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% |