Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: A4HMK4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.328 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.322 |
DEG_ODPH_VHL_1 | 113 | 126 | PF01847 | 0.234 |
DOC_CYCLIN_RxL_1 | 424 | 432 | PF00134 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.292 |
DOC_MAPK_gen_1 | 100 | 110 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 437 | 444 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.266 |
DOC_MAPK_RevD_3 | 526 | 540 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 438 | 445 | PF00149 | 0.290 |
DOC_PP1_SILK_1 | 332 | 337 | PF00149 | 0.400 |
DOC_PP4_FxxP_1 | 421 | 424 | PF00568 | 0.309 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.255 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.485 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.296 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 391 | 395 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 569 | 575 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 619 | 627 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 648 | 654 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 80 | 88 | PF00244 | 0.435 |
LIG_Actin_WH2_2 | 195 | 213 | PF00022 | 0.429 |
LIG_Actin_WH2_2 | 66 | 82 | PF00022 | 0.360 |
LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 507 | 511 | PF00533 | 0.278 |
LIG_BRCT_BRCA1_1 | 671 | 675 | PF00533 | 0.453 |
LIG_Clathr_ClatBox_1 | 133 | 137 | PF01394 | 0.312 |
LIG_deltaCOP1_diTrp_1 | 688 | 695 | PF00928 | 0.301 |
LIG_EH_1 | 30 | 34 | PF12763 | 0.465 |
LIG_eIF4E_1 | 611 | 617 | PF01652 | 0.350 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.223 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.448 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.483 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.564 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.332 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.349 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.463 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.427 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.334 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.370 |
LIG_GBD_Chelix_1 | 233 | 241 | PF00786 | 0.423 |
LIG_IBAR_NPY_1 | 602 | 604 | PF08397 | 0.376 |
LIG_LIR_Apic_2 | 418 | 424 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 122 | 130 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 482 | 490 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 584 | 588 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 626 | 630 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 705 | 710 | PF02991 | 0.324 |
LIG_LYPXL_yS_3 | 656 | 659 | PF13949 | 0.225 |
LIG_NRBOX | 527 | 533 | PF00104 | 0.343 |
LIG_Pex14_2 | 249 | 253 | PF04695 | 0.449 |
LIG_Pex14_2 | 417 | 421 | PF04695 | 0.429 |
LIG_Pex14_2 | 623 | 627 | PF04695 | 0.300 |
LIG_PTB_Apo_2 | 141 | 148 | PF02174 | 0.429 |
LIG_PTB_Phospho_1 | 141 | 147 | PF10480 | 0.433 |
LIG_REV1ctd_RIR_1 | 441 | 450 | PF16727 | 0.337 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.435 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.287 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 123 | 126 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.545 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.445 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.465 |
LIG_SH2_SRC | 604 | 607 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 392 | 395 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.187 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.364 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.409 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.433 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.435 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.354 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 551 | 557 | PF11976 | 0.354 |
LIG_TRAF2_1 | 642 | 645 | PF00917 | 0.328 |
LIG_TYR_ITIM | 121 | 126 | PF00017 | 0.462 |
LIG_TYR_ITIM | 183 | 188 | PF00017 | 0.439 |
LIG_TYR_ITSM | 372 | 379 | PF00017 | 0.449 |
LIG_UBA3_1 | 531 | 540 | PF00899 | 0.409 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 466 | 471 | PF05994 | 0.265 |
MOD_CDK_SPxxK_3 | 420 | 427 | PF00069 | 0.298 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.372 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.494 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.405 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.310 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.377 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.453 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.436 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.340 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.327 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.396 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.496 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.287 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.319 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.283 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.443 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.327 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.433 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.388 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.462 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.371 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.425 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.417 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.325 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.387 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.361 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.343 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.249 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.322 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.561 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.334 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.310 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.503 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.363 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.471 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.410 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.307 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.270 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.319 |
MOD_PKA_2 | 684 | 690 | PF00069 | 0.426 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.444 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.357 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.308 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.422 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.550 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.324 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.430 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.297 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.185 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.294 |
MOD_SUMO_rev_2 | 168 | 178 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 364 | 374 | PF00179 | 0.387 |
TRG_DiLeu_BaEn_1 | 198 | 203 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_1 | 527 | 532 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 147 | 152 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 158 | 163 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 268 | 273 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4C7 | Leptomonas seymouri | 84% | 100% |
A0A0S4ILQ1 | Bodo saltans | 58% | 99% |
A0A1X0P5V8 | Trypanosomatidae | 65% | 100% |
A0A3Q8IHX6 | Leishmania donovani | 93% | 100% |
A0A422NNY1 | Trypanosoma rangeli | 68% | 100% |
A4IB83 | Leishmania infantum | 93% | 100% |
C9ZZK8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AF04 | Leishmania major | 93% | 100% |
E9B660 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D9G0 | Trypanosoma cruzi | 67% | 100% |