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:0016020 | membrane | 2 | 31 |
GO:0110165 | cellular anatomical entity | 1 | 31 |
Related structures:
AlphaFold database: A4HQ67
Term | Name | Level | Count |
---|---|---|---|
GO:0038023 | signaling receptor activity | 2 | 3 |
GO:0060089 | molecular transducer activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.525 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.141 |
DOC_AGCK_PIF_1 | 169 | 174 | PF00069 | 0.208 |
DOC_CYCLIN_RxL_1 | 293 | 300 | PF00134 | 0.325 |
DOC_CYCLIN_RxL_1 | 9 | 17 | PF00134 | 0.558 |
DOC_MAPK_DCC_7 | 161 | 169 | PF00069 | 0.141 |
DOC_MAPK_gen_1 | 147 | 157 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.177 |
DOC_MAPK_MEF2A_6 | 161 | 169 | PF00069 | 0.333 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.474 |
DOC_PP2B_PxIxI_1 | 277 | 283 | PF00149 | 0.237 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.468 |
DOC_USP7_MATH_2 | 41 | 47 | PF00917 | 0.511 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 253 | 260 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.707 |
LIG_APCC_ABBA_1 | 104 | 109 | PF00400 | 0.416 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.241 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.408 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.480 |
LIG_EH1_1 | 206 | 214 | PF00400 | 0.258 |
LIG_EH1_1 | 241 | 249 | PF00400 | 0.216 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.337 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.429 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.360 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.305 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.453 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.271 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.538 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.502 |
LIG_IRF3_LxIS_1 | 286 | 291 | PF10401 | 0.333 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.217 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 345 | 355 | PF02991 | 0.318 |
LIG_LIR_LC3C_4 | 210 | 214 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.318 |
LIG_PDZ_Class_2 | 358 | 363 | PF00595 | 0.276 |
LIG_Pex14_1 | 231 | 235 | PF04695 | 0.236 |
LIG_Pex14_2 | 251 | 255 | PF04695 | 0.444 |
LIG_Pex14_2 | 310 | 314 | PF04695 | 0.302 |
LIG_Pex14_2 | 325 | 329 | PF04695 | 0.414 |
LIG_REV1ctd_RIR_1 | 249 | 257 | PF16727 | 0.300 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.218 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.209 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.218 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.147 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.481 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.580 |
LIG_SUMO_SIM_anti_2 | 210 | 216 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 210 | 216 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 286 | 291 | PF11976 | 0.339 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.288 |
LIG_WRC_WIRS_1 | 186 | 191 | PF05994 | 0.482 |
LIG_WRC_WIRS_1 | 214 | 219 | PF05994 | 0.291 |
LIG_WRC_WIRS_1 | 239 | 244 | PF05994 | 0.375 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.292 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.547 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.651 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.505 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.304 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.278 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.434 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.569 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.532 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.283 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.352 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.314 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.238 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.509 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.372 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.281 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.227 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.288 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.283 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.276 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.450 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.557 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.348 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.423 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.342 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.454 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.601 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.281 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.283 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.265 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.334 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.305 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.545 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.673 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.733 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.210 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.141 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I280 | Leptomonas seymouri | 64% | 100% |
A0A0N1I909 | Leptomonas seymouri | 37% | 100% |
A0A0N1PEB9 | Leptomonas seymouri | 37% | 67% |
A0A0S4J7T5 | Bodo saltans | 37% | 98% |
A0A0S4J8V2 | Bodo saltans | 42% | 100% |
A0A0S4JQM0 | Bodo saltans | 42% | 100% |
A0A0S4JWI8 | Bodo saltans | 37% | 100% |
A0A0S4KIQ2 | Bodo saltans | 36% | 100% |
A0A1X0P1D6 | Trypanosomatidae | 34% | 100% |
A0A1X0P1Q2 | Trypanosomatidae | 47% | 100% |
A0A3R7L1Y6 | Trypanosoma rangeli | 49% | 100% |
A0A3S5ISE8 | Trypanosoma rangeli | 21% | 100% |
A0A3S7XBT4 | Leishmania donovani | 79% | 100% |
A0A3S7XBU6 | Leishmania donovani | 35% | 71% |
A0A3S7XC05 | Leishmania donovani | 37% | 100% |
A4HQ64 | Leishmania braziliensis | 36% | 71% |
A4HQ68 | Leishmania braziliensis | 36% | 100% |
A4IDW4 | Leishmania infantum | 79% | 100% |
A4IDW5 | Leishmania infantum | 35% | 71% |
A4IDW6 | Leishmania infantum | 37% | 100% |
B7F9G7 | Oryza sativa subsp. japonica | 29% | 97% |
D0A450 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A451 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ATY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9ATY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 73% |
E9ATY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q03419 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q07959 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 67% |
Q09749 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
Q09910 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 82% |
Q12442 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q4Q0K9 | Leishmania major | 38% | 100% |
Q4Q0L0 | Leishmania major | 35% | 72% |
Q4Q0L1 | Leishmania major | 77% | 100% |
Q6DC77 | Danio rerio | 26% | 100% |
Q6TCG5 | Mus musculus | 28% | 100% |
Q6TCG8 | Mus musculus | 31% | 100% |
Q6TCH4 | Homo sapiens | 27% | 100% |
Q6TCH7 | Homo sapiens | 31% | 100% |
Q6ZVX9 | Homo sapiens | 26% | 96% |
Q753H5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 100% |
Q75F81 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 87% |
Q801D8 | Cynoscion nebulosus | 24% | 100% |
Q84N34 | Arabidopsis thaliana | 30% | 100% |
Q86V24 | Homo sapiens | 32% | 94% |
Q8BQS5 | Mus musculus | 32% | 94% |
Q91VH1 | Mus musculus | 32% | 97% |
Q93ZH9 | Arabidopsis thaliana | 29% | 100% |
Q94177 | Caenorhabditis elegans | 30% | 84% |
Q96A54 | Homo sapiens | 32% | 97% |
Q9JJE4 | Mus musculus | 26% | 100% |
Q9SVF3 | Arabidopsis thaliana | 30% | 97% |
Q9SZG0 | Arabidopsis thaliana | 30% | 94% |
Q9VCY8 | Drosophila melanogaster | 32% | 82% |
Q9ZUH8 | Arabidopsis thaliana | 30% | 100% |
V5BJ57 | Trypanosoma cruzi | 33% | 100% |
V5DK49 | Trypanosoma cruzi | 51% | 100% |