| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S7X093
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.572 |
| CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.509 |
| CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.544 |
| CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.683 |
| CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.546 |
| CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.503 |
| CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.466 |
| CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.440 |
| CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.717 |
| CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.461 |
| CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.570 |
| CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.425 |
| DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.436 |
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.563 |
| DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.615 |
| DOC_USP7_UBL2_3 | 78 | 82 | PF12436 | 0.562 |
| DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.563 |
| LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.430 |
| LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.350 |
| LIG_Actin_WH2_2 | 102 | 120 | PF00022 | 0.476 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.428 |
| LIG_FHA_1 | 24 | 30 | PF00498 | 0.501 |
| LIG_FHA_1 | 49 | 55 | PF00498 | 0.542 |
| LIG_SH2_GRB2like | 91 | 94 | PF00017 | 0.553 |
| LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.553 |
| LIG_SH3_3 | 113 | 119 | PF00018 | 0.537 |
| LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.378 |
| LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.618 |
| LIG_SUMO_SIM_par_1 | 60 | 66 | PF11976 | 0.479 |
| LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.389 |
| LIG_UBA3_1 | 72 | 78 | PF00899 | 0.474 |
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.547 |
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.554 |
| MOD_CK2_1 | 25 | 31 | PF00069 | 0.387 |
| MOD_Cter_Amidation | 146 | 149 | PF01082 | 0.753 |
| MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.447 |
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.531 |
| MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.606 |
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.627 |
| MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.489 |
| MOD_NEK2_2 | 124 | 129 | PF00069 | 0.463 |
| MOD_PKA_2 | 117 | 123 | PF00069 | 0.630 |
| MOD_PKA_2 | 96 | 102 | PF00069 | 0.535 |
| MOD_Plk_1 | 48 | 54 | PF00069 | 0.535 |
| MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.558 |
| MOD_SUMO_rev_2 | 49 | 59 | PF00179 | 0.571 |
| TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.613 |
| TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.426 |
| TRG_DiLeu_LyEn_5 | 49 | 54 | PF01217 | 0.464 |
| TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.555 |
| TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.466 |
| TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.476 |
| TRG_ER_diLys_1 | 148 | 151 | PF00400 | 0.598 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PDC7 | Leptomonas seymouri | 76% | 100% |
| A0A0S4JH37 | Bodo saltans | 37% | 100% |
| A0A1X0NEM8 | Trypanosomatidae | 52% | 100% |
| A0A3R7R8R4 | Trypanosoma rangeli | 52% | 100% |
| A4HFA2 | Leishmania braziliensis | 83% | 100% |
| C9ZX03 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 97% |
| E9AYN9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| Q4Q8T3 | Leishmania major | 96% | 100% |