| 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 |
Related structures:
AlphaFold database: E9ATX2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 8 |
| GO:0006793 | phosphorus metabolic process | 3 | 8 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
| GO:0008152 | metabolic process | 1 | 8 |
| GO:0009987 | cellular process | 1 | 8 |
| GO:0016311 | dephosphorylation | 5 | 8 |
| GO:0019538 | protein metabolic process | 3 | 8 |
| GO:0036211 | protein modification process | 4 | 8 |
| GO:0043170 | macromolecule metabolic process | 3 | 8 |
| GO:0043412 | macromolecule modification | 4 | 8 |
| GO:0044237 | cellular metabolic process | 2 | 8 |
| GO:0044238 | primary metabolic process | 2 | 8 |
| GO:0071704 | organic substance metabolic process | 2 | 8 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 8 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 8 |
| GO:0004725 | protein tyrosine phosphatase activity | 4 | 8 |
| GO:0016787 | hydrolase activity | 2 | 8 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
| GO:0016791 | phosphatase activity | 5 | 8 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.333 |
| CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.572 |
| CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.327 |
| CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.320 |
| CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.454 |
| CLV_PCSK_FUR_1 | 484 | 488 | PF00082 | 0.600 |
| CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.485 |
| CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.327 |
| CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.454 |
| CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.577 |
| CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.615 |
| CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.256 |
| CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.339 |
| CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.443 |
| CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.489 |
| DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.339 |
| DEG_APCC_KENBOX_2 | 140 | 144 | PF00400 | 0.313 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.355 |
| DOC_CYCLIN_RxL_1 | 174 | 186 | PF00134 | 0.379 |
| DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.663 |
| DOC_MAPK_DCC_7 | 99 | 109 | PF00069 | 0.363 |
| DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.369 |
| DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.433 |
| DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.363 |
| DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.363 |
| DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.303 |
| DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.762 |
| DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.303 |
| DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.506 |
| DOC_SPAK_OSR1_1 | 101 | 105 | PF12202 | 0.196 |
| DOC_SPAK_OSR1_1 | 11 | 15 | PF12202 | 0.413 |
| DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.347 |
| DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.646 |
| DOC_USP7_MATH_2 | 364 | 370 | PF00917 | 0.626 |
| DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.339 |
| DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.340 |
| DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.371 |
| DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.321 |
| DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.643 |
| DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.702 |
| DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.725 |
| DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.626 |
| DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.718 |
| DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.622 |
| LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.495 |
| LIG_14-3-3_CanoR_1 | 226 | 234 | PF00244 | 0.333 |
| LIG_14-3-3_CanoR_1 | 299 | 308 | PF00244 | 0.431 |
| LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.665 |
| LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.693 |
| LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.641 |
| LIG_14-3-3_CanoR_1 | 467 | 472 | PF00244 | 0.533 |
| LIG_Actin_WH2_2 | 102 | 118 | PF00022 | 0.196 |
| LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.600 |
| LIG_DLG_GKlike_1 | 412 | 419 | PF00625 | 0.503 |
| LIG_FHA_1 | 275 | 281 | PF00498 | 0.339 |
| LIG_FHA_1 | 331 | 337 | PF00498 | 0.659 |
| LIG_FHA_1 | 460 | 466 | PF00498 | 0.679 |
| LIG_FHA_1 | 467 | 473 | PF00498 | 0.557 |
| LIG_FHA_2 | 116 | 122 | PF00498 | 0.276 |
| LIG_FHA_2 | 211 | 217 | PF00498 | 0.382 |
| LIG_FHA_2 | 321 | 327 | PF00498 | 0.666 |
| LIG_LIR_Apic_2 | 100 | 105 | PF02991 | 0.363 |
| LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.303 |
| LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.303 |
| LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.466 |
| LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.284 |
| LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.427 |
| LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.363 |
| LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.303 |
| LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.547 |
| LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.609 |
| LIG_LYPXL_S_1 | 23 | 27 | PF13949 | 0.491 |
| LIG_LYPXL_yS_3 | 24 | 27 | PF13949 | 0.493 |
| LIG_OCRL_FandH_1 | 245 | 257 | PF00620 | 0.363 |
| LIG_PCNA_yPIPBox_3 | 294 | 305 | PF02747 | 0.382 |
| LIG_PDZ_Class_1 | 488 | 493 | PF00595 | 0.604 |
| LIG_Pex14_1 | 123 | 127 | PF04695 | 0.303 |
