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: E9B2W3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.527 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.719 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.561 |
DEG_SCF_TRCP1_1 | 320 | 326 | PF00400 | 0.612 |
DOC_ANK_TNKS_1 | 37 | 44 | PF00023 | 0.548 |
DOC_CYCLIN_RxL_1 | 355 | 365 | PF00134 | 0.718 |
DOC_CYCLIN_RxL_1 | 405 | 414 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 160 | PF00134 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 393 | 399 | PF00134 | 0.697 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.702 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.620 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.703 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.697 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.643 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.699 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 95 | 105 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.695 |
LIG_ActinCP_TwfCPI_2 | 29 | 38 | PF01115 | 0.556 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.670 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.613 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.693 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.727 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.636 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.734 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.510 |
LIG_FXI_DFP_1 | 172 | 176 | PF00024 | 0.676 |
LIG_Integrin_isoDGR_2 | 310 | 312 | PF01839 | 0.529 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 28 | 32 | PF02991 | 0.586 |
LIG_LIR_Apic_2 | 50 | 54 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.640 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.637 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.773 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.685 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 192 | 196 | PF00017 | 0.688 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.529 |
LIG_SH3_1 | 179 | 185 | PF00018 | 0.681 |
LIG_SH3_2 | 396 | 401 | PF14604 | 0.629 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.681 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.710 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.625 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.582 |
LIG_SUMO_SIM_par_1 | 156 | 162 | PF11976 | 0.633 |
LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.470 |
LIG_TYR_ITSM | 188 | 195 | PF00017 | 0.734 |
LIG_UBA3_1 | 22 | 31 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 26 | 31 | PF05994 | 0.575 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.553 |
MOD_CDC14_SPxK_1 | 282 | 285 | PF00782 | 0.525 |
MOD_CDK_SPxK_1 | 279 | 285 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 261 | 268 | PF00069 | 0.439 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.705 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.748 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.606 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.659 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.576 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.572 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.776 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.701 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.734 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.748 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.531 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.589 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.710 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.702 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.694 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.715 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.653 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.785 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.680 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.668 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.463 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.584 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.594 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.763 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.610 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.750 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.622 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.622 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.547 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.737 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.562 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.790 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.486 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.638 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.719 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.735 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.770 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.681 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.522 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.513 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.542 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.613 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.759 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.677 |
MOD_SUMO_rev_2 | 36 | 45 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 369 | 375 | PF00179 | 0.706 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.725 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.730 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I475 | Leptomonas seymouri | 57% | 100% |
A0A1X0NUD6 | Trypanosomatidae | 32% | 100% |
A0A3Q8IGT2 | Leishmania donovani | 86% | 100% |
A4I801 | Leishmania infantum | 86% | 100% |
Q4Q593 | Leishmania major | 85% | 100% |
V5BF21 | Trypanosoma cruzi | 27% | 100% |