| 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) | yes | yes: 3 |
| 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: 23 |
| NetGPI | no | yes: 0, no: 23 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 24 |
| GO:0110165 | cellular anatomical entity | 1 | 24 |
Related structures:
AlphaFold database: A4HUP5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 24 |
| GO:0006811 | monoatomic ion transport | 4 | 24 |
| GO:0006817 | phosphate ion transport | 7 | 24 |
| GO:0006820 | monoatomic anion transport | 5 | 24 |
| GO:0015698 | inorganic anion transport | 6 | 24 |
| GO:0051179 | localization | 1 | 24 |
| GO:0051234 | establishment of localization | 2 | 24 |
| GO:0009987 | cellular process | 1 | 3 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
| GO:0035435 | phosphate ion transmembrane transport | 6 | 3 |
| GO:0055085 | transmembrane transport | 2 | 3 |
| GO:0098656 | monoatomic anion transmembrane transport | 4 | 3 |
| GO:0098660 | inorganic ion transmembrane transport | 4 | 3 |
| GO:0098661 | inorganic anion transmembrane transport | 5 | 3 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 24 |
| GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 24 |
| GO:0015291 | secondary active transmembrane transporter activity | 4 | 24 |
| GO:0015293 | symporter activity | 5 | 24 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 24 |
| GO:0022804 | active transmembrane transporter activity | 3 | 24 |
| GO:0022857 | transmembrane transporter activity | 2 | 24 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.522 |
| CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.501 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.240 |
| CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.458 |
| CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.263 |
| CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.463 |
| CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.286 |
| CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.458 |
| CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.245 |
| CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.463 |
| CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.339 |
| CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.471 |
| CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.369 |
| CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.263 |
| CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.316 |
| DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.290 |
| DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.334 |
| DOC_CKS1_1 | 407 | 412 | PF01111 | 0.573 |
| DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.463 |
| DOC_MAPK_gen_1 | 324 | 334 | PF00069 | 0.445 |
| DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.455 |
| DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.353 |
| DOC_MAPK_MEF2A_6 | 458 | 465 | PF00069 | 0.581 |
| DOC_MAPK_NFAT4_5 | 458 | 466 | PF00069 | 0.568 |
| DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.299 |
| DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.479 |
| DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.319 |
| DOC_SPAK_OSR1_1 | 177 | 181 | PF12202 | 0.513 |
| DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.319 |
| DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.334 |
| DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.438 |
| DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.263 |
| DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.263 |
| DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.319 |
| DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.487 |
| LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.463 |
| LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.494 |
| LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.306 |
| LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.526 |
| LIG_Actin_WH2_2 | 203 | 221 | PF00022 | 0.280 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.392 |
| LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.348 |
| LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.340 |
| LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.375 |
| LIG_CaM_NSCaTE_8 | 377 | 384 | PF13499 | 0.349 |
| LIG_deltaCOP1_diTrp_1 | 322 | 329 | PF00928 | 0.463 |
| LIG_FHA_1 | 114 | 120 | PF00498 | 0.302 |
| LIG_FHA_1 | 163 | 169 | PF00498 | 0.425 |
| LIG_FHA_1 | 191 | 197 | PF00498 | 0.531 |
| LIG_FHA_1 | 288 | 294 | PF00498 | 0.460 |
| LIG_FHA_1 | 363 | 369 | PF00498 | 0.327 |
| LIG_FHA_1 | 390 | 396 | PF00498 | 0.313 |
| LIG_FHA_1 | 435 | 441 | PF00498 | 0.345 |
| LIG_FHA_1 | 44 | 50 | PF00498 | 0.411 |
| LIG_FHA_1 | 470 | 476 | PF00498 | 0.328 |
| LIG_FHA_1 | 66 | 72 | PF00498 | 0.272 |
| LIG_GBD_Chelix_1 | 196 | 204 | PF00786 | 0.334 |
| LIG_IBAR_NPY_1 | 5 | 7 | PF08397 | 0.367 |
| LIG_LIR_Apic_2 | 157 | 162 | PF02991 | 0.319 |
| LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.334 |
| LIG_LIR_Gen_1 | 107 | 113 | PF02991 | 0.535 |
| LIG_LIR_Gen_1 | 205 | 214 | PF02991 | 0.319 |
| LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.300 |
| LIG_LIR_LC3C_4 | 419 | 424 | PF02991 | 0.346 |
| LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.535 |
| LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.272 |
| LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.324 |
| LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.359 |
| LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.476 |
| LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.311 |
| LIG_Pex14_2 | 203 | 207 | PF04695 | 0.320 |
| LIG_SH2_CRK | 173 | 177 | PF00017 | 0.264 |
