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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HD29
Term | Name | Level | Count |
---|---|---|---|
GO:0003341 | cilium movement | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0030030 | cell projection organization | 4 | 12 |
GO:0030031 | cell projection assembly | 5 | 12 |
GO:0044782 | cilium organization | 5 | 12 |
GO:0060271 | cilium assembly | 6 | 12 |
GO:0070925 | organelle assembly | 5 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 12 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.190 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.453 |
CLV_PCSK_FUR_1 | 112 | 116 | PF00082 | 0.581 |
CLV_PCSK_FUR_1 | 14 | 18 | PF00082 | 0.509 |
CLV_PCSK_FUR_1 | 410 | 414 | PF00082 | 0.301 |
CLV_PCSK_FUR_1 | 71 | 75 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.201 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.547 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.443 |
DOC_CDC14_PxL_1 | 475 | 483 | PF14671 | 0.486 |
DOC_MAPK_gen_1 | 471 | 480 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 3 | 10 | PF00069 | 0.444 |
DOC_MAPK_NFAT4_5 | 3 | 11 | PF00069 | 0.437 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.487 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 255 | 272 | PF00022 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 342 | 352 | PF00928 | 0.491 |
LIG_eIF4E_1 | 475 | 481 | PF01652 | 0.477 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.428 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.400 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 276 | 284 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 55 | 62 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.544 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.496 |
LIG_PCNA_yPIPBox_3 | 43 | 57 | PF02747 | 0.584 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.639 |
LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.400 |
LIG_RPA_C_Fungi | 68 | 80 | PF08784 | 0.333 |
LIG_RPA_C_Plants | 303 | 314 | PF08784 | 0.378 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.449 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 155 | 159 | PF00017 | 0.223 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.344 |
LIG_SH3_1 | 476 | 482 | PF00018 | 0.454 |
LIG_SH3_2 | 479 | 484 | PF14604 | 0.507 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.454 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.223 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.605 |
LIG_UBA3_1 | 262 | 270 | PF00899 | 0.449 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.665 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.627 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.669 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.382 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.634 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.223 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.223 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.223 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.413 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.423 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.606 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.392 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.627 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.223 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.575 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.475 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.381 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.625 |
MOD_PKB_1 | 410 | 418 | PF00069 | 0.223 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.505 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.223 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.627 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.223 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.691 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.576 |
MOD_SUMO_for_1 | 113 | 116 | PF00179 | 0.509 |
MOD_SUMO_for_1 | 280 | 283 | PF00179 | 0.466 |
MOD_SUMO_for_1 | 470 | 473 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 116 | 121 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 193 | 199 | PF00179 | 0.223 |
MOD_SUMO_rev_2 | 264 | 272 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 46 | 53 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_1 | 232 | 237 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 476 | 481 | PF01217 | 0.482 |
TRG_DiLeu_LyEn_5 | 232 | 237 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.453 |
TRG_NLS_MonoExtN_4 | 197 | 204 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 482 | 487 | PF00514 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 388 | 393 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD5 | Leptomonas seymouri | 73% | 100% |
A0A0S4IRE4 | Bodo saltans | 38% | 99% |
A0A1X0NWN4 | Trypanosomatidae | 49% | 100% |
A0A3Q8IMD7 | Leishmania donovani | 85% | 100% |
A0A422NJE4 | Trypanosoma rangeli | 49% | 100% |
A4I0L6 | Leishmania infantum | 85% | 100% |
C9ZNQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AWH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QAZ3 | Leishmania major | 85% | 100% |
V5D760 | Trypanosoma cruzi | 51% | 100% |