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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 9, no: 2 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WTD0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.122 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.306 |
CLV_PCSK_FUR_1 | 226 | 230 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.384 |
DEG_APCC_DBOX_1 | 22 | 30 | PF00400 | 0.471 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.366 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.555 |
DOC_CYCLIN_RxL_1 | 19 | 28 | PF00134 | 0.471 |
DOC_CYCLIN_RxL_1 | 279 | 289 | PF00134 | 0.411 |
DOC_CYCLIN_RxL_1 | 431 | 443 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.452 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.498 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 152 | 156 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.306 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 176 | 184 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.526 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.453 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.521 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.374 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.372 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.527 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 181 | 187 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 316 | 327 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.468 |
LIG_LIR_LC3C_4 | 28 | 32 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.518 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.347 |
LIG_NRBOX | 25 | 31 | PF00104 | 0.585 |
LIG_Pex14_2 | 519 | 523 | PF04695 | 0.695 |
LIG_Pex14_2 | 527 | 531 | PF04695 | 0.668 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.666 |
LIG_Pex14_2 | 543 | 547 | PF04695 | 0.437 |
LIG_REV1ctd_RIR_1 | 562 | 570 | PF16727 | 0.634 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.553 |
LIG_SH2_CRK | 435 | 439 | PF00017 | 0.306 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.306 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.507 |
LIG_SH2_GRB2like | 501 | 504 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 17 | 21 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.549 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.360 |
LIG_SH2_SRC | 501 | 504 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 338 | 341 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.362 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.587 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.537 |
LIG_SUMO_SIM_anti_2 | 206 | 212 | PF11976 | 0.384 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.622 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.397 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.520 |
LIG_UBA3_1 | 113 | 118 | PF00899 | 0.368 |
LIG_UBA3_1 | 306 | 312 | PF00899 | 0.438 |
LIG_UBA3_1 | 437 | 442 | PF00899 | 0.426 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.457 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.570 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.532 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.568 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.515 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.517 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.307 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.344 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.272 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.567 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.376 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.577 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.370 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.649 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.398 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.306 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.364 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.398 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.664 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.589 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.504 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.568 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.303 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.227 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.748 |
MOD_NEK2_2 | 349 | 354 | PF00069 | 0.399 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.455 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.527 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.566 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.498 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.526 |
MOD_PK_1 | 216 | 222 | PF00069 | 0.313 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.400 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.515 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.640 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.420 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.450 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.517 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.467 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.592 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.500 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.394 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.559 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.437 |
MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.573 |
MOD_SUMO_for_1 | 84 | 87 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 139 | 147 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 311 | 319 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 407 | 415 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 484 | 491 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 494 | 499 | PF00179 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.297 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.341 |
TRG_NES_CRM1_1 | 209 | 224 | PF08389 | 0.436 |
TRG_NES_CRM1_1 | 275 | 289 | PF08389 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 282 | 287 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0D1E2P6 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 98% |
A0A0D2XVZ5 | Fusarium oxysporum f. sp. lycopersici (strain 4287 / CBS 123668 / FGSC 9935 / NRRL 34936) | 28% | 100% |
A0A0N1PCC0 | Leptomonas seymouri | 66% | 100% |
A0A0N1PF59 | Leptomonas seymouri | 26% | 100% |
A0A0P0VG31 | Oryza sativa subsp. japonica | 29% | 100% |
A0A0S4JQ76 | Bodo saltans | 45% | 100% |
A0A1X0NP19 | Trypanosomatidae | 44% | 100% |
A0A422NFP3 | Trypanosoma rangeli | 48% | 100% |
A4H7V3 | Leishmania braziliensis | 85% | 100% |
A4HW79 | Leishmania infantum | 99% | 100% |
C9ZST7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9APY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
J9VKM5 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 27% | 100% |
Q13217 | Homo sapiens | 29% | 100% |
Q27968 | Bos taurus | 28% | 100% |
Q4QFK1 | Leishmania major | 93% | 99% |
Q54M21 | Dictyostelium discoideum | 26% | 100% |
Q5JNB5 | Oryza sativa subsp. japonica | 29% | 100% |
Q5R8D8 | Pongo abelii | 23% | 100% |
Q5ZI13 | Gallus gallus | 28% | 100% |
Q91YW3 | Mus musculus | 28% | 100% |
Q99615 | Homo sapiens | 23% | 100% |
Q9QYI3 | Mus musculus | 23% | 100% |
Q9R0T3 | Rattus norvegicus | 28% | 100% |
V5BKH0 | Trypanosoma cruzi | 48% | 100% |