF00244 | 0.338 |
| LIG_14-3-3_CanoR_1 | 246 | 253 | PF00244 | 0.539 |
| LIG_14-3-3_CanoR_1 | 87 | 96 | PF00244 | 0.445 |
| LIG_Actin_WH2_2 | 70 | 88 | PF00022 | 0.401 |
| LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.365 |
| LIG_CtBP_PxDLS_1 | 278 | 282 | PF00389 | 0.457 |
| LIG_deltaCOP1_diTrp_1 | 219 | 225 | PF00928 | 0.461 |
| LIG_deltaCOP1_diTrp_1 | 407 | 415 | PF00928 | 0.406 |
| LIG_eIF4E_1 | 356 | 362 | PF01652 | 0.330 |
| LIG_eIF4E_1 | 471 | 477 | PF01652 | 0.518 |
| LIG_FHA_1 | 107 | 113 | PF00498 | 0.340 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.263 |
| LIG_FHA_1 | 236 | 242 | PF00498 | 0.298 |
| LIG_FHA_1 | 315 | 321 | PF00498 | 0.470 |
| LIG_FHA_1 | 418 | 424 | PF00498 | 0.377 |
| LIG_FHA_1 | 471 | 477 | PF00498 | 0.396 |
| LIG_FHA_1 | 50 | 56 | PF00498 | 0.488 |
| LIG_FHA_1 | 58 | 64 | PF00498 | 0.464 |
| LIG_FHA_2 | 247 | 253 | PF00498 | 0.411 |
| LIG_FHA_2 | 261 | 267 | PF00498 | 0.460 |
| LIG_FHA_2 | 291 | 297 | PF00498 | 0.306 |
| LIG_FHA_2 | 3 | 9 | PF00498 | 0.359 |
| LIG_LIR_Apic_2 | 314 | 318 | PF02991 | 0.406 |
| LIG_LIR_Gen_1 | 122 | 130 | PF02991 | 0.533 |
| LIG_LIR_Gen_1 | 299 | 306 | PF02991 | 0.398 |
| LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.320 |
| LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.409 |
| LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.488 |
| LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.429 |
| LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.421 |
| LIG_NRBOX | 16 | 22 | PF00104 | 0.349 |
| LIG_PCNA_PIPBox_1 | 210 | 219 | PF02747 | 0.417 |
| LIG_PCNA_yPIPBox_3 | 382 | 392 | PF02747 | 0.400 |
| LIG_Pex14_1 | 221 | 225 | PF04695 | 0.309 |
| LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.390 |
| LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.330 |
| LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.452 |
| LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.403 |
| LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.330 |
| LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.331 |
| LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.358 |
| LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.358 |
| LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.401 |
| LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.524 |
| LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.404 |
| LIG_SH3_3 | 195 | 201 | PF00018 | 0.309 |
| LIG_SH3_3 | 351 | 357 | PF00018 | 0.404 |
| LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.502 |
| LIG_UBA3_1 | 431 | 436 | PF00899 | 0.518 |
| LIG_WRC_WIRS_1 | 123 | 128 | PF05994 | 0.436 |
| MOD_CDK_SPxxK_3 | 314 | 321 | PF00069 | 0.324 |
| MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.306 |
| MOD_CK1_1 | 107 | 113 | PF00069 | 0.480 |
| MOD_CK1_1 | 145 | 151 | PF00069 | 0.358 |
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.338 |
| MOD_CK1_1 | 245 | 251 | PF00069 | 0.330 |
| MOD_CK1_1 | 422 | 428 | PF00069 | 0.317 |
| MOD_CK1_1 | 57 | 63 | PF00069 | 0.348 |
| MOD_CK2_1 | 2 | 8 | PF00069 | 0.518 |
| MOD_CK2_1 | 260 | 266 | PF00069 | 0.533 |
| MOD_CK2_1 | 267 | 273 | PF00069 | 0.572 |
| MOD_CK2_1 | 290 | 296 | PF00069 | 0.309 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.495 |
| MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.459 |
| MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.306 |
| MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.391 |
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.379 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.460 |
| MOD_GSK3_1 | 242 | 249 | PF00069 | 0.529 |
| MOD_GSK3_1 | 260 | 267 | PF00069 | 0.506 |
