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: A0A3S7X8J7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.678 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.624 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.410 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.651 |
DOC_CYCLIN_RxL_1 | 16 | 25 | PF00134 | 0.573 |
DOC_CYCLIN_RxL_1 | 394 | 404 | PF00134 | 0.408 |
DOC_MAPK_DCC_7 | 28 | 37 | PF00069 | 0.635 |
DOC_MAPK_DCC_7 | 397 | 405 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 353 | 359 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 394 | 402 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 28 | 37 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 397 | 405 | PF00069 | 0.434 |
DOC_MIT_MIM_1 | 134 | 142 | PF04212 | 0.570 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.545 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.545 |
LIG_Actin_WH2_2 | 392 | 410 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 90 | 107 | PF00022 | 0.607 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.630 |
LIG_CaM_IQ_9 | 206 | 221 | PF13499 | 0.522 |
LIG_CaM_IQ_9 | 90 | 105 | PF13499 | 0.642 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.551 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.702 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.687 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.562 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.543 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.547 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.601 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.561 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.727 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.451 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.678 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 382 | 390 | PF00786 | 0.480 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.615 |
LIG_NRBOX | 282 | 288 | PF00104 | 0.584 |
LIG_NRBOX | 402 | 408 | PF00104 | 0.335 |
LIG_RPA_C_Fungi | 348 | 360 | PF08784 | 0.561 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.335 |
LIG_SUMO_SIM_par_1 | 4 | 9 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 57 | 62 | PF11976 | 0.465 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.590 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.623 |
LIG_TRAF2_2 | 68 | 73 | PF00917 | 0.643 |
LIG_UBA3_1 | 399 | 408 | PF00899 | 0.447 |
MOD_CDC14_SPxK_1 | 78 | 81 | PF00782 | 0.610 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.619 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.569 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.655 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.545 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.626 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.688 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.669 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.745 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.660 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.654 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.692 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.456 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.571 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.749 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.601 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.456 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.591 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.516 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.647 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.503 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.585 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.552 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.617 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.610 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.497 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.420 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.502 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.570 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.669 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.555 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.578 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.615 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.515 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.712 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.552 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.621 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.591 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.498 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.468 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.502 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.476 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.519 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.640 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.684 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.358 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.542 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.670 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.753 |
MOD_SUMO_rev_2 | 155 | 165 | PF00179 | 0.637 |
MOD_SUMO_rev_2 | 250 | 258 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.597 |
TRG_DiLeu_BaEn_1 | 282 | 287 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 281 | 285 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF68 | Leptomonas seymouri | 40% | 90% |
A0A0S4KIU3 | Bodo saltans | 28% | 91% |
A0A1X0PB65 | Trypanosomatidae | 24% | 92% |
A4HBD2 | Leishmania braziliensis | 66% | 100% |
A4IAI0 | Leishmania infantum | 99% | 100% |
C9ZLQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 92% |
E9B5K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q2D2 | Leishmania major | 84% | 100% |
V5BW28 | Trypanosoma cruzi | 29% | 89% |