| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B0K1
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.488 |
| CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.601 |
| CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.548 |
| CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.494 |
| CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.623 |
| CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.754 |
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.652 |
| CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.636 |
| CLV_PCSK_PC1ET2_1 | 55 | 57 | PF00082 | 0.598 |
| CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.652 |
| CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.592 |
| CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.552 |
| DEG_COP1_1 | 69 | 78 | PF00400 | 0.513 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.678 |
| DEG_SCF_FBW7_1 | 68 | 74 | PF00400 | 0.558 |
| DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.502 |
| DOC_CKS1_1 | 68 | 73 | PF01111 | 0.480 |
| DOC_PP1_RVXF_1 | 12 | 19 | PF00149 | 0.671 |
| DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.549 |
| DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.545 |
| DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.782 |
| DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.673 |
| DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.641 |
| DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.590 |
| LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.427 |
| LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.607 |
| LIG_FHA_1 | 113 | 119 | PF00498 | 0.692 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.413 |
| LIG_FHA_1 | 99 | 105 | PF00498 | 0.484 |
| LIG_LIR_Gen_1 | 146 | 155 | PF02991 | 0.531 |
| LIG_LIR_Gen_1 | 214 | 225 | PF02991 | 0.381 |
| LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.534 |
| LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.327 |
| LIG_NRBOX | 103 | 109 | PF00104 | 0.548 |
| LIG_SH2_CRK | 205 | 209 | PF00017 | 0.372 |
| LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.357 |
| LIG_SH2_PTP2 | 263 | 266 | PF00017 | 0.471 |
| LIG_SH2_SRC | 123 | 126 | PF00017 | 0.610 |
| LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.521 |
| LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.471 |
| LIG_SH3_3 | 175 | 181 | PF00018 | 0.433 |
| LIG_SH3_3 | 184 | 190 | PF00018 | 0.485 |
| LIG_SH3_3 | 65 | 71 | PF00018 | 0.691 |
| LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.574 |
| LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.651 |
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.554 |
| MOD_CK1_1 | 166 | 172 | PF00069 | 0.488 |
| MOD_CK1_1 | 64 | 70 | PF00069 | 0.690 |
| MOD_CK2_1 | 131 | 137 | PF00069 | 0.461 |
| MOD_CK2_1 | 140 | 146 | PF00069 | 0.470 |
| MOD_CK2_1 | 150 | 156 | PF00069 | 0.462 |
| MOD_CMANNOS | 15 | 18 | PF00535 | 0.600 |
| MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.663 |
| MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.432 |
| MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.581 |
| MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.390 |
| MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.723 |
| MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.644 |
| MOD_GSK3_1 | 108 | 115 | PF00069 | 0.606 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.600 |
| MOD_GSK3_1 | 166 | 173 | PF00069 | 0.497 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.346 |
| MOD_GSK3_1 | 219 | 226 | PF00069 | 0.432 |
| MOD_GSK3_1 | 248 | 255 | PF00069 | 0.336 |
| MOD_GSK3_1 | 62 | 69 | PF00069 | 0.693 |
| MOD_GSK3_1 | 74 | 81 | PF00069 | 0.624 |
| MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.513 |
| MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.328 |
| MOD_NEK2_1 | 108 | 113 | PF00069 | 0.513 |
| MOD_NEK2_1 | 150 | 155 | PF00069 | 0.640 |
| MOD_NEK2_1 | 163 | 168 | PF00069 | 0.502 |
| MOD_NEK2_1 | 212 | 217 | PF00069 | 0.497 |
| MOD_NEK2_1 | 61 | 66 | PF00069 | 0.709 |
| MOD_NEK2_2 | 47 | 52 | PF00069 | 0.659 |
| MOD_PK_1 | 22 | 28 | PF00069 | 0.750 |
| MOD_PKA_1 | 55 | 61 | PF00069 | 0.609 |
| MOD_PKA_2 | 112 | 118 | PF00069 | 0.549 |
| MOD_PKA_2 | 163 | 169 | PF00069 | 0.606 |
| MOD_PKA_2 | 55 | 61 | PF00069 | 0.522 |
| MOD_PKB_1 | 5 | 13 | PF00069 | 0.481 |
| MOD_Plk_1 | 269 | 275 | PF00069 | 0.335 |
| MOD_Plk_1 | 47 | 53 | PF00069 | 0.670 |
| MOD_Plk_4 | 128 | 134 | PF00069 | 0.651 |
| MOD_Plk_4 | 170 | 176 | PF00069 | 0.435 |
| MOD_Plk_4 | 212 | 218 | PF00069 | 0.294 |
| MOD_Plk_4 | 22 | 28 | PF00069 | 0.637 |
| MOD_Plk_4 | 269 | 275 | PF00069 | 0.423 |
| MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.644 |
| MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.588 |
| MOD_SUMO_rev_2 | 77 | 83 | PF00179 | 0.515 |
| TRG_DiLeu_BaEn_1 | 103 | 108 | PF01217 | 0.571 |
| TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.621 |
| TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.662 |
| TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.618 |
| TRG_NLS_MonoExtC_3 | 90 | 95 | PF00514 | 0.497 |
| TRG_NLS_MonoExtN_4 | 89 | 95 | PF00514 | 0.496 |
| TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.488 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PFH4 | Leptomonas seymouri | 50% | 100% |
| A0A0S4JGE4 | Bodo saltans | 30% | 81% |
| A0A1X0P245 | Trypanosomatidae | 33% | 89% |
| A0A3S7X369 | Leishmania donovani | 93% | 100% |
| A0A422P4T3 | Trypanosoma rangeli | 35% | 99% |
| A4HI29 | Leishmania braziliensis | 83% | 100% |
| A4I5A5 | Leishmania infantum | 92% | 100% |
| C9ZQN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 97% |
| Q4Q7N1 | Leishmania major | 92% | 100% |
| V5BUA0 | Trypanosoma cruzi | 36% | 99% |