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: A4I8I8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 680 | 684 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.312 |
CLV_Separin_Metazoa | 559 | 563 | PF03568 | 0.611 |
DEG_APCC_DBOX_1 | 25 | 33 | PF00400 | 0.545 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.555 |
DEG_SCF_FBW7_1 | 529 | 536 | PF00400 | 0.485 |
DEG_SPOP_SBC_1 | 581 | 585 | PF00917 | 0.603 |
DOC_AGCK_PIF_3 | 724 | 727 | PF00069 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 659 | 665 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 38 | 45 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 524 | 531 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 38 | 45 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 562 | 570 | PF00069 | 0.686 |
DOC_PP1_RVXF_1 | 248 | 255 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 525 | 532 | PF00149 | 0.372 |
DOC_PP1_RVXF_1 | 641 | 648 | PF00149 | 0.613 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.719 |
DOC_USP7_MATH_2 | 337 | 343 | PF00917 | 0.608 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 599 | 603 | PF12436 | 0.402 |
DOC_USP7_UBL2_3 | 673 | 677 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 680 | 684 | PF12436 | 0.435 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 390 | 408 | PF00022 | 0.559 |
LIG_BIR_III_4 | 166 | 170 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.561 |
LIG_EVH1_2 | 41 | 45 | PF00568 | 0.633 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.620 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.383 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.453 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.447 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.472 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.599 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.659 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.699 |
LIG_Integrin_RGD_1 | 203 | 205 | PF01839 | 0.595 |
LIG_LIR_Apic_2 | 44 | 48 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 52 | 56 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 635 | 641 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 393 | 398 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 484 | 493 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.710 |
LIG_LIR_Nem_3 | 721 | 727 | PF02991 | 0.483 |
LIG_MYND_3 | 283 | 287 | PF01753 | 0.595 |
LIG_PCNA_yPIPBox_3 | 361 | 370 | PF02747 | 0.411 |
LIG_PDZ_Class_2 | 722 | 727 | PF00595 | 0.635 |
LIG_Pex14_2 | 306 | 310 | PF04695 | 0.669 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 708 | 712 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 259 | 262 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.431 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.599 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.460 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.573 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.567 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 269 | 276 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 543 | 548 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.413 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.697 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.597 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.614 |
LIG_TYR_ITIM | 363 | 368 | PF00017 | 0.438 |
MOD_CDK_SPK_2 | 415 | 420 | PF00069 | 0.538 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.726 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.694 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.533 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.495 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.463 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.704 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.601 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.494 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.593 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.460 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.693 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.653 |
MOD_Cter_Amidation | 525 | 528 | PF01082 | 0.422 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.583 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.582 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.431 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.382 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.623 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.612 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.745 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.653 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.669 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.469 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.450 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.639 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.604 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.745 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.485 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.455 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.490 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.503 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.740 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.462 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.592 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.394 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.560 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.413 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.469 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.608 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.509 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.618 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.595 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.619 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.558 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.419 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.472 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.644 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.393 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.575 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.465 |
MOD_Plk_2-3 | 288 | 294 | PF00069 | 0.426 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.467 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.593 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.473 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.549 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.572 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.534 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.629 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.526 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 706 | 709 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 161 | 170 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 436 | 441 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 592 | 601 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_2 | 620 | 626 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_3 | 225 | 231 | PF01217 | 0.354 |
TRG_DiLeu_LyEn_5 | 437 | 442 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.424 |
TRG_NLS_MonoExtC_3 | 523 | 528 | PF00514 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 439 | 443 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 607 | 612 | PF00026 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P501 | Leptomonas seymouri | 63% | 86% |
A0A0S4JJK2 | Bodo saltans | 33% | 89% |
A0A1X0NRY5 | Trypanosomatidae | 42% | 99% |
A0A3S5H7T3 | Leishmania donovani | 100% | 100% |
A4HL07 | Leishmania braziliensis | 81% | 100% |
D0AAM9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 98% |
E9B3E8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
Q4Q4Q2 | Leishmania major | 95% | 100% |
V5BLC8 | Trypanosoma cruzi | 41% | 98% |