| 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: 4 |
| Pissara et al. | no | yes: 20 |
| 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: 24 |
| NetGPI | no | yes: 0, no: 24 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005929 | cilium | 4 | 2 |
| GO:0031514 | motile cilium | 5 | 2 |
| GO:0042995 | cell projection | 2 | 2 |
| GO:0043226 | organelle | 2 | 2 |
| GO:0043227 | membrane-bounded organelle | 3 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 4 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
| GO:0005815 | microtubule organizing center | 2 | 1 |
| GO:0005816 | spindle pole body | 3 | 1 |
| GO:0036064 | ciliary basal body | 3 | 1 |
| GO:0044732 | mitotic spindle pole body | 4 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AVX2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 1 |
| GO:0006897 | endocytosis | 5 | 1 |
| GO:0016192 | vesicle-mediated transport | 4 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.258 |
| CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.608 |
| CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.483 |
| CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.662 |
| CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.369 |
| CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.418 |
| CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.418 |
| CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.313 |
| CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.369 |
| CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.418 |
| CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.313 |
| CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.701 |
| CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.615 |
| DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.545 |
| DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.617 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.356 |
| DOC_CYCLIN_RxL_1 | 5 | 16 | PF00134 | 0.600 |
| DOC_CYCLIN_yCln2_LP_2 | 11 | 17 | PF00134 | 0.615 |
| DOC_MAPK_FxFP_2 | 93 | 96 | PF00069 | 0.523 |
| DOC_MAPK_gen_1 | 234 | 243 | PF00069 | 0.201 |
| DOC_PP1_RVXF_1 | 20 | 26 | PF00149 | 0.424 |
| DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.523 |
| DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.317 |
| DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.474 |
| DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.492 |
| DOC_USP7_UBL2_3 | 159 | 163 | PF12436 | 0.394 |
| LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.363 |
| LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.552 |
| LIG_deltaCOP1_diTrp_1 | 293 | 299 | PF00928 | 0.381 |
| LIG_deltaCOP1_diTrp_1 | 31 | 37 | PF00928 | 0.311 |
| LIG_FHA_1 | 302 | 308 | PF00498 | 0.490 |
| LIG_FHA_1 | 397 | 403 | PF00498 | 0.670 |
| LIG_FHA_2 | 215 | 221 | PF00498 | 0.256 |
| LIG_Integrin_RGDW_4 | 197 | 200 | PF00362 | 0.377 |
| LIG_LIR_Apic_2 | 210 | 214 | PF02991 | 0.381 |
| LIG_LIR_Apic_2 | 304 | 308 | PF02991 | 0.462 |
| LIG_LIR_Apic_2 | 92 | 96 | PF02991 | 0.526 |
| LIG_LIR_Gen_1 | 88 | 96 | PF02991 | 0.444 |
| LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.445 |
| LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.426 |
| LIG_SH2_CRK | 147 | 151 | PF00017 | 0.498 |
| LIG_SH2_CRK | 273 | 277 | PF00017 | 0.396 |
| LIG_SH2_GRB2like | 321 | 324 | PF00017 | 0.258 |
| LIG_SH2_SRC | 211 | 214 | PF00017 | 0.369 |
| LIG_SH2_SRC | 321 | 324 | PF00017 | 0.258 |
| LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.297 |
| LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.363 |
| LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.274 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.313 |
| LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.343 |
| LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.314 |
| LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.511 |
| LIG_SH2_STAT6 | 89 | 93 | PF00017 | 0.518 |
| LIG_SUMO_SIM_par_1 | 65 | 73 | PF11976 | 0.481 |
| LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.499 |
| MOD_CK1_1 | 256 | 262 | PF00069 | 0.438 |
| MOD_CK1_1 | 335 | 341 | PF00069 | 0.521 |
| MOD_CK2_1 | 214 | 220 | PF00069 | 0.237 |
| MOD_Cter_Amidation | 323 | 326 | PF01082 | 0.348 |
| MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.420 |
| MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.357 |
| MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.323 |
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.285 |
| MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.339 |
| MOD_GSK3_1 | 255 | 262 | PF00069 | 0.452 |
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.524 |
| MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.407 |
| MOD_NEK2_1 | 117 | 122 | PF00069 | 0.505 |
| MOD_NEK2_2 | 272 | 277 | PF00069 | 0.278 |
| MOD_PIKK_1 | 117 | 123 | PF00454 | 0.343 |
| MOD_PKA_1 | 315 | 321 | PF00069 | 0.264 |
| MOD_PKA_2 | 117 | 123 | PF00069 | 0.496 |
| MOD_PKA_2 | 230 | 236 | PF00069 | 0.318 |
| MOD_PKA_2 | 265 | 271 | PF00069 | 0.512 |
| MOD_PKA_2 | 301 | 307 | PF00069 | 0.481 |
| MOD_PKA_2 | 315 | 321 | PF00069 | 0.346 |
| MOD_PKA_2 | 80 | 86 | PF00069 | 0.502 |
| MOD_PKB_1 | 79 | 87 | PF00069 | 0.550 |
| MOD_Plk_1 | 178 | 184 | PF00069 | 0.387 |
| MOD_Plk_1 | 5 | 11 | PF00069 | 0.609 |
| MOD_Plk_4 | 151 | 157 | PF00069 | 0.320 |
| MOD_Plk_4 | 207 | 213 | PF00069 | 0.313 |
| MOD_SUMO_rev_2 | 144 | 150 | PF00179 | 0.411 |
| MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.354 |
| TRG_DiLeu_BaLyEn_6 | 410 | 415 | PF01217 | 0.559 |
| TRG_DiLeu_BaLyEn_6 | 6 | 11 | PF01217 | 0.616 |
| TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.478 |
| TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.425 |
| TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.434 |
| TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.377 |
| TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.258 |
| TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.419 |
| TRG_LysEnd_GGAAcLL_1 | 411 | 417 | PF00790 | 0.494 |
| TRG_NES_CRM1_1 | 66 | 80 | PF08389 | 0.492 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IIF6 | Leptomonas seymouri | 77% | 73% |
| A0A0N1IIK8 | Leptomonas seymouri | 36% | 100% |
| A0A0S4J443 | Bodo saltans | 26% | 94% |
| A0A0S4JES9 | Bodo saltans | 30% | 82% |
| A0A0S4KIY0 | Bodo saltans | 35% | 100% |
| A0A0S4KKM9 | Bodo saltans | 30% | 78% |
| A0A1X0NTG8 | Trypanosomatidae | 43% | 95% |
| A0A1X0P1A5 | Trypanosomatidae | 37% | 100% |
| A0A3R7NAK8 | Trypanosoma rangeli | 45% | 100% |
| A0A3S7WXA1 | Leishmania donovani | 93% | 79% |
| A0A3S7X3U7 | Leishmania donovani | 36% | 100% |
| A0A422P0W0 | Trypanosoma rangeli | 35% | 100% |
| A4HCH7 | Leishmania braziliensis | 88% | 100% |
| A4HIR9 | Leishmania braziliensis | 36% | 100% |
| A4HZZ9 | Leishmania infantum | 93% | 79% |
| A4I615 | Leishmania infantum | 36% | 100% |
| C9ZRE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
| C9ZSQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 95% |
| E9ATG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| E9B1A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| Q4Q137 | Leishmania major | 24% | 100% |
| Q4Q6V8 | Leishmania major | 36% | 100% |
| Q4QBK7 | Leishmania major | 92% | 100% |