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: E9AF20
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.550 |
CLV_PCSK_FUR_1 | 32 | 36 | PF00082 | 0.443 |
CLV_PCSK_FUR_1 | 550 | 554 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 552 | 554 | PF00082 | 0.581 |
CLV_PCSK_PC7_1 | 298 | 304 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.589 |
DEG_APCC_DBOX_1 | 128 | 136 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.590 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.681 |
DEG_SCF_FBW7_1 | 532 | 539 | PF00400 | 0.574 |
DOC_ANK_TNKS_1 | 301 | 308 | PF00023 | 0.713 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.469 |
DOC_MAPK_DCC_7 | 324 | 332 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 321 | 330 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.544 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.727 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 103 | 108 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 450 | 454 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.501 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.606 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.644 |
LIG_Clathr_ClatBox_1 | 278 | 282 | PF01394 | 0.424 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.535 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.454 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.431 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.432 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.476 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.511 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.467 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.679 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.561 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.678 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.442 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.462 |
LIG_LIR_Apic_2 | 73 | 78 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 407 | 416 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.447 |
LIG_NRP_CendR_1 | 588 | 589 | PF00754 | 0.588 |
LIG_Pex14_2 | 42 | 46 | PF04695 | 0.503 |
LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.530 |
LIG_PTB_Apo_2 | 495 | 502 | PF02174 | 0.725 |
LIG_PTB_Phospho_1 | 151 | 157 | PF10480 | 0.553 |
LIG_PTB_Phospho_1 | 495 | 501 | PF10480 | 0.620 |
LIG_SH2_GRB2like | 345 | 348 | PF00017 | 0.698 |
LIG_SH2_GRB2like | 410 | 413 | PF00017 | 0.763 |
LIG_SH2_NCK_1 | 410 | 414 | PF00017 | 0.688 |
LIG_SH2_NCK_1 | 514 | 518 | PF00017 | 0.699 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.434 |
LIG_SH2_SRC | 410 | 413 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.699 |
LIG_SH2_STAT3 | 81 | 84 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.336 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.514 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.548 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.429 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.743 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.375 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.486 |
LIG_SH3_4 | 394 | 401 | PF00018 | 0.669 |
LIG_SUMO_SIM_par_1 | 194 | 200 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 276 | 282 | PF11976 | 0.420 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.694 |
LIG_WRC_WIRS_1 | 383 | 388 | PF05994 | 0.799 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.735 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.762 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.469 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.411 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.487 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.441 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.710 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.521 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.580 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.612 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.638 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.554 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.701 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.635 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.695 |
MOD_GlcNHglycan | 579 | 585 | PF01048 | 0.560 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.595 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.434 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.429 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.688 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.767 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.582 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.796 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.556 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.484 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.511 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.587 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.607 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.733 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.755 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.487 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.710 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.442 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.399 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.427 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.391 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.563 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.655 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.382 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.780 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.617 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.547 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.457 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.491 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.782 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.583 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.400 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.643 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.643 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.700 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.760 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.591 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.511 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.461 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.633 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.403 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.632 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.750 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.495 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.417 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.711 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.577 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.721 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.651 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.721 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.628 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.821 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.546 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 144 | 150 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 184 | 193 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 255 | 262 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 331 | 340 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 436 | 443 | PF00179 | 0.600 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.646 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.576 |
TRG_NES_CRM1_1 | 97 | 108 | PF08389 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 431 | 436 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P326 | Leptomonas seymouri | 79% | 97% |
A0A0S4JIC7 | Bodo saltans | 56% | 100% |
A0A1X0P7C6 | Trypanosomatidae | 68% | 100% |
A0A3Q8IM74 | Leishmania donovani | 97% | 100% |
A4HML8 | Leishmania braziliensis | 91% | 100% |
A4IB96 | Leishmania infantum | 97% | 100% |
C9ZZM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9B676 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5ATF8 | Trypanosoma cruzi | 68% | 100% |