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: E9B5K4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.641 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.444 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.545 |
DOC_CDC14_PxL_1 | 22 | 30 | PF14671 | 0.374 |
DOC_CYCLIN_RxL_1 | 16 | 23 | PF00134 | 0.562 |
DOC_CYCLIN_RxL_1 | 399 | 409 | PF00134 | 0.401 |
DOC_MAPK_DCC_7 | 402 | 410 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 358 | 364 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 399 | 407 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.429 |
DOC_MIT_MIM_1 | 127 | 135 | PF04212 | 0.567 |
DOC_PP1_RVXF_1 | 342 | 348 | PF00149 | 0.545 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.767 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.572 |
LIG_Actin_WH2_2 | 320 | 336 | PF00022 | 0.443 |
LIG_Actin_WH2_2 | 397 | 415 | PF00022 | 0.444 |
LIG_Actin_WH2_2 | 83 | 100 | PF00022 | 0.602 |
LIG_BIR_III_2 | 242 | 246 | PF00653 | 0.455 |
LIG_BIR_III_4 | 303 | 307 | PF00653 | 0.492 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.583 |
LIG_CaM_IQ_9 | 83 | 98 | PF13499 | 0.646 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.624 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.564 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.679 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.540 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.532 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.600 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.750 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.449 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.681 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.513 |
LIG_GBD_Chelix_1 | 387 | 395 | PF00786 | 0.485 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 346 | 355 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 346 | 350 | PF02991 | 0.612 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.571 |
LIG_NRBOX | 407 | 413 | PF00104 | 0.344 |
LIG_RPA_C_Fungi | 353 | 365 | PF08784 | 0.564 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.610 |
LIG_SH2_STAT3 | 29 | 32 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.344 |
LIG_SUMO_SIM_par_1 | 323 | 330 | PF11976 | 0.416 |
LIG_UBA3_1 | 404 | 413 | PF00899 | 0.444 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.564 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.565 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.649 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.552 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.620 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.692 |
MOD_GlcNHglycan | 237 | 241 | PF01048 | 0.496 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.693 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.643 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.555 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.492 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.710 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.713 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.442 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.585 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.790 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.642 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.493 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.587 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.657 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.515 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.481 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.583 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.511 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.431 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.606 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.594 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.497 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.414 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.538 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.568 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.649 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.516 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.336 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.551 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.335 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.620 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.553 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.628 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.620 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.503 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.453 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.491 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.509 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.518 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.681 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.428 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.372 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.687 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.585 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.547 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.741 |
MOD_SUMO_rev_2 | 255 | 263 | PF00179 | 0.477 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.680 |
TRG_NLS_MonoExtC_3 | 128 | 134 | PF00514 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF68 | Leptomonas seymouri | 41% | 92% |
A0A1X0PB65 | Trypanosomatidae | 25% | 95% |
A0A3S7X8J7 | Leishmania donovani | 83% | 100% |
A4HBD2 | Leishmania braziliensis | 64% | 100% |
A4IAI0 | Leishmania infantum | 83% | 89% |
C9ZLQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 94% |
Q4Q2D2 | Leishmania major | 82% | 100% |
V5BW28 | Trypanosoma cruzi | 28% | 91% |