Leucine-rich repeat proteins with a hydrophobic terminal helix. Unlike its distant animal relatives, this cytoplasmic sensor protein might be anchored to the membrane.
Uncharacterized Protein, Uncharacterized
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: A0A3S7WZL6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.321 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 280 | 288 | PF00400 | 0.452 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.617 |
DOC_ANK_TNKS_1 | 120 | 127 | PF00023 | 0.516 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.385 |
DOC_CYCLIN_RxL_1 | 15 | 24 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 192 | 202 | PF00069 | 0.400 |
DOC_MIT_MIM_1 | 226 | 235 | PF04212 | 0.366 |
DOC_PP1_SILK_1 | 159 | 164 | PF00149 | 0.438 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.400 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.394 |
LIG_Actin_RPEL_3 | 16 | 35 | PF02755 | 0.456 |
LIG_Actin_WH2_2 | 298 | 315 | PF00022 | 0.490 |
LIG_DLG_GKlike_1 | 104 | 112 | PF00625 | 0.513 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.420 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.495 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.416 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.519 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.252 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.493 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.321 |
LIG_GBD_Chelix_1 | 302 | 310 | PF00786 | 0.404 |
LIG_LIR_Apic_2 | 22 | 28 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.458 |
LIG_NRBOX | 385 | 391 | PF00104 | 0.494 |
LIG_PCNA_yPIPBox_3 | 364 | 372 | PF02747 | 0.454 |
LIG_PCNA_yPIPBox_3 | 380 | 390 | PF02747 | 0.291 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.468 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.559 |
LIG_SUMO_SIM_anti_2 | 252 | 258 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 31 | 36 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 339 | 344 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 182 | 189 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 338 | 344 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.437 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.413 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.386 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.423 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.461 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.471 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.316 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.321 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.490 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.286 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.452 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.419 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.339 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.426 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.390 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.458 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.346 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.442 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.682 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.478 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.374 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.325 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.582 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.460 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.281 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.387 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.398 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.444 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.326 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.390 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.305 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.376 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.506 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.396 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.371 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.316 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.399 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.372 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.339 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.351 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.337 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.493 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.472 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.344 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.510 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.413 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.464 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.510 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.303 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.284 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.390 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.488 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.356 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.378 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.526 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUH0 | Leptomonas seymouri | 77% | 91% |
A0A0N1I317 | Leptomonas seymouri | 28% | 100% |
A0A0N1PD72 | Leptomonas seymouri | 25% | 96% |
A0A0S4JGH2 | Bodo saltans | 27% | 100% |
A0A0S4JL85 | Bodo saltans | 25% | 100% |
A0A0S4JPV3 | Bodo saltans | 38% | 89% |
A0A0S4JXN4 | Bodo saltans | 26% | 99% |
A0A0S4KL56 | Bodo saltans | 29% | 89% |
A0A1X0NTY3 | Trypanosomatidae | 54% | 96% |
A0A1X0P2M5 | Trypanosomatidae | 30% | 100% |
A0A1X0P364 | Trypanosomatidae | 25% | 100% |
A0A3Q8IDE6 | Leishmania donovani | 26% | 100% |
A0A3R7L7Y9 | Trypanosoma rangeli | 53% | 96% |
A0A3R7P015 | Trypanosoma rangeli | 25% | 91% |
A0A3S5H5G2 | Leishmania donovani | 28% | 100% |
A0A3S7WXH1 | Leishmania donovani | 26% | 100% |
A0JPI9 | Rattus norvegicus | 30% | 90% |
A4H461 | Leishmania braziliensis | 28% | 100% |
A4HCM9 | Leishmania braziliensis | 25% | 100% |
A4HEQ6 | Leishmania braziliensis | 79% | 100% |
A4HFQ6 | Leishmania braziliensis | 24% | 100% |
A4HHW0 | Leishmania braziliensis | 30% | 100% |
A4HSD0 | Leishmania infantum | 29% | 100% |
A4I053 | Leishmania infantum | 26% | 100% |
A4I1Y5 | Leishmania infantum | 100% | 100% |
A4I2T1 | Leishmania infantum | 26% | 100% |
C9ZPX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 99% |
C9ZS33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
E9ADA9 | Leishmania major | 28% | 100% |
E9AKB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AN05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AW16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AY32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AZ34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
O13066 | Xenopus laevis | 24% | 74% |
P10775 | Sus scrofa | 28% | 94% |
P13489 | Homo sapiens | 25% | 93% |
P46060 | Homo sapiens | 25% | 73% |
P46061 | Mus musculus | 25% | 73% |
Q0VAA2 | Homo sapiens | 26% | 88% |
Q4Q9E1 | Leishmania major | 95% | 100% |
Q4QBG0 | Leishmania major | 23% | 100% |
Q4QJI8 | Leishmania major | 28% | 100% |
Q4V8D9 | Rattus norvegicus | 25% | 100% |
Q6ZQY2 | Homo sapiens | 31% | 100% |
Q8HZP9 | Pan troglodytes | 25% | 93% |
Q8IZ02 | Homo sapiens | 25% | 92% |
Q91VI7 | Mus musculus | 27% | 94% |
Q9DAM1 | Mus musculus | 25% | 100% |
Q9LE82 | Arabidopsis thaliana | 27% | 80% |
Q9M651 | Arabidopsis thaliana | 25% | 79% |
Q9VIW3 | Drosophila melanogaster | 24% | 72% |
V5BJF0 | Trypanosoma cruzi | 25% | 87% |
V5BN05 | Trypanosoma cruzi | 25% | 72% |
V5BPZ7 | Trypanosoma cruzi | 55% | 96% |