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:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005840 | ribosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4QF17
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008213 | protein alkylation | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018195 | peptidyl-arginine modification | 6 | 12 |
GO:0018216 | peptidyl-arginine methylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019919 | peptidyl-arginine methylation, to asymmetrical-dimethyl arginine | 8 | 2 |
GO:0032259 | methylation | 2 | 12 |
GO:0034969 | histone arginine methylation | 6 | 2 |
GO:0035246 | peptidyl-arginine N-methylation | 6 | 2 |
GO:0035247 | peptidyl-arginine omega-N-methylation | 7 | 2 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008169 | C-methyltransferase activity | 5 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008276 | protein methyltransferase activity | 3 | 12 |
GO:0008469 | histone arginine N-methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016273 | arginine N-methyltransferase activity | 6 | 12 |
GO:0016274 | protein-arginine N-methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0035244 | protein-arginine C-methyltransferase activity | 4 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.372 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.324 |
DEG_MDM2_SWIB_1 | 198 | 205 | PF02201 | 0.437 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.678 |
DEG_ODPH_VHL_1 | 310 | 323 | PF01847 | 0.376 |
DOC_ANK_TNKS_1 | 285 | 292 | PF00023 | 0.333 |
DOC_ANK_TNKS_1 | 46 | 53 | PF00023 | 0.405 |
DOC_CYCLIN_RxL_1 | 232 | 240 | PF00134 | 0.428 |
DOC_CYCLIN_RxL_1 | 36 | 48 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.319 |
DOC_MAPK_DCC_7 | 182 | 190 | PF00069 | 0.257 |
DOC_MAPK_gen_1 | 32 | 39 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 325 | 335 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.481 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.389 |
DOC_PP1_RVXF_1 | 357 | 363 | PF00149 | 0.486 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.318 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.495 |
DOC_SPAK_OSR1_1 | 286 | 290 | PF12202 | 0.273 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 278 | 282 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 286 | 290 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 331 | 349 | PF00022 | 0.344 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 139 | 146 | PF00928 | 0.258 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.454 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.461 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.394 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.247 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.390 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.410 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.479 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.369 |
LIG_Pex14_1 | 140 | 144 | PF04695 | 0.261 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.422 |
LIG_Pex14_2 | 198 | 202 | PF04695 | 0.460 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.280 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.430 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.358 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.321 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.282 |
LIG_SUMO_SIM_anti_2 | 99 | 108 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 76 | 81 | PF11976 | 0.482 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.267 |
LIG_WW_3 | 232 | 236 | PF00397 | 0.409 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.291 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.471 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.535 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.549 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.569 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.385 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.443 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.216 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.216 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.452 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.451 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.365 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.377 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.202 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.397 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.440 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.440 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.425 |
