Appears to be unique to Kinetoplastids, with very unclear topology, localization and function.. Despite the topology, no signal peptides are present, although a mitochondrial transit signal cannot be excluded
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HJS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.419 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.347 |
DEG_SPOP_SBC_1 | 149 | 153 | PF00917 | 0.557 |
DOC_ANK_TNKS_1 | 354 | 361 | PF00023 | 0.648 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.371 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.539 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.334 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.332 |
DOC_USP7_MATH_2 | 89 | 95 | PF00917 | 0.371 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.373 |
LIG_Actin_WH2_2 | 17 | 34 | PF00022 | 0.319 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.345 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.401 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.418 |
LIG_Clathr_ClatBox_1 | 330 | 334 | PF01394 | 0.559 |
LIG_deltaCOP1_diTrp_1 | 287 | 293 | PF00928 | 0.492 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.507 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.677 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.509 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.376 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.573 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.595 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.718 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.490 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.630 |
LIG_GBD_Chelix_1 | 322 | 330 | PF00786 | 0.313 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 372 | 380 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.677 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.348 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.314 |
LIG_REV1ctd_RIR_1 | 127 | 138 | PF16727 | 0.480 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.764 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 192 | 196 | PF00017 | 0.769 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.366 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.709 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.230 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.411 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.611 |
LIG_SUMO_SIM_anti_2 | 157 | 164 | PF11976 | 0.605 |
LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 157 | 164 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 221 | 227 | PF11976 | 0.346 |
LIG_UBA3_1 | 330 | 335 | PF00899 | 0.564 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.346 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.371 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.338 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.432 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.430 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.580 |
MOD_Cter_Amidation | 214 | 217 | PF01082 | 0.314 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.492 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.423 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.464 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.506 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.606 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.364 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.594 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.518 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.460 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.714 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.559 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.444 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.330 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.389 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.349 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.381 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.584 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.309 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.408 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.368 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.545 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.420 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.310 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.474 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.290 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.658 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.576 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.380 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.649 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.665 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.330 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.617 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.700 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.325 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.634 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.646 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.363 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.263 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.342 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.503 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.327 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.534 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.235 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.371 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.633 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.619 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.373 |
MOD_SUMO_for_1 | 331 | 334 | PF00179 | 0.542 |
MOD_SUMO_rev_2 | 362 | 367 | PF00179 | 0.681 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.700 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4U5 | Leptomonas seymouri | 69% | 100% |
A0A0S4JIB3 | Bodo saltans | 33% | 100% |
A0A1X0NIE1 | Trypanosomatidae | 45% | 100% |
A0A3R7NC34 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X4W5 | Leishmania donovani | 80% | 100% |
A4I788 | Leishmania infantum | 80% | 100% |
C9ZMG7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZWL8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B283 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
Q4Q5X5 | Leishmania major | 71% | 100% |
V5BC20 | Trypanosoma cruzi | 42% | 100% |