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: A4HHV6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.279 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.374 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.310 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.328 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.633 |
DOC_ANK_TNKS_1 | 97 | 104 | PF00023 | 0.331 |
DOC_CDC14_PxL_1 | 225 | 233 | PF14671 | 0.489 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.554 |
DOC_CYCLIN_RxL_1 | 370 | 383 | PF00134 | 0.329 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.330 |
DOC_MAPK_FxFP_2 | 410 | 413 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 220 | 230 | PF00069 | 0.283 |
DOC_MAPK_gen_1 | 384 | 391 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 69 | 77 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 69 | 77 | PF00069 | 0.555 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.524 |
DOC_USP7_MATH_2 | 170 | 176 | PF00917 | 0.327 |
DOC_USP7_MATH_2 | 289 | 295 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 148 | 155 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 186 | 195 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 375 | 380 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 396 | 401 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.483 |
LIG_Actin_WH2_1 | 264 | 280 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 273 | 290 | PF00022 | 0.273 |
LIG_BRCT_BRCA1_1 | 406 | 410 | PF00533 | 0.569 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.320 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.488 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.484 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.464 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.535 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.510 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.513 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.502 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.435 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.482 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.408 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.511 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.519 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.514 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.537 |
LIG_LIR_Apic_2 | 196 | 200 | PF02991 | 0.484 |
LIG_LIR_Apic_2 | 407 | 413 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.496 |
LIG_LIR_LC3C_4 | 175 | 178 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.485 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.475 |
LIG_Rb_LxCxE_1 | 378 | 394 | PF01857 | 0.298 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.548 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.517 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.556 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.538 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.414 |
LIG_SH3_4 | 199 | 206 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 263 | 269 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 163 | 169 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 232 | 238 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 375 | 380 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 421 | 427 | PF11976 | 0.328 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.419 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.542 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.505 |
MOD_CDK_SPxxK_3 | 368 | 375 | PF00069 | 0.301 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.504 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.493 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.537 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.542 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.340 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.522 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.554 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.443 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.518 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.538 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.532 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.466 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.522 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.500 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.505 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.408 |
MOD_GlcNHglycan | 49 | 53 | PF01048 | 0.594 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.523 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.530 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.467 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.532 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.442 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.302 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.528 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.470 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.497 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.610 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.485 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.514 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.483 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.444 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.496 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.429 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.420 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.455 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.449 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.412 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.540 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.448 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.508 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.449 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.320 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.552 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.275 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.518 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.427 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.480 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.476 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.532 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.482 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.418 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.540 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.279 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.507 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.506 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.448 |
MOD_PKB_1 | 42 | 50 | PF00069 | 0.415 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.502 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.541 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.528 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.479 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.477 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.487 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.338 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.562 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.544 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.551 |
TRG_DiLeu_BaEn_1 | 172 | 177 | PF01217 | 0.311 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_2 | 290 | 296 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 261 | 266 | PF01217 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.561 |
TRG_DiLeu_LyEn_5 | 180 | 185 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.538 |
TRG_NES_CRM1_1 | 270 | 281 | PF08389 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2N3 | Leptomonas seymouri | 47% | 99% |
A0A1X0P2E5 | Trypanosomatidae | 27% | 100% |
A0A3Q8IEP2 | Leishmania donovani | 78% | 100% |
A4I506 | Leishmania infantum | 78% | 100% |
C9ZQF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 98% |
E9B0D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q7U4 | Leishmania major | 79% | 100% |
V5BLE7 | Trypanosoma cruzi | 27% | 100% |