Forms a well-defined channel with 6 helices. Some paralogs tend to have an additional hydrophobic segment that might be a transit or signal peptide. It is unclear if the N-peptide is a signal or transit peptide. Localization: Mitochondrial (by homology)
| 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: 8 | 
| NetGPI | no | yes: 0, no: 8 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005743 | mitochondrial inner membrane | 5 | 8 | 
| GO:0016020 | membrane | 2 | 8 | 
| GO:0019866 | organelle inner membrane | 4 | 8 | 
| GO:0031090 | organelle membrane | 3 | 8 | 
| GO:0031966 | mitochondrial membrane | 4 | 8 | 
| GO:0110165 | cellular anatomical entity | 1 | 9 | 
| GO:0005737 | cytoplasm | 2 | 1 | 
Related structures:
AlphaFold database: A0A3S7WP13
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006810 | transport | 3 | 9 | 
| GO:0006811 | monoatomic ion transport | 4 | 9 | 
| GO:0006817 | phosphate ion transport | 7 | 9 | 
| GO:0006820 | monoatomic anion transport | 5 | 9 | 
| GO:0009987 | cellular process | 1 | 9 | 
| GO:0015698 | inorganic anion transport | 6 | 9 | 
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 9 | 
| GO:0035435 | phosphate ion transmembrane transport | 6 | 9 | 
| GO:0051179 | localization | 1 | 9 | 
| GO:0051234 | establishment of localization | 2 | 9 | 
| GO:0055085 | transmembrane transport | 2 | 9 | 
| GO:0098656 | monoatomic anion transmembrane transport | 4 | 9 | 
| GO:0098660 | inorganic ion transmembrane transport | 4 | 9 | 
| GO:0098661 | inorganic anion transmembrane transport | 5 | 9 | 
| GO:1990542 | mitochondrial transmembrane transport | 3 | 9 | 
| GO:1990547 | mitochondrial phosphate ion transmembrane transport | 4 | 9 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 9 | 
| GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 9 | 
| GO:0015291 | secondary active transmembrane transporter activity | 4 | 9 | 
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 9 | 
| GO:0022804 | active transmembrane transporter activity | 3 | 9 | 
| GO:0022857 | transmembrane transporter activity | 2 | 9 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.523 | 
| CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.765 | 
| CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.494 | 
| CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.294 | 
| CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.273 | 
| CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.377 | 
| DEG_APCC_DBOX_1 | 192 | 200 | PF00400 | 0.577 | 
| DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.577 | 
| DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.522 | 
| DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.680 | 
| DOC_AGCK_PIF_2 | 332 | 337 | PF00069 | 0.471 | 
| DOC_CYCLIN_yCln2_LP_2 | 61 | 64 | PF00134 | 0.748 | 
| DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.515 | 
| DOC_MAPK_MEF2A_6 | 217 | 224 | PF00069 | 0.517 | 
| DOC_MAPK_MEF2A_6 | 448 | 456 | PF00069 | 0.539 | 
| DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.625 | 
| DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.748 | 
| DOC_PP4_FxxP_1 | 2 | 5 | PF00568 | 0.605 | 
| DOC_PP4_FxxP_1 | 224 | 227 | PF00568 | 0.645 | 
| DOC_PP4_FxxP_1 | 75 | 78 | PF00568 | 0.637 | 
| DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.495 | 
| DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.700 | 
| DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.686 | 
| DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.527 | 
| DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.273 | 
| DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.577 | 
| DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.709 | 
| LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.397 | 
| LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.539 | 
| LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.712 | 
| LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.577 | 
| LIG_AP2alpha_1 | 168 | 172 | PF02296 | 0.508 | 
| LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.539 | 
| LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.517 | 
| LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.471 | 
| LIG_Clathr_ClatBox_1 | 175 | 179 | PF01394 | 0.522 | 
| LIG_deltaCOP1_diTrp_1 | 440 | 447 | PF00928 | 0.527 | 
| LIG_eIF4E_1 | 185 | 191 | PF01652 | 0.522 | 
| LIG_FHA_1 | 120 | 126 | PF00498 | 0.395 | 
| LIG_FHA_1 | 305 | 311 | PF00498 | 0.587 | 
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.690 | 
| LIG_FHA_2 | 407 | 413 | PF00498 | 0.522 | 
| LIG_FHA_2 | 46 | 52 | PF00498 | 0.694 | 
| LIG_FHA_2 | 477 | 483 | PF00498 | 0.464 | 
| LIG_GBD_Chelix_1 | 364 | 372 | PF00786 | 0.360 | 
| LIG_LIR_Apic_2 | 74 | 78 | PF02991 | 0.634 | 
| LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.282 | 
| LIG_LIR_Gen_1 | 170 | 180 | PF02991 | 0.539 | 
| LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.577 | 
| LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.500 | 
| LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.339 | 
| LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.466 | 
| LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.282 | 
| LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.539 | 
| LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.506 | 
| LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.509 | 
| LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.539 | 
| LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.569 | 
| LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.339 | 
| LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.422 | 
| LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.377 | 
| LIG_NRBOX | 371 | 377 | PF00104 | 0.433 | 
| LIG_Pex14_2 | 133 | 137 | PF04695 | 0.370 | 
| LIG_Pex14_2 | 168 | 172 | PF04695 | 0.547 | 
| LIG_Pex14_2 | 191 | 195 | PF04695 | 0.524 | 
| LIG_Pex14_2 | 260 | 264 | PF04695 | 0.577 | 
| LIG_REV1ctd_RIR_1 | 189 | 196 | PF16727 | 0.522 | 
| LIG_SH2_CRK | 135 | 139 | PF00017 | 0.417 | 
| LIG_SH2_CRK | 185 | 189 | PF00017 | 0.522 | 
| LIG_SH2_CRK | 314 | 318 | PF00017 | 0.495 | 
| LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.522 | 
| LIG_SH2_SRC | 213 | 216 | PF00017 | 0.494 | 
| LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.489 | 
| LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.504 | 
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.532 | 
| LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.312 | 
| LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.522 | 
| LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.341 | 
| LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.336 | 
| LIG_SH3_3 | 146 | 152 | PF00018 | 0.335 | 
| LIG_SH3_3 | 288 | 294 | PF00018 | 0.575 | 
| LIG_SH3_3 | 377 | 383 | PF00018 | 0.336 | 
| LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.387 | 
| LIG_SUMO_SIM_par_1 | 453 | 459 | PF11976 | 0.417 | 
| LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.545 | 
| LIG_WRC_WIRS_1 | 165 | 170 | PF05994 | 0.577 | 
| LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.336 | 
| MOD_CK1_1 | 17 | 23 | PF00069 | 0.760 | 
| MOD_CK1_1 | 244 | 250 | PF00069 | 0.604 | 
| MOD_CK1_1 | 389 | 395 | PF00069 | 0.400 | 
| MOD_CK1_1 | 396 | 402 | PF00069 | 0.553 | 
| MOD_CK1_1 | 74 | 80 | PF00069 | 0.674 | 
| MOD_CK2_1 | 208 | 214 | PF00069 | 0.564 | 
| MOD_CK2_1 | 330 | 336 | PF00069 | 0.380 | 
| MOD_CK2_1 | 43 | 49 | PF00069 | 0.650 | 
| MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.653 | 
| MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.465 | 
| MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.394 | 
| MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.326 | 
| MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.377 | 
| MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.361 | 
| MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.605 | 
| MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.512 | 
| MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.371 | 
| MOD_GSK3_1 | 204 | 211 | PF00069 | 0.556 | 
| MOD_GSK3_1 | 241 | 248 | PF00069 | 0.661 | 
| MOD_GSK3_1 | 341 | 348 | PF00069 | 0.446 | 
