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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H6S2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.471 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.497 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.446 |
CLV_PCSK_FUR_1 | 339 | 343 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 569 | 571 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 207 | 213 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 253 | 259 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.609 |
CLV_Separin_Metazoa | 185 | 189 | PF03568 | 0.358 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.445 |
DOC_ANK_TNKS_1 | 569 | 576 | PF00023 | 0.405 |
DOC_CDC14_PxL_1 | 368 | 376 | PF14671 | 0.458 |
DOC_CYCLIN_RxL_1 | 15 | 24 | PF00134 | 0.371 |
DOC_CYCLIN_RxL_1 | 178 | 189 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 482 | 488 | PF00134 | 0.457 |
DOC_MAPK_DCC_7 | 474 | 483 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 445 | 453 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 474 | 483 | PF00069 | 0.579 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.414 |
DOC_USP7_UBL2_3 | 549 | 553 | PF12436 | 0.351 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 526 | 530 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 559 | 563 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 587 | 597 | PF00244 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 235 | 241 | PF00400 | 0.415 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.395 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.525 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.463 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.726 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.653 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.616 |
LIG_LIR_Gen_1 | 375 | 384 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.466 |
LIG_NRBOX | 186 | 192 | PF00104 | 0.357 |
LIG_NRBOX | 21 | 27 | PF00104 | 0.369 |
LIG_Pex14_2 | 37 | 41 | PF04695 | 0.396 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.448 |
LIG_PTB_Phospho_1 | 108 | 114 | PF10480 | 0.454 |
LIG_Rb_pABgroove_1 | 371 | 379 | PF01858 | 0.491 |
LIG_RPA_C_Fungi | 336 | 348 | PF08784 | 0.582 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.383 |
LIG_SH2_CRK | 597 | 601 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 114 | 118 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 222 | 226 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 427 | 431 | PF00017 | 0.505 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.409 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.433 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 267 | 273 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 267 | 273 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 372 | 379 | PF11976 | 0.521 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.357 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.547 |
LIG_TRAF2_1 | 539 | 542 | PF00917 | 0.303 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.651 |
LIG_TYR_ITIM | 53 | 58 | PF00017 | 0.404 |
LIG_WRC_WIRS_1 | 432 | 437 | PF05994 | 0.444 |
MOD_CDK_SPK_2 | 486 | 491 | PF00069 | 0.429 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.520 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.481 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.694 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.499 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.518 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.495 |
MOD_Cter_Amidation | 617 | 620 | PF01082 | 0.475 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.445 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.443 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.505 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.496 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.733 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.610 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.532 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.434 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.538 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.420 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.369 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.506 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.594 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.625 |
MOD_OFUCOSY | 93 | 100 | PF10250 | 0.652 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.636 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.482 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.503 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.632 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.526 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.467 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.454 |
MOD_PKB_1 | 419 | 427 | PF00069 | 0.365 |
MOD_PKB_1 | 472 | 480 | PF00069 | 0.591 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.506 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.622 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.480 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.348 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.505 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.500 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.424 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.550 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.579 |
MOD_SUMO_for_1 | 200 | 203 | PF00179 | 0.389 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 301 | 309 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 489 | 498 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 542 | 551 | PF00179 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 477 | 482 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 558 | 560 | PF00400 | 0.533 |
TRG_NLS_Bipartite_1 | 552 | 573 | PF00514 | 0.582 |
TRG_NLS_MonoExtC_3 | 568 | 574 | PF00514 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 560 | 565 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK43 | Leptomonas seymouri | 46% | 100% |
A0A1X0NM25 | Trypanosomatidae | 26% | 100% |
A0A3Q8I971 | Leishmania donovani | 72% | 100% |
A0A422N6D2 | Trypanosoma rangeli | 28% | 100% |
A4HV51 | Leishmania infantum | 72% | 100% |
E9ANT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QGT6 | Leishmania major | 70% | 100% |