| 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: A4H714
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.434 |
| CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.541 |
| CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.584 |
| CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.494 |
| CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.653 |
| CLV_PCSK_FUR_1 | 159 | 163 | PF00082 | 0.632 |
| CLV_PCSK_FUR_1 | 66 | 70 | PF00082 | 0.633 |
| CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.435 |
| CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.525 |
| CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.402 |
| CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.533 |
| CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.568 |
| CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.520 |
| CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.565 |
| CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.593 |
| CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.470 |
| CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.564 |
| CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.533 |
| CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.572 |
| CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.407 |
| CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.563 |
| CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.670 |
| CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.650 |
| DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.522 |
| DEG_SPOP_SBC_1 | 222 | 226 | PF00917 | 0.505 |
| DOC_CYCLIN_RxL_1 | 86 | 95 | PF00134 | 0.685 |
| DOC_MAPK_DCC_7 | 89 | 98 | PF00069 | 0.453 |
| DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.565 |
| DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.592 |
| DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.623 |
| DOC_MAPK_MEF2A_6 | 89 | 98 | PF00069 | 0.575 |
| DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.681 |
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.715 |
| DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.636 |
| DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.690 |
| DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.434 |
| DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.644 |
| DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.638 |
| DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.747 |
| DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.634 |
| LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.610 |
| LIG_14-3-3_CanoR_1 | 177 | 181 | PF00244 | 0.659 |
| LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.626 |
| LIG_14-3-3_CanoR_1 | 320 | 330 | PF00244 | 0.558 |
| LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.624 |
| LIG_14-3-3_CanoR_1 | 69 | 76 | PF00244 | 0.604 |
| LIG_APCC_ABBA_1 | 411 | 416 | PF00400 | 0.470 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.641 |
| LIG_FHA_1 | 22 | 28 | PF00498 | 0.704 |
| LIG_FHA_1 | 268 | 274 | PF00498 | 0.644 |
| LIG_FHA_1 | 41 | 47 | PF00498 | 0.517 |
| LIG_FHA_1 | 93 | 99 | PF00498 | 0.655 |
| LIG_FHA_2 | 282 | 288 | PF00498 | 0.634 |
| LIG_FHA_2 | 42 | 48 | PF00498 | 0.438 |
| LIG_FHA_2 | 446 | 452 | PF00498 | 0.687 |
| LIG_Integrin_RGD_1 | 281 | 283 | PF01839 | 0.698 |
| LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.756 |
| LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.639 |
| LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.749 |
| LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.614 |
| LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.477 |
| LIG_PDZ_Class_1 | 455 | 460 | PF00595 | 0.547 |
| LIG_SH2_CRK | 237 | 241 | PF00017 | 0.615 |
| LIG_SH2_CRK | 53 | 57 | PF00017 | 0.581 |
| LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.459 |
| LIG_SH3_2 | 33 | 38 | PF14604 | 0.634 |
| LIG_SH3_3 | 30 | 36 | PF00018 | 0.634 |
| LIG_SH3_3 | 376 | 382 | PF00018 | 0.515 |
| LIG_SH3_3 | 397 | 403 | PF00018 | 0.477 |
| LIG_SH3_3 | 77 | 83 | PF00018 | 0.664 |
| LIG_SUMO_SIM_anti_2 | 427 | 434 | PF11976 | 0.621 |
| LIG_SUMO_SIM_par_1 | 427 | 434 | PF11976 | 0.609 |
| LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.662 |
| LIG_TYR_ITIM | 51 | 56 | PF00017 | 0.587 |
| MOD_CK1_1 | 11 | 17 | PF00069 | 0.701 |
| MOD_CK1_1 | 223 | 229 | PF00069 | 0.594 |
| MOD_CK1_1 | 233 | 239 | PF00069 | 0.621 |
| MOD_CK1_1 | 324 | 330 | PF00069 | 0.526 |
| MOD_CK1_1 | 381 | 387 | PF00069 | 0.689 |
| MOD_CK1_1 | 39 | 45 | PF00069 | 0.639 |
| MOD_CK2_1 | 259 | 265 | PF00069 | 0.701 |
| MOD_CK2_1 | 281 | 287 | PF00069 | 0.554 |
| MOD_CK2_1 | 313 | 319 | PF00069 | 0.720 |
| MOD_CK2_1 | 385 | 391 | PF00069 | 0.650 |
| MOD_CK2_1 | 41 | 47 | PF00069 | 0.627 |
| MOD_DYRK1A_RPxSP_1 | 81 | 85 | PF00069 | 0.700 |
| MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.664 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.578 |
| MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.671 |
| MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.601 |
| MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.526 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.497 |
| MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.633 |
| MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.539 |
| MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.686 |
| MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.660 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.453 |
| MOD_GSK3_1 | 17 | 24 | PF00069 | 0.708 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.607 |
| MOD_GSK3_1 | 205 | 212 | PF00069 | 0.573 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.517 |
| MOD_GSK3_1 | 267 | 274 | PF00069 | 0.691 |
| MOD_GSK3_1 | 36 | 43 | PF00069 | 0.619 |
| MOD_GSK3_1 | 377 | 384 | PF00069 | 0.742 |
| MOD_GSK3_1 | 452 | 459 | PF00069 | 0.756 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.618 |
| MOD_GSK3_1 | 94 | 101 | PF00069 | 0.645 |
| MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.684 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.735 |
| MOD_NEK2_1 | 16 | 21 | PF00069 | 0.511 |
| MOD_NEK2_2 | 176 | 181 | PF00069 | 0.610 |
| MOD_NEK2_2 | 94 | 99 | PF00069 | 0.433 |
| MOD_PKA_1 | 68 | 74 | PF00069 | 0.641 |
| MOD_PKA_2 | 111 | 117 | PF00069 | 0.574 |
| MOD_PKA_2 | 176 | 182 | PF00069 | 0.634 |
| MOD_PKA_2 | 205 | 211 | PF00069 | 0.612 |
| MOD_PKA_2 | 319 | 325 | PF00069 | 0.595 |
| MOD_PKA_2 | 68 | 74 | PF00069 | 0.560 |
| MOD_PKB_1 | 370 | 378 | PF00069 | 0.538 |
| MOD_Plk_1 | 304 | 310 | PF00069 | 0.554 |
| MOD_Plk_1 | 452 | 458 | PF00069 | 0.659 |
| MOD_Plk_4 | 381 | 387 | PF00069 | 0.727 |
| MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.435 |
| MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.643 |
| MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.639 |
| MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.745 |
| MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.637 |
| TRG_DiLeu_BaLyEn_6 | 285 | 290 | PF01217 | 0.571 |
| TRG_DiLeu_BaLyEn_6 | 46 | 51 | PF01217 | 0.511 |
| TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.547 |
| TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.580 |
| TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.427 |
| TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.551 |
| TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.634 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1S5 | Leptomonas seymouri | 49% | 100% |
| A0A0S4IQ31 | Bodo saltans | 26% | 70% |
| A0A0S4JQK5 | Bodo saltans | 26% | 88% |
| A0A1X0NNN8 | Trypanosomatidae | 27% | 84% |
| A0A3R7MBM6 | Trypanosoma rangeli | 26% | 90% |
| A0A3S5H6M8 | Leishmania donovani | 73% | 83% |
| A4HVE2 | Leishmania infantum | 73% | 83% |
| E9AP40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
| Q4QGE8 | Leishmania major | 72% | 100% |