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: A4HH92
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.446 |
DEG_SCF_FBW7_2 | 248 | 253 | PF00400 | 0.357 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 168 | 176 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.556 |
DOC_MAPK_RevD_3 | 170 | 184 | PF00069 | 0.432 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.444 |
DOC_PP2B_PxIxI_1 | 106 | 112 | PF00149 | 0.410 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.319 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.653 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.505 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.712 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.385 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.335 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.565 |
LIG_APCC_ABBA_1 | 73 | 78 | PF00400 | 0.342 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BIR_III_2 | 285 | 289 | PF00653 | 0.269 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.543 |
LIG_CaM_NSCaTE_8 | 347 | 354 | PF13499 | 0.355 |
LIG_CSL_BTD_1 | 209 | 212 | PF09270 | 0.651 |
LIG_DLG_GKlike_1 | 123 | 130 | PF00625 | 0.496 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.480 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.279 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.276 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.342 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.654 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 49 | 54 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 381 | 389 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.373 |
LIG_PDZ_Class_2 | 386 | 391 | PF00595 | 0.410 |
LIG_Pex14_1 | 201 | 205 | PF04695 | 0.616 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.535 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.615 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.355 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.448 |
LIG_Rb_LxCxE_1 | 20 | 35 | PF01857 | 0.472 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.201 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.328 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.410 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.577 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.381 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.578 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.296 |
LIG_SUMO_SIM_anti_2 | 171 | 176 | PF11976 | 0.379 |
LIG_SUMO_SIM_anti_2 | 98 | 104 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 173 | 179 | PF11976 | 0.344 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.325 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.311 |
LIG_WW_2 | 212 | 215 | PF00397 | 0.648 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.617 |
MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.624 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.417 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.291 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.476 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.420 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.634 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.411 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.308 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.353 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.513 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.210 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.393 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.270 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.614 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.432 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.344 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.340 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.334 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.512 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.334 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.389 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.498 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.515 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.327 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.513 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.320 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.250 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.404 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.474 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.242 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.297 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.327 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.653 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.382 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.513 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEY8 | Leptomonas seymouri | 61% | 100% |
A0A1X0P088 | Trypanosomatidae | 33% | 100% |
A0A3Q8IH62 | Leishmania donovani | 83% | 100% |
A0A3R7MU19 | Trypanosoma rangeli | 37% | 92% |
A4I4D8 | Leishmania infantum | 83% | 100% |
C9ZL26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9ADT7 | Leishmania major | 84% | 100% |
E9ALZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BH42 | Trypanosoma cruzi | 31% | 100% |