| 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: 1, no: 5 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AUI2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 7 |
| GO:0005488 | binding | 1 | 7 |
| GO:0016787 | hydrolase activity | 2 | 7 |
| GO:0043167 | ion binding | 2 | 7 |
| GO:0043169 | cation binding | 3 | 7 |
| GO:0046872 | metal ion binding | 4 | 7 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.507 |
| CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.557 |
| CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.648 |
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.557 |
| CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.444 |
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.557 |
| CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.444 |
| CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.422 |
| CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.422 |
| CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.631 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.707 |
| CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.636 |
| CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.699 |
| DEG_APCC_KENBOX_2 | 39 | 43 | PF00400 | 0.380 |
| DEG_ODPH_VHL_1 | 287 | 300 | PF01847 | 0.518 |
| DOC_CKS1_1 | 173 | 178 | PF01111 | 0.580 |
| DOC_CYCLIN_yCln2_LP_2 | 315 | 321 | PF00134 | 0.467 |
| DOC_MAPK_gen_1 | 54 | 63 | PF00069 | 0.376 |
| DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.542 |
| DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.403 |
| DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.501 |
| DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.677 |
| DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.367 |
| DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.420 |
| DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.371 |
| DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.547 |
| DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.458 |
| DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.664 |
| DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.461 |
| DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.407 |
| DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.671 |
| LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.413 |
| LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.465 |
| LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.481 |
| LIG_Actin_WH2_2 | 175 | 191 | PF00022 | 0.467 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
| LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.474 |
| LIG_deltaCOP1_diTrp_1 | 146 | 152 | PF00928 | 0.501 |
| LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.380 |
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.391 |
| LIG_FHA_1 | 131 | 137 | PF00498 | 0.347 |
| LIG_FHA_1 | 164 | 170 | PF00498 | 0.669 |
| LIG_FHA_1 | 289 | 295 | PF00498 | 0.390 |
| LIG_FHA_2 | 341 | 347 | PF00498 | 0.689 |
| LIG_FHA_2 | 395 | 401 | PF00498 | 0.647 |
| LIG_FHA_2 | 96 | 102 | PF00498 | 0.672 |
| LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.399 |
| LIG_LIR_Apic_2 | 353 | 357 | PF02991 | 0.463 |
| LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.660 |
| LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.397 |
| LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.401 |
| LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.440 |
| LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.460 |
| LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.440 |
| LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.383 |
| LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.469 |
| LIG_Pex14_2 | 386 | 390 | PF04695 | 0.605 |
| LIG_Rb_LxCxE_1 | 332 | 353 | PF01857 | 0.539 |
| LIG_SH2_CRK | 209 | 213 | PF00017 | 0.374 |
| LIG_SH2_CRK | 331 | 335 | PF00017 | 0.451 |
| LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.391 |
| LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.387 |
| LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.405 |
| LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.374 |
| LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.451 |
| LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.384 |
| LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.501 |
| LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.565 |
| LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.609 |
| LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.532 |
| LIG_SH3_3 | 170 | 176 | PF00018 | 0.558 |
| LIG_SH3_3 | 20 | 26 | PF00018 | 0.472 |
| LIG_SH3_3 | 315 | 321 | PF00018 | 0.657 |
| LIG_SH3_3 | 4 | 10 | PF00018 | 0.485 |
| LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.423 |
| LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.574 |
| LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.581 |
| LIG_TRFH_1 | 285 | 289 | PF08558 | 0.397 |
| LIG_TYR_ITIM | 329 | 334 | PF00017 | 0.465 |
| LIG_WW_1 | 289 | 292 | PF00397 | 0.512 |
| MOD_CDK_SPK_2 | 193 | 198 | PF00069 | 0.461 |
| MOD_CK1_1 | 183 | 189 | PF00069 | 0.411 |
| MOD_CK1_1 | 261 | 267 | PF00069 | 0.558 |
| MOD_CK1_1 | 303 | 309 | PF00069 | 0.523 |
| MOD_CK1_1 | 342 | 348 | PF00069 | 0.569 |
| MOD_CK2_1 | 107 | 113 | PF00069 | 0.597 |
| MOD_CK2_1 | 142 | 148 | PF00069 | 0.403 |
| MOD_CK2_1 | 233 | 239 | PF00069 | 0.702 |
| MOD_CK2_1 | 340 | 346 | PF00069 | 0.643 |
| MOD_CMANNOS | 149 | 152 | PF00535 | 0.563 |
| MOD_DYRK1A_RPxSP_1 | 172 | 176 | PF00069 | 0.551 |
| MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.569 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.648 |
| MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.609 |
| MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.541 |
| MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.458 |
| MOD_GSK3_1 | 163 | 170 | PF00069 | 0.656 |
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.398 |
| MOD_GSK3_1 | 193 | 200 | PF00069 | 0.471 |
| MOD_GSK3_1 | 212 | 219 | PF00069 | 0.576 |
| MOD_GSK3_1 | 228 | 235 | PF00069 | 0.537 |
| MOD_GSK3_1 | 279 | 286 | PF00069 | 0.468 |
| MOD_GSK3_1 | 296 | 303 | PF00069 | 0.473 |
| MOD_GSK3_1 | 394 | 401 | PF00069 | 0.482 |
| MOD_LATS_1 | 88 | 94 | PF00433 | 0.433 |
| MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.307 |
| MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.524 |
| MOD_NEK2_1 | 102 | 107 | PF00069 | 0.638 |
| MOD_NEK2_1 | 12 | 17 | PF00069 | 0.418 |
| MOD_NEK2_1 | 212 | 217 | PF00069 | 0.529 |
| MOD_NEK2_1 | 361 | 366 | PF00069 | 0.748 |
| MOD_NEK2_2 | 184 | 189 | PF00069 | 0.537 |
| MOD_PIKK_1 | 229 | 235 | PF00454 | 0.704 |
| MOD_PIKK_1 | 96 | 102 | PF00454 | 0.701 |
| MOD_PKA_2 | 197 | 203 | PF00069 | 0.553 |
| MOD_PKA_2 | 398 | 404 | PF00069 | 0.465 |
| MOD_Plk_1 | 180 | 186 | PF00069 | 0.390 |
| MOD_Plk_1 | 283 | 289 | PF00069 | 0.300 |
| MOD_Plk_4 | 12 | 18 | PF00069 | 0.413 |
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.408 |
| MOD_Plk_4 | 288 | 294 | PF00069 | 0.391 |
| MOD_Plk_4 | 330 | 336 | PF00069 | 0.548 |
| MOD_Plk_4 | 406 | 412 | PF00069 | 0.590 |
| MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.651 |
| MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.466 |
| MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.414 |
| MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.675 |
| TRG_DiLeu_BaEn_1 | 262 | 267 | PF01217 | 0.427 |
| TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.563 |
| TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.377 |
| TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.509 |
| TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.460 |
| TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.532 |
| TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.441 |
| TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.391 |
| TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.490 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IIQ0 | Leptomonas seymouri | 51% | 100% |
| A0A3S7WVU6 | Leishmania donovani | 89% | 100% |
| A4HYN2 | Leishmania infantum | 89% | 100% |
| E9AI97 | Leishmania braziliensis | 73% | 100% |
| Q4QD02 | Leishmania major | 88% | 100% |