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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 10 |
GO:0042995 | cell projection | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 10 |
Related structures:
AlphaFold database: A0A3Q8IEP2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.484 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.599 |
DEG_SCF_FBW7_1 | 368 | 375 | PF00400 | 0.468 |
DOC_CDC14_PxL_1 | 225 | 233 | PF14671 | 0.488 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 390 | 400 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 393 | 403 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 69 | 77 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 69 | 77 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 391 | 398 | PF00149 | 0.488 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 148 | 155 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 186 | 195 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 396 | 402 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.497 |
LIG_Actin_WH2_1 | 264 | 280 | PF00022 | 0.532 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.515 |
LIG_eIF4E_1 | 410 | 416 | PF01652 | 0.384 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.551 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.464 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.470 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.529 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.520 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.636 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.501 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.539 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.459 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.503 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.462 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.476 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.489 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.512 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.492 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.554 |
LIG_LIR_Apic_2 | 407 | 413 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.502 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.466 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.539 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.561 |
LIG_SH2_SRC | 54 | 57 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.557 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.543 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.440 |
LIG_SH3_4 | 199 | 206 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 163 | 169 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 263 | 269 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 421 | 427 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 163 | 169 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 232 | 238 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 278 | 283 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 371 | 378 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.488 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.554 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.503 |
MOD_CDC14_SPxK_1 | 39 | 42 | PF00782 | 0.517 |
MOD_CDK_SPxK_1 | 36 | 42 | PF00069 | 0.503 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.510 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.423 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.546 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.431 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.588 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.530 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.520 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.382 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.340 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.418 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.481 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.541 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.447 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.603 |
MOD_GlcNHglycan | 281 | 285 | PF01048 | 0.443 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.526 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.514 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.453 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.433 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.544 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.446 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.517 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.541 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.477 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.458 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.537 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.519 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.519 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.447 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.515 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.459 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.424 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.405 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.382 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.216 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.477 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.459 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.506 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.456 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.538 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.421 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.520 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.580 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.472 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.483 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.531 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.538 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.483 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.533 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.464 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.484 |
MOD_PKB_1 | 137 | 145 | PF00069 | 0.526 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.523 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.647 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.565 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.481 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.476 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.428 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.399 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.561 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.550 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.539 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.507 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.547 |
MOD_SUMO_rev_2 | 57 | 62 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_1 | 363 | 368 | PF01217 | 0.325 |
TRG_DiLeu_BaEn_2 | 290 | 296 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 180 | 185 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 270 | 281 | PF08389 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2N3 | Leptomonas seymouri | 49% | 99% |
A0A1X0P2E5 | Trypanosomatidae | 27% | 100% |
A4HHV6 | Leishmania braziliensis | 78% | 100% |
A4I506 | Leishmania infantum | 99% | 100% |
C9ZQF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 98% |
E9B0D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q7U4 | Leishmania major | 93% | 100% |
V5BLE7 | Trypanosoma cruzi | 26% | 100% |