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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H7P2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 540 | 544 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.479 |
CLV_PCSK_FUR_1 | 440 | 444 | PF00082 | 0.574 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 626 | 628 | PF00082 | 0.532 |
CLV_PCSK_PC7_1 | 591 | 597 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.437 |
CLV_Separin_Metazoa | 209 | 213 | PF03568 | 0.538 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.513 |
DEG_SCF_FBW7_2 | 130 | 137 | PF00400 | 0.316 |
DEG_SCF_FBW7_2 | 375 | 382 | PF00400 | 0.662 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.566 |
DOC_ANK_TNKS_1 | 349 | 356 | PF00023 | 0.480 |
DOC_CDC14_PxL_1 | 124 | 132 | PF14671 | 0.478 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.547 |
DOC_CYCLIN_RxL_1 | 63 | 72 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 450 | 460 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 63 | 70 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 533 | 539 | PF00149 | 0.601 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.437 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.565 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 535 | 539 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 601 | 609 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 619 | 623 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 390 | 407 | PF00022 | 0.537 |
LIG_BRCT_BRCA1_1 | 543 | 547 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.297 |
LIG_deltaCOP1_diTrp_1 | 91 | 98 | PF00928 | 0.450 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.575 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.485 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.693 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.386 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.317 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.647 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.303 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.512 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.467 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.489 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.788 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 96 | 106 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.296 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.419 |
LIG_Pex14_2 | 523 | 527 | PF04695 | 0.557 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.402 |
LIG_REV1ctd_RIR_1 | 44 | 53 | PF16727 | 0.362 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 423 | 426 | PF00017 | 0.568 |
LIG_SH2_GRB2like | 530 | 533 | PF00017 | 0.343 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.611 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 214 | 217 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 531 | 534 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.616 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.613 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.387 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.706 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.515 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.728 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.667 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.615 |
LIG_SUMO_SIM_anti_2 | 356 | 365 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 356 | 365 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 66 | 72 | PF11976 | 0.448 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.566 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.429 |
LIG_TRAF2_1 | 406 | 409 | PF00917 | 0.337 |
MOD_CDK_SPK_2 | 201 | 206 | PF00069 | 0.553 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.709 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.650 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.596 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.628 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.500 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.365 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.579 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.704 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.485 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.484 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.652 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.320 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.466 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.491 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.538 |
MOD_Cter_Amidation | 589 | 592 | PF01082 | 0.663 |
MOD_Cter_Amidation | 593 | 596 | PF01082 | 0.623 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.644 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.525 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.539 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.676 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.686 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.522 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.694 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.388 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.429 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.691 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.697 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.621 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.461 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.782 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.589 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.578 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.418 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.496 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.529 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.665 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.615 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.589 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.541 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.500 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.633 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.535 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.613 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.692 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.574 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.575 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.507 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.554 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.545 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.504 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.479 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.705 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.681 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.651 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.508 |
MOD_PKA_1 | 432 | 438 | PF00069 | 0.523 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.608 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.525 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.560 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.538 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.622 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.557 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.597 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.475 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.640 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.686 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.739 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.503 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.561 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.329 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.448 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.313 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.547 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.628 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.723 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.619 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.612 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.595 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.522 |
MOD_SUMO_rev_2 | 226 | 235 | PF00179 | 0.648 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_4 | 230 | 236 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 554 | 559 | PF01217 | 0.645 |
TRG_DiLeu_BaLyEn_6 | 593 | 598 | PF01217 | 0.722 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 591 | 593 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.435 |
TRG_NLS_MonoExtC_3 | 438 | 443 | PF00514 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKL8 | Leptomonas seymouri | 54% | 94% |
A0A1X0NP41 | Trypanosomatidae | 28% | 100% |
A0A3S7WT20 | Leishmania donovani | 74% | 96% |
A0A422N7R9 | Trypanosoma rangeli | 29% | 100% |
A4HW32 | Leishmania infantum | 75% | 96% |
C9ZSZ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9APT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 95% |
Q4QFP6 | Leishmania major | 72% | 100% |
V5AYY7 | Trypanosoma cruzi | 27% | 70% |