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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AUY1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 621 | 625 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.655 |
CLV_PCSK_FUR_1 | 156 | 160 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 569 | 575 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.333 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.428 |
DEG_SCF_FBW7_1 | 364 | 371 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.376 |
DEG_SPOP_SBC_1 | 41 | 45 | PF00917 | 0.450 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.483 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.384 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.448 |
DOC_CYCLIN_RxL_1 | 155 | 165 | PF00134 | 0.351 |
DOC_CYCLIN_RxL_1 | 369 | 380 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 101 | 110 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 250 | 256 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 156 | 163 | PF00149 | 0.385 |
DOC_PP1_RVXF_1 | 210 | 216 | PF00149 | 0.366 |
DOC_PP1_RVXF_1 | 220 | 226 | PF00149 | 0.348 |
DOC_PP1_RVXF_1 | 262 | 269 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 370 | 377 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 450 | 457 | PF00149 | 0.380 |
DOC_PP4_FxxP_1 | 344 | 347 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.471 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.389 |
LIG_14-3-3_CanoR_1 | 112 | 121 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 241 | 245 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 396 | 401 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 68 | 84 | PF00022 | 0.571 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.354 |
LIG_CaM_IQ_9 | 90 | 106 | PF13499 | 0.383 |
LIG_deltaCOP1_diTrp_1 | 149 | 157 | PF00928 | 0.298 |
LIG_deltaCOP1_diTrp_1 | 437 | 443 | PF00928 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 455 | 461 | PF00928 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 509 | 517 | PF00928 | 0.491 |
LIG_EVH1_2 | 294 | 298 | PF00568 | 0.479 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.452 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.372 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.308 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.293 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.680 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.404 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.393 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.465 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.542 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.457 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.483 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.544 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 560 | 565 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 171 | 180 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 399 | 408 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 455 | 464 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.427 |
LIG_NRP_CendR_1 | 640 | 642 | PF00754 | 0.574 |
LIG_PCNA_PIPBox_1 | 299 | 308 | PF02747 | 0.330 |
LIG_PCNA_yPIPBox_3 | 396 | 404 | PF02747 | 0.564 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.483 |
LIG_REV1ctd_RIR_1 | 373 | 383 | PF16727 | 0.386 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 582 | 586 | PF00017 | 0.541 |
LIG_SH2_PTP2 | 562 | 565 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 582 | 586 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.430 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.438 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.359 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.409 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.582 |
LIG_SUMO_SIM_par_1 | 313 | 321 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 525 | 531 | PF11976 | 0.337 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.535 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.444 |
LIG_TRAF2_2 | 58 | 63 | PF00917 | 0.513 |
LIG_TYR_ITIM | 218 | 223 | PF00017 | 0.354 |
LIG_UBA3_1 | 619 | 623 | PF00899 | 0.476 |
MOD_CDK_SPK_2 | 468 | 473 | PF00069 | 0.327 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.468 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.621 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.617 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.568 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.463 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.543 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.581 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.485 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.577 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.358 |
MOD_GlcNHglycan | 437 | 441 | PF01048 | 0.475 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.743 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.596 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.448 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.294 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.366 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.615 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.546 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.598 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.389 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.602 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.462 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.454 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.357 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.335 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.630 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.388 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.607 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.445 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.367 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.441 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.509 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.548 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.452 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.435 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.341 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.552 |
MOD_PK_1 | 189 | 195 | PF00069 | 0.333 |
MOD_PK_1 | 396 | 402 | PF00069 | 0.463 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.550 |
MOD_PKB_1 | 187 | 195 | PF00069 | 0.438 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.318 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.463 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.452 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.503 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.320 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.599 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.463 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.428 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.383 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.540 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.424 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.709 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.525 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.370 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.432 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.323 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.385 |
MOD_SUMO_rev_2 | 471 | 480 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 618 | 625 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_1 | 601 | 606 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_2 | 459 | 465 | PF01217 | 0.312 |
TRG_DiLeu_BaEn_2 | 488 | 494 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_3 | 91 | 97 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_4 | 427 | 433 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 497 | 502 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.202 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 573 | 575 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 639 | 642 | PF00400 | 0.733 |
TRG_NES_CRM1_1 | 547 | 560 | PF08389 | 0.502 |
TRG_NLS_MonoExtN_4 | 414 | 421 | PF00514 | 0.483 |
TRG_NLS_MonoExtN_4 | 512 | 519 | PF00514 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 357 | 362 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4X2 | Leptomonas seymouri | 69% | 96% |
A0A0S4IQX1 | Bodo saltans | 45% | 100% |
A0A1X0NXS1 | Trypanosomatidae | 63% | 94% |
A0A3S7WWA1 | Leishmania donovani | 96% | 100% |
A4HBL3 | Leishmania braziliensis | 92% | 100% |
A4HZJ6 | Leishmania infantum | 96% | 95% |
D0A1K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 99% |
Q4QCK1 | Leishmania major | 94% | 100% |
V5DGX7 | Trypanosoma cruzi | 61% | 95% |