| LIG_Pex14_2 | 102 | 106 | PF04695 | 0.303 |
| LIG_Pex14_2 | 488 | 492 | PF04695 | 0.600 |
| LIG_PTAP_UEV_1 | 367 | 372 | PF05743 | 0.507 |
| LIG_PTB_Apo_2 | 89 | 96 | PF02174 | 0.303 |
| LIG_PTB_Phospho_1 | 89 | 95 | PF10480 | 0.276 |
| LIG_SH2_GRB2like | 127 | 130 | PF00017 | 0.363 |
| LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.303 |
| LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.363 |
| LIG_SH2_SRC | 90 | 93 | PF00017 | 0.339 |
| LIG_SH2_SRC | 95 | 98 | PF00017 | 0.339 |
| LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.384 |
| LIG_SH2_STAT3 | 195 | 198 | PF00017 | 0.282 |
| LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.339 |
| LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.287 |
| LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.595 |
| LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.420 |
| LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.339 |
| LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.339 |
| LIG_SH3_3 | 197 | 203 | PF00018 | 0.339 |
| LIG_SH3_3 | 365 | 371 | PF00018 | 0.503 |
| LIG_SUMO_SIM_anti_2 | 165 | 171 | PF11976 | 0.339 |
| LIG_SUMO_SIM_anti_2 | 210 | 216 | PF11976 | 0.383 |
| LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.363 |
| LIG_UBA3_1 | 214 | 223 | PF00899 | 0.303 |
| MOD_CDK_SPK_2 | 221 | 226 | PF00069 | 0.383 |
| MOD_CK1_1 | 210 | 216 | PF00069 | 0.383 |
| MOD_CK1_1 | 224 | 230 | PF00069 | 0.303 |
| MOD_CK1_1 | 303 | 309 | PF00069 | 0.378 |
| MOD_CK1_1 | 358 | 364 | PF00069 | 0.676 |
| MOD_CK1_1 | 396 | 402 | PF00069 | 0.705 |
| MOD_CK1_1 | 429 | 435 | PF00069 | 0.709 |
| MOD_CK1_1 | 451 | 457 | PF00069 | 0.683 |
| MOD_CK1_1 | 459 | 465 | PF00069 | 0.636 |
| MOD_CK1_1 | 56 | 62 | PF00069 | 0.413 |
| MOD_CK2_1 | 210 | 216 | PF00069 | 0.363 |
| MOD_CK2_1 | 320 | 326 | PF00069 | 0.659 |
| MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.398 |
| MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.335 |
| MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.635 |
| MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.534 |
| MOD_GSK3_1 | 147 | 154 | PF00069 | 0.196 |
| MOD_GSK3_1 | 217 | 224 | PF00069 | 0.370 |
| MOD_GSK3_1 | 327 | 334 | PF00069 | 0.668 |
| MOD_GSK3_1 | 358 | 365 | PF00069 | 0.579 |
| MOD_GSK3_1 | 396 | 403 | PF00069 | 0.777 |
| MOD_GSK3_1 | 424 | 431 | PF00069 | 0.631 |
| MOD_GSK3_1 | 447 | 454 | PF00069 | 0.652 |
| MOD_GSK3_1 | 53 | 60 | PF00069 | 0.395 |
| MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.383 |
| MOD_NEK2_1 | 115 | 120 | PF00069 | 0.317 |
| MOD_NEK2_1 | 164 | 169 | PF00069 | 0.394 |
| MOD_NEK2_1 | 183 | 188 | PF00069 | 0.363 |
| MOD_NEK2_1 | 217 | 222 | PF00069 | 0.377 |
| MOD_NEK2_1 | 300 | 305 | PF00069 | 0.439 |
| MOD_NEK2_1 | 310 | 315 | PF00069 | 0.594 |
| MOD_NEK2_1 | 356 | 361 | PF00069 | 0.643 |
| MOD_NEK2_1 | 423 | 428 | PF00069 | 0.691 |
| MOD_NEK2_1 | 433 | 438 | PF00069 | 0.764 |
| MOD_NEK2_1 | 458 | 463 | PF00069 | 0.693 |
| MOD_NEK2_1 | 466 | 471 | PF00069 | 0.696 |
| MOD_NEK2_1 | 57 | 62 | PF00069 | 0.446 |
| MOD_NEK2_1 | 79 | 84 | PF00069 | 0.473 |
| MOD_PIKK_1 | 108 | 114 | PF00454 | 0.303 |
| MOD_PIKK_1 | 225 | 231 | PF00454 | 0.333 |
| MOD_PIKK_1 | 300 | 306 | PF00454 | 0.501 |
| MOD_PIKK_1 | 327 | 333 | PF00454 | 0.744 |
| MOD_PIKK_1 | 81 | 87 | PF00454 | 0.333 |
| MOD_PK_1 | 174 | 180 | PF00069 | 0.339 |
| MOD_PKA_2 | 225 | 231 | PF00069 | 0.383 |
| MOD_PKA_2 | 315 | 321 | PF00069 | 0.618 |
| MOD_PKA_2 | 356 | 362 | PF00069 | 0.637 |
| MOD_PKA_2 | 423 | 429 | PF00069 | 0.691 |
| MOD_PKA_2 | 466 | 472 | PF00069 | 0.508 |
| MOD_Plk_1 | 128 | 134 | PF00069 | 0.383 |
| MOD_Plk_1 | 410 | 416 | PF00069 | 0.722 |
| MOD_Plk_2-3 | 383 | 389 | PF00069 | 0.699 |
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.319 |
| MOD_Plk_4 | 147 | 153 | PF00069 | 0.363 |
| MOD_Plk_4 | 164 | 170 | PF00069 | 0.363 |
| MOD_Plk_4 | 210 | 216 | PF00069 | 0.363 |
| MOD_Plk_4 | 453 | 459 | PF00069 | 0.657 |
| MOD_Plk_4 | 467 | 473 | PF00069 | 0.500 |
| MOD_Plk_4 | 72 | 78 | PF00069 | 0.379 |
| MOD_Plk_4 | 86 | 92 | PF00069 | 0.303 |
| MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.371 |
| MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.642 |
| MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.705 |
| MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.626 |
| MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.719 |
| MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.623 |
| MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.363 |
| TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.333 |
| TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.683 |
| TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.608 |
| TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.493 |
| TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.303 |
| TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.303 |
| TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.512 |
| TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.327 |
| TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.587 |
| TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.444 |
| TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.373 |
| TRG_Pf-PMV_PEXEL_1 | 4 | 8 | PF00026 | 0.574 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P9E1 | Leptomonas seymouri | 67% | 96% |
| A0A3Q8ILM2 | Leishmania donovani | 92% | 100% |
| A4HQ52 | Leishmania braziliensis | 76% | 100% |
| A4IDV1 | Leishmania infantum | 91% | 100% |
| Q4Q0M4 | Leishmania major | 91% | 100% |
| V5B554 | Trypanosoma cruzi | 54% | 74% |