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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S7WQU1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.733 |
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.579 |
CLV_MEL_PAP_1 | 417 | 423 | PF00089 | 0.670 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.589 |
DEG_ODPH_VHL_1 | 247 | 260 | PF01847 | 0.531 |
DEG_SPOP_SBC_1 | 515 | 519 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.756 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 609 | 616 | PF00069 | 0.616 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.586 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.545 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 570 | 576 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 579 | 585 | PF00244 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_BIR_III_2 | 187 | 191 | PF00653 | 0.570 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.659 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.628 |
LIG_Clathr_ClatBox_1 | 103 | 107 | PF01394 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 197 | 205 | PF00928 | 0.729 |
LIG_DLG_GKlike_1 | 420 | 428 | PF00625 | 0.680 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.512 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.607 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.613 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.551 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.684 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.691 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.571 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.673 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.502 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.525 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.755 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.704 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.537 |
LIG_LIR_Nem_3 | 583 | 587 | PF02991 | 0.676 |
LIG_LYPXL_SIV_4 | 595 | 603 | PF13949 | 0.622 |
LIG_MYND_1 | 576 | 580 | PF01753 | 0.616 |
LIG_PDZ_Class_2 | 611 | 616 | PF00595 | 0.462 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.406 |
LIG_Pex14_2 | 542 | 546 | PF04695 | 0.504 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.742 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.768 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.538 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.714 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 259 | 264 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 41 | 49 | PF11976 | 0.735 |
LIG_SUMO_SIM_anti_2 | 549 | 556 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 86 | 97 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 157 | 162 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 261 | 268 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 549 | 556 | PF11976 | 0.481 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.769 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.807 |
LIG_TRAF2_1 | 556 | 559 | PF00917 | 0.435 |
LIG_TRAF2_2 | 452 | 457 | PF00917 | 0.690 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.533 |
LIG_TYR_ITIM | 412 | 417 | PF00017 | 0.657 |
LIG_WRC_WIRS_1 | 581 | 586 | PF05994 | 0.697 |
MOD_CDC14_SPxK_1 | 478 | 481 | PF00782 | 0.578 |
MOD_CDK_SPxK_1 | 475 | 481 | PF00069 | 0.581 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.477 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.781 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.716 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.521 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.699 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.494 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.748 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.713 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.650 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.687 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.658 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.677 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.601 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.452 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.767 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.505 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.605 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.622 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.639 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.537 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.729 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.542 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.446 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.692 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.665 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.553 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.714 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.712 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.757 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.609 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.594 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.731 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.670 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.644 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.527 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.418 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.550 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.445 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.557 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.720 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.768 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.629 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.699 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.694 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.656 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.694 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.622 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.711 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.618 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.739 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.732 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.643 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.476 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.352 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.716 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.516 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.342 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.727 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.610 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.591 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.695 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.571 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.629 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.527 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.648 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.561 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.604 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.503 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.673 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.539 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.637 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.539 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.620 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.707 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.785 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.674 |
TRG_DiLeu_BaEn_1 | 41 | 46 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.666 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.494 |
TRG_NES_CRM1_1 | 34 | 49 | PF08389 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H8 | Leptomonas seymouri | 48% | 81% |
A0A1X0NMF5 | Trypanosomatidae | 30% | 100% |
A4H5S4 | Leishmania braziliensis | 77% | 100% |
A4HU17 | Leishmania infantum | 100% | 100% |
D0A9I5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AMU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHS8 | Leishmania major | 91% | 100% |
V5B2B3 | Trypanosoma cruzi | 32% | 100% |