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: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 30 |
GO:0042995 | cell projection | 2 | 30 |
GO:0043226 | organelle | 2 | 30 |
GO:0043227 | membrane-bounded organelle | 3 | 30 |
GO:0110165 | cellular anatomical entity | 1 | 31 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 30 |
GO:0016020 | membrane | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
Related structures:
AlphaFold database: A4H461
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.307 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.389 |
DOC_CYCLIN_RxL_1 | 276 | 285 | PF00134 | 0.290 |
DOC_MAPK_gen_1 | 378 | 385 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.388 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.610 |
DOC_USP7_UBL2_3 | 436 | 440 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.335 |
LIG_14-3-3_CanoR_1 | 130 | 136 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 237 | 245 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 265 | 273 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 361 | 367 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 61 | 65 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 88 | 96 | PF00244 | 0.407 |
LIG_APCC_ABBAyCdc20_2 | 406 | 412 | PF00400 | 0.388 |
LIG_BIR_III_4 | 105 | 109 | PF00653 | 0.153 |
LIG_BIR_III_4 | 401 | 405 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.344 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.283 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.246 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.312 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.391 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.413 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.467 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.523 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.561 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.407 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.336 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.408 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.371 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.502 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.367 |
LIG_GBD_Chelix_1 | 296 | 304 | PF00786 | 0.404 |
LIG_LIR_Gen_1 | 131 | 138 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 164 | 172 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 63 | 70 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.308 |
LIG_MYND_3 | 304 | 308 | PF01753 | 0.217 |
LIG_PCNA_yPIPBox_3 | 129 | 141 | PF02747 | 0.254 |
LIG_SH2_GRB2like | 95 | 98 | PF00017 | 0.246 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.182 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.182 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.305 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 134 | 139 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 333 | 339 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 380 | 389 | PF11976 | 0.527 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.421 |
LIG_TYR_ITIM | 93 | 98 | PF00017 | 0.304 |
LIG_UBA3_1 | 408 | 413 | PF00899 | 0.637 |
LIG_WRC_WIRS_1 | 64 | 69 | PF05994 | 0.153 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.160 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.421 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.497 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.407 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.228 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.386 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.499 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.690 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.509 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.421 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.285 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.368 |
MOD_LATS_1 | 377 | 383 | PF00433 | 0.504 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.457 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.356 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.331 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.340 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.290 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.393 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.312 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.481 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.331 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.326 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.309 |
MOD_NEK2_2 | 128 | 133 | PF00069 | 0.366 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.421 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.536 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.532 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.526 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.407 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.158 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.359 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.322 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.288 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.316 |
MOD_Plk_2-3 | 303 | 309 | PF00069 | 0.304 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.326 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.471 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.369 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.458 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.458 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.342 |
MOD_SUMO_rev_2 | 308 | 318 | PF00179 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.304 |
TRG_ER_diLys_1 | 437 | 442 | PF00400 | 0.582 |
TRG_NES_CRM1_1 | 303 | 314 | PF08389 | 0.344 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.527 |
TRG_NLS_MonoExtC_3 | 435 | 440 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 28 | 33 | PF00514 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4N0 | Leptomonas seymouri | 25% | 100% |
A0A0N1HUH0 | Leptomonas seymouri | 29% | 94% |
A0A0N1I317 | Leptomonas seymouri | 26% | 100% |
A0A0N1PD72 | Leptomonas seymouri | 70% | 99% |
A0A0S4IT30 | Bodo saltans | 25% | 66% |
A0A0S4JGH2 | Bodo saltans | 26% | 100% |
A0A0S4JL85 | Bodo saltans | 46% | 100% |
A0A0S4JPV3 | Bodo saltans | 29% | 92% |
A0A1X0NTY3 | Trypanosomatidae | 28% | 98% |
A0A1X0P364 | Trypanosomatidae | 50% | 100% |
A0A3Q8IDE6 | Leishmania donovani | 28% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 28% | 99% |
A0A3R7P015 | Trypanosoma rangeli | 51% | 93% |
A0A3S5H5G2 | Leishmania donovani | 87% | 100% |
A0A3S7WZL6 | Leishmania donovani | 28% | 100% |
A4HEQ6 | Leishmania braziliensis | 29% | 100% |
A4HFQ6 | Leishmania braziliensis | 27% | 100% |
A4HHW0 | Leishmania braziliensis | 26% | 100% |
A4HSD0 | Leishmania infantum | 87% | 100% |
A4I1Y5 | Leishmania infantum | 28% | 100% |
A4I2T1 | Leishmania infantum | 28% | 100% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 99% |
E9ADA9 | Leishmania major | 28% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AY32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 93% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P10775 | Sus scrofa | 26% | 97% |
Q0VAA2 | Homo sapiens | 24% | 91% |
Q4Q9E1 | Leishmania major | 28% | 100% |
Q4QBG0 | Leishmania major | 24% | 100% |
Q4QJI8 | Leishmania major | 88% | 100% |
Q8IZ02 | Homo sapiens | 22% | 95% |
Q9LE82 | Arabidopsis thaliana | 26% | 83% |
Q9M651 | Arabidopsis thaliana | 26% | 81% |
V5BC66 | Trypanosoma cruzi | 29% | 67% |
V5BJF0 | Trypanosoma cruzi | 52% | 89% |
V5BPZ7 | Trypanosoma cruzi | 29% | 98% |
V5DHF2 | Trypanosoma cruzi | 24% | 100% |