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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
Related structures:
AlphaFold database: A4HEQ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.258 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.504 |
DEG_APCC_DBOX_1 | 280 | 288 | PF00400 | 0.525 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.479 |
DOC_ANK_TNKS_1 | 120 | 127 | PF00023 | 0.452 |
DOC_CYCLIN_RxL_1 | 250 | 263 | PF00134 | 0.199 |
DOC_CYCLIN_yCln2_LP_2 | 162 | 168 | PF00134 | 0.294 |
DOC_MAPK_gen_1 | 192 | 202 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 304 | 312 | PF00069 | 0.260 |
DOC_MIT_MIM_1 | 226 | 235 | PF04212 | 0.366 |
DOC_PP1_RVXF_1 | 28 | 35 | PF00149 | 0.290 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 199 | 203 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 255 | 260 | PF00244 | 0.199 |
LIG_14-3-3_CanoR_1 | 304 | 309 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 46 | 55 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 93 | 103 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 298 | 315 | PF00022 | 0.425 |
LIG_Actin_WH2_2 | 32 | 48 | PF00022 | 0.271 |
LIG_DLG_GKlike_1 | 104 | 112 | PF00625 | 0.512 |
LIG_DLG_GKlike_1 | 304 | 312 | PF00625 | 0.314 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.352 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.482 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.357 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.329 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.480 |
LIG_PCNA_yPIPBox_3 | 364 | 372 | PF02747 | 0.447 |
LIG_PCNA_yPIPBox_3 | 380 | 390 | PF02747 | 0.264 |
LIG_PDZ_Class_1 | 412 | 417 | PF00595 | 0.574 |
LIG_PTB_Apo_2 | 217 | 224 | PF02174 | 0.245 |
LIG_PTB_Phospho_1 | 217 | 223 | PF10480 | 0.244 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.389 |
LIG_SH2_STAT3 | 407 | 410 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.331 |
LIG_SUMO_SIM_anti_2 | 339 | 344 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.329 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.382 |
LIG_UBA3_1 | 305 | 313 | PF00899 | 0.260 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.258 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.362 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.363 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.469 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.315 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.320 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.486 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.452 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.339 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.204 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.435 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.390 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.446 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.377 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.346 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.366 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.441 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.660 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.482 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.374 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.327 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.452 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.281 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.337 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.356 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.439 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.390 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.305 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.484 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.395 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.371 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.320 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.304 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.302 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.280 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.372 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.328 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.323 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.260 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.244 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.492 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.343 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.511 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.511 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.488 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.343 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.360 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.261 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.294 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.390 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.482 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.424 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.349 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.399 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.447 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.219 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.391 |
TRG_NES_CRM1_1 | 301 | 314 | PF08389 | 0.199 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4N0 | Leptomonas seymouri | 29% | 100% |
A0A0N0P7L1 | Leptomonas seymouri | 24% | 80% |
A0A0N1HUH0 | Leptomonas seymouri | 74% | 89% |
A0A0N1PD72 | Leptomonas seymouri | 26% | 93% |
A0A0S4IK39 | Bodo saltans | 24% | 66% |
A0A0S4JGH2 | Bodo saltans | 27% | 100% |
A0A0S4JHR1 | Bodo saltans | 25% | 67% |
A0A0S4JL85 | Bodo saltans | 23% | 98% |
A0A0S4JPV3 | Bodo saltans | 39% | 86% |
A0A0S4JXN4 | Bodo saltans | 28% | 97% |
A0A1X0NTY3 | Trypanosomatidae | 55% | 93% |
A0A1X0P2M5 | Trypanosomatidae | 29% | 100% |
A0A1X0P364 | Trypanosomatidae | 25% | 97% |
A0A3Q8IDE6 | Leishmania donovani | 25% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 54% | 94% |
A0A3R7P015 | Trypanosoma rangeli | 25% | 88% |
A0A3S5H5G2 | Leishmania donovani | 26% | 95% |
A0A3S7WXH1 | Leishmania donovani | 26% | 100% |
A0A3S7WZL6 | Leishmania donovani | 79% | 97% |
A0JPI9 | Rattus norvegicus | 29% | 87% |
A4H461 | Leishmania braziliensis | 29% | 100% |
A4HCM9 | Leishmania braziliensis | 27% | 100% |
A4HFQ6 | Leishmania braziliensis | 25% | 100% |
A4HHW0 | Leishmania braziliensis | 27% | 100% |
A4HSD0 | Leishmania infantum | 26% | 95% |
A4I053 | Leishmania infantum | 26% | 100% |
A4I1Y5 | Leishmania infantum | 79% | 97% |
A4I2T1 | Leishmania infantum | 25% | 100% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 97% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 93% |
D0A5Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ADA9 | Leishmania major | 24% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 94% |
E9AW16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AY32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 88% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
O13066 | Xenopus laevis | 26% | 72% |
P10775 | Sus scrofa | 29% | 91% |
P13489 | Homo sapiens | 26% | 90% |
P29315 | Rattus norvegicus | 27% | 91% |
P46060 | Homo sapiens | 27% | 71% |
P46061 | Mus musculus | 27% | 71% |
Q0VAA2 | Homo sapiens | 29% | 85% |
Q14BP6 | Mus musculus | 31% | 100% |
Q4Q9E1 | Leishmania major | 79% | 100% |
Q4QBG0 | Leishmania major | 26% | 100% |
Q4QJI8 | Leishmania major | 25% | 100% |
Q6ZQY2 | Homo sapiens | 28% | 100% |
Q8HZP9 | Pan troglodytes | 26% | 90% |
Q8IZ02 | Homo sapiens | 28% | 90% |
Q91VI7 | Mus musculus | 27% | 91% |
Q9LE82 | Arabidopsis thaliana | 27% | 78% |
Q9M651 | Arabidopsis thaliana | 26% | 77% |
Q9VIW3 | Drosophila melanogaster | 24% | 70% |
V5BJF0 | Trypanosoma cruzi | 25% | 84% |
V5BN36 | Trypanosoma cruzi | 28% | 100% |
V5BPZ7 | Trypanosoma cruzi | 56% | 93% |
V5DHF2 | Trypanosoma cruzi | 28% | 100% |