MOD_LATS_1 | 315 | 321 | PF00433 | 0.334 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.421 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.345 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.447 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.295 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.356 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.517 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.483 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.511 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.230 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.472 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.502 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.378 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.365 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.516 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.537 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.423 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.320 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.416 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.456 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.274 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.306 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.494 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.333 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.396 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.320 |
MOD_SUMO_rev_2 | 326 | 333 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 46 | 55 | PF00179 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 235 | 240 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3A7 | Leptomonas seymouri | 24% | 91% |
A0A0N0P6T9 | Leptomonas seymouri | 32% | 100% |
A0A0N0P7Z0 | Leptomonas seymouri | 65% | 100% |
A0A0S4JQD8 | Bodo saltans | 38% | 98% |
A0A0S4JWH9 | Bodo saltans | 30% | 100% |
A0A1X0NMC6 | Trypanosomatidae | 30% | 100% |
A0A1X0P0F1 | Trypanosomatidae | 45% | 99% |
A0A3R7MAM8 | Trypanosoma rangeli | 46% | 99% |
A0A3S5H6M7 | Leishmania donovani | 31% | 100% |
A0A3S7WTR5 | Leishmania donovani | 94% | 100% |
A0A451EJR0 | Leishmania donovani | 23% | 100% |
A2XYY8 | Oryza sativa subsp. indica | 28% | 96% |
A2Y953 | Oryza sativa subsp. indica | 29% | 96% |
A2YPT7 | Oryza sativa subsp. indica | 34% | 69% |
A2Z0C0 | Oryza sativa subsp. indica | 30% | 94% |
A2Z8S0 | Oryza sativa subsp. indica | 28% | 92% |
A3KPF2 | Arabidopsis thaliana | 31% | 69% |
A4H8A2 | Leishmania braziliensis | 22% | 90% |
A4H8D0 | Leishmania braziliensis | 85% | 100% |
A4HWQ2 | Leishmania infantum | 94% | 100% |
A8IEF3 | Chlamydomonas reinhardtii | 32% | 100% |
B0JYW5 | Xenopus tropicalis | 31% | 100% |
B3DLB3 | Xenopus tropicalis | 30% | 84% |
B3M1E1 | Drosophila ananassae | 31% | 69% |
B3P4N5 | Drosophila erecta | 31% | 69% |
B4GZ20 | Drosophila persimilis | 32% | 69% |
B4HJC0 | Drosophila sechellia | 31% | 69% |
B4JXV2 | Drosophila grimshawi | 30% | 67% |
B4KA23 | Drosophila mojavensis | 31% | 68% |
B4LVS8 | Drosophila virilis | 31% | 68% |
B4NKI9 | Drosophila willistoni | 31% | 68% |
B4PVH6 | Drosophila yakuba | 32% | 69% |
B4QVW6 | Drosophila simulans | 31% | 69% |
C9ZI39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZPS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 99% |
D9IVE5 | Xenopus laevis | 29% | 84% |
E9ACK5 | Leishmania major | 22% | 90% |
E9AGI9 | Leishmania infantum | 31% | 100% |
E9AIN9 | Leishmania braziliensis | 32% | 99% |
E9AJU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 91% |
E9AP27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AQF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O13648 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 67% |
O60678 | Homo sapiens | 29% | 69% |
O70467 | Rattus norvegicus | 28% | 69% |
O82210 | Arabidopsis thaliana | 30% | 100% |
P38074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P55345 | Homo sapiens | 28% | 84% |
Q08A71 | Arabidopsis thaliana | 30% | 84% |
Q0J2C6 | Oryza sativa subsp. japonica | 30% | 94% |
Q28F07 | Xenopus tropicalis | 30% | 100% |
Q29B63 | Drosophila pseudoobscura pseudoobscura | 32% | 69% |
Q4QGG2 | Leishmania major | 31% | 100% |
Q54EF2 | Dictyostelium discoideum | 27% | 100% |
Q54HI0 | Dictyostelium discoideum | 29% | 71% |
Q5E9L5 | Bos taurus | 32% | 97% |
Q5RGQ2 | Danio rerio | 29% | 87% |
Q63009 | Rattus norvegicus | 30% | 100% |
Q68EZ3 | Xenopus laevis | 31% | 100% |
Q6NWG4 | Danio rerio | 30% | 100% |
Q6NZB1 | Mus musculus | 32% | 97% |
Q6PAK3 | Mus musculus | 29% | 93% |
Q6VRB0 | Xenopus laevis | 30% | 100% |
Q75G68 | Oryza sativa subsp. japonica | 28% | 92% |
Q7XI75 | Oryza sativa subsp. japonica | 34% | 69% |
Q7XKC0 | Oryza sativa subsp. japonica | 28% | 93% |
Q84W92 | Arabidopsis thaliana | 32% | 68% |
Q8AV13 | Xenopus laevis | 30% | 99% |
Q922H1 | Mus musculus | 28% | 69% |
Q96LA8 | Homo sapiens | 31% | 97% |
Q99873 | Homo sapiens | 30% | 98% |
Q9JIF0 | Mus musculus | 30% | 98% |
Q9NR22 | Homo sapiens | 29% | 93% |
Q9R144 | Mus musculus | 29% | 81% |
Q9SNQ2 | Oryza sativa subsp. japonica | 29% | 96% |
Q9SU94 | Arabidopsis thaliana | 31% | 94% |
Q9U2X0 | Caenorhabditis elegans | 32% | 100% |
Q9URX7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q9VH48 | Drosophila melanogaster | 31% | 69% |
V5ARC3 | Trypanosoma cruzi | 48% | 93% |
V5BF38 | Trypanosoma cruzi | 29% | 100% |