| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q226
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.448 |
| CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.510 |
| CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.489 |
| CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.574 |
| CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.519 |
| CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.501 |
| CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.472 |
| CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.742 |
| CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.456 |
| CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.462 |
| CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.488 |
| CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.472 |
| CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.512 |
| CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.456 |
| CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.546 |
| CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.530 |
| CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.623 |
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.678 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.519 |
| DOC_MAPK_gen_1 | 200 | 207 | PF00069 | 0.403 |
| DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.504 |
| DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.449 |
| DOC_PP1_RVXF_1 | 313 | 320 | PF00149 | 0.400 |
| DOC_PP2B_PxIxI_1 | 328 | 334 | PF00149 | 0.561 |
| DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.479 |
| DOC_PP4_FxxP_1 | 268 | 271 | PF00568 | 0.423 |
| DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.553 |
| DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.514 |
| DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.447 |
| DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.594 |
| LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.347 |
| LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.556 |
| LIG_14-3-3_CanoR_1 | 315 | 320 | PF00244 | 0.520 |
| LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.611 |
| LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.564 |
| LIG_Actin_WH2_2 | 125 | 143 | PF00022 | 0.396 |
| LIG_Actin_WH2_2 | 22 | 40 | PF00022 | 0.518 |
| LIG_Actin_WH2_2 | 376 | 394 | PF00022 | 0.478 |
| LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.422 |
| LIG_Clathr_ClatBox_1 | 380 | 384 | PF01394 | 0.490 |
| LIG_EH1_1 | 206 | 214 | PF00400 | 0.394 |
| LIG_FHA_1 | 134 | 140 | PF00498 | 0.418 |
| LIG_FHA_1 | 222 | 228 | PF00498 | 0.405 |
| LIG_FHA_1 | 271 | 277 | PF00498 | 0.468 |
| LIG_FHA_1 | 319 | 325 | PF00498 | 0.662 |
| LIG_FHA_2 | 265 | 271 | PF00498 | 0.447 |
| LIG_FHA_2 | 399 | 405 | PF00498 | 0.376 |
| LIG_GBD_Chelix_1 | 10 | 18 | PF00786 | 0.445 |
| LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.488 |
| LIG_LIR_Gen_1 | 128 | 134 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 244 | 255 | PF02991 | 0.400 |
| LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.381 |
| LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.458 |
| LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.343 |
| LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.594 |
| LIG_NRBOX | 128 | 134 | PF00104 | 0.404 |
| LIG_Pex14_2 | 247 | 251 | PF04695 | 0.463 |
| LIG_Pex14_2 | 264 | 268 | PF04695 | 0.346 |
| LIG_PTB_Apo_2 | 306 | 313 | PF02174 | 0.512 |
| LIG_PTB_Phospho_1 | 306 | 312 | PF10480 | 0.517 |
| LIG_Rb_LxCxE_1 | 249 | 267 | PF01857 | 0.432 |
| LIG_SH2_CRK | 283 | 287 | PF00017 | 0.562 |
| LIG_SH2_SRC | 269 | 272 | PF00017 | 0.468 |
| LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.384 |
| LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.590 |
| LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.456 |
| LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.408 |
| LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.467 |
| LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.448 |
| LIG_SH3_3 | 215 | 221 | PF00018 | 0.532 |
| LIG_SH3_3 | 26 | 32 | PF00018 | 0.470 |
| LIG_SH3_3 | 276 | 282 | PF00018 | 0.449 |
| LIG_SH3_3 | 283 | 289 | PF00018 | 0.486 |
| LIG_SH3_3 | 342 | 348 | PF00018 | 0.710 |
| LIG_SUMO_SIM_anti_2 | 376 | 382 | PF11976 | 0.483 |
| LIG_SUMO_SIM_par_1 | 379 | 384 | PF11976 | 0.488 |
| LIG_UBA3_1 | 356 | 360 | PF00899 | 0.485 |
| LIG_WRC_WIRS_1 | 265 | 270 | PF05994 | 0.529 |
| LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.495 |
| MOD_CK1_1 | 119 | 125 | PF00069 | 0.421 |
| MOD_CK1_1 | 318 | 324 | PF00069 | 0.537 |
| MOD_CK1_1 | 337 | 343 | PF00069 | 0.457 |
| MOD_CK1_1 | 396 | 402 | PF00069 | 0.509 |
| MOD_CK1_1 | 58 | 64 | PF00069 | 0.760 |
| MOD_CK2_1 | 352 | 358 | PF00069 | 0.468 |
| MOD_CK2_1 | 398 | 404 | PF00069 | 0.428 |
| MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.499 |
| MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.644 |
| MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.418 |
| MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.443 |
| MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.684 |
| MOD_GSK3_1 | 115 | 122 | PF00069 | 0.379 |
| MOD_GSK3_1 | 237 | 244 | PF00069 | 0.501 |
| MOD_GSK3_1 | 318 | 325 | PF00069 | 0.631 |
| MOD_GSK3_1 | 348 | 355 | PF00069 | 0.506 |
| MOD_GSK3_1 | 67 | 74 | PF00069 | 0.679 |
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.564 |
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.722 |
| MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.496 |
| MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.514 |
| MOD_NEK2_1 | 133 | 138 | PF00069 | 0.481 |
| MOD_NEK2_1 | 140 | 145 | PF00069 | 0.529 |
| MOD_NEK2_1 | 185 | 190 | PF00069 | 0.536 |
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.601 |
| MOD_NEK2_1 | 299 | 304 | PF00069 | 0.496 |
| MOD_NEK2_1 | 398 | 403 | PF00069 | 0.461 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.708 |
| MOD_NEK2_1 | 90 | 95 | PF00069 | 0.745 |
| MOD_NEK2_2 | 21 | 26 | PF00069 | 0.514 |
| MOD_NEK2_2 | 221 | 226 | PF00069 | 0.383 |
| MOD_NEK2_2 | 246 | 251 | PF00069 | 0.483 |
| MOD_OFUCOSY | 100 | 107 | PF10250 | 0.546 |
| MOD_PIKK_1 | 119 | 125 | PF00454 | 0.463 |
| MOD_PIKK_1 | 270 | 276 | PF00454 | 0.445 |
| MOD_PKA_1 | 322 | 328 | PF00069 | 0.634 |
| MOD_PKA_1 | 334 | 340 | PF00069 | 0.556 |
| MOD_PKA_2 | 140 | 146 | PF00069 | 0.471 |
| MOD_PKA_2 | 199 | 205 | PF00069 | 0.407 |
| MOD_PKA_2 | 334 | 340 | PF00069 | 0.540 |
| MOD_Plk_1 | 241 | 247 | PF00069 | 0.414 |
| MOD_Plk_1 | 42 | 48 | PF00069 | 0.568 |
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.410 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.463 |
| MOD_Plk_4 | 264 | 270 | PF00069 | 0.575 |
| MOD_Plk_4 | 294 | 300 | PF00069 | 0.487 |
| MOD_Plk_4 | 315 | 321 | PF00069 | 0.518 |
| MOD_Plk_4 | 352 | 358 | PF00069 | 0.552 |
| MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.594 |
| MOD_SUMO_for_1 | 4 | 7 | PF00179 | 0.440 |
| MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.413 |
| MOD_SUMO_rev_2 | 355 | 361 | PF00179 | 0.478 |
| MOD_SUMO_rev_2 | 384 | 394 | PF00179 | 0.396 |
| TRG_DiLeu_BaEn_1 | 376 | 381 | PF01217 | 0.359 |
| TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.496 |
| TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.419 |
| TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.443 |
| TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.328 |
| TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.344 |
| TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.562 |
| TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.496 |
| TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.519 |
| TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.411 |
| TRG_NES_CRM1_1 | 28 | 43 | PF08389 | 0.432 |
| TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.438 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0S4JPJ4 | Bodo saltans | 34% | 86% |
| A0A1X0P9M8 | Trypanosomatidae | 36% | 100% |
| A0A3Q8IFS3 | Leishmania donovani | 93% | 100% |
| A0A422P297 | Trypanosoma rangeli | 36% | 99% |
| A4HNR0 | Leishmania braziliensis | 72% | 100% |
| A4ICT5 | Leishmania infantum | 93% | 100% |
| D0A2L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| E9ASG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |