Uncharacterized Protein, Uncharacterized
| 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: 9 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.493 | 
| CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.406 | 
| CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.643 | 
| CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.550 | 
| CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.518 | 
| CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.436 | 
| CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.632 | 
| CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.397 | 
| CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.644 | 
| CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.611 | 
| CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.365 | 
| CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.474 | 
| CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.530 | 
| CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.516 | 
| CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.439 | 
| CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.436 | 
| CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.496 | 
| CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.644 | 
| CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.619 | 
| CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.604 | 
| CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.369 | 
| CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.474 | 
| CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.439 | 
| CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.615 | 
| CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.604 | 
| CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.381 | 
| CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.484 | 
| CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.363 | 
| CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.430 | 
| CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.318 | 
| CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.406 | 
| CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.575 | 
| CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.531 | 
| DOC_CKS1_1 | 31 | 36 | PF01111 | 0.375 | 
| DOC_CYCLIN_RxL_1 | 112 | 125 | PF00134 | 0.406 | 
| DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.404 | 
| DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.589 | 
| DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.382 | 
| DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.448 | 
| DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.637 | 
| DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.564 | 
| DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.701 | 
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.392 | 
| DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.720 | 
| DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.616 | 
| DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.628 | 
| LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.360 | 
| LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.574 | 
| LIG_FHA_1 | 27 | 33 | PF00498 | 0.404 | 
| LIG_FHA_1 | 401 | 407 | PF00498 | 0.612 | 
| LIG_FHA_2 | 212 | 218 | PF00498 | 0.576 | 
| LIG_FHA_2 | 276 | 282 | PF00498 | 0.501 | 
| LIG_LIR_Apic_2 | 214 | 219 | PF02991 | 0.598 | 
| LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.383 | 
| LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.631 | 
| LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.368 | 
| LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.365 | 
| LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.372 | 
| LIG_MYND_3 | 183 | 187 | PF01753 | 0.445 | 
| LIG_MYND_3 | 379 | 383 | PF01753 | 0.619 | 
| LIG_PDZ_Class_3 | 421 | 426 | PF00595 | 0.601 | 
| LIG_Pex14_1 | 65 | 69 | PF04695 | 0.358 | 
| LIG_SH2_CRK | 16 | 20 | PF00017 | 0.423 | 
| LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.431 | 
| LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.353 | 
| LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.407 | 
| LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.544 | 
| LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.432 | 
| LIG_SH2_STAT3 | 61 | 64 | PF00017 | 0.367 | 
| LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.397 | 
| LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.391 | 
| LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.511 | 
| LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.371 | 
| LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.465 | 
| LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.548 | 
| LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.594 | 
| LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.651 | 
| LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.544 | 
| LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.361 | 
| MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.385 | 
| MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.629 | 
| MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.627 | 
| MOD_CK1_1 | 152 | 158 | PF00069 | 0.517 | 
| MOD_CK1_1 | 381 | 387 | PF00069 | 0.662 | 
| MOD_CK2_1 | 152 | 158 | PF00069 | 0.473 | 
| MOD_CK2_1 | 17 | 23 | PF00069 | 0.483 | 
| MOD_CK2_1 | 211 | 217 | PF00069 | 0.554 | 
| MOD_CK2_1 | 232 | 238 | PF00069 | 0.556 | 
| MOD_CK2_1 | 271 | 277 | PF00069 | 0.620 | 
| MOD_Cter_Amidation | 24 | 27 | PF01082 | 0.455 | 
| MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.496 | 
| MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.675 | 
| MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.625 | 
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.509 | 
| MOD_GSK3_1 | 195 | 202 | PF00069 | 0.525 | 
| MOD_GSK3_1 | 245 | 252 | PF00069 | 0.500 | 
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.394 | 
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.492 | 
| MOD_GSK3_1 | 292 | 299 | PF00069 | 0.533 | 
| MOD_GSK3_1 | 312 | 319 | PF00069 | 0.577 | 
| MOD_GSK3_1 | 381 | 388 | PF00069 | 0.636 | 
| MOD_LATS_1 | 24 | 30 | PF00433 | 0.432 | 
| MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.367 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.563 | 
| MOD_NEK2_1 | 232 | 237 | PF00069 | 0.501 | 
| MOD_NEK2_2 | 211 | 216 | PF00069 | 0.594 | 
| MOD_NEK2_2 | 296 | 301 | PF00069 | 0.581 | 
| MOD_NEK2_2 | 65 | 70 | PF00069 | 0.362 | 
| MOD_PIKK_1 | 102 | 108 | PF00454 | 0.531 | 
| MOD_PIKK_1 | 149 | 155 | PF00454 | 0.419 | 
| MOD_PKA_1 | 102 | 108 | PF00069 | 0.531 | 
| MOD_PKA_1 | 26 | 32 | PF00069 | 0.414 | 
| MOD_PKA_1 | 324 | 330 | PF00069 | 0.658 | 
| MOD_PKA_2 | 102 | 108 | PF00069 | 0.531 | 
| MOD_PKA_2 | 136 | 142 | PF00069 | 0.355 | 
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.500 | 
| MOD_PKA_2 | 26 | 32 | PF00069 | 0.542 | 
| MOD_PKA_2 | 324 | 330 | PF00069 | 0.670 | 
| MOD_PKB_1 | 100 | 108 | PF00069 | 0.516 | 
| MOD_Plk_1 | 353 | 359 | PF00069 | 0.600 | 
| MOD_Plk_4 | 211 | 217 | PF00069 | 0.567 | 
| MOD_Plk_4 | 296 | 302 | PF00069 | 0.620 | 
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.385 | 
| MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.724 | 
| MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.615 | 
| MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.630 | 
| MOD_SUMO_for_1 | 351 | 354 | PF00179 | 0.564 | 
| MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.628 | 
| TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.431 | 
| TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.518 | 
| TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.569 | 
| TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.538 | 
| TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.655 | 
| TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.542 | 
| TRG_NLS_Bipartite_1 | 100 | 120 | PF00514 | 0.436 | 
| TRG_NLS_MonoCore_2 | 322 | 327 | PF00514 | 0.623 | 
| TRG_NLS_MonoExtC_3 | 115 | 121 | PF00514 | 0.411 | 
| TRG_NLS_MonoExtC_3 | 324 | 330 | PF00514 | 0.539 | 
| TRG_NLS_MonoExtN_4 | 321 | 327 | PF00514 | 0.568 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P2P6 | Leptomonas seymouri | 78% | 100% | 
| A0A0S4IKL5 | Bodo saltans | 51% | 91% | 
| A0A1X0P5A6 | Trypanosomatidae | 61% | 96% | 
| A0A3Q8IPV2 | Leishmania donovani | 100% | 100% | 
| A0A3R7NKQ1 | Trypanosoma rangeli | 62% | 97% | 
| A4HN18 | Leishmania braziliensis | 93% | 100% | 
| C9ZYZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 97% | 
| E9AFH3 | Leishmania major | 97% | 100% | 
| E9B6M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% | 
| V5BY99 | Trypanosoma cruzi | 61% | 96% |