This protein is only found among Kinetoplastds. However, its function is unclear, could be a transporter or channel protein.
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9ALZ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.387 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.320 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.402 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.589 |
DOC_MAPK_RevD_3 | 170 | 184 | PF00069 | 0.430 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.464 |
DOC_PP2B_PxIxI_1 | 106 | 112 | PF00149 | 0.447 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.370 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.681 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.693 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.373 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.429 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.330 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.515 |
LIG_Actin_WH2_2 | 311 | 328 | PF00022 | 0.188 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.572 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.590 |
LIG_CaM_NSCaTE_8 | 347 | 354 | PF13499 | 0.480 |
LIG_CSL_BTD_1 | 209 | 212 | PF09270 | 0.670 |
LIG_DLG_GKlike_1 | 123 | 130 | PF00625 | 0.586 |
LIG_EVH1_1 | 87 | 91 | PF00568 | 0.364 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.468 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.335 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.441 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.395 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.331 |
LIG_IRF3_LxIS_1 | 159 | 166 | PF10401 | 0.285 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.682 |
LIG_LIR_Apic_2 | 49 | 54 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.397 |
LIG_PDZ_Class_2 | 386 | 391 | PF00595 | 0.447 |
LIG_Pex14_1 | 201 | 205 | PF04695 | 0.643 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.578 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.484 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 384 | 391 | PF02174 | 0.402 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.335 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.416 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.632 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.358 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.595 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.386 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 171 | 176 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 98 | 104 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 173 | 179 | PF11976 | 0.360 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.381 |
LIG_UBA3_1 | 57 | 66 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.368 |
LIG_WW_2 | 212 | 215 | PF00397 | 0.659 |
MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.655 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.451 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.328 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.500 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.480 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.545 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.612 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.396 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.414 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.337 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.377 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.375 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.523 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.435 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.435 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.639 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.341 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.417 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.374 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.379 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.376 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.475 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.572 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.366 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.405 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.402 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.290 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.645 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.514 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.292 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.295 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.381 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.678 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.556 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.330 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEY8 | Leptomonas seymouri | 60% | 100% |
A0A1X0P088 | Trypanosomatidae | 34% | 100% |
A0A3Q8IH62 | Leishmania donovani | 93% | 100% |
A0A3R7MU19 | Trypanosoma rangeli | 37% | 92% |
A4HH92 | Leishmania braziliensis | 84% | 100% |
A4I4D8 | Leishmania infantum | 93% | 100% |
C9ZL26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ADT7 | Leishmania major | 94% | 100% |
V5BH42 | Trypanosoma cruzi | 33% | 100% |