| 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: 3 |
| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H5L9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 9 |
| GO:0003677 | DNA binding | 4 | 9 |
| GO:0005488 | binding | 1 | 9 |
| GO:0097159 | organic cyclic compound binding | 2 | 9 |
| GO:1901363 | heterocyclic compound binding | 2 | 9 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.210 |
| CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.531 |
| CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.521 |
| CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.264 |
| CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.385 |
| CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.519 |
| CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.264 |
| CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.385 |
| CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.698 |
| CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.291 |
| DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.356 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.536 |
| DEG_SIAH_1 | 212 | 220 | PF03145 | 0.532 |
| DOC_CYCLIN_RxL_1 | 39 | 49 | PF00134 | 0.294 |
| DOC_CYCLIN_yCln2_LP_2 | 216 | 219 | PF00134 | 0.701 |
| DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.367 |
| DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.735 |
| DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.291 |
| DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.385 |
| DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.291 |
| DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.461 |
| DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.571 |
| DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.647 |
| DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.517 |
| DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.540 |
| DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.521 |
| DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.658 |
| DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.521 |
| DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.527 |
| LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.407 |
| LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.711 |
| LIG_14-3-3_CanoR_1 | 448 | 457 | PF00244 | 0.320 |
| LIG_14-3-3_CanoR_1 | 58 | 68 | PF00244 | 0.367 |
| LIG_BIR_III_4 | 379 | 383 | PF00653 | 0.467 |
| LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.709 |
| LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.210 |
| LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.255 |
| LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.471 |
| LIG_FHA_1 | 137 | 143 | PF00498 | 0.524 |
| LIG_FHA_1 | 420 | 426 | PF00498 | 0.385 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.351 |
| LIG_FHA_2 | 124 | 130 | PF00498 | 0.479 |
| LIG_FHA_2 | 350 | 356 | PF00498 | 0.464 |
| LIG_FHA_2 | 47 | 53 | PF00498 | 0.461 |
| LIG_FHA_2 | 61 | 67 | PF00498 | 0.203 |
| LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.453 |
| LIG_LIR_Gen_1 | 37 | 48 | PF02991 | 0.272 |
| LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.291 |
| LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.260 |
| LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.298 |
| LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.373 |
| LIG_PDZ_Class_3 | 455 | 460 | PF00595 | 0.555 |
| LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.688 |
| LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.210 |
| LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.664 |
| LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.445 |
| LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.291 |
| LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.291 |
| LIG_SH3_3 | 371 | 377 | PF00018 | 0.456 |
| LIG_SH3_3 | 436 | 442 | PF00018 | 0.481 |
| LIG_SUMO_SIM_anti_2 | 422 | 427 | PF11976 | 0.385 |
| LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.372 |
| LIG_TRAF2_2 | 218 | 223 | PF00917 | 0.530 |
| MOD_CDK_SPK_2 | 209 | 214 | PF00069 | 0.538 |
| MOD_CDK_SPxxK_3 | 256 | 263 | PF00069 | 0.525 |
| MOD_CK1_1 | 105 | 111 | PF00069 | 0.370 |
| MOD_CK1_1 | 136 | 142 | PF00069 | 0.338 |
| MOD_CK1_1 | 160 | 166 | PF00069 | 0.660 |
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.434 |
| MOD_CK1_1 | 209 | 215 | PF00069 | 0.715 |
| MOD_CK1_1 | 243 | 249 | PF00069 | 0.582 |
| MOD_CK1_1 | 259 | 265 | PF00069 | 0.678 |
| MOD_CK1_1 | 32 | 38 | PF00069 | 0.309 |
| MOD_CK1_1 | 327 | 333 | PF00069 | 0.701 |
| MOD_CK1_1 | 449 | 455 | PF00069 | 0.341 |
| MOD_CK1_1 | 69 | 75 | PF00069 | 0.385 |
| MOD_CK2_1 | 105 | 111 | PF00069 | 0.370 |
| MOD_CK2_1 | 123 | 129 | PF00069 | 0.541 |
| MOD_CK2_1 | 292 | 298 | PF00069 | 0.687 |
| MOD_CK2_1 | 349 | 355 | PF00069 | 0.505 |
| MOD_CK2_1 | 46 | 52 | PF00069 | 0.465 |
| MOD_CK2_1 | 60 | 66 | PF00069 | 0.205 |
| MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.611 |
| MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.786 |
| MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.789 |
| MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.540 |
| MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.265 |
| MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.295 |
| MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.385 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.291 |
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.541 |
| MOD_GSK3_1 | 204 | 211 | PF00069 | 0.629 |
| MOD_GSK3_1 | 236 | 243 | PF00069 | 0.693 |
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.696 |
| MOD_GSK3_1 | 259 | 266 | PF00069 | 0.722 |
| MOD_GSK3_1 | 288 | 295 | PF00069 | 0.739 |
| MOD_GSK3_1 | 30 | 37 | PF00069 | 0.240 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.414 |
| MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.385 |
| MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.653 |
| MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.539 |
| MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.540 |
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.653 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.699 |
| MOD_NEK2_1 | 334 | 339 | PF00069 | 0.697 |
| MOD_OFUCOSY | 434 | 441 | PF10250 | 0.340 |
| MOD_PIKK_1 | 160 | 166 | PF00454 | 0.781 |
| MOD_PIKK_1 | 179 | 185 | PF00454 | 0.503 |
| MOD_PIKK_1 | 218 | 224 | PF00454 | 0.728 |
| MOD_PIKK_1 | 73 | 79 | PF00454 | 0.282 |
| MOD_PKA_2 | 19 | 25 | PF00069 | 0.385 |
| MOD_PKA_2 | 204 | 210 | PF00069 | 0.716 |
| MOD_PKA_2 | 236 | 242 | PF00069 | 0.679 |
| MOD_PKA_2 | 342 | 348 | PF00069 | 0.564 |
| MOD_PKB_1 | 149 | 157 | PF00069 | 0.618 |
| MOD_Plk_1 | 105 | 111 | PF00069 | 0.385 |
| MOD_Plk_1 | 4 | 10 | PF00069 | 0.483 |
| MOD_Plk_4 | 271 | 277 | PF00069 | 0.708 |
| MOD_Plk_4 | 336 | 342 | PF00069 | 0.652 |
| MOD_Plk_4 | 419 | 425 | PF00069 | 0.291 |
| MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.658 |
| MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.522 |
| MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.528 |
| TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.526 |
| TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.298 |
| TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.291 |
| TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.573 |
| TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.544 |
| TRG_Pf-PMV_PEXEL_1 | 359 | 364 | PF00026 | 0.464 |
| TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.513 |
| TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.291 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I698 | Leptomonas seymouri | 59% | 96% |
| A0A3S5H6D0 | Leishmania donovani | 75% | 99% |
| A0A422NV73 | Trypanosoma rangeli | 37% | 100% |
| A4HTV7 | Leishmania infantum | 75% | 99% |
| E9AMP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 96% |
| Q4QHY1 | Leishmania major | 73% | 99% |
| V5BIH0 | Trypanosoma cruzi | 39% | 100% |