| LIG_SH2_CRK | 192 | 196 | PF00017 | 0.264 |
| LIG_SH2_CRK | 430 | 434 | PF00017 | 0.379 |
| LIG_SH2_CRK | 90 | 94 | PF00017 | 0.354 |
| LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.469 |
| LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.436 |
| LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.311 |
| LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.339 |
| LIG_SH3_3 | 177 | 183 | PF00018 | 0.437 |
| LIG_SH3_3 | 404 | 410 | PF00018 | 0.573 |
| LIG_SH3_3 | 72 | 78 | PF00018 | 0.363 |
| LIG_Sin3_3 | 420 | 427 | PF02671 | 0.435 |
| LIG_SUMO_SIM_anti_2 | 403 | 409 | PF11976 | 0.573 |
| LIG_SUMO_SIM_anti_2 | 46 | 53 | PF11976 | 0.431 |
| LIG_SUMO_SIM_par_1 | 41 | 46 | PF11976 | 0.498 |
| LIG_SUMO_SIM_par_1 | 443 | 448 | PF11976 | 0.334 |
| LIG_SUMO_SIM_par_1 | 47 | 53 | PF11976 | 0.308 |
| LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.347 |
| LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.411 |
| LIG_UBA3_1 | 460 | 464 | PF00899 | 0.327 |
| LIG_ULM_U2AF65_1 | 216 | 221 | PF00076 | 0.280 |
| LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.347 |
| LIG_WRC_WIRS_1 | 204 | 209 | PF05994 | 0.276 |
| LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.379 |
| LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.348 |
| MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.334 |
| MOD_CK1_1 | 115 | 121 | PF00069 | 0.290 |
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.342 |
| MOD_CK1_1 | 297 | 303 | PF00069 | 0.356 |
| MOD_CK1_1 | 347 | 353 | PF00069 | 0.323 |
| MOD_CK1_1 | 425 | 431 | PF00069 | 0.345 |
| MOD_CK1_1 | 69 | 75 | PF00069 | 0.317 |
| MOD_CK2_1 | 264 | 270 | PF00069 | 0.287 |
| MOD_CK2_1 | 292 | 298 | PF00069 | 0.388 |
| MOD_CK2_1 | 50 | 56 | PF00069 | 0.331 |
| MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.509 |
| MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.169 |
| MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.472 |
| MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.314 |
| MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.312 |
| MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.283 |
| MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.336 |
| MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.484 |
| MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.309 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.326 |
| MOD_GSK3_1 | 154 | 161 | PF00069 | 0.329 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.319 |
| MOD_GSK3_1 | 265 | 272 | PF00069 | 0.424 |
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.344 |
| MOD_GSK3_1 | 434 | 441 | PF00069 | 0.318 |
| MOD_GSK3_1 | 469 | 476 | PF00069 | 0.351 |
| MOD_GSK3_1 | 65 | 72 | PF00069 | 0.340 |
| MOD_NEK2_1 | 203 | 208 | PF00069 | 0.295 |
| MOD_NEK2_1 | 218 | 223 | PF00069 | 0.382 |
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.364 |
| MOD_NEK2_1 | 388 | 393 | PF00069 | 0.348 |
| MOD_NEK2_1 | 422 | 427 | PF00069 | 0.334 |
| MOD_NEK2_1 | 43 | 48 | PF00069 | 0.392 |
| MOD_NEK2_1 | 473 | 478 | PF00069 | 0.371 |
| MOD_PIKK_1 | 270 | 276 | PF00454 | 0.278 |
| MOD_PIKK_1 | 292 | 298 | PF00454 | 0.276 |
| MOD_PIKK_1 | 43 | 49 | PF00454 | 0.435 |
| MOD_PK_1 | 370 | 376 | PF00069 | 0.300 |
| MOD_PKA_2 | 264 | 270 | PF00069 | 0.421 |
| MOD_Plk_1 | 403 | 409 | PF00069 | 0.310 |
| MOD_Plk_4 | 104 | 110 | PF00069 | 0.339 |
| MOD_Plk_4 | 15 | 21 | PF00069 | 0.347 |
| MOD_Plk_4 | 154 | 160 | PF00069 | 0.305 |
| MOD_Plk_4 | 171 | 177 | PF00069 | 0.305 |
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.321 |
| MOD_Plk_4 | 403 | 409 | PF00069 | 0.411 |
| MOD_Plk_4 | 445 | 451 | PF00069 | 0.300 |
| MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.319 |
| MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.334 |
| MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.300 |
| TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.304 |
| TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.270 |
| TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.289 |
| TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.311 |
| TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.321 |
| TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.315 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P4S5 | Leptomonas seymouri | 68% | 94% |
| A0A1X0NXY5 | Trypanosomatidae | 60% | 93% |
| A0A3Q8I8Y3 | Leishmania donovani | 100% | 100% |
| A0A3Q8IBK1 | Leishmania donovani | 62% | 91% |
| A0A3R7K4N2 | Trypanosoma rangeli | 58% | 100% |
| A0A3S5H545 | Leishmania donovani | 48% | 86% |
| A4H5Y5 | Leishmania braziliensis | 92% | 100% |
| A4H6C2 | Leishmania braziliensis | 92% | 100% |
| A4HBH2 | Leishmania braziliensis | 61% | 100% |
| A4HH06 | Leishmania braziliensis | 49% | 100% |
| A4HYJ6 | Leishmania infantum | 62% | 91% |
| C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 96% |
| C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 96% |
| E9ACJ5 | Leishmania major | 48% | 100% |
| E9AG39 | Leishmania infantum | 48% | 86% |
| E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
| E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
| O84698 | Chlamydia trachomatis (strain D/UW-3/Cx) | 32% | 100% |
| P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 86% |
| Q38954 | Arabidopsis thaliana | 33% | 84% |
| Q4QH82 | Leishmania major | 99% | 100% |
| Q4QHL7 | Leishmania major | 99% | 100% |
| Q6PFM1 | Danio rerio | 31% | 74% |
| Q9PLN5 | Chlamydia muridarum (strain MoPn / Nigg) | 32% | 100% |
| Q9Z7M4 | Chlamydia pneumoniae | 31% | 100% |
| Q9ZJC8 | Helicobacter pylori (strain J99 / ATCC 700824) | 30% | 92% |
| V5DS90 | Trypanosoma cruzi | 59% | 100% |