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: 3 |
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: Q4QDG9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 470 | 474 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 136 | 140 | PF00082 | 0.709 |
CLV_PCSK_FUR_1 | 288 | 292 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.706 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.466 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.417 |
DEG_SCF_TRCP1_1 | 79 | 84 | PF00400 | 0.622 |
DOC_ANK_TNKS_1 | 438 | 445 | PF00023 | 0.371 |
DOC_MAPK_gen_1 | 424 | 432 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 521 | 530 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 424 | 432 | PF00069 | 0.528 |
DOC_MAPK_RevD_3 | 419 | 434 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.501 |
DOC_PP1_RVXF_1 | 252 | 259 | PF00149 | 0.510 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.617 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.480 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.673 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 524 | 529 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 165 | 181 | PF00022 | 0.520 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_BIR_III_2 | 62 | 66 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.703 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.724 |
LIG_CaM_IQ_9 | 192 | 207 | PF13499 | 0.515 |
LIG_CaM_IQ_9 | 249 | 265 | PF13499 | 0.428 |
LIG_CaM_IQ_9 | 425 | 441 | PF13499 | 0.599 |
LIG_eIF4E_1 | 118 | 124 | PF01652 | 0.577 |
LIG_EVH1_2 | 105 | 109 | PF00568 | 0.577 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.554 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.623 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.496 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.561 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.662 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.521 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.483 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.576 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.545 |
LIG_GBD_Chelix_1 | 422 | 430 | PF00786 | 0.359 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 497 | 505 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 522 | 531 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.477 |
LIG_PCNA_yPIPBox_3 | 157 | 169 | PF02747 | 0.476 |
LIG_PDZ_Class_1 | 564 | 569 | PF00595 | 0.549 |
LIG_REV1ctd_RIR_1 | 291 | 298 | PF16727 | 0.462 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.478 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.516 |
LIG_SH2_GRB2like | 147 | 150 | PF00017 | 0.592 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 498 | 502 | PF00017 | 0.552 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.640 |
LIG_SH2_SRC | 245 | 248 | PF00017 | 0.487 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.671 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.577 |
LIG_SH3_1 | 12 | 18 | PF00018 | 0.619 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.619 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.573 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.581 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.713 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.490 |
LIG_WW_3 | 133 | 137 | PF00397 | 0.623 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.578 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.669 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.529 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.516 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.503 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.516 |
MOD_GlcNHglycan | 473 | 477 | PF01048 | 0.539 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.773 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.732 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.758 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.644 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.638 |
MOD_N-GLC_2 | 95 | 97 | PF02516 | 0.604 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.553 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.529 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.468 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.546 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.664 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.634 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.312 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.628 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.425 |
MOD_PK_1 | 34 | 40 | PF00069 | 0.606 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.436 |
MOD_PKB_1 | 406 | 414 | PF00069 | 0.518 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.529 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.623 |
MOD_Plk_2-3 | 313 | 319 | PF00069 | 0.527 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.565 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.723 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 461 | 464 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 114 | 119 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 368 | 377 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 443 | 448 | PF00179 | 0.500 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 439 | 442 | PF00400 | 0.492 |
TRG_NLS_MonoCore_2 | 287 | 292 | PF00514 | 0.650 |
TRG_NLS_MonoExtC_3 | 287 | 292 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 285 | 292 | PF00514 | 0.581 |
TRG_NLS_MonoExtN_4 | 433 | 440 | PF00514 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 408 | 413 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 424 | 429 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9S0 | Leptomonas seymouri | 45% | 95% |
A0A1X0P7R9 | Trypanosomatidae | 33% | 100% |
A0A3S7WVD7 | Leishmania donovani | 91% | 100% |
A0A422P367 | Trypanosoma rangeli | 34% | 100% |
A4HA10 | Leishmania braziliensis | 65% | 95% |
A4HY74 | Leishmania infantum | 90% | 100% |
D0A0J3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AS04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BSD1 | Trypanosoma cruzi | 35% | 100% |