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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
GO:0005929 | cilium | 4 | 17 |
GO:0042995 | cell projection | 2 | 17 |
GO:0043226 | organelle | 2 | 17 |
GO:0043227 | membrane-bounded organelle | 3 | 17 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 17 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QJI8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.387 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.626 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.394 |
DOC_MAPK_gen_1 | 377 | 384 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 377 | 384 | PF00069 | 0.508 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.345 |
DOC_USP7_UBL2_3 | 27 | 31 | PF12436 | 0.486 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 223 | 229 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 264 | 272 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 377 | 381 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.329 |
LIG_BIR_III_4 | 400 | 404 | PF00653 | 0.657 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.367 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.258 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.334 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.398 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.286 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.384 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.407 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.437 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.416 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.536 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.669 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.655 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.370 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.336 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.496 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.332 |
LIG_LIR_Gen_1 | 130 | 137 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.466 |
LIG_NRP_CendR_1 | 438 | 441 | PF00754 | 0.467 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.260 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.513 |
LIG_SUMO_SIM_anti_2 | 133 | 138 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 332 | 338 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 379 | 388 | PF11976 | 0.518 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.428 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.459 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.349 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.319 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.457 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.719 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.513 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.362 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.398 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.349 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.425 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.357 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.530 |
MOD_LATS_1 | 376 | 382 | PF00433 | 0.494 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.464 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.381 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.393 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.459 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.354 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.287 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.354 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.396 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.326 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.330 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.547 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.317 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.340 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.499 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.392 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.351 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.260 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.498 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.312 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.128 |
MOD_PK_1 | 29 | 35 | PF00069 | 0.343 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.404 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.342 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.282 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.281 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.391 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.329 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.381 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.470 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.506 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.413 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.437 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.517 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 307 | 317 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.335 |
TRG_ER_diLys_1 | 436 | 441 | PF00400 | 0.568 |
TRG_NLS_MonoExtC_3 | 26 | 31 | PF00514 | 0.517 |
TRG_NLS_MonoExtC_3 | 434 | 439 | PF00514 | 0.497 |
TRG_NLS_MonoExtN_4 | 27 | 32 | PF00514 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUH0 | Leptomonas seymouri | 26% | 94% |
A0A0N1I317 | Leptomonas seymouri | 26% | 100% |
A0A0N1PD72 | Leptomonas seymouri | 71% | 99% |
A0A0S4IK39 | Bodo saltans | 25% | 70% |
A0A0S4IT30 | Bodo saltans | 26% | 66% |
A0A0S4JGH2 | Bodo saltans | 25% | 100% |
A0A0S4JL85 | Bodo saltans | 48% | 100% |
A0A0S4JPV3 | Bodo saltans | 28% | 91% |
A0A1X0NTY3 | Trypanosomatidae | 29% | 98% |
A0A1X0P364 | Trypanosomatidae | 52% | 100% |
A0A3Q8IDE6 | Leishmania donovani | 28% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 28% | 99% |
A0A3R7P015 | Trypanosoma rangeli | 52% | 93% |
A0A3S5H5G2 | Leishmania donovani | 97% | 100% |
A0A3S7WZL6 | Leishmania donovani | 28% | 100% |
A4H461 | Leishmania braziliensis | 88% | 100% |
A4HEQ6 | Leishmania braziliensis | 25% | 100% |
A4HFQ6 | Leishmania braziliensis | 28% | 100% |
A4HHW0 | Leishmania braziliensis | 27% | 100% |
A4HSD0 | Leishmania infantum | 97% | 100% |
A4I1Y5 | Leishmania infantum | 28% | 100% |
A4I2T1 | Leishmania infantum | 28% | 100% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 98% |
E9ADA9 | Leishmania major | 28% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AY32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 93% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P10775 | Sus scrofa | 24% | 97% |
Q4Q9E1 | Leishmania major | 27% | 100% |
Q4QBG0 | Leishmania major | 24% | 100% |
Q4V8D9 | Rattus norvegicus | 22% | 100% |
Q8IZ02 | Homo sapiens | 25% | 95% |
Q91VI7 | Mus musculus | 23% | 97% |
Q9DAM1 | Mus musculus | 23% | 100% |
Q9LE82 | Arabidopsis thaliana | 26% | 82% |
Q9M651 | Arabidopsis thaliana | 26% | 81% |
Q9VIW3 | Drosophila melanogaster | 28% | 74% |
V5BC66 | Trypanosoma cruzi | 28% | 67% |
V5BJF0 | Trypanosoma cruzi | 53% | 89% |
V5BPZ7 | Trypanosoma cruzi | 29% | 98% |