Leucine-rich repeat proteins with a hydrophobic terminal helix. Unlike its distant animal relatives, this cytoplasmic sensor protein might be anchored to the membrane.
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 16 |
GO:0042995 | cell projection | 2 | 16 |
GO:0043226 | organelle | 2 | 16 |
GO:0043227 | membrane-bounded organelle | 3 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 16 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AY32
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.265 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.380 |
CLV_PCSK_PC7_1 | 429 | 435 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.639 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.281 |
DOC_ANK_TNKS_1 | 169 | 176 | PF00023 | 0.281 |
DOC_CYCLIN_RxL_1 | 159 | 168 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 241 | 251 | PF00069 | 0.347 |
DOC_MIT_MIM_1 | 275 | 284 | PF04212 | 0.313 |
DOC_PP1_SILK_1 | 208 | 213 | PF00149 | 0.302 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 185 | 189 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 7 | 14 | PF00244 | 0.745 |
LIG_Actin_WH2_2 | 347 | 364 | PF00022 | 0.453 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.153 |
LIG_DLG_GKlike_1 | 153 | 161 | PF00625 | 0.341 |
LIG_EH1_1 | 348 | 356 | PF00400 | 0.203 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.750 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.399 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.478 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.468 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.482 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.337 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.575 |
LIG_NRBOX | 434 | 440 | PF00104 | 0.377 |
LIG_PCNA_yPIPBox_3 | 413 | 421 | PF02747 | 0.416 |
LIG_PCNA_yPIPBox_3 | 429 | 439 | PF02747 | 0.288 |
LIG_SH2_NCK_1 | 112 | 116 | PF00017 | 0.339 |
LIG_SH2_STAT3 | 456 | 459 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.447 |
LIG_SUMO_SIM_anti_2 | 213 | 219 | PF11976 | 0.258 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.247 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 231 | 238 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 304 | 309 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.323 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.377 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.362 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.596 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.447 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.377 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.454 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.442 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.314 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.319 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.472 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.245 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.410 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.362 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.283 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.422 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.770 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.411 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.343 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.287 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.426 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.625 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.345 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.318 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.510 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.407 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.357 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.425 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.438 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.541 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.398 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.350 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.304 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.377 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.303 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.353 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.284 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.510 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.335 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.302 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.338 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.376 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.685 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.460 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.288 |
MOD_PKA_1 | 247 | 253 | PF00069 | 0.483 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.396 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.332 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.483 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.532 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.466 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.241 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.273 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.363 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.446 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.361 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.493 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.359 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.633 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.412 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.593 |
TRG_DiLeu_BaEn_1 | 174 | 179 | PF01217 | 0.187 |
TRG_DiLeu_BaLyEn_6 | 147 | 152 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.406 |
TRG_NES_CRM1_1 | 205 | 219 | PF08389 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUH0 | Leptomonas seymouri | 75% | 100% |
A0A0N1PD72 | Leptomonas seymouri | 27% | 100% |
A0A0S4IIC5 | Bodo saltans | 26% | 67% |
A0A0S4IT30 | Bodo saltans | 24% | 71% |
A0A0S4JDM4 | Bodo saltans | 27% | 70% |
A0A0S4JHR1 | Bodo saltans | 24% | 76% |
A0A0S4JL85 | Bodo saltans | 24% | 100% |
A0A0S4JPV3 | Bodo saltans | 39% | 98% |
A0A1X0NTY3 | Trypanosomatidae | 52% | 100% |
A0A1X0P364 | Trypanosomatidae | 21% | 100% |
A0A3Q8IDE6 | Leishmania donovani | 26% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 54% | 100% |
A0A3R7P015 | Trypanosoma rangeli | 25% | 100% |
A0A3S5H5G2 | Leishmania donovani | 29% | 100% |
A0A3S5H6F0 | Leishmania donovani | 24% | 100% |
A0A3S7WXH1 | Leishmania donovani | 24% | 100% |
A0A3S7WZL6 | Leishmania donovani | 92% | 100% |
A0A422NBD9 | Trypanosoma rangeli | 25% | 69% |
A4H461 | Leishmania braziliensis | 29% | 100% |
A4HCM9 | Leishmania braziliensis | 27% | 100% |
A4HEQ6 | Leishmania braziliensis | 79% | 100% |
A4HFQ6 | Leishmania braziliensis | 26% | 100% |
A4HHW0 | Leishmania braziliensis | 30% | 100% |
A4HSD0 | Leishmania infantum | 29% | 100% |
A4HU75 | Leishmania infantum | 24% | 100% |
A4I053 | Leishmania infantum | 25% | 100% |
A4I1Y5 | Leishmania infantum | 92% | 100% |
A4I2T1 | Leishmania infantum | 26% | 100% |
A7Z026 | Bos taurus | 28% | 68% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ADA9 | Leishmania major | 27% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AN05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AW16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
O75864 | Homo sapiens | 27% | 68% |
P10775 | Sus scrofa | 28% | 100% |
P13489 | Homo sapiens | 25% | 100% |
P41391 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P46060 | Homo sapiens | 25% | 81% |
P46061 | Mus musculus | 25% | 80% |
Q4Q9E1 | Leishmania major | 90% | 100% |
Q4QBG0 | Leishmania major | 24% | 100% |
Q4QJI8 | Leishmania major | 28% | 100% |
Q8HZP9 | Pan troglodytes | 25% | 100% |
Q9VIW3 | Drosophila melanogaster | 23% | 79% |
V5BC30 | Trypanosoma cruzi | 23% | 68% |
V5BC66 | Trypanosoma cruzi | 27% | 72% |
V5BJF0 | Trypanosoma cruzi | 24% | 96% |
V5BPZ7 | Trypanosoma cruzi | 54% | 100% |