Uncharacterized Protein, Uncharacterized
| 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: A4IAJ5
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.498 |
| CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.660 |
| CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.694 |
| CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.647 |
| CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.585 |
| CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.418 |
| CLV_PCSK_FUR_1 | 196 | 200 | PF00082 | 0.572 |
| CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.731 |
| CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.680 |
| CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.522 |
| CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.319 |
| CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.580 |
| CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.609 |
| CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.286 |
| CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.344 |
| CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.323 |
| DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.553 |
| DOC_CKS1_1 | 286 | 291 | PF01111 | 0.487 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 34 | 43 | PF00134 | 0.410 |
| DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.410 |
| DOC_MAPK_gen_1 | 132 | 139 | PF00069 | 0.644 |
| DOC_MAPK_gen_1 | 287 | 295 | PF00069 | 0.439 |
| DOC_MAPK_MEF2A_6 | 297 | 304 | PF00069 | 0.559 |
| DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.294 |
| DOC_PP1_RVXF_1 | 95 | 101 | PF00149 | 0.373 |
| DOC_PP1_SILK_1 | 399 | 404 | PF00149 | 0.455 |
| DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.724 |
| DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.420 |
| DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.545 |
| DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.741 |
| DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.657 |
| DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.496 |
| DOC_USP7_MATH_2 | 30 | 36 | PF00917 | 0.355 |
| DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.668 |
| DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.574 |
| DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.441 |
| DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.474 |
| DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.317 |
| DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.391 |
| LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.584 |
| LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.357 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.565 |
| LIG_BIR_III_2 | 344 | 348 | PF00653 | 0.427 |
| LIG_FHA_1 | 132 | 138 | PF00498 | 0.653 |
| LIG_FHA_1 | 148 | 154 | PF00498 | 0.431 |
| LIG_FHA_1 | 257 | 263 | PF00498 | 0.458 |
| LIG_FHA_1 | 361 | 367 | PF00498 | 0.476 |
| LIG_FHA_2 | 107 | 113 | PF00498 | 0.503 |
| LIG_FHA_2 | 209 | 215 | PF00498 | 0.631 |
| LIG_FHA_2 | 246 | 252 | PF00498 | 0.496 |
| LIG_FHA_2 | 330 | 336 | PF00498 | 0.360 |
| LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.503 |
| LIG_LIR_Gen_1 | 3 | 10 | PF02991 | 0.452 |
| LIG_LIR_Gen_1 | 35 | 44 | PF02991 | 0.300 |
| LIG_LIR_Gen_1 | 395 | 406 | PF02991 | 0.351 |
| LIG_LIR_Gen_1 | 72 | 80 | PF02991 | 0.311 |
| LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.443 |
| LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.300 |
| LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.353 |
| LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.318 |
| LIG_PDZ_Class_3 | 405 | 410 | PF00595 | 0.495 |
| LIG_PTAP_UEV_1 | 200 | 205 | PF05743 | 0.619 |
| LIG_Rb_pABgroove_1 | 392 | 400 | PF01858 | 0.475 |
| LIG_SH2_CRK | 398 | 402 | PF00017 | 0.368 |
| LIG_SH2_CRK | 6 | 10 | PF00017 | 0.398 |
| LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.403 |
| LIG_SH2_NCK_1 | 6 | 10 | PF00017 | 0.391 |
| LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.328 |
| LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.446 |
| LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.489 |
| LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.605 |
| LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.501 |
| LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.421 |
| LIG_SH3_1 | 198 | 204 | PF00018 | 0.644 |
| LIG_SH3_2 | 204 | 209 | PF14604 | 0.632 |
| LIG_SH3_3 | 114 | 120 | PF00018 | 0.712 |
| LIG_SH3_3 | 198 | 204 | PF00018 | 0.673 |
| LIG_SH3_3 | 278 | 284 | PF00018 | 0.445 |
| LIG_Sin3_3 | 276 | 283 | PF02671 | 0.401 |
| LIG_SUMO_SIM_par_1 | 300 | 305 | PF11976 | 0.496 |
| LIG_TRFH_1 | 90 | 94 | PF08558 | 0.322 |
| LIG_TYR_ITSM | 2 | 9 | PF00017 | 0.434 |
| LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.368 |
| MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.442 |
| MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.636 |
| MOD_CDK_SPxxK_3 | 202 | 209 | PF00069 | 0.671 |
| MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.410 |
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.574 |
| MOD_CK1_1 | 360 | 366 | PF00069 | 0.501 |
| MOD_CK2_1 | 106 | 112 | PF00069 | 0.515 |
| MOD_CK2_1 | 208 | 214 | PF00069 | 0.567 |
| MOD_CK2_1 | 329 | 335 | PF00069 | 0.390 |
| MOD_CK2_1 | 371 | 377 | PF00069 | 0.461 |
| MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.657 |
| MOD_GlcNHglycan | 171 | 175 | PF01048 | 0.753 |
| MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.614 |
| MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.545 |
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.587 |
| MOD_GSK3_1 | 170 | 177 | PF00069 | 0.622 |
| MOD_GSK3_1 | 183 | 190 | PF00069 | 0.573 |
| MOD_GSK3_1 | 208 | 215 | PF00069 | 0.626 |
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.463 |
| MOD_GSK3_1 | 245 | 252 | PF00069 | 0.381 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.431 |
| MOD_GSK3_1 | 358 | 365 | PF00069 | 0.449 |
| MOD_GSK3_1 | 61 | 68 | PF00069 | 0.282 |
| MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.284 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.474 |
| MOD_NEK2_1 | 143 | 148 | PF00069 | 0.668 |
| MOD_NEK2_1 | 170 | 175 | PF00069 | 0.618 |
| MOD_NEK2_1 | 183 | 188 | PF00069 | 0.640 |
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.690 |
| MOD_NEK2_1 | 397 | 402 | PF00069 | 0.441 |
| MOD_NEK2_2 | 218 | 223 | PF00069 | 0.736 |
| MOD_PK_1 | 362 | 368 | PF00069 | 0.422 |
| MOD_PKA_2 | 131 | 137 | PF00069 | 0.652 |
| MOD_PKA_2 | 183 | 189 | PF00069 | 0.755 |
| MOD_PKA_2 | 25 | 31 | PF00069 | 0.410 |
| MOD_Plk_4 | 32 | 38 | PF00069 | 0.306 |
| MOD_Plk_4 | 397 | 403 | PF00069 | 0.414 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.297 |
| MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.673 |
| MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.576 |
| MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.441 |
| MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.465 |
| MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.317 |
| MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.391 |
| MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.585 |
| TRG_DiLeu_BaEn_2 | 31 | 37 | PF01217 | 0.410 |
| TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.473 |
| TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.352 |
| TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.341 |
| TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.394 |
| TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.763 |
| TRG_NLS_Bipartite_1 | 191 | 213 | PF00514 | 0.630 |
| TRG_NLS_MonoExtC_3 | 208 | 214 | PF00514 | 0.595 |
| TRG_NLS_MonoExtN_4 | 206 | 213 | PF00514 | 0.602 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1ILS6 | Leptomonas seymouri | 59% | 96% |
| A0A0S4IL96 | Bodo saltans | 30% | 86% |
| A0A3R7KTI0 | Trypanosoma rangeli | 36% | 100% |
| A0A3S7X8R1 | Leishmania donovani | 100% | 100% |
| A4HBE7 | Leishmania braziliensis | 80% | 100% |
| C9ZLP5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 95% |
| E9B5L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
| Q4Q2B7 | Leishmania major | 92% | 100% |
| V5BW13 | Trypanosoma cruzi | 39% | 100% |