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. | yes | 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: A0A3S7X4W5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.528 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.542 |
DOC_ANK_TNKS_1 | 299 | 306 | PF00023 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.446 |
DOC_SPAK_OSR1_1 | 193 | 197 | PF12202 | 0.429 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.660 |
LIG_AP2alpha_2 | 4 | 6 | PF02296 | 0.384 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.481 |
LIG_Clathr_ClatBox_1 | 275 | 279 | PF01394 | 0.651 |
LIG_deltaCOP1_diTrp_1 | 232 | 238 | PF00928 | 0.511 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.535 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.692 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.539 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.388 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.601 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.598 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.617 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.554 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.502 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.641 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.732 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.746 |
LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.738 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.384 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.381 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.366 |
LIG_REV1ctd_RIR_1 | 72 | 83 | PF16727 | 0.510 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.775 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.605 |
LIG_SH2_NCK_1 | 137 | 141 | PF00017 | 0.783 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.404 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.724 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.638 |
LIG_SUMO_SIM_anti_2 | 102 | 109 | PF11976 | 0.624 |
LIG_SUMO_SIM_anti_2 | 166 | 172 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 102 | 109 | PF11976 | 0.637 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.472 |
LIG_UBA3_1 | 275 | 280 | PF00899 | 0.656 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.571 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.719 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.608 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.445 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.488 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.517 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.627 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.640 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.516 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.567 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.716 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.741 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.560 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.679 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.614 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.403 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.415 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.569 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.198 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.194 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.422 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.439 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.658 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.611 |
MOD_PKA_1 | 310 | 316 | PF00069 | 0.732 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.692 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.653 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.732 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.462 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.648 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.729 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.657 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.382 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.572 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.708 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.477 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.446 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.655 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.258 |
TRG_DiLeu_BaLyEn_6 | 34 | 39 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.734 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.628 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4U5 | Leptomonas seymouri | 70% | 100% |
A0A0S4JIB3 | Bodo saltans | 32% | 100% |
A0A1X0NIE1 | Trypanosomatidae | 44% | 100% |
A0A3R7NC34 | Trypanosoma rangeli | 43% | 100% |
A4HJS2 | Leishmania braziliensis | 80% | 100% |
A4I788 | Leishmania infantum | 99% | 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) | 89% | 100% |
Q4Q5X5 | Leishmania major | 95% | 100% |
V5BC20 | Trypanosoma cruzi | 43% | 100% |