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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AF73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.795 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.703 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.795 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.603 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.431 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.533 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.664 |
DOC_CYCLIN_yCln2_LP_2 | 311 | 317 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 46 | PF00134 | 0.723 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.603 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.593 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.594 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.628 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.397 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 282 | 292 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 337 | 347 | PF00244 | 0.455 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.517 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.555 |
LIG_CSL_BTD_1 | 227 | 230 | PF09270 | 0.631 |
LIG_deltaCOP1_diTrp_1 | 226 | 235 | PF00928 | 0.621 |
LIG_eIF4E_1 | 38 | 44 | PF01652 | 0.518 |
LIG_EVH1_1 | 44 | 48 | PF00568 | 0.586 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.609 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.525 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.639 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.635 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.464 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.572 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.750 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.659 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.581 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.687 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.549 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.610 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.557 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.534 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.537 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.586 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 286 | 291 | PF02991 | 0.522 |
LIG_LIR_Apic_2 | 30 | 36 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 160 | 168 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.498 |
LIG_MYND_1 | 41 | 45 | PF01753 | 0.543 |
LIG_PCNA_PIPBox_1 | 516 | 525 | PF02747 | 0.459 |
LIG_Pex14_1 | 479 | 483 | PF04695 | 0.393 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 424 | 428 | PF00017 | 0.487 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.503 |
LIG_SH2_SRC | 424 | 427 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.507 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.591 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.691 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.654 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.496 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.537 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.703 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.547 |
LIG_Sin3_3 | 344 | 351 | PF02671 | 0.338 |
LIG_SUMO_SIM_anti_2 | 507 | 514 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.631 |
LIG_SUMO_SIM_par_1 | 507 | 514 | PF11976 | 0.509 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.611 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.536 |
LIG_WW_1 | 35 | 38 | PF00397 | 0.508 |
LIG_WW_2 | 52 | 55 | PF00397 | 0.662 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.551 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.708 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.619 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.456 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.597 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.578 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.556 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.567 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.638 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.716 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.641 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.672 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.559 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.534 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.784 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.585 |
MOD_Cter_Amidation | 442 | 445 | PF01082 | 0.639 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.493 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.740 |
MOD_GlcNHglycan | 245 | 249 | PF01048 | 0.592 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.498 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.658 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.463 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.658 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.598 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.731 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.746 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.687 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.605 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.664 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.552 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.687 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.518 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.524 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.610 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.520 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.452 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.688 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.584 |
MOD_PKA_1 | 213 | 219 | PF00069 | 0.690 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.595 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.486 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.580 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.472 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.701 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.519 |
MOD_Plk_2-3 | 446 | 452 | PF00069 | 0.642 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.490 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.455 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.528 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.468 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.788 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.653 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.560 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.443 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.580 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.607 |
MOD_SUMO_for_1 | 548 | 551 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 185 | 192 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_3 | 153 | 159 | PF01217 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 113 | 118 | PF01217 | 0.600 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.584 |
TRG_NLS_MonoExtC_3 | 212 | 217 | PF00514 | 0.755 |
TRG_NLS_MonoExtN_4 | 210 | 217 | PF00514 | 0.754 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.638 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG0 | Leptomonas seymouri | 61% | 100% |
A0A1X0P5K7 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJ29 | Leishmania donovani | 93% | 100% |
A0A3R7KY71 | Trypanosoma rangeli | 36% | 100% |
A4HMS3 | Leishmania braziliensis | 80% | 100% |
A4IBF9 | Leishmania infantum | 94% | 100% |
C9ZZA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B6C9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DK90 | Trypanosoma cruzi | 35% | 100% |