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: A0A3Q8IEA8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.561 |
CLV_MEL_PAP_1 | 348 | 354 | PF00089 | 0.362 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.687 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.634 |
CLV_PCSK_PC7_1 | 93 | 99 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.521 |
DEG_APCC_KENBOX_2 | 150 | 154 | PF00400 | 0.533 |
DEG_SPOP_SBC_1 | 272 | 276 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.531 |
DOC_CYCLIN_RxL_1 | 540 | 550 | PF00134 | 0.435 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 212 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 493 | 499 | PF00134 | 0.576 |
DOC_MAPK_DCC_7 | 204 | 214 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 592 | 601 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 377 | 385 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 202 | 209 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 541 | 548 | PF00149 | 0.540 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.496 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.719 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 351 | 359 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 456 | 465 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 546 | 555 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 280 | 295 | PF00022 | 0.561 |
LIG_APCC_ABBAyCdc20_2 | 495 | 501 | PF00400 | 0.505 |
LIG_BIR_III_4 | 341 | 345 | PF00653 | 0.577 |
LIG_BIR_III_4 | 577 | 581 | PF00653 | 0.612 |
LIG_Clathr_ClatBox_1 | 326 | 330 | PF01394 | 0.379 |
LIG_deltaCOP1_diTrp_1 | 299 | 307 | PF00928 | 0.329 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.711 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.679 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.430 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.540 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.445 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.453 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.538 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.508 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.679 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.730 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.393 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.637 |
LIG_LIR_Apic_2 | 510 | 516 | PF02991 | 0.502 |
LIG_LIR_Apic_2 | 549 | 554 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.448 |
LIG_LYPXL_yS_3 | 255 | 258 | PF13949 | 0.630 |
LIG_PCNA_yPIPBox_3 | 293 | 301 | PF02747 | 0.469 |
LIG_Pex14_2 | 547 | 551 | PF04695 | 0.446 |
LIG_SH2_CRK | 378 | 382 | PF00017 | 0.494 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.471 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.444 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.593 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.678 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.426 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.728 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.602 |
LIG_Sin3_3 | 8 | 15 | PF02671 | 0.423 |
LIG_SUMO_SIM_anti_2 | 193 | 199 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.630 |
LIG_TRAF2_1 | 559 | 562 | PF00917 | 0.469 |
LIG_TRAF2_2 | 242 | 247 | PF00917 | 0.487 |
LIG_UBA3_1 | 83 | 92 | PF00899 | 0.521 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.805 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.787 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.423 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.673 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.593 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.500 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.556 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.586 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.572 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.692 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.750 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.667 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.623 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.602 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.745 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.369 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.666 |
MOD_Cter_Amidation | 93 | 96 | PF01082 | 0.619 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.794 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.526 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.666 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.734 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.544 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.642 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.461 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.705 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.650 |
MOD_GlcNHglycan | 278 | 282 | PF01048 | 0.590 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.409 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.534 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.505 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.673 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.695 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.709 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.767 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.790 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.674 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.534 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.492 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.568 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.651 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.719 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.555 |
MOD_N-GLC_1 | 507 | 512 | PF02516 | 0.436 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.617 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.715 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.765 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.620 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.474 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.482 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.502 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.359 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.484 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.567 |
MOD_NEK2_2 | 541 | 546 | PF00069 | 0.379 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.538 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.435 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.347 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.545 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.517 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.441 |
MOD_PIKK_1 | 700 | 706 | PF00454 | 0.656 |
MOD_PK_1 | 146 | 152 | PF00069 | 0.599 |
MOD_PKA_1 | 146 | 152 | PF00069 | 0.608 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.683 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.725 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.686 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.569 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.584 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.422 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.407 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.639 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.447 |
MOD_PKB_1 | 96 | 104 | PF00069 | 0.610 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.482 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.410 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.536 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.428 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.445 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.547 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.409 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.464 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.437 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.490 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.585 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.574 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.485 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.567 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.673 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 415 | 420 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE66 | Leptomonas seymouri | 40% | 100% |
A0A1X0NZK2 | Trypanosomatidae | 25% | 100% |
A0A3R7NL89 | Trypanosoma rangeli | 26% | 100% |
A4HH77 | Leishmania braziliensis | 67% | 97% |
A4I4C3 | Leishmania infantum | 99% | 100% |
E9ADS2 | Leishmania major | 89% | 100% |
E9AM08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |