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: A4HBD8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.426 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 615 | 617 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.679 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.269 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.483 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.502 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.330 |
DOC_CDC14_PxL_1 | 586 | 594 | PF14671 | 0.378 |
DOC_CYCLIN_RxL_1 | 127 | 136 | PF00134 | 0.370 |
DOC_CYCLIN_RxL_1 | 219 | 229 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 346 | 354 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 365 | 374 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 585 | 593 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 184 | 190 | PF00149 | 0.323 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.320 |
DOC_SPAK_OSR1_1 | 54 | 58 | PF12202 | 0.380 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.461 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 405 | 415 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 527 | 535 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 616 | 626 | PF00244 | 0.438 |
LIG_BIR_III_2 | 446 | 450 | PF00653 | 0.715 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 313 | 317 | PF01394 | 0.275 |
LIG_deltaCOP1_diTrp_1 | 23 | 29 | PF00928 | 0.477 |
LIG_deltaCOP1_diTrp_1 | 390 | 394 | PF00928 | 0.350 |
LIG_EVH1_1 | 42 | 46 | PF00568 | 0.377 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.554 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.463 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.423 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.504 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.534 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.447 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.468 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.319 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 305 | 313 | PF00786 | 0.430 |
LIG_LIR_Apic_2 | 602 | 607 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 368 | 376 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 64 | 72 | PF02991 | 0.335 |
LIG_LIR_LC3C_4 | 311 | 315 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.320 |
LIG_LYPXL_yS_3 | 42 | 45 | PF13949 | 0.558 |
LIG_PDZ_Class_2 | 644 | 649 | PF00595 | 0.458 |
LIG_PTB_Apo_2 | 114 | 121 | PF02174 | 0.395 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.402 |
LIG_SH2_GRB2like | 115 | 118 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 324 | 327 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.559 |
LIG_SH3_2 | 461 | 466 | PF14604 | 0.467 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.483 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.465 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.548 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.735 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.500 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.339 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.402 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.391 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.424 |
LIG_SUMO_SIM_anti_2 | 311 | 318 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 311 | 318 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 330 | 338 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.470 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.469 |
LIG_WW_3 | 434 | 438 | PF00397 | 0.594 |
MOD_CDK_SPK_2 | 214 | 219 | PF00069 | 0.635 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.510 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.318 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.671 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.684 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.482 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.447 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.529 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.701 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.456 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.445 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.323 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.540 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.645 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.622 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.524 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.647 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.751 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.638 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.549 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.484 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.364 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.447 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.378 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.521 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.505 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.307 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.603 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.378 |
MOD_LATS_1 | 404 | 410 | PF00433 | 0.319 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.602 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.602 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.539 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.521 |
MOD_N-GLC_2 | 180 | 182 | PF02516 | 0.519 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.508 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.478 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.572 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.483 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.444 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.468 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.528 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.564 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.307 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.447 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.647 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.394 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.560 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.307 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.502 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.442 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.361 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.395 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.513 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.538 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.260 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.424 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.399 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.384 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.344 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.619 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.493 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.493 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.434 |
MOD_SUMO_rev_2 | 145 | 150 | PF00179 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 490 | 495 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 530 | 543 | PF08389 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 223 | 228 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E9 | Leptomonas seymouri | 51% | 98% |
A0A0S4KIT9 | Bodo saltans | 28% | 95% |
A0A1X0PA76 | Trypanosomatidae | 32% | 100% |
A0A3Q8IHL1 | Leishmania donovani | 76% | 99% |
A0A422NVA9 | Trypanosoma rangeli | 35% | 100% |
A4IAI6 | Leishmania infantum | 76% | 99% |
C9ZLQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B5L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q2C6 | Leishmania major | 76% | 100% |
V5DMS9 | Trypanosoma cruzi | 32% | 100% |