| 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: 22 | 
| NetGPI | no | yes: 0, no: 22 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 23 | 
| GO:0110165 | cellular anatomical entity | 1 | 23 | 
| GO:0000323 | lytic vacuole | 6 | 1 | 
| GO:0005764 | lysosome | 7 | 1 | 
| GO:0005773 | vacuole | 5 | 1 | 
| GO:0020022 | acidocalcisome | 5 | 1 | 
| GO:0043226 | organelle | 2 | 1 | 
| GO:0043227 | membrane-bounded organelle | 3 | 1 | 
| GO:0043229 | intracellular organelle | 3 | 1 | 
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 | 
Related structures:
AlphaFold database: A0A3S7WRN2
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 23 | 
| GO:0015203 | polyamine transmembrane transporter activity | 3 | 23 | 
| GO:0022857 | transmembrane transporter activity | 2 | 23 | 
| GO:0003824 | catalytic activity | 1 | 5 | 
| GO:0016787 | hydrolase activity | 2 | 5 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.224 | 
| CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.482 | 
| CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.284 | 
| CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.291 | 
| CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.286 | 
| CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.499 | 
| CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.276 | 
| CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.390 | 
| CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.409 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.286 | 
| DOC_CYCLIN_yClb1_LxF_4 | 252 | 258 | PF00134 | 0.182 | 
| DOC_CYCLIN_yCln2_LP_2 | 361 | 367 | PF00134 | 0.446 | 
| DOC_MAPK_gen_1 | 107 | 116 | PF00069 | 0.280 | 
| DOC_MAPK_MEF2A_6 | 343 | 351 | PF00069 | 0.321 | 
| DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.516 | 
| DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.326 | 
| DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.532 | 
| DOC_PP1_RVXF_1 | 427 | 434 | PF00149 | 0.556 | 
| DOC_PP1_RVXF_1 | 59 | 65 | PF00149 | 0.339 | 
| DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.457 | 
| DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.367 | 
| DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.364 | 
| DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.356 | 
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.448 | 
| DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.403 | 
| DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.697 | 
| LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.164 | 
| LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.528 | 
| LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.650 | 
| LIG_Actin_WH2_2 | 139 | 155 | PF00022 | 0.182 | 
| LIG_APCC_ABBA_1 | 391 | 396 | PF00400 | 0.319 | 
| LIG_Clathr_ClatBox_1 | 332 | 336 | PF01394 | 0.353 | 
| LIG_CtBP_PxDLS_1 | 232 | 236 | PF00389 | 0.224 | 
| LIG_deltaCOP1_diTrp_1 | 171 | 175 | PF00928 | 0.473 | 
| LIG_FHA_1 | 1 | 7 | PF00498 | 0.347 | 
| LIG_FHA_1 | 115 | 121 | PF00498 | 0.267 | 
| LIG_FHA_1 | 129 | 135 | PF00498 | 0.328 | 
| LIG_FHA_1 | 171 | 177 | PF00498 | 0.538 | 
| LIG_FHA_1 | 276 | 282 | PF00498 | 0.422 | 
| LIG_FHA_1 | 397 | 403 | PF00498 | 0.277 | 
| LIG_FHA_1 | 451 | 457 | PF00498 | 0.742 | 
| LIG_FHA_2 | 189 | 195 | PF00498 | 0.502 | 
| LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.320 | 
| LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.488 | 
| LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.296 | 
| LIG_LIR_Gen_1 | 312 | 323 | PF02991 | 0.372 | 
| LIG_LIR_Gen_1 | 414 | 421 | PF02991 | 0.410 | 
| LIG_LIR_Gen_1 | 432 | 438 | PF02991 | 0.641 | 
| LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.310 | 
| LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.457 | 
| LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.284 | 
| LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.312 | 
| LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.280 | 
| LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.368 | 
| LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.311 | 
| LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.616 | 
| LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.325 | 
| LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.188 | 
| LIG_LYPXL_S_1 | 357 | 361 | PF13949 | 0.318 | 
| LIG_LYPXL_S_1 | 86 | 90 | PF13949 | 0.477 | 
| LIG_LYPXL_yS_3 | 358 | 361 | PF13949 | 0.442 | 
| LIG_LYPXL_yS_3 | 87 | 90 | PF13949 | 0.262 | 
| LIG_MAD2 | 429 | 437 | PF02301 | 0.545 | 
| LIG_NRBOX | 110 | 116 | PF00104 | 0.338 | 
| LIG_NRBOX | 144 | 150 | PF00104 | 0.375 | 
| LIG_Pex14_1 | 238 | 242 | PF04695 | 0.262 | 
| LIG_Pex14_1 | 311 | 315 | PF04695 | 0.404 | 
| LIG_Pex14_2 | 156 | 160 | PF04695 | 0.465 | 
| LIG_Pex14_2 | 365 | 369 | PF04695 | 0.476 | 
| LIG_Pex14_2 | 411 | 415 | PF04695 | 0.330 | 
| LIG_PTB_Apo_2 | 81 | 88 | PF02174 | 0.250 | 
| LIG_PTB_Phospho_1 | 81 | 87 | PF10480 | 0.262 | 
| LIG_SH2_GRB2like | 157 | 160 | PF00017 | 0.469 | 
| LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.320 | 
| LIG_SH2_PTP2 | 79 | 82 | PF00017 | 0.224 | 
| LIG_SH2_SRC | 165 | 168 | PF00017 | 0.498 | 
| LIG_SH2_SRC | 218 | 221 | PF00017 | 0.320 | 
| LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.308 | 
| LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.331 | 
| LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.394 | 
| LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.468 | 
| LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.451 | 
| LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.458 | 
| LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.319 | 
| LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.335 | 
| LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.490 | 
| LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.380 | 
| LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.299 | 
| LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.246 | 
| LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.225 | 
| LIG_SH3_1 | 455 | 461 | PF00018 | 0.602 | 
| LIG_SH3_3 | 155 | 161 | PF00018 | 0.498 | 
| LIG_SH3_3 | 356 | 362 | PF00018 | 0.460 | 
| LIG_SH3_3 | 431 | 437 | PF00018 | 0.662 | 
| LIG_SH3_3 | 455 | 461 | PF00018 | 0.780 | 
| LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.413 | 
| LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.340 | 
| LIG_SUMO_SIM_anti_2 | 396 | 402 | PF11976 | 0.308 | 
| LIG_SUMO_SIM_par_1 | 131 | 139 | PF11976 | 0.374 | 
| LIG_SUMO_SIM_par_1 | 21 | 27 | PF11976 | 0.324 | 
| LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.349 | 
| LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.312 | 
| LIG_SUMO_SIM_par_1 | 344 | 350 | PF11976 | 0.412 | 
| LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.530 | 
| LIG_SxIP_EBH_1 | 201 | 214 | PF03271 | 0.394 | 
| LIG_TYR_ITIM | 77 | 82 | PF00017 | 0.267 | 
| LIG_UBA3_1 | 57 | 61 | PF00899 | 0.530 | 
| LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.389 | 
| LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.399 | 
| LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.419 | 
| LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.619 | 
| MOD_CK1_1 | 177 | 183 | PF00069 | 0.470 | 
| MOD_CK1_1 | 199 | 205 | PF00069 | 0.566 | 
| MOD_CK1_1 | 439 | 445 | PF00069 | 0.712 | 
| MOD_CK2_1 | 181 | 187 | PF00069 | 0.464 | 
| MOD_CK2_1 | 188 | 194 | PF00069 | 0.432 | 
| MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.286 | 
| MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.276 | 
| MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.236 | 
| MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.280 | 
| MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.467 | 
| MOD_GSK3_1 | 129 | 136 | PF00069 | 0.321 | 
| MOD_GSK3_1 | 166 | 173 | PF00069 | 0.473 | 
