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. | yes | yes: 25 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A0A451EJR0
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0008213 | protein alkylation | 5 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0018193 | peptidyl-amino acid modification | 5 | 13 |
GO:0018195 | peptidyl-arginine modification | 6 | 13 |
GO:0018216 | peptidyl-arginine methylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0032259 | methylation | 2 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0043414 | macromolecule methylation | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0008168 | methyltransferase activity | 4 | 13 |
GO:0008170 | N-methyltransferase activity | 5 | 13 |
GO:0008276 | protein methyltransferase activity | 3 | 13 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 13 |
GO:0016273 | arginine N-methyltransferase activity | 6 | 13 |
GO:0016274 | protein-arginine N-methyltransferase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.356 |
CLV_Separin_Metazoa | 221 | 225 | PF03568 | 0.587 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.433 |
DOC_CDC14_PxL_1 | 237 | 245 | PF14671 | 0.467 |
DOC_CKS1_1 | 368 | 373 | PF01111 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 350 | 356 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 374 | 383 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 66 | 74 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 75 | 85 | PF00069 | 0.281 |
DOC_MAPK_HePTP_8 | 95 | 107 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 98 | 107 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.495 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 164 | 171 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 187 | 191 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.507 |
LIG_deltaCOP1_diTrp_1 | 205 | 214 | PF00928 | 0.422 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.457 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.457 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.715 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.514 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.318 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.566 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.578 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.588 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.539 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 154 | 158 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.556 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.431 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.353 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 70 | 74 | PF00017 | 0.546 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 212 | 215 | PF00017 | 0.605 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.468 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.556 |
LIG_SUMO_SIM_par_1 | 157 | 163 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 300 | 305 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 379 | 384 | PF11976 | 0.514 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.635 |
LIG_WRC_WIRS_1 | 312 | 317 | PF05994 | 0.416 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.612 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.448 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.582 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.578 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.480 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.363 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.491 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.655 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.535 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.459 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.537 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.449 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.570 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.559 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.427 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.513 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.874 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.522 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.604 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.527 |
MOD_N-GLC_2 | 22 | 24 | PF02516 | 0.556 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.582 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.423 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.680 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.566 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.846 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.450 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.477 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.482 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.374 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.396 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.440 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.593 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.551 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.584 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.384 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.533 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.551 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.409 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.314 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.604 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3A7 | Leptomonas seymouri | 81% | 100% |
A0A0S4JDH7 | Bodo saltans | 43% | 100% |
A0A0S4JWH9 | Bodo saltans | 27% | 100% |
A0A1X0NMC6 | Trypanosomatidae | 29% | 100% |
A0A1X0PA69 | Trypanosomatidae | 51% | 97% |
A0A3R7NHM3 | Trypanosoma rangeli | 51% | 100% |
A0A3S5H6M7 | Leishmania donovani | 25% | 97% |
A2XYY8 | Oryza sativa subsp. indica | 23% | 100% |
A2Y953 | Oryza sativa subsp. indica | 26% | 100% |
A2YPT7 | Oryza sativa subsp. indica | 25% | 77% |
A2Z0C0 | Oryza sativa subsp. indica | 26% | 100% |
A2Z8S0 | Oryza sativa subsp. indica | 26% | 100% |
A3KPF2 | Arabidopsis thaliana | 25% | 77% |
A4H8A2 | Leishmania braziliensis | 90% | 100% |
A4H8D0 | Leishmania braziliensis | 23% | 100% |
A8IEF3 | Chlamydomonas reinhardtii | 26% | 100% |
B0JYW5 | Xenopus tropicalis | 24% | 100% |
B0W3L6 | Culex quinquefasciatus | 25% | 68% |
B3DLB3 | Xenopus tropicalis | 27% | 94% |
B3M1E1 | Drosophila ananassae | 23% | 76% |
B3P4N5 | Drosophila erecta | 23% | 76% |
B4GZ20 | Drosophila persimilis | 23% | 76% |
B4HJC0 | Drosophila sechellia | 23% | 76% |
B4JXV2 | Drosophila grimshawi | 23% | 74% |
B4KA23 | Drosophila mojavensis | 23% | 75% |
B4LVS8 | Drosophila virilis | 23% | 75% |
B4NKI9 | Drosophila willistoni | 23% | 76% |
B4PVH6 | Drosophila yakuba | 23% | 76% |
B4QVW6 | Drosophila simulans | 23% | 76% |
C9ZI39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A264 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D9IVE5 | Xenopus laevis | 26% | 94% |
E9ACK5 | Leishmania major | 96% | 100% |
E9AG49 | Leishmania infantum | 100% | 100% |
E9AGI9 | Leishmania infantum | 25% | 97% |
E9AIN9 | Leishmania braziliensis | 25% | 99% |
E9AJU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AP27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9AQF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
O13648 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 75% |
O60678 | Homo sapiens | 28% | 76% |
O70467 | Rattus norvegicus | 27% | 77% |
O82210 | Arabidopsis thaliana | 26% | 100% |
P55345 | Homo sapiens | 25% | 94% |
Q08A71 | Arabidopsis thaliana | 27% | 93% |
Q0J2C6 | Oryza sativa subsp. japonica | 26% | 100% |
Q0WVD6 | Arabidopsis thaliana | 24% | 67% |
Q174R2 | Aedes aegypti | 24% | 68% |
Q28F07 | Xenopus tropicalis | 27% | 100% |
Q29B63 | Drosophila pseudoobscura pseudoobscura | 23% | 76% |
Q4QF17 | Leishmania major | 23% | 100% |
Q4QGG2 | Leishmania major | 26% | 100% |
Q54EF2 | Dictyostelium discoideum | 27% | 100% |
Q5E9L5 | Bos taurus | 26% | 100% |
Q5RGQ2 | Danio rerio | 28% | 97% |
Q5XK84 | Xenopus laevis | 22% | 67% |
Q63009 | Rattus norvegicus | 26% | 100% |
Q68EZ3 | Xenopus laevis | 24% | 100% |
Q6DC04 | Danio rerio | 24% | 69% |
Q6NWG4 | Danio rerio | 23% | 100% |
Q6NZB1 | Mus musculus | 27% | 100% |
Q6PAK3 | Mus musculus | 28% | 100% |
Q6VRB0 | Xenopus laevis | 27% | 100% |
Q75G68 | Oryza sativa subsp. japonica | 26% | 100% |
Q7XI75 | Oryza sativa subsp. japonica | 25% | 77% |
Q7XKC0 | Oryza sativa subsp. japonica | 23% | 100% |
Q84W92 | Arabidopsis thaliana | 24% | 76% |
Q86X55 | Homo sapiens | 24% | 67% |
Q8AV13 | Xenopus laevis | 27% | 100% |
Q922H1 | Mus musculus | 27% | 77% |
Q96LA8 | Homo sapiens | 27% | 100% |
Q99873 | Homo sapiens | 26% | 100% |
Q9JIF0 | Mus musculus | 26% | 100% |
Q9NR22 | Homo sapiens | 28% | 100% |
Q9R144 | Mus musculus | 26% | 90% |
Q9SNQ2 | Oryza sativa subsp. japonica | 26% | 100% |
Q9SU94 | Arabidopsis thaliana | 26% | 100% |
Q9U2X0 | Caenorhabditis elegans | 24% | 100% |
Q9URX7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
Q9VH48 | Drosophila melanogaster | 23% | 76% |
Q9WVG6 | Mus musculus | 24% | 67% |
V5BXE6 | Trypanosoma cruzi | 51% | 100% |