This protein is only found among Kinetoplastds. However, its function is unclear, could be a transporter or channel protein.
| 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 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 9 |
| GO:0110165 | cellular anatomical entity | 1 | 9 |
| GO:0005635 | nuclear envelope | 4 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0005819 | spindle | 5 | 1 |
| GO:0031967 | organelle envelope | 3 | 1 |
| GO:0031975 | envelope | 2 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IH62
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.382 |
| CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.434 |
| CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.382 |
| CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.415 |
| CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.488 |
| CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.339 |
| DOC_CKS1_1 | 369 | 374 | PF01111 | 0.318 |
| DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.489 |
| DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.479 |
| DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.565 |
| DOC_MAPK_RevD_3 | 170 | 184 | PF00069 | 0.406 |
| DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.430 |
| DOC_PP2B_PxIxI_1 | 106 | 112 | PF00149 | 0.415 |
| DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.320 |
| DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.652 |
| DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.538 |
| DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.699 |
| DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.323 |
| DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.298 |
| DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.432 |
| DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.315 |
| DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.390 |
| DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.331 |
| DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.659 |
| DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.532 |
| DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.517 |
| DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.270 |
| DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.442 |
| LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.580 |
| LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.480 |
| LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.503 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
| LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.459 |
| LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.549 |
| LIG_CaM_NSCaTE_8 | 347 | 354 | PF13499 | 0.370 |
| LIG_CSL_BTD_1 | 209 | 212 | PF09270 | 0.662 |
| LIG_DLG_GKlike_1 | 123 | 130 | PF00625 | 0.507 |
| LIG_EVH1_1 | 87 | 91 | PF00568 | 0.320 |
| LIG_FHA_1 | 159 | 165 | PF00498 | 0.444 |
| LIG_FHA_1 | 216 | 222 | PF00498 | 0.292 |
| LIG_FHA_1 | 369 | 375 | PF00498 | 0.344 |
| LIG_FHA_1 | 47 | 53 | PF00498 | 0.348 |
| LIG_FHA_1 | 96 | 102 | PF00498 | 0.281 |
| LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.654 |
| LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.572 |
| LIG_LIR_Apic_2 | 49 | 54 | PF02991 | 0.329 |
| LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.319 |
| LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.519 |
| LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.314 |
| LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.370 |
| LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.366 |
| LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.660 |
| LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.345 |
| LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.540 |
| LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.642 |
| LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.350 |
| LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.324 |
| LIG_PDZ_Class_2 | 386 | 391 | PF00595 | 0.415 |
| LIG_Pex14_1 | 201 | 205 | PF04695 | 0.615 |
| LIG_Pex14_2 | 114 | 118 | PF04695 | 0.537 |
| LIG_Pex14_2 | 333 | 337 | PF04695 | 0.616 |
| LIG_Pex14_2 | 46 | 50 | PF04695 | 0.474 |
| LIG_Pex14_2 | 51 | 55 | PF04695 | 0.438 |
| LIG_PTB_Apo_2 | 384 | 391 | PF02174 | 0.318 |
| LIG_SH2_CRK | 279 | 283 | PF00017 | 0.329 |
| LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.318 |
| LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.397 |
| LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.561 |
| LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.344 |
| LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.490 |
| LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.408 |
| LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.285 |
| LIG_SH3_3 | 107 | 113 | PF00018 | 0.374 |
| LIG_SH3_3 | 206 | 212 | PF00018 | 0.622 |
| LIG_SH3_3 | 214 | 220 | PF00018 | 0.350 |
| LIG_SH3_3 | 338 | 344 | PF00018 | 0.570 |
| LIG_SH3_3 | 366 | 372 | PF00018 | 0.307 |
| LIG_SH3_3 | 85 | 91 | PF00018 | 0.416 |
| LIG_SUMO_SIM_anti_2 | 98 | 104 | PF11976 | 0.363 |
| LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.331 |
| LIG_UBA3_1 | 57 | 66 | PF00899 | 0.318 |
| LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.317 |
| LIG_WW_2 | 212 | 215 | PF00397 | 0.648 |
| MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.621 |
| MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.627 |
| MOD_CK1_1 | 126 | 132 | PF00069 | 0.421 |
| MOD_CK1_1 | 79 | 85 | PF00069 | 0.451 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.375 |
| MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.629 |
| MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.462 |
| MOD_GSK3_1 | 139 | 146 | PF00069 | 0.314 |
| MOD_GSK3_1 | 255 | 262 | PF00069 | 0.423 |
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.301 |
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.334 |
| MOD_GSK3_1 | 347 | 354 | PF00069 | 0.324 |
| MOD_GSK3_1 | 76 | 83 | PF00069 | 0.474 |
| MOD_NEK2_1 | 153 | 158 | PF00069 | 0.399 |
| MOD_NEK2_1 | 163 | 168 | PF00069 | 0.410 |
| MOD_NEK2_1 | 200 | 205 | PF00069 | 0.609 |
| MOD_NEK2_1 | 255 | 260 | PF00069 | 0.423 |
| MOD_NEK2_1 | 270 | 275 | PF00069 | 0.381 |
| MOD_NEK2_1 | 351 | 356 | PF00069 | 0.330 |
| MOD_NEK2_1 | 46 | 51 | PF00069 | 0.326 |
| MOD_NEK2_2 | 304 | 309 | PF00069 | 0.205 |
| MOD_Plk_4 | 123 | 129 | PF00069 | 0.554 |
| MOD_Plk_4 | 131 | 137 | PF00069 | 0.315 |
| MOD_Plk_4 | 246 | 252 | PF00069 | 0.386 |
| MOD_Plk_4 | 285 | 291 | PF00069 | 0.369 |
| MOD_Plk_4 | 304 | 310 | PF00069 | 0.254 |
| MOD_Plk_4 | 32 | 38 | PF00069 | 0.604 |
| MOD_Plk_4 | 342 | 348 | PF00069 | 0.479 |
| MOD_Plk_4 | 357 | 363 | PF00069 | 0.246 |
| MOD_Plk_4 | 46 | 52 | PF00069 | 0.249 |
| MOD_Plk_4 | 71 | 77 | PF00069 | 0.359 |
| MOD_Plk_4 | 95 | 101 | PF00069 | 0.331 |
| MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.652 |
| MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.529 |
| MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.517 |
| MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.270 |
| MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.439 |
| MOD_SUMO_rev_2 | 2 | 11 | PF00179 | 0.661 |
| TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.446 |
| TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.328 |
| TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.285 |
| TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.556 |
| TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.409 |
| TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.436 |
| TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.304 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PEY8 | Leptomonas seymouri | 59% | 100% |
| A0A1X0P088 | Trypanosomatidae | 35% | 100% |
| A0A3R7MU19 | Trypanosoma rangeli | 37% | 92% |
| A4HH92 | Leishmania braziliensis | 83% | 100% |
| A4I4D8 | Leishmania infantum | 100% | 100% |
| C9ZL26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
| E9ADT7 | Leishmania major | 96% | 100% |
| E9ALZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| V5BH42 | Trypanosoma cruzi | 33% | 100% |