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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QFP6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.530 |
CLV_PCSK_FUR_1 | 469 | 473 | PF00082 | 0.600 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 625 | 627 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 461 | 463 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 621 | 627 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.581 |
CLV_Separin_Metazoa | 221 | 225 | PF03568 | 0.488 |
DEG_APCC_DBOX_1 | 330 | 338 | PF00400 | 0.638 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.538 |
DEG_SCF_FBW7_2 | 404 | 411 | PF00400 | 0.681 |
DEG_SCF_TRCP1_1 | 173 | 179 | PF00400 | 0.510 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.598 |
DOC_CDC14_PxL_1 | 124 | 132 | PF14671 | 0.458 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 63 | 72 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 248 | 256 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 63 | 70 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.462 |
DOC_PP1_RVXF_1 | 562 | 568 | PF00149 | 0.542 |
DOC_PP1_RVXF_1 | 93 | 99 | PF00149 | 0.398 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.632 |
DOC_USP7_MATH_2 | 381 | 387 | PF00917 | 0.594 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 109 | 116 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 331 | 339 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 564 | 568 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 631 | 639 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 649 | 653 | PF00244 | 0.482 |
LIG_Actin_WH2_2 | 419 | 436 | PF00022 | 0.550 |
LIG_BIR_III_2 | 596 | 600 | PF00653 | 0.519 |
LIG_BRCT_BRCA1_1 | 572 | 576 | PF00533 | 0.608 |
LIG_deltaCOP1_diTrp_1 | 91 | 98 | PF00928 | 0.455 |
LIG_DLG_GKlike_1 | 250 | 258 | PF00625 | 0.438 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.345 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.548 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.569 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.591 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.530 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.558 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.683 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.460 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.520 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.626 |
LIG_LIR_Gen_1 | 396 | 404 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.406 |
LIG_MYND_3 | 189 | 193 | PF01753 | 0.521 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.395 |
LIG_Pex14_2 | 552 | 556 | PF04695 | 0.508 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.404 |
LIG_REV1ctd_RIR_1 | 44 | 53 | PF16727 | 0.349 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.537 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 452 | 455 | PF00017 | 0.503 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.621 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 226 | 229 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 560 | 563 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.571 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.389 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.412 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.630 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.532 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.663 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.656 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.557 |
LIG_Sin3_3 | 590 | 597 | PF02671 | 0.508 |
LIG_SUMO_SIM_anti_2 | 386 | 393 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 168 | 174 | PF11976 | 0.691 |
LIG_SUMO_SIM_par_1 | 386 | 393 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 66 | 72 | PF11976 | 0.396 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.407 |
LIG_TRAF2_1 | 658 | 661 | PF00917 | 0.569 |
MOD_CDK_SPK_2 | 213 | 218 | PF00069 | 0.630 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.689 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.716 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.690 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.698 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.496 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.655 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.654 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.637 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.485 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.679 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.520 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.560 |
MOD_Cter_Amidation | 273 | 276 | PF01082 | 0.509 |
MOD_Cter_Amidation | 34 | 37 | PF01082 | 0.449 |
MOD_Cter_Amidation | 619 | 622 | PF01082 | 0.660 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.714 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.503 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.738 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.655 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.627 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.669 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.737 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.678 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.667 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.694 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.608 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.483 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.666 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.487 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.557 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.691 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.718 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.687 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.506 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.538 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.648 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.636 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.589 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.624 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.634 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.431 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.655 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.624 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.752 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.654 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.557 |
MOD_NEK2_2 | 116 | 121 | PF00069 | 0.577 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.537 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.502 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.367 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.678 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.707 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.669 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.506 |
MOD_PKA_1 | 461 | 467 | PF00069 | 0.533 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.608 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.573 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.635 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.521 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.554 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.559 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.523 |
MOD_PKB_1 | 248 | 256 | PF00069 | 0.518 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.608 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.471 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.611 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.592 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.720 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.461 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.625 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.641 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.567 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.631 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.676 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.683 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.725 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.483 |
MOD_SUMO_for_1 | 120 | 123 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 238 | 247 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_4 | 242 | 248 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 623 | 628 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 469 | 472 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 621 | 623 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKL8 | Leptomonas seymouri | 54% | 99% |
A0A3S7WT20 | Leishmania donovani | 92% | 100% |
A0A422N7R9 | Trypanosoma rangeli | 27% | 100% |
A4H7P2 | Leishmania braziliensis | 72% | 100% |
A4HW32 | Leishmania infantum | 92% | 100% |
E9APT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |