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:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005743 | mitochondrial inner membrane | 5 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0019866 | organelle inner membrane | 4 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0031966 | mitochondrial membrane | 4 | 7 |
Related structures:
AlphaFold database: Q4QJH3
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 | 20 | 24 | PF00656 | 0.717 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 479 | 483 | PF00656 | 0.302 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.334 |
DEG_APCC_DBOX_1 | 192 | 200 | PF00400 | 0.534 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.489 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.651 |
DOC_AGCK_PIF_2 | 332 | 337 | PF00069 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.587 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 64 | PF00134 | 0.706 |
DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 448 | 456 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.624 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.600 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.706 |
DOC_PP4_FxxP_1 | 75 | 78 | PF00568 | 0.637 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.288 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.569 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.450 |
LIG_Clathr_ClatBox_1 | 175 | 179 | PF01394 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 440 | 447 | PF00928 | 0.501 |
LIG_eIF4E_1 | 185 | 191 | PF01652 | 0.489 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.399 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.419 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.581 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.694 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.385 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.489 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.690 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.429 |
LIG_GBD_Chelix_1 | 364 | 372 | PF00786 | 0.335 |
LIG_GBD_Chelix_1 | 96 | 104 | PF00786 | 0.221 |
LIG_LIR_Apic_2 | 72 | 78 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 170 | 180 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.335 |
LIG_LIR_LC3C_4 | 101 | 106 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.371 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.380 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.329 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.527 |
LIG_Pex14_2 | 191 | 195 | PF04695 | 0.498 |
LIG_Pex14_2 | 260 | 264 | PF04695 | 0.534 |
LIG_REV1ctd_RIR_1 | 189 | 196 | PF16727 | 0.489 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.386 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.489 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.465 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.489 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.371 |
LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.294 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.567 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.301 |
LIG_SUMO_SIM_anti_2 | 101 | 107 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 453 | 459 | PF11976 | 0.386 |
LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.524 |
LIG_WRC_WIRS_1 | 165 | 170 | PF05994 | 0.534 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.312 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.788 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.526 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.689 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.398 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.551 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.386 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.635 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.424 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.385 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.318 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.334 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.180 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.282 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.463 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.534 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.413 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.541 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.712 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.558 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.335 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.698 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.446 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.451 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.342 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.286 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.504 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.337 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.327 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.489 |
MOD_NEK2_2 | 341 | 346 | PF00069 | 0.494 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.780 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.566 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.534 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.668 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.534 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.365 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.493 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.522 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.707 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.294 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.382 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.327 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.371 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.699 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.648 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.534 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 226 | 234 | PF00179 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 450 | 455 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.263 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3H8 | Leptomonas seymouri | 53% | 100% |
A0A0S4JBC4 | Bodo saltans | 41% | 100% |
A0A0S4JNX4 | Bodo saltans | 32% | 100% |
A0A3S7WP13 | Leishmania donovani | 93% | 100% |
A0A3S7WVJ8 | Leishmania donovani | 21% | 100% |
A4H474 | Leishmania braziliensis | 72% | 97% |
A4HSE9 | Leishmania infantum | 93% | 100% |
A4HYC8 | Leishmania infantum | 21% | 100% |
A4IA82 | Leishmania infantum | 23% | 100% |
A4RPU0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 22% | 100% |
B4F8I5 | Zea mays | 25% | 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) | 88% | 100% |
E9AS62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 100% |
O04619 | Arabidopsis thaliana | 23% | 100% |
O61703 | Choristoneura fumiferana | 35% | 100% |
O94502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
P12234 | Bos taurus | 35% | 100% |
P16036 | Rattus norvegicus | 33% | 100% |
P40614 | Caenorhabditis elegans | 38% | 100% |
Q00325 | Homo sapiens | 34% | 100% |
Q287T7 | Danio rerio | 23% | 100% |
Q2H608 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 21% | 100% |
Q4QDA4 | Leishmania major | 22% | 100% |
Q54S10 | Dictyostelium discoideum | 21% | 100% |
Q552L9 | Dictyostelium discoideum | 23% | 100% |
Q5R7W2 | Pongo abelii | 33% | 100% |
Q7S2H8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 100% |
Q7T292 | Danio rerio | 23% | 100% |
Q8R0Z5 | Mus musculus | 22% | 100% |
Q8RXZ9 | Arabidopsis thaliana | 21% | 100% |
Q8VEM8 | Mus musculus | 34% | 100% |
Q96A46 | Homo sapiens | 22% | 100% |
Q96U08 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 100% |
Q9FI73 | Arabidopsis thaliana | 22% | 100% |
Q9FLS8 | Arabidopsis thaliana | 22% | 100% |
Q9FMU6 | Arabidopsis thaliana | 33% | 100% |
Q9M2Z8 | Arabidopsis thaliana | 33% | 100% |
Q9NYZ2 | Homo sapiens | 23% | 100% |
Q9Z2B2 | Mus musculus | 23% | 100% |