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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B161
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 603 | 607 | PF00656 | 0.465 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.428 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.528 |
CLV_PCSK_PC7_1 | 648 | 654 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.438 |
CLV_Separin_Metazoa | 155 | 159 | PF03568 | 0.495 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.599 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.488 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.612 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.571 |
DOC_CYCLIN_RxL_1 | 305 | 313 | PF00134 | 0.526 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.431 |
DOC_MAPK_DCC_7 | 535 | 543 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 592 | 599 | PF00069 | 0.512 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.599 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.597 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.451 |
LIG_14-3-3_CanoR_1 | 128 | 132 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 158 | 166 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 183 | 193 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 441 | 449 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 55 | 63 | PF00244 | 0.626 |
LIG_14-3-3_CterR_2 | 668 | 673 | PF00244 | 0.507 |
LIG_Actin_WH2_2 | 13 | 30 | PF00022 | 0.432 |
LIG_BRCT_BRCA1_1 | 630 | 634 | PF00533 | 0.476 |
LIG_eIF4E_1 | 289 | 295 | PF01652 | 0.382 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.688 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.485 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.417 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.389 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.525 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.518 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.490 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.478 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.600 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.478 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.501 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.452 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.380 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.455 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.398 |
LIG_LIR_Apic_2 | 129 | 134 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 434 | 443 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.447 |
LIG_LIR_LC3C_4 | 270 | 275 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 62 | 66 | PF02991 | 0.446 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.434 |
LIG_NRBOX | 6 | 12 | PF00104 | 0.426 |
LIG_Rb_LxCxE_1 | 278 | 290 | PF01857 | 0.504 |
LIG_REV1ctd_RIR_1 | 363 | 372 | PF16727 | 0.372 |
LIG_SH2_CRK | 436 | 440 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 350 | 353 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.465 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.398 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.365 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 397 | 403 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 472 | 479 | PF11976 | 0.346 |
LIG_SxIP_EBH_1 | 165 | 177 | PF03271 | 0.505 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.542 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.529 |
LIG_UBA3_1 | 510 | 516 | PF00899 | 0.353 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.354 |
MOD_CDK_SPxxK_3 | 237 | 244 | PF00069 | 0.271 |
MOD_CDK_SPxxK_3 | 641 | 648 | PF00069 | 0.466 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.661 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.547 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.600 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.481 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.390 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.486 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.689 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.715 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.667 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.495 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.370 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.455 |
MOD_DYRK1A_RPxSP_1 | 641 | 645 | PF00069 | 0.536 |
MOD_DYRK1A_RPxSP_1 | 656 | 660 | PF00069 | 0.562 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.658 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.376 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.399 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.384 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.475 |
MOD_GlcNHglycan | 479 | 483 | PF01048 | 0.450 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.419 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.660 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.747 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.767 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.670 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.781 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.451 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.293 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.347 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.622 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.436 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.418 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.471 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.570 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.630 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.470 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.706 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.646 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.277 |
MOD_N-GLC_1 | 611 | 616 | PF02516 | 0.355 |
MOD_N-GLC_2 | 21 | 23 | PF02516 | 0.392 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.521 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.607 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.472 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.544 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.243 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.393 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.455 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.421 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.297 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.338 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.473 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.369 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.449 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.493 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.460 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.777 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.693 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.556 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.596 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.517 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.463 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.516 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.386 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.532 |
MOD_PKA_1 | 652 | 658 | PF00069 | 0.366 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.657 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.578 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.577 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.549 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.582 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.490 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.406 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.421 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.516 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.483 |
MOD_Plk_2-3 | 473 | 479 | PF00069 | 0.489 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.550 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.519 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.382 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.397 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.292 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.422 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.412 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.332 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.400 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.322 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.463 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 389 | 393 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 639 | 641 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 651 | 653 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I481 | Leptomonas seymouri | 70% | 98% |
A0A0S4IPG5 | Bodo saltans | 36% | 100% |
A0A1X0P1H7 | Trypanosomatidae | 49% | 100% |
A0A3Q8IG13 | Leishmania donovani | 95% | 100% |
A0A3R7JPV2 | Trypanosoma rangeli | 49% | 100% |
A4HIM2 | Leishmania braziliensis | 86% | 100% |
A4I5W7 | Leishmania infantum | 95% | 100% |
C9ZR90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
Q4Q704 | Leishmania major | 94% | 100% |
V5B7A2 | Trypanosoma cruzi | 49% | 100% |