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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AFT7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.471 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.590 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.495 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.481 |
DEG_SPOP_SBC_1 | 505 | 509 | PF00917 | 0.655 |
DOC_CYCLIN_RxL_1 | 197 | 207 | PF00134 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.457 |
DOC_MAPK_gen_1 | 261 | 270 | PF00069 | 0.519 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.614 |
DOC_USP7_MATH_2 | 123 | 129 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 393 | 397 | PF12436 | 0.587 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.548 |
LIG_Actin_WH2_2 | 70 | 85 | PF00022 | 0.617 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.566 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_eIF4E_1 | 26 | 32 | PF01652 | 0.545 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.557 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.512 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.674 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.544 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.539 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.630 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.556 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.608 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 309 | 312 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.456 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.566 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.613 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.641 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.651 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.501 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.615 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.567 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.577 |
LIG_UBA3_1 | 112 | 119 | PF00899 | 0.516 |
LIG_UBA3_1 | 191 | 200 | PF00899 | 0.596 |
LIG_UBA3_1 | 78 | 83 | PF00899 | 0.532 |
MOD_CDC14_SPxK_1 | 155 | 158 | PF00782 | 0.525 |
MOD_CDK_SPxK_1 | 152 | 158 | PF00069 | 0.682 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.594 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.568 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.675 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.627 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.547 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.550 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.529 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.648 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.516 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.533 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.588 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.683 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.699 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.540 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.552 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.614 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.666 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.512 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.690 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.722 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.621 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.380 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.641 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.484 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.595 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.728 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.562 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.653 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.642 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.670 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.767 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.621 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.617 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.598 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.553 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.613 |
MOD_NEK2_2 | 392 | 397 | PF00069 | 0.471 |
MOD_NEK2_2 | 69 | 74 | PF00069 | 0.523 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.490 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.495 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.540 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.685 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.595 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.709 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.571 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.445 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.635 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.536 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.442 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.682 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.631 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.597 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.637 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.595 |
MOD_SUMO_rev_2 | 124 | 129 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 420 | 428 | PF00179 | 0.634 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.627 |
TRG_DiLeu_BaEn_4 | 298 | 304 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 471 | 474 | PF00400 | 0.464 |
TRG_NES_CRM1_1 | 379 | 394 | PF08389 | 0.446 |
TRG_NES_CRM1_1 | 441 | 455 | PF08389 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 426 | 430 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P962 | Leptomonas seymouri | 47% | 91% |
A0A1X0P582 | Trypanosomatidae | 25% | 100% |
A0A3R7P212 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X9X8 | Leishmania donovani | 91% | 100% |
A4HNC7 | Leishmania braziliensis | 68% | 98% |
A4IC00 | Leishmania infantum | 92% | 100% |
E9B6Y9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5C2K9 | Trypanosoma cruzi | 26% | 100% |