| MOD_GSK3_1 | 27 | 34 | PF00069 | 0.504 |
| MOD_GSK3_1 | 290 | 297 | PF00069 | 0.480 |
| MOD_GSK3_1 | 49 | 56 | PF00069 | 0.448 |
| MOD_LATS_1 | 269 | 275 | PF00433 | 0.330 |
| MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.474 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.494 |
| MOD_NEK2_1 | 260 | 265 | PF00069 | 0.424 |
| MOD_NEK2_1 | 338 | 343 | PF00069 | 0.515 |
| MOD_NEK2_1 | 431 | 436 | PF00069 | 0.328 |
| MOD_PIKK_1 | 2 | 8 | PF00454 | 0.389 |
| MOD_PIKK_1 | 294 | 300 | PF00454 | 0.464 |
| MOD_PIKK_1 | 463 | 469 | PF00454 | 0.515 |
| MOD_PIKK_1 | 88 | 94 | PF00454 | 0.578 |
| MOD_PKA_2 | 15 | 21 | PF00069 | 0.257 |
| MOD_PKA_2 | 245 | 251 | PF00069 | 0.397 |
| MOD_Plk_1 | 242 | 248 | PF00069 | 0.342 |
| MOD_Plk_1 | 338 | 344 | PF00069 | 0.465 |
| MOD_Plk_1 | 440 | 446 | PF00069 | 0.330 |
| MOD_Plk_1 | 72 | 78 | PF00069 | 0.485 |
| MOD_Plk_4 | 122 | 128 | PF00069 | 0.525 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.408 |
| MOD_Plk_4 | 27 | 33 | PF00069 | 0.408 |
| MOD_Plk_4 | 422 | 428 | PF00069 | 0.427 |
| MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.310 |
| MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.435 |
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.399 |
| MOD_SUMO_for_1 | 435 | 438 | PF00179 | 0.330 |
| MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.561 |
| MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.449 |
| MOD_SUMO_rev_2 | 22 | 31 | PF00179 | 0.317 |
| TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.330 |
| TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.495 |
| TRG_DiLeu_BaLyEn_6 | 108 | 113 | PF01217 | 0.330 |
| TRG_DiLeu_BaLyEn_6 | 315 | 320 | PF01217 | 0.447 |
| TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.398 |
| TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.400 |
| TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.448 |
| TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.501 |
| TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.400 |
| TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.407 |
| TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.330 |
| TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.398 |
| TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.390 |
| TRG_Pf-PMV_PEXEL_1 | 497 | 501 | PF00026 | 0.564 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0S4IZ28 | Bodo saltans | 45% | 100% |
| A0A1X0NY67 | Trypanosomatidae | 53% | 99% |
| A0A1X0P441 | Trypanosomatidae | 55% | 100% |
| A0A1X0P598 | Trypanosomatidae | 57% | 100% |
| A0A3Q8IBW2 | Leishmania donovani | 53% | 100% |
| A0A3Q8IJY8 | Leishmania donovani | 47% | 100% |
| A0A3Q8IU74 | Leishmania donovani | 55% | 100% |
| A0A3S7WSA3 | Leishmania donovani | 96% | 100% |
| A0A422P042 | Trypanosoma rangeli | 54% | 100% |
| A0A422P4R1 | Trypanosoma rangeli | 54% | 100% |
| A4H716 | Leishmania braziliensis | 80% | 100% |
| A4HLW4 | Leishmania braziliensis | 56% | 100% |
| A4HVE5 | Leishmania infantum | 95% | 100% |
| A4HVW0 | Leishmania infantum | 53% | 100% |
| A4I993 | Leishmania infantum | 55% | 100% |
| A4IC85 | Leishmania infantum | 47% | 100% |
| D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
| E9AP43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
| P42663 | Thermus aquaticus | 36% | 98% |
| P50848 | Bacillus subtilis (strain 168) | 34% | 100% |
| Q4Q0D4 | Leishmania major | 51% | 100% |
| Q4Q3T3 | Leishmania major | 55% | 100% |
| Q4QFW7 | Leishmania major | 53% | 100% |
| Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 35% | 99% |
| Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 34% | 100% |
| V5DQA0 | Trypanosoma cruzi | 55% | 100% |