| 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: 1, no: 7 |
| NetGPI | no | yes: 0, no: 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.633 |
| CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.544 |
| CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.540 |
| CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.752 |
| CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.664 |
| CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.601 |
| CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.765 |
| CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.529 |
| CLV_PCSK_FUR_1 | 37 | 41 | PF00082 | 0.773 |
| CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.462 |
| CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.447 |
| CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.566 |
| CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.591 |
| CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.601 |
| CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.756 |
| CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.762 |
| CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.530 |
| CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.450 |
| CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.638 |
| CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.671 |
| CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.467 |
| CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.596 |
| CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.700 |
| DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.698 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.736 |
| DOC_CDC14_PxL_1 | 300 | 308 | PF14671 | 0.477 |
| DOC_CYCLIN_RxL_1 | 195 | 205 | PF00134 | 0.582 |
| DOC_MAPK_gen_1 | 188 | 198 | PF00069 | 0.584 |
| DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.432 |
| DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.635 |
| DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.497 |
| DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.490 |
| DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.476 |
| DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.519 |
| DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.518 |
| LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.554 |
| LIG_BIR_III_4 | 29 | 33 | PF00653 | 0.566 |
| LIG_CtBP_PxDLS_1 | 76 | 80 | PF00389 | 0.627 |
| LIG_eIF4E_1 | 105 | 111 | PF01652 | 0.452 |
| LIG_FHA_1 | 324 | 330 | PF00498 | 0.588 |
| LIG_FHA_1 | 48 | 54 | PF00498 | 0.706 |
| LIG_FHA_2 | 123 | 129 | PF00498 | 0.478 |
| LIG_FHA_2 | 200 | 206 | PF00498 | 0.427 |
| LIG_LIR_Apic_2 | 70 | 76 | PF02991 | 0.531 |
| LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.517 |
| LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.553 |
| LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.570 |
| LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.540 |
| LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.558 |
| LIG_PCNA_TLS_4 | 201 | 208 | PF02747 | 0.466 |
| LIG_RPA_C_Fungi | 122 | 134 | PF08784 | 0.463 |
| LIG_SH2_CRK | 193 | 197 | PF00017 | 0.542 |
| LIG_SH2_SRC | 207 | 210 | PF00017 | 0.615 |
| LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.588 |
| LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.533 |
| LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.504 |
| LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.434 |
| LIG_SH3_2 | 262 | 267 | PF14604 | 0.565 |
| LIG_SH3_3 | 203 | 209 | PF00018 | 0.475 |
| LIG_SH3_3 | 259 | 265 | PF00018 | 0.575 |
| LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.593 |
| LIG_TRFH_1 | 105 | 109 | PF08558 | 0.445 |
| LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.435 |
| MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.510 |
| MOD_CK1_1 | 246 | 252 | PF00069 | 0.742 |
| MOD_CK1_1 | 46 | 52 | PF00069 | 0.676 |
| MOD_CK1_1 | 63 | 69 | PF00069 | 0.498 |
| MOD_CK2_1 | 199 | 205 | PF00069 | 0.488 |
| MOD_CK2_1 | 93 | 99 | PF00069 | 0.523 |
| MOD_Cter_Amidation | 252 | 255 | PF01082 | 0.584 |
| MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.603 |
| MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.783 |
| MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.674 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.690 |
| MOD_GSK3_1 | 239 | 246 | PF00069 | 0.630 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.601 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.681 |
| MOD_GSK3_1 | 63 | 70 | PF00069 | 0.361 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.637 |
| MOD_GSK3_1 | 84 | 91 | PF00069 | 0.495 |
| MOD_NEK2_1 | 110 | 115 | PF00069 | 0.497 |
| MOD_NEK2_1 | 122 | 127 | PF00069 | 0.474 |
| MOD_NEK2_1 | 16 | 21 | PF00069 | 0.701 |
| MOD_NEK2_1 | 164 | 169 | PF00069 | 0.603 |
| MOD_NEK2_1 | 241 | 246 | PF00069 | 0.606 |
| MOD_NEK2_1 | 47 | 52 | PF00069 | 0.610 |
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.536 |
| MOD_PIKK_1 | 20 | 26 | PF00454 | 0.525 |
| MOD_PKA_1 | 188 | 194 | PF00069 | 0.569 |
| MOD_PKA_1 | 254 | 260 | PF00069 | 0.587 |
| MOD_PKA_1 | 40 | 46 | PF00069 | 0.540 |
| MOD_PKA_2 | 188 | 194 | PF00069 | 0.602 |
| MOD_PKA_2 | 254 | 260 | PF00069 | 0.731 |
| MOD_PKA_2 | 327 | 333 | PF00069 | 0.592 |
| MOD_PKA_2 | 40 | 46 | PF00069 | 0.540 |
| MOD_PKA_2 | 67 | 73 | PF00069 | 0.544 |
| MOD_PKB_1 | 38 | 46 | PF00069 | 0.542 |
| MOD_Plk_1 | 222 | 228 | PF00069 | 0.403 |
| MOD_Plk_4 | 222 | 228 | PF00069 | 0.472 |
| MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.469 |
| MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.517 |
| MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.513 |
| MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.498 |
| TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.590 |
| TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.543 |
| TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.434 |
| TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.480 |
| TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.556 |
| TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.752 |
| TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.760 |
| TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.448 |
| TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.467 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PCF7 | Leptomonas seymouri | 57% | 100% |
| A0A1X0NWV8 | Trypanosomatidae | 34% | 100% |
| A0A3S7WYC1 | Leishmania donovani | 90% | 100% |
| A4I0S5 | Leishmania infantum | 90% | 100% |
| D0A755 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| E9AIG8 | Leishmania braziliensis | 74% | 85% |
| E9AWS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |