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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I801
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.757 |
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.696 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.629 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.523 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.723 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.545 |
DEG_SCF_TRCP1_1 | 311 | 316 | PF00400 | 0.646 |
DOC_ANK_TNKS_1 | 37 | 44 | PF00023 | 0.515 |
DOC_CYCLIN_RxL_1 | 355 | 365 | PF00134 | 0.720 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 160 | PF00134 | 0.647 |
DOC_CYCLIN_yCln2_LP_2 | 393 | 399 | PF00134 | 0.645 |
DOC_CYCLIN_yCln2_LP_2 | 85 | 91 | PF00134 | 0.527 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.712 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.652 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.456 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.704 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.468 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.634 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 95 | 105 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.667 |
LIG_Actin_WH2_2 | 79 | 97 | PF00022 | 0.537 |
LIG_ActinCP_TwfCPI_2 | 29 | 38 | PF01115 | 0.487 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.635 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.739 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.484 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.594 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.750 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.438 |
LIG_FXI_DFP_1 | 172 | 176 | PF00024 | 0.644 |
LIG_IRF3_LxIS_1 | 289 | 296 | PF10401 | 0.740 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.711 |
LIG_LIR_Apic_2 | 28 | 32 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 50 | 54 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 189 | 197 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 267 | 274 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.578 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.599 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.539 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.765 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.691 |
LIG_SH2_STAP1 | 192 | 196 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.715 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.650 |
LIG_SH3_1 | 179 | 185 | PF00018 | 0.688 |
LIG_SH3_2 | 396 | 401 | PF14604 | 0.593 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.688 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.710 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.572 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.576 |
LIG_SUMO_SIM_par_1 | 156 | 162 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.395 |
LIG_TYR_ITSM | 188 | 195 | PF00017 | 0.748 |
LIG_WRC_WIRS_1 | 26 | 31 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.502 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.719 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.737 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.737 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.555 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.596 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.724 |
MOD_GlcNHglycan | 129 | 134 | PF01048 | 0.548 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.707 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.664 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.726 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.721 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.717 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.738 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.518 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.581 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.647 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.767 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.610 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.694 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.641 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.720 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.773 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.648 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.624 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.707 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.531 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.774 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.558 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.606 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.688 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.591 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.584 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.541 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.610 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.555 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.799 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.544 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.634 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.634 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.750 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.767 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.671 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.472 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.438 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.544 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.752 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.550 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.669 |
MOD_SUMO_rev_2 | 125 | 132 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 36 | 45 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 369 | 375 | PF00179 | 0.719 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.691 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.724 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I475 | Leptomonas seymouri | 56% | 100% |
A0A1X0NUD6 | Trypanosomatidae | 31% | 100% |
A0A3Q8IGT2 | Leishmania donovani | 100% | 100% |
E9B2W3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q593 | Leishmania major | 89% | 100% |
V5BF21 | Trypanosoma cruzi | 29% | 100% |