| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 2 |
| Forrest at al. (procyclic) | no | yes: 2 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 12 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 1, no: 10 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000813 | ESCRT I complex | 3 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0036452 | ESCRT complex | 2 | 12 |
| GO:0098796 | membrane protein complex | 2 | 12 |
Related structures:
AlphaFold database: A4HG97
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 12 |
| GO:0008104 | protein localization | 4 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009056 | catabolic process | 2 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0015031 | protein transport | 4 | 12 |
| GO:0033036 | macromolecule localization | 2 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044248 | cellular catabolic process | 3 | 12 |
| GO:0045184 | establishment of protein localization | 3 | 12 |
| GO:0051179 | localization | 1 | 12 |
| GO:0051234 | establishment of localization | 2 | 12 |
| GO:0051641 | cellular localization | 2 | 12 |
| GO:0070727 | cellular macromolecule localization | 3 | 12 |
| GO:0071702 | organic substance transport | 4 | 12 |
| GO:0071705 | nitrogen compound transport | 4 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.559 |
| CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.484 |
| CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.473 |
| CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.556 |
| CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.379 |
| CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.439 |
| CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.414 |
| CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.455 |
| CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.518 |
| DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.328 |
| DOC_CKS1_1 | 216 | 221 | PF01111 | 0.392 |
| DOC_CKS1_1 | 74 | 79 | PF01111 | 0.547 |
| DOC_MAPK_gen_1 | 231 | 240 | PF00069 | 0.376 |
| DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.540 |
| DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.223 |
| DOC_USP7_UBL2_3 | 263 | 267 | PF12436 | 0.401 |
| DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.458 |
| DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.362 |
| DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.551 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.493 |
| LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.437 |
| LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.557 |
| LIG_FHA_1 | 122 | 128 | PF00498 | 0.553 |
| LIG_FHA_1 | 129 | 135 | PF00498 | 0.519 |
| LIG_FHA_1 | 17 | 23 | PF00498 | 0.584 |
| LIG_FHA_1 | 92 | 98 | PF00498 | 0.501 |
| LIG_FHA_2 | 163 | 169 | PF00498 | 0.369 |
| LIG_FHA_2 | 223 | 229 | PF00498 | 0.469 |
| LIG_FHA_2 | 94 | 100 | PF00498 | 0.508 |
| LIG_IRF3_LxIS_1 | 33 | 40 | PF10401 | 0.459 |
| LIG_LIR_Gen_1 | 254 | 262 | PF02991 | 0.358 |
| LIG_LIR_Gen_1 | 48 | 58 | PF02991 | 0.425 |
| LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.502 |
| LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.358 |
| LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.409 |
| LIG_PCNA_yPIPBox_3 | 151 | 163 | PF02747 | 0.475 |
| LIG_SH2_CRK | 150 | 154 | PF00017 | 0.344 |
| LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.431 |
| LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.426 |
| LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.344 |
| LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.410 |
| LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.528 |
| LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.449 |
| LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.413 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.355 |
| LIG_SH3_3 | 111 | 117 | PF00018 | 0.481 |
| LIG_SH3_3 | 136 | 142 | PF00018 | 0.385 |
| LIG_SH3_3 | 213 | 219 | PF00018 | 0.410 |
| LIG_SH3_3 | 48 | 54 | PF00018 | 0.424 |
| LIG_SH3_3 | 71 | 77 | PF00018 | 0.561 |
| LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.600 |
| LIG_UBA3_1 | 271 | 275 | PF00899 | 0.399 |
| MOD_CK1_1 | 119 | 125 | PF00069 | 0.509 |
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.474 |
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.385 |
| MOD_CK1_1 | 20 | 26 | PF00069 | 0.520 |
| MOD_CK1_1 | 215 | 221 | PF00069 | 0.385 |
| MOD_CK1_1 | 91 | 97 | PF00069 | 0.539 |
| MOD_CK2_1 | 162 | 168 | PF00069 | 0.417 |
| MOD_CK2_1 | 22 | 28 | PF00069 | 0.489 |
| MOD_CK2_1 | 93 | 99 | PF00069 | 0.524 |
| MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.446 |
| MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.578 |
| MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.546 |
| MOD_GSK3_1 | 121 | 128 | PF00069 | 0.544 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.511 |
| MOD_GSK3_1 | 211 | 218 | PF00069 | 0.312 |
| MOD_GSK3_1 | 45 | 52 | PF00069 | 0.487 |
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.582 |
| MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.449 |
| MOD_NEK2_1 | 212 | 217 | PF00069 | 0.354 |
| MOD_NEK2_1 | 49 | 54 | PF00069 | 0.426 |
| MOD_NEK2_2 | 45 | 50 | PF00069 | 0.477 |
| MOD_PIKK_1 | 199 | 205 | PF00454 | 0.449 |
| MOD_PKA_1 | 159 | 165 | PF00069 | 0.223 |
| MOD_PKA_1 | 231 | 237 | PF00069 | 0.456 |
| MOD_PKA_1 | 275 | 281 | PF00069 | 0.562 |
| MOD_PKA_2 | 162 | 168 | PF00069 | 0.453 |
| MOD_PKA_2 | 275 | 281 | PF00069 | 0.562 |
| MOD_Plk_1 | 174 | 180 | PF00069 | 0.409 |
| MOD_Plk_2-3 | 182 | 188 | PF00069 | 0.463 |
| MOD_Plk_4 | 17 | 23 | PF00069 | 0.496 |
| MOD_Plk_4 | 26 | 32 | PF00069 | 0.431 |
| MOD_Plk_4 | 45 | 51 | PF00069 | 0.204 |
| MOD_Plk_4 | 93 | 99 | PF00069 | 0.468 |
| MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.362 |
| MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.549 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.503 |
| MOD_SUMO_rev_2 | 182 | 190 | PF00179 | 0.223 |
| MOD_SUMO_rev_2 | 268 | 277 | PF00179 | 0.203 |
| TRG_DiLeu_BaEn_1 | 130 | 135 | PF01217 | 0.575 |
| TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.213 |
| TRG_DiLeu_LyEn_5 | 130 | 135 | PF01217 | 0.575 |
| TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.403 |
| TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.539 |
| TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.449 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1Q4 | Leptomonas seymouri | 78% | 100% |
| A0A0S4JBQ7 | Bodo saltans | 30% | 100% |
| A0A1X0NYI9 | Trypanosomatidae | 42% | 100% |
| A0A3S7X186 | Leishmania donovani | 86% | 100% |
| A0A422P1P4 | Trypanosoma rangeli | 38% | 100% |
| A4I3D0 | Leishmania infantum | 86% | 100% |
| D0A814 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| E9AZL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
| Q4Q8L4 | Leishmania major | 85% | 100% |
| V5DH66 | Trypanosoma cruzi | 41% | 93% |