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: A4HHK0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 440 | 446 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.556 |
CLV_Separin_Metazoa | 211 | 215 | PF03568 | 0.331 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.351 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.640 |
DEG_SCF_FBW7_2 | 541 | 546 | PF00400 | 0.634 |
DEG_SPOP_SBC_1 | 635 | 639 | PF00917 | 0.407 |
DOC_CKS1_1 | 497 | 502 | PF01111 | 0.548 |
DOC_CYCLIN_RxL_1 | 116 | 127 | PF00134 | 0.537 |
DOC_CYCLIN_yCln2_LP_2 | 670 | 676 | PF00134 | 0.638 |
DOC_MAPK_gen_1 | 116 | 124 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 463 | 469 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 653 | 661 | PF00069 | 0.519 |
DOC_PP1_RVXF_1 | 118 | 125 | PF00149 | 0.531 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.424 |
DOC_PP2B_LxvP_1 | 670 | 673 | PF13499 | 0.497 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.526 |
DOC_USP7_UBL2_3 | 528 | 532 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 606 | 614 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 616 | 624 | PF00244 | 0.384 |
LIG_APCC_ABBA_1 | 191 | 196 | PF00400 | 0.445 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.484 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.629 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.419 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.504 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.565 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.482 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.522 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.505 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.508 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.464 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.580 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.590 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.435 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 419 | 429 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 598 | 604 | PF02991 | 0.552 |
LIG_PCNA_yPIPBox_3 | 379 | 391 | PF02747 | 0.550 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.371 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.475 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.343 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 429 | 433 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 482 | 485 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 663 | 666 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.458 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.476 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.446 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.550 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.421 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.591 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.408 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.517 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.543 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.523 |
LIG_TYR_ITIM | 207 | 212 | PF00017 | 0.424 |
LIG_TYR_ITSM | 309 | 316 | PF00017 | 0.487 |
LIG_UBA3_1 | 212 | 220 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 375 | 380 | PF05994 | 0.436 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.513 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.410 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.681 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.488 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.458 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.522 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.414 |
MOD_Cter_Amidation | 23 | 26 | PF01082 | 0.551 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.615 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.746 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.334 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.599 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.543 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.409 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.481 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.660 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.560 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.491 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.576 |
MOD_N-GLC_2 | 179 | 181 | PF02516 | 0.332 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.661 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.421 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.356 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.452 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.452 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.605 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.525 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.535 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.462 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.410 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.413 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.527 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.685 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.480 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.498 |
MOD_PK_1 | 610 | 616 | PF00069 | 0.542 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.648 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.623 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.406 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.487 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.341 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.700 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.480 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.384 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.660 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.474 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.516 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.456 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.426 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.393 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.445 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.533 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.427 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.511 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.606 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.434 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.718 |
MOD_SUMO_for_1 | 469 | 472 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 127 | 134 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 334 | 339 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 34 | 39 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 511 | 516 | PF01217 | 0.647 |
TRG_DiLeu_BaEn_4 | 472 | 478 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 437 | 442 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 517 | 522 | PF01217 | 0.663 |
TRG_DiLeu_LyEn_5 | 211 | 216 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 50 | 64 | PF08389 | 0.559 |
TRG_NLS_Bipartite_1 | 9 | 29 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.431 |
TRG_PTS1 | 695 | 698 | PF00515 | 0.634 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5R0 | Leptomonas seymouri | 71% | 97% |
A0A0S4IQD8 | Bodo saltans | 36% | 94% |
A0A1X0P086 | Trypanosomatidae | 45% | 100% |
A0A3S7X2T2 | Leishmania donovani | 87% | 100% |
A0A422NKV6 | Trypanosoma rangeli | 43% | 100% |
A4I4Q8 | Leishmania infantum | 87% | 100% |
C9ZLE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AE63 | Leishmania major | 85% | 100% |
E9ALM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BGI2 | Trypanosoma cruzi | 45% | 95% |