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 |
Related structures:
AlphaFold database: E9AUA6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.433 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.423 |
DEG_SCF_FBW7_1 | 435 | 441 | PF00400 | 0.449 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.629 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.612 |
DOC_CDC14_PxL_1 | 252 | 260 | PF14671 | 0.597 |
DOC_CKS1_1 | 407 | 412 | PF01111 | 0.451 |
DOC_CKS1_1 | 435 | 440 | PF01111 | 0.449 |
DOC_CYCLIN_RxL_1 | 182 | 195 | PF00134 | 0.572 |
DOC_CYCLIN_RxL_1 | 390 | 402 | PF00134 | 0.422 |
DOC_CYCLIN_RxL_1 | 458 | 469 | PF00134 | 0.594 |
DOC_MAPK_DCC_7 | 250 | 260 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 144 | 151 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 393 | 400 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.580 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 144 | 148 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 333 | 343 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 443 | 448 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.623 |
LIG_Actin_WH2_2 | 145 | 160 | PF00022 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 178 | 184 | PF00928 | 0.437 |
LIG_eIF4E_1 | 72 | 78 | PF01652 | 0.483 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.560 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.627 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.540 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.581 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.580 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.458 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.366 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.288 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.562 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.661 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.419 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.609 |
LIG_GBD_Chelix_1 | 459 | 467 | PF00786 | 0.390 |
LIG_GLEBS_BUB3_1 | 123 | 131 | PF00400 | 0.588 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 466 | 473 | PF02991 | 0.662 |
LIG_LIR_LC3C_4 | 111 | 116 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.650 |
LIG_PDZ_Class_2 | 468 | 473 | PF00595 | 0.573 |
LIG_Pex14_1 | 132 | 136 | PF04695 | 0.629 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.535 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.638 |
LIG_Rb_pABgroove_1 | 395 | 403 | PF01858 | 0.397 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.630 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.593 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 18 | 21 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.528 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.569 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.641 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.649 |
LIG_TRFH_1 | 468 | 472 | PF08558 | 0.453 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.413 |
LIG_WW_1 | 370 | 373 | PF00397 | 0.573 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.771 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.481 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.409 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.681 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.584 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.583 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.273 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.580 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.549 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.455 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.362 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.592 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.378 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.604 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.687 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.622 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.682 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.654 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.428 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.280 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.668 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.537 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.329 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.420 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.681 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.400 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.426 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.505 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.631 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.599 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.351 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.610 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.505 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.448 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.439 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.753 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.388 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.470 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.560 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.543 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.510 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.504 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.560 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.519 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.263 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.405 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.498 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.519 |
MOD_PKB_1 | 82 | 90 | PF00069 | 0.626 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.688 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.528 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.440 |
MOD_Plk_2-3 | 172 | 178 | PF00069 | 0.262 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.511 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.435 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.431 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.327 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.520 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.566 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.480 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.464 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.277 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.576 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.449 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 365 | 371 | PF00179 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 245 | 249 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 84 | 89 | PF00026 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR4 | Leptomonas seymouri | 66% | 98% |
A0A0S4ISX7 | Bodo saltans | 27% | 98% |
A0A1X0NN06 | Trypanosomatidae | 44% | 100% |
A0A3Q8IM62 | Leishmania donovani | 93% | 100% |
A0A3R7MQC3 | Trypanosoma rangeli | 44% | 100% |
A4HQJ3 | Leishmania braziliensis | 83% | 100% |
D0A3P1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AI02 | Leishmania infantum | 93% | 100% |
Q4Q085 | Leishmania major | 92% | 100% |
V5BHM6 | Trypanosoma cruzi | 42% | 100% |