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: A4HBL3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.399 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 495 | 501 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.341 |
CLV_Separin_Metazoa | 5 | 9 | PF03568 | 0.382 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.347 |
DEG_APCC_DBOX_1 | 542 | 550 | PF00400 | 0.454 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.370 |
DEG_ODPH_VHL_1 | 10 | 22 | PF01847 | 0.329 |
DEG_SCF_FBW7_1 | 290 | 297 | PF00400 | 0.455 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.483 |
DEG_SPOP_SBC_1 | 256 | 260 | PF00917 | 0.395 |
DOC_CKS1_1 | 291 | 296 | PF01111 | 0.462 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.432 |
DOC_CYCLIN_RxL_1 | 295 | 304 | PF00134 | 0.529 |
DOC_CYCLIN_RxL_1 | 81 | 91 | PF00134 | 0.356 |
DOC_MAPK_gen_1 | 176 | 182 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 27 | 36 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 542 | 549 | PF00069 | 0.460 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 146 | 152 | PF00149 | 0.354 |
DOC_PP1_RVXF_1 | 188 | 195 | PF00149 | 0.470 |
DOC_PP1_RVXF_1 | 296 | 303 | PF00149 | 0.400 |
DOC_PP1_RVXF_1 | 376 | 383 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 82 | 89 | PF00149 | 0.390 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.527 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.418 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 542 | 547 | PF00244 | 0.505 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.346 |
LIG_deltaCOP1_diTrp_1 | 363 | 369 | PF00928 | 0.377 |
LIG_deltaCOP1_diTrp_1 | 381 | 387 | PF00928 | 0.375 |
LIG_deltaCOP1_diTrp_1 | 435 | 443 | PF00928 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 75 | 83 | PF00928 | 0.305 |
LIG_EVH1_2 | 220 | 224 | PF00568 | 0.489 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.383 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.554 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.315 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.295 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.413 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.410 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.542 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.487 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.331 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.491 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.490 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.559 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.488 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.442 |
LIG_LIR_Apic_2 | 486 | 491 | PF02991 | 0.376 |
LIG_LIR_Apic_2 | 505 | 511 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.367 |
LIG_PCNA_PIPBox_1 | 225 | 234 | PF02747 | 0.337 |
LIG_PCNA_yPIPBox_3 | 322 | 330 | PF02747 | 0.558 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.485 |
LIG_REV1ctd_RIR_1 | 299 | 309 | PF16727 | 0.456 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.348 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 303 | 307 | PF00017 | 0.316 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.232 |
LIG_SH2_PTP2 | 488 | 491 | PF00017 | 0.367 |
LIG_SH2_SRC | 566 | 569 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.429 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.448 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.430 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.412 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 239 | 247 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 451 | 457 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 545 | 552 | PF11976 | 0.392 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.457 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.532 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.352 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.360 |
LIG_UBA3_1 | 19 | 27 | PF00899 | 0.377 |
MOD_CDK_SPK_2 | 394 | 399 | PF00069 | 0.337 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.477 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.490 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.627 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.587 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.502 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.558 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.582 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.377 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.447 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.607 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.342 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.369 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.561 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.455 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.456 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.449 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.338 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.552 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.457 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.489 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.306 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.213 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.372 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.443 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.361 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.454 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.347 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.308 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.565 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.459 |
MOD_PKA_1 | 542 | 548 | PF00069 | 0.406 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.559 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.317 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.406 |
MOD_PKB_1 | 113 | 121 | PF00069 | 0.439 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.404 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.459 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.375 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.505 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.324 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.459 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.311 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.383 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.544 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.424 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.589 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.435 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.416 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.332 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.379 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.461 |
MOD_SUMO_rev_2 | 397 | 406 | PF00179 | 0.368 |
MOD_SUMO_rev_2 | 510 | 519 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 545 | 552 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 402 | 407 | PF01217 | 0.345 |
TRG_DiLeu_BaEn_1 | 528 | 533 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_2 | 385 | 391 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_3 | 17 | 23 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_4 | 353 | 359 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 423 | 428 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.230 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 499 | 501 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.396 |
TRG_NES_CRM1_1 | 473 | 486 | PF08389 | 0.508 |
TRG_NLS_MonoExtN_4 | 340 | 347 | PF00514 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 283 | 288 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4X2 | Leptomonas seymouri | 76% | 85% |
A0A0S4IQX1 | Bodo saltans | 45% | 100% |
A0A1X0NXS1 | Trypanosomatidae | 64% | 83% |
A0A3S7WWA1 | Leishmania donovani | 93% | 89% |
A4HZJ6 | Leishmania infantum | 93% | 84% |
D0A1K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 88% |
E9AUY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 89% |
Q4QCK1 | Leishmania major | 91% | 100% |
V5DGX7 | Trypanosoma cruzi | 64% | 84% |