| MOD_GSK3_1 | 389 | 396 | PF00069 | 0.507 | 
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.676 | 
| MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.613 | 
| MOD_NEK2_1 | 104 | 109 | PF00069 | 0.375 | 
| MOD_NEK2_1 | 245 | 250 | PF00069 | 0.663 | 
| MOD_NEK2_1 | 262 | 267 | PF00069 | 0.476 | 
| MOD_NEK2_1 | 330 | 335 | PF00069 | 0.394 | 
| MOD_NEK2_1 | 345 | 350 | PF00069 | 0.373 | 
| MOD_NEK2_1 | 363 | 368 | PF00069 | 0.337 | 
| MOD_NEK2_1 | 406 | 411 | PF00069 | 0.529 | 
| MOD_NEK2_1 | 456 | 461 | PF00069 | 0.333 | 
| MOD_NEK2_2 | 180 | 185 | PF00069 | 0.529 | 
| MOD_NEK2_2 | 341 | 346 | PF00069 | 0.530 | 
| MOD_PIKK_1 | 389 | 395 | PF00454 | 0.369 | 
| MOD_PKA_2 | 12 | 18 | PF00069 | 0.764 | 
| MOD_PKA_2 | 31 | 37 | PF00069 | 0.563 | 
| MOD_PKA_2 | 393 | 399 | PF00069 | 0.577 | 
| MOD_Plk_1 | 30 | 36 | PF00069 | 0.750 | 
| MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.577 | 
| MOD_Plk_4 | 104 | 110 | PF00069 | 0.370 | 
| MOD_Plk_4 | 180 | 186 | PF00069 | 0.520 | 
| MOD_Plk_4 | 31 | 37 | PF00069 | 0.760 | 
| MOD_Plk_4 | 325 | 331 | PF00069 | 0.329 | 
| MOD_Plk_4 | 341 | 347 | PF00069 | 0.475 | 
| MOD_Plk_4 | 363 | 369 | PF00069 | 0.362 | 
| MOD_Plk_4 | 383 | 389 | PF00069 | 0.386 | 
| MOD_Plk_4 | 57 | 63 | PF00069 | 0.725 | 
| MOD_Plk_4 | 71 | 77 | PF00069 | 0.590 | 
| MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.577 | 
| MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.700 | 
| MOD_SUMO_rev_2 | 226 | 234 | PF00179 | 0.603 | 
| TRG_DiLeu_BaLyEn_6 | 450 | 455 | PF01217 | 0.417 | 
| TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.376 | 
| TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.504 | 
| TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.522 | 
| TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.480 | 
| TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.480 | 
| TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.602 | 
| TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.495 | 
| TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.294 | 
| TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.280 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P3H8 | Leptomonas seymouri | 53% | 100% | 
| A0A0S4JBC4 | Bodo saltans | 40% | 100% | 
| A0A0S4JNX4 | Bodo saltans | 32% | 100% | 
| A0A1D6N272 | Zea mays | 22% | 100% | 
| A0A3S7WVJ8 | Leishmania donovani | 22% | 100% | 
| A4H474 | Leishmania braziliensis | 73% | 100% | 
| A4HSE9 | Leishmania infantum | 100% | 100% | 
| A4HYC8 | Leishmania infantum | 22% | 100% | 
| A4RPU0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 22% | 100% | 
| B4F8I5 | Zea mays | 24% | 100% | 
| D0A4I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% | 
| E9AFR9 | Leishmania major | 31% | 93% | 
| E9AKD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% | 
| O61703 | Choristoneura fumiferana | 35% | 100% | 
| O94502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% | 
| P12234 | Bos taurus | 34% | 100% | 
| P16036 | Rattus norvegicus | 33% | 100% | 
| P40614 | Caenorhabditis elegans | 38% | 100% | 
| Q00325 | Homo sapiens | 33% | 100% | 
| Q19529 | Caenorhabditis elegans | 22% | 91% | 
| Q2H608 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 24% | 100% | 
| Q4QDA4 | Leishmania major | 23% | 100% | 
| Q4QJH3 | Leishmania major | 93% | 100% | 
| Q54S10 | Dictyostelium discoideum | 21% | 100% | 
| Q5R7W2 | Pongo abelii | 33% | 100% | 
| Q628Z2 | Caenorhabditis briggsae | 22% | 91% | 
| Q7S2H8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% | 
| Q7T292 | Danio rerio | 23% | 100% | 
| Q8RXZ9 | Arabidopsis thaliana | 22% | 100% | 
| Q8VEM8 | Mus musculus | 34% | 100% | 
| Q96U08 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 100% | 
| Q9FI73 | Arabidopsis thaliana | 23% | 100% | 
| Q9FLS8 | Arabidopsis thaliana | 23% | 100% | 
| Q9FMU6 | Arabidopsis thaliana | 32% | 100% | 
| Q9LJX5 | Arabidopsis thaliana | 21% | 100% | 
| Q9LY28 | Arabidopsis thaliana | 23% | 100% | 
| Q9M2Z8 | Arabidopsis thaliana | 33% | 100% | 
| Q9NYZ2 | Homo sapiens | 23% | 100% | 
| Q9Z2B2 | Mus musculus | 22% | 100% |