| MOD_GSK3_1 | 177 | 184 | PF00069 | 0.456 | 
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.486 | 
| MOD_GSK3_1 | 233 | 240 | PF00069 | 0.282 | 
| MOD_GSK3_1 | 270 | 277 | PF00069 | 0.298 | 
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.459 | 
| MOD_GSK3_1 | 317 | 324 | PF00069 | 0.310 | 
| MOD_GSK3_1 | 382 | 389 | PF00069 | 0.290 | 
| MOD_GSK3_1 | 407 | 414 | PF00069 | 0.389 | 
| MOD_GSK3_1 | 450 | 457 | PF00069 | 0.792 | 
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.233 | 
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.245 | 
| MOD_NEK2_1 | 175 | 180 | PF00069 | 0.463 | 
| MOD_NEK2_1 | 233 | 238 | PF00069 | 0.349 | 
| MOD_NEK2_1 | 268 | 273 | PF00069 | 0.278 | 
| MOD_NEK2_1 | 275 | 280 | PF00069 | 0.417 | 
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.331 | 
| MOD_NEK2_1 | 382 | 387 | PF00069 | 0.338 | 
| MOD_NEK2_1 | 4 | 9 | PF00069 | 0.312 | 
| MOD_NEK2_1 | 411 | 416 | PF00069 | 0.394 | 
| MOD_NEK2_1 | 95 | 100 | PF00069 | 0.322 | 
| MOD_PIKK_1 | 196 | 202 | PF00454 | 0.379 | 
| MOD_PKA_2 | 439 | 445 | PF00069 | 0.720 | 
| MOD_PKA_2 | 99 | 105 | PF00069 | 0.194 | 
| MOD_Plk_1 | 170 | 176 | PF00069 | 0.448 | 
| MOD_Plk_1 | 244 | 250 | PF00069 | 0.314 | 
| MOD_Plk_4 | 129 | 135 | PF00069 | 0.322 | 
| MOD_Plk_4 | 188 | 194 | PF00069 | 0.497 | 
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.440 | 
| MOD_Plk_4 | 21 | 27 | PF00069 | 0.304 | 
| MOD_Plk_4 | 314 | 320 | PF00069 | 0.318 | 
| MOD_Plk_4 | 322 | 328 | PF00069 | 0.317 | 
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.304 | 
| MOD_Plk_4 | 396 | 402 | PF00069 | 0.261 | 
| MOD_Plk_4 | 407 | 413 | PF00069 | 0.321 | 
| MOD_Plk_4 | 429 | 435 | PF00069 | 0.636 | 
| MOD_Plk_4 | 73 | 79 | PF00069 | 0.287 | 
| MOD_Plk_4 | 86 | 92 | PF00069 | 0.257 | 
| MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.696 | 
| TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.317 | 
| TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.452 | 
| TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.360 | 
| TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.290 | 
| TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.246 | 
| TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.238 | 
| TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.689 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I2T0 | Leptomonas seymouri | 69% | 80% | 
| A0A0N1PGN1 | Leptomonas seymouri | 34% | 89% | 
| A0A0S4IJF6 | Bodo saltans | 25% | 80% | 
| A0A0S4ISA5 | Bodo saltans | 23% | 81% | 
| A0A0S4JBT0 | Bodo saltans | 25% | 90% | 
| A0A1X0NNQ0 | Trypanosomatidae | 31% | 74% | 
| A0A1X0NV66 | Trypanosomatidae | 51% | 89% | 
| A0A1X0P501 | Trypanosomatidae | 36% | 86% | 
| A0A3R7M6P3 | Trypanosoma rangeli | 32% | 76% | 
| A0A3R7N0T9 | Trypanosoma rangeli | 52% | 92% | 
| A0A3S5IRV3 | Trypanosoma rangeli | 35% | 92% | 
| A0A3S7XA01 | Leishmania donovani | 35% | 90% | 
| A2X8M8 | Oryza sativa subsp. indica | 28% | 88% | 
| A4H6H7 | Leishmania braziliensis | 84% | 100% | 
| A4HNB0 | Leishmania braziliensis | 36% | 100% | 
| A4HUW5 | Leishmania infantum | 100% | 100% | 
| A4IBY1 | Leishmania infantum | 35% | 100% | 
| C9ZYM5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 95% | 
| D0A7J0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 92% | 
| E9AFR8 | Leishmania major | 35% | 100% | 
| E9ANJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% | 
| E9B6X1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% | 
| Q4QH28 | Leishmania major | 95% | 100% | 
| Q6Z8D0 | Oryza sativa subsp. japonica | 28% | 88% | 
| Q9C6S4 | Arabidopsis thaliana | 27% | 97% | 
| Q9C6S5 | Arabidopsis thaliana | 28% | 94% | 
| Q9FFL1 | Arabidopsis thaliana | 30% | 95% | 
| Q9LH39 | Arabidopsis thaliana | 28% | 97% | 
| Q9LHN7 | Arabidopsis thaliana | 26% | 97% | 
| V5BCQ1 | Trypanosoma cruzi | 37% | 100% | 
| V5DDZ5 | Trypanosoma cruzi | 31% | 74% |