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:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ATF3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 12 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 316 | 320 | PF03568 | 0.404 |
DEG_ODPH_VHL_1 | 352 | 364 | PF01847 | 0.409 |
DEG_ODPH_VHL_1 | 389 | 401 | PF01847 | 0.346 |
DOC_CYCLIN_RxL_1 | 334 | 347 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 102 | 109 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.567 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.429 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.360 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.405 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 311 | 318 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.444 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.478 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 62 | 66 | PF01394 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 279 | 285 | PF00928 | 0.301 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.411 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.322 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.401 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.350 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.342 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.507 |
LIG_LIR_Apic_2 | 298 | 304 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 279 | 290 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 368 | 378 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 446 | 451 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.447 |
LIG_MYND_1 | