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: E9B676
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.574 |
CLV_PCSK_FUR_1 | 32 | 36 | PF00082 | 0.451 |
CLV_PCSK_FUR_1 | 549 | 553 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 551 | 553 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 298 | 304 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 128 | 136 | PF00400 | 0.437 |
DEG_APCC_DBOX_1 | 450 | 458 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.682 |
DOC_ANK_TNKS_1 | 301 | 308 | PF00023 | 0.675 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.495 |
DOC_MAPK_DCC_7 | 325 | 333 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.638 |
DOC_MAPK_gen_1 | 322 | 331 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.621 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.721 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.822 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 103 | 108 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 205 | 210 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 451 | 455 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.520 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.518 |
LIG_AP_GAE_1 | 475 | 481 | PF02883 | 0.545 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.624 |
LIG_Clathr_ClatBox_1 | 278 | 282 | PF01394 | 0.447 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.557 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.450 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.436 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.436 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.522 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.473 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.670 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.571 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.680 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.469 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 73 | 78 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 483 | 487 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.493 |
LIG_NRP_CendR_1 | 587 | 588 | PF00754 | 0.591 |
LIG_Pex14_2 | 42 | 46 | PF04695 | 0.504 |
LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.521 |
LIG_PTB_Phospho_1 | 151 | 157 | PF10480 | 0.546 |
LIG_SH2_GRB2like | 346 | 349 | PF00017 | 0.702 |
LIG_SH2_GRB2like | 411 | 414 | PF00017 | 0.756 |
LIG_SH2_NCK_1 | 411 | 415 | PF00017 | 0.683 |
LIG_SH2_NCK_1 | 515 | 519 | PF00017 | 0.683 |
LIG_SH2_SRC | 411 | 414 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.683 |
LIG_SH2_STAT3 | 81 | 84 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.518 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.600 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.441 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.736 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.390 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.539 |
LIG_SH3_4 | 395 | 402 | PF00018 | 0.672 |
LIG_SUMO_SIM_par_1 | 194 | 200 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 276 | 282 | PF11976 | 0.448 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.688 |
LIG_TRFH_1 | 157 | 161 | PF08558 | 0.457 |
LIG_UBA3_1 | 274 | 283 | PF00899 | 0.494 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.793 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.574 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.733 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.760 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.503 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.413 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.448 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.707 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.526 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.581 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.610 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.609 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.554 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.544 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.705 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.664 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.625 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.575 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.436 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.434 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.686 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.765 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.575 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.796 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.538 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.531 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.548 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.583 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.614 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.728 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.670 |
MOD_N-GLC_1 | 542 | 547 | PF02516 | 0.750 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.533 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.706 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.439 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.397 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.433 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.396 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.607 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.629 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.385 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.780 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.613 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.535 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.474 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.489 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.779 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.584 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.408 |
MOD_PK_1 | 205 | 211 | PF00069 | 0.293 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.638 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.638 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.696 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.757 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.594 |
MOD_PKB_1 | 203 | 211 | PF00069 | 0.507 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.544 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.623 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.406 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.637 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.748 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.494 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.415 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.706 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.595 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.717 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.645 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.720 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.633 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.649 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.822 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 144 | 150 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 184 | 193 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 255 | 262 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 332 | 341 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 437 | 444 | PF00179 | 0.601 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 565 | 568 | PF00400 | 0.612 |
TRG_NES_CRM1_1 | 97 | 108 | PF08389 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 432 | 437 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P326 | Leptomonas seymouri | 79% | 97% |
A0A0S4JIC7 | Bodo saltans | 56% | 100% |
A0A1X0P7C6 | Trypanosomatidae | 68% | 100% |
A0A3Q8IM74 | Leishmania donovani | 96% | 100% |
A4HML8 | Leishmania braziliensis | 91% | 100% |
A4IB96 | Leishmania infantum | 95% | 100% |
C9ZZM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AF20 | Leishmania major | 96% | 100% |
V5ATF8 | Trypanosoma cruzi | 67% | 100% |