| 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: 5 |
| 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 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q301
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0019538 | protein metabolic process | 3 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0008233 | peptidase activity | 3 | 12 |
| GO:0008234 | cysteine-type peptidase activity | 4 | 12 |
| GO:0008242 | omega peptidase activity | 4 | 2 |
| GO:0016787 | hydrolase activity | 2 | 12 |
| GO:0016920 | pyroglutamyl-peptidase activity | 5 | 2 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.683 |
| CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.573 |
| CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.573 |
| CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.416 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.709 |
| DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.526 |
| DOC_MAPK_MEF2A_6 | 5 | 12 | PF00069 | 0.397 |
| DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.561 |
| DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.542 |
| LIG_14-3-3_CanoR_1 | 240 | 249 | PF00244 | 0.603 |
| LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.491 |
| LIG_APCC_ABBA_1 | 132 | 137 | PF00400 | 0.524 |
| LIG_APCC_ABBA_1 | 88 | 93 | PF00400 | 0.496 |
| LIG_Clathr_ClatBox_1 | 97 | 101 | PF01394 | 0.444 |
| LIG_deltaCOP1_diTrp_1 | 164 | 169 | PF00928 | 0.407 |
| LIG_FHA_1 | 169 | 175 | PF00498 | 0.601 |
| LIG_FHA_1 | 18 | 24 | PF00498 | 0.590 |
| LIG_FHA_1 | 67 | 73 | PF00498 | 0.560 |
| LIG_FHA_1 | 92 | 98 | PF00498 | 0.521 |
| LIG_FHA_2 | 159 | 165 | PF00498 | 0.579 |
| LIG_FHA_2 | 173 | 179 | PF00498 | 0.474 |
| LIG_FHA_2 | 241 | 247 | PF00498 | 0.610 |
| LIG_FHA_2 | 47 | 53 | PF00498 | 0.526 |
| LIG_LIR_Apic_2 | 193 | 197 | PF02991 | 0.376 |
| LIG_LIR_Gen_1 | 107 | 115 | PF02991 | 0.536 |
| LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.477 |
| LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.530 |
| LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.377 |
| LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.478 |
| LIG_Pex14_2 | 135 | 139 | PF04695 | 0.530 |
| LIG_SH2_CRK | 215 | 219 | PF00017 | 0.373 |
| LIG_SH2_CRK | 253 | 257 | PF00017 | 0.322 |
| LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.322 |
| LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.347 |
| LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.491 |
| LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.295 |
| LIG_SH3_3 | 121 | 127 | PF00018 | 0.508 |
| LIG_SH3_3 | 232 | 238 | PF00018 | 0.396 |
| LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.501 |
| LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.423 |
| LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.402 |
| MOD_CK1_1 | 181 | 187 | PF00069 | 0.649 |
| MOD_CK1_1 | 199 | 205 | PF00069 | 0.376 |
| MOD_CK1_1 | 54 | 60 | PF00069 | 0.494 |
| MOD_CK2_1 | 158 | 164 | PF00069 | 0.543 |
| MOD_CK2_1 | 172 | 178 | PF00069 | 0.568 |
| MOD_CK2_1 | 240 | 246 | PF00069 | 0.554 |
| MOD_CMANNOS | 166 | 169 | PF00535 | 0.409 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.749 |
| MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.241 |
| MOD_GSK3_1 | 158 | 165 | PF00069 | 0.501 |
| MOD_GSK3_1 | 168 | 175 | PF00069 | 0.579 |
| MOD_GSK3_1 | 177 | 184 | PF00069 | 0.547 |
| MOD_GSK3_1 | 195 | 202 | PF00069 | 0.549 |
| MOD_GSK3_1 | 254 | 261 | PF00069 | 0.507 |
| MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.533 |
| MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.478 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.548 |
| MOD_NEK2_1 | 108 | 113 | PF00069 | 0.530 |
| MOD_NEK2_1 | 135 | 140 | PF00069 | 0.500 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.472 |
| MOD_NEK2_2 | 17 | 22 | PF00069 | 0.589 |
| MOD_PKA_2 | 46 | 52 | PF00069 | 0.550 |
| MOD_PKA_2 | 66 | 72 | PF00069 | 0.331 |
| MOD_Plk_1 | 158 | 164 | PF00069 | 0.578 |
| MOD_Plk_1 | 51 | 57 | PF00069 | 0.432 |
| MOD_Plk_4 | 135 | 141 | PF00069 | 0.427 |
| MOD_Plk_4 | 254 | 260 | PF00069 | 0.466 |
| MOD_Plk_4 | 270 | 276 | PF00069 | 0.397 |
| MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.536 |
| MOD_SUMO_rev_2 | 110 | 120 | PF00179 | 0.602 |
| MOD_SUMO_rev_2 | 181 | 189 | PF00179 | 0.732 |
| TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.531 |
| TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.482 |
| TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.355 |
| TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.243 |
| TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.457 |
| TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.546 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8X3 | Leptomonas seymouri | 55% | 99% |
| A0A0S4JYF2 | Bodo saltans | 28% | 95% |
| A0A1X0P9S4 | Trypanosomatidae | 34% | 100% |
| A0A3R7R5B2 | Trypanosoma rangeli | 29% | 100% |
| A0A3S5H7W7 | Leishmania donovani | 89% | 100% |
| A4HAR3 | Leishmania braziliensis | 71% | 100% |
| A4I9X7 | Leishmania infantum | 90% | 100% |
| C9ZMR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| E9B4Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
| V5BNH8 | Trypanosoma cruzi | 29% | 100% |