| 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: 5 |
| NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AM37
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 6 |
| GO:0043167 | ion binding | 2 | 6 |
| GO:0043169 | cation binding | 3 | 6 |
| GO:0046872 | metal ion binding | 4 | 6 |
| GO:0003676 | nucleic acid binding | 3 | 1 |
| GO:0003723 | RNA binding | 4 | 1 |
| GO:0097159 | organic cyclic compound binding | 2 | 1 |
| GO:1901363 | heterocyclic compound binding | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.546 |
| CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.569 |
| CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.520 |
| CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.695 |
| CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.520 |
| CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.617 |
| CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.535 |
| CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.437 |
| CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.562 |
| DEG_APCC_DBOX_1 | 218 | 226 | PF00400 | 0.521 |
| DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.478 |
| DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.634 |
| DOC_CKS1_1 | 102 | 107 | PF01111 | 0.682 |
| DOC_CKS1_1 | 198 | 203 | PF01111 | 0.526 |
| DOC_CYCLIN_RxL_1 | 297 | 305 | PF00134 | 0.522 |
| DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.616 |
| DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.621 |
| DOC_MAPK_gen_1 | 57 | 68 | PF00069 | 0.613 |
| DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.504 |
| DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.502 |
| DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.578 |
| DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.606 |
| DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.732 |
| DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.673 |
| DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.681 |
| DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.581 |
| DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.512 |
| DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.524 |
| DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.483 |
| DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.476 |
| DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.474 |
| DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.625 |
| DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.709 |
| DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.541 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.505 |
| DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.652 |
| LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.597 |
| LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.646 |
| LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.593 |
| LIG_Actin_WH2_2 | 206 | 221 | PF00022 | 0.443 |
| LIG_Actin_WH2_2 | 272 | 290 | PF00022 | 0.467 |
| LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.506 |
| LIG_CSL_BTD_1 | 142 | 145 | PF09270 | 0.502 |
| LIG_FHA_1 | 12 | 18 | PF00498 | 0.615 |
| LIG_FHA_1 | 191 | 197 | PF00498 | 0.651 |
| LIG_FHA_1 | 22 | 28 | PF00498 | 0.437 |
| LIG_FHA_1 | 224 | 230 | PF00498 | 0.612 |
| LIG_FHA_1 | 373 | 379 | PF00498 | 0.467 |
| LIG_FHA_2 | 243 | 249 | PF00498 | 0.629 |
| LIG_FHA_2 | 273 | 279 | PF00498 | 0.647 |
| LIG_FHA_2 | 362 | 368 | PF00498 | 0.682 |
| LIG_FHA_2 | 377 | 383 | PF00498 | 0.587 |
| LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.593 |
| LIG_LIR_Apic_2 | 282 | 286 | PF02991 | 0.631 |
| LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.476 |
| LIG_LIR_Gen_1 | 315 | 324 | PF02991 | 0.611 |
| LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.472 |
| LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.670 |
| LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.651 |
| LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.557 |
| LIG_NRBOX | 379 | 385 | PF00104 | 0.628 |
| LIG_SH2_CRK | 317 | 321 | PF00017 | 0.655 |
| LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.625 |
| LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.690 |
| LIG_SH2_STAT3 | 281 | 284 | PF00017 | 0.651 |
| LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.515 |
| LIG_SH3_2 | 102 | 107 | PF14604 | 0.682 |
| LIG_SH3_3 | 144 | 150 | PF00018 | 0.565 |
| LIG_SH3_3 | 238 | 244 | PF00018 | 0.539 |
| LIG_SH3_3 | 396 | 402 | PF00018 | 0.588 |
| LIG_SH3_3 | 99 | 105 | PF00018 | 0.665 |
| LIG_SH3_4 | 5 | 12 | PF00018 | 0.735 |
| LIG_SUMO_SIM_anti_2 | 379 | 387 | PF11976 | 0.626 |
| LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.549 |
| LIG_SUMO_SIM_par_1 | 220 | 226 | PF11976 | 0.506 |
| LIG_SUMO_SIM_par_1 | 375 | 382 | PF11976 | 0.574 |
| LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.528 |
| LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.509 |
| LIG_WW_3 | 143 | 147 | PF00397 | 0.501 |
| MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.680 |
| MOD_CK1_1 | 190 | 196 | PF00069 | 0.643 |
| MOD_CK1_1 | 203 | 209 | PF00069 | 0.672 |
| MOD_CK1_1 | 236 | 242 | PF00069 | 0.503 |
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.476 |
| MOD_CK2_1 | 287 | 293 | PF00069 | 0.577 |
| MOD_DYRK1A_RPxSP_1 | 146 | 150 | PF00069 | 0.504 |
| MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.762 |
| MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.642 |
| MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.603 |
| MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.653 |
| MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.537 |
| MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.466 |
| MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.523 |
| MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.566 |
| MOD_GlcNHglycan | 394 | 399 | PF01048 | 0.550 |
| MOD_GlcNHglycan | 97 | 101 | PF01048 | 0.495 |
| MOD_GSK3_1 | 169 | 176 | PF00069 | 0.676 |
| MOD_GSK3_1 | 187 | 194 | PF00069 | 0.657 |
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.523 |
| MOD_GSK3_1 | 217 | 224 | PF00069 | 0.484 |
| MOD_GSK3_1 | 357 | 364 | PF00069 | 0.617 |
| MOD_GSK3_1 | 372 | 379 | PF00069 | 0.528 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.436 |
| MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.629 |
| MOD_NEK2_1 | 119 | 124 | PF00069 | 0.722 |
| MOD_NEK2_1 | 287 | 292 | PF00069 | 0.582 |
| MOD_NEK2_1 | 316 | 321 | PF00069 | 0.509 |
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.646 |
| MOD_NEK2_2 | 179 | 184 | PF00069 | 0.511 |
| MOD_NEK2_2 | 328 | 333 | PF00069 | 0.503 |
| MOD_PIKK_1 | 251 | 257 | PF00454 | 0.700 |
| MOD_PIKK_1 | 338 | 344 | PF00454 | 0.513 |
| MOD_PIKK_1 | 44 | 50 | PF00454 | 0.494 |
| MOD_PKA_2 | 145 | 151 | PF00069 | 0.502 |
| MOD_PKA_2 | 272 | 278 | PF00069 | 0.644 |
| MOD_PKA_2 | 322 | 328 | PF00069 | 0.596 |
| MOD_Plk_1 | 163 | 169 | PF00069 | 0.681 |
| MOD_Plk_1 | 62 | 68 | PF00069 | 0.509 |
| MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.644 |
| MOD_Plk_4 | 13 | 19 | PF00069 | 0.623 |
| MOD_Plk_4 | 138 | 144 | PF00069 | 0.515 |
| MOD_Plk_4 | 208 | 214 | PF00069 | 0.484 |
| MOD_Plk_4 | 298 | 304 | PF00069 | 0.514 |
| MOD_Plk_4 | 376 | 382 | PF00069 | 0.622 |
| MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.712 |
| MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.539 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.507 |
| MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.657 |
| MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.682 |
| MOD_SUMO_rev_2 | 162 | 167 | PF00179 | 0.686 |
| TRG_DiLeu_BaEn_4 | 162 | 168 | PF01217 | 0.518 |
| TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.659 |
| TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.516 |
| TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.698 |
| TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.517 |
| TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.411 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3S7X275 | Leishmania donovani | 88% | 100% |
| A4HH43 | Leishmania braziliensis | 68% | 100% |
| A4I496 | Leishmania infantum | 88% | 100% |
| E9ADP3 | Leishmania major | 88% | 100% |