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: A4H474
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 | 185 | 189 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.436 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.346 |
CLV_Separin_Metazoa | 449 | 453 | PF03568 | 0.425 |
DEG_APCC_DBOX_1 | 210 | 218 | PF00400 | 0.578 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.578 |
DEG_MDM2_SWIB_1 | 349 | 357 | PF02201 | 0.306 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.503 |
DOC_AGCK_PIF_2 | 228 | 233 | PF00069 | 0.397 |
DOC_AGCK_PIF_2 | 344 | 349 | PF00069 | 0.472 |
DOC_CDC14_PxL_1 | 203 | 211 | PF14671 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 82 | PF00134 | 0.785 |
DOC_MAPK_MEF2A_6 | 461 | 469 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 101 | 107 | PF00149 | 0.631 |
DOC_PP1_RVXF_1 | 450 | 457 | PF00149 | 0.442 |
DOC_PP1_SILK_1 | 200 | 205 | PF00149 | 0.397 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.785 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 129 | 138 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 307 | 317 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 406 | 414 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 434 | 444 | PF00244 | 0.397 |
LIG_Actin_RPEL_3 | 450 | 469 | PF02755 | 0.397 |
LIG_AP2alpha_1 | 186 | 190 | PF02296 | 0.508 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.625 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.472 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.418 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.424 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.349 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.397 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.762 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.764 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.451 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.753 |
LIG_GBD_Chelix_1 | 376 | 384 | PF00786 | 0.360 |
LIG_IRF3_LxIS_1 | 234 | 241 | PF10401 | 0.397 |
LIG_LIR_Apic_2 | 7 | 13 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 147 | 156 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.321 |
LIG_LIR_LC3C_4 | 372 | 377 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.378 |
LIG_NBox_RRM_1 | 440 | 450 | PF00076 | 0.397 |
LIG_NRBOX | 383 | 389 | PF00104 | 0.433 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.605 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.370 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.548 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.578 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.306 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.418 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.477 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.496 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.285 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.319 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.336 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.665 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.576 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.337 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.397 |
LIG_SUMO_SIM_par_1 | 466 | 472 | PF11976 | 0.418 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.546 |
LIG_TYR_ITIM | 337 | 342 | PF00017 | 0.249 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.502 |
LIG_WRC_WIRS_1 | 145 | 150 | PF05994 | 0.298 |
LIG_WRC_WIRS_1 | 183 | 188 | PF05994 | 0.578 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.337 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.326 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.805 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.568 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.778 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.720 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.565 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.418 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.586 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.635 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.492 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.471 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.378 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.305 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.590 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.452 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.439 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.289 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.578 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.653 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.505 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.401 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.781 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.581 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.609 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.535 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.365 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.376 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.481 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.477 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.323 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.475 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.376 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.283 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.530 |
MOD_PKA_1 | 18 | 24 | PF00069 | 0.631 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.341 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.578 |
MOD_Plk_2-3 | 182 | 188 | PF00069 | 0.578 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.457 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.401 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.511 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.486 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.331 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.316 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.369 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.374 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.742 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.788 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.628 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.578 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.546 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.738 |
TRG_DiLeu_BaEn_2 | 181 | 187 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.281 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3H8 | Leptomonas seymouri | 48% | 100% |
A0A0S4JBC4 | Bodo saltans | 40% | 100% |
A0A0S4JNX4 | Bodo saltans | 31% | 100% |
A0A1D6N272 | Zea mays | 24% | 100% |
A0A3S7WP13 | Leishmania donovani | 73% | 100% |
A4HSE9 | Leishmania infantum | 73% | 100% |
A4RPU0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 22% | 100% |
B4FIJ0 | Zea mays | 24% | 100% |
D0A4I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AFR9 | Leishmania major | 31% | 85% |
E9AKD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
O04619 | Arabidopsis thaliana | 25% | 100% |
O61703 | Choristoneura fumiferana | 34% | 100% |
O75746 | Homo sapiens | 23% | 73% |
P12234 | Bos taurus | 35% | 100% |
P16036 | Rattus norvegicus | 34% | 100% |
P40614 | Caenorhabditis elegans | 37% | 100% |
Q00325 | Homo sapiens | 34% | 100% |
Q287T7 | Danio rerio | 24% | 100% |
Q2H608 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 24% | 100% |
Q4QJH3 | Leishmania major | 72% | 100% |
Q54VX4 | Dictyostelium discoideum | 22% | 100% |
Q5R7W2 | Pongo abelii | 34% | 100% |
Q5RBC8 | Pongo abelii | 23% | 73% |
Q628Z2 | Caenorhabditis briggsae | 21% | 94% |
Q66H23 | Rattus norvegicus | 23% | 100% |
Q6DHC3 | Danio rerio | 20% | 100% |
Q6P316 | Xenopus tropicalis | 21% | 100% |
Q7T292 | Danio rerio | 25% | 100% |
Q8R0Z5 | Mus musculus | 25% | 100% |
Q8RXZ9 | Arabidopsis thaliana | 21% | 100% |
Q8VEM8 | Mus musculus | 35% | 100% |
Q920G8 | Mus musculus | 24% | 100% |
Q96A46 | Homo sapiens | 25% | 100% |
Q96U08 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 100% |
Q9FI73 | Arabidopsis thaliana | 24% | 100% |
Q9FLS8 | Arabidopsis thaliana | 23% | 100% |
Q9FMU6 | Arabidopsis thaliana | 34% | 100% |
Q9M2Z8 | Arabidopsis thaliana | 34% | 100% |
Q9NYZ2 | Homo sapiens | 24% | 100% |
Q9VAY3 | Drosophila melanogaster | 21% | 100% |