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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 14 |
GO:0042995 | cell projection | 2 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043227 | membrane-bounded organelle | 3 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 14 |
Related structures:
AlphaFold database: A4HFQ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.325 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.665 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.354 |
DEG_ODPH_VHL_1 | 188 | 199 | PF01847 | 0.477 |
DOC_CKS1_1 | 133 | 138 | PF01111 | 0.463 |
DOC_CYCLIN_RxL_1 | 192 | 201 | PF00134 | 0.352 |
DOC_MIT_MIM_1 | 37 | 49 | PF04212 | 0.602 |
DOC_PP1_RVXF_1 | 229 | 235 | PF00149 | 0.328 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.383 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.323 |
LIG_14-3-3_CanoR_1 | 119 | 128 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 248 | 263 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 350 | 367 | PF00022 | 0.394 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 |
LIG_BIR_III_4 | 61 | 65 | PF00653 | 0.482 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.442 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.454 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.405 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.466 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.491 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.496 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.438 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.650 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.457 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.499 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.230 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.375 |
LIG_LRP6_Inhibitor_1 | 274 | 280 | PF00058 | 0.322 |
LIG_LYPXL_SIV_4 | 67 | 75 | PF13949 | 0.429 |
LIG_MAD2 | 251 | 259 | PF02301 | 0.463 |
LIG_PDZ_Class_3 | 394 | 399 | PF00595 | 0.528 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.496 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.249 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.409 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 52 | 56 | PF00017 | 0.546 |
LIG_SH2_PTP2 | 133 | 136 | PF00017 | 0.385 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.363 |
LIG_SH3_1 | 52 | 58 | PF00018 | 0.650 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.526 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.365 |
LIG_SUMO_SIM_anti_2 | 126 | 131 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 335 | 340 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 95 | 102 | PF11976 | 0.457 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.561 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.336 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.491 |
LIG_TYR_ITIM | 101 | 106 | PF00017 | 0.480 |
LIG_TYR_ITIM | 146 | 151 | PF00017 | 0.245 |
LIG_TYR_ITIM | 227 | 232 | PF00017 | 0.362 |
LIG_UBA3_1 | 151 | 159 | PF00899 | 0.396 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.284 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.477 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.500 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.546 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.517 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.315 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.637 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.467 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.383 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.425 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.479 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.361 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.284 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.422 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.522 |
MOD_GlcNHglycan | 61 | 65 | PF01048 | 0.414 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.430 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.363 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.543 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.397 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.456 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.458 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.480 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.362 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.371 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.320 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.464 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.361 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.533 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.392 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.202 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.504 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.577 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.435 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.355 |
MOD_NEK2_2 | 190 | 195 | PF00069 | 0.416 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.313 |
MOD_OFUCOSY | 282 | 287 | PF10250 | 0.444 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.606 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.335 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.448 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.292 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.244 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.374 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.533 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.368 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.327 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.323 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.285 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.368 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.319 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.697 |
TRG_NLS_Bipartite_1 | 32 | 52 | PF00514 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 251 | 256 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.357 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUH0 | Leptomonas seymouri | 27% | 85% |
A0A0N1I317 | Leptomonas seymouri | 74% | 100% |
A0A0S4JL85 | Bodo saltans | 27% | 94% |
A0A0S4JV86 | Bodo saltans | 41% | 100% |
A0A1X0NTY3 | Trypanosomatidae | 26% | 89% |
A0A1X0P364 | Trypanosomatidae | 24% | 93% |
A0A1X0P4Z4 | Trypanosomatidae | 50% | 100% |
A0A3Q8IDE6 | Leishmania donovani | 85% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 25% | 90% |
A0A3R7NL91 | Trypanosoma rangeli | 49% | 100% |
A0A3S5H5G2 | Leishmania donovani | 27% | 90% |
A0A3S7WXH1 | Leishmania donovani | 24% | 100% |
A0A3S7WZL6 | Leishmania donovani | 24% | 93% |
A4H461 | Leishmania braziliensis | 27% | 90% |
A4HEQ6 | Leishmania braziliensis | 25% | 100% |
A4HSD0 | Leishmania infantum | 27% | 90% |
A4I053 | Leishmania infantum | 24% | 100% |
A4I1Y5 | Leishmania infantum | 24% | 93% |
A4I2T1 | Leishmania infantum | 85% | 100% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 92% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 89% |
D0A5Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 96% |
E9ADA9 | Leishmania major | 87% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 90% |
E9AW16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AY32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
P10775 | Sus scrofa | 27% | 88% |
P13489 | Homo sapiens | 25% | 87% |
P29315 | Rattus norvegicus | 24% | 88% |
Q0VAA2 | Homo sapiens | 28% | 82% |
Q14BP6 | Mus musculus | 28% | 100% |
Q4Q9E1 | Leishmania major | 26% | 100% |
Q4QJI8 | Leishmania major | 28% | 90% |
Q6ZQY2 | Homo sapiens | 29% | 100% |
Q8HZP9 | Pan troglodytes | 26% | 87% |
Q91VI7 | Mus musculus | 24% | 88% |
Q9LE82 | Arabidopsis thaliana | 26% | 75% |
Q9M651 | Arabidopsis thaliana | 26% | 73% |
V5BPZ7 | Trypanosoma cruzi | 26% | 89% |
V5DHF2 | Trypanosoma cruzi | 49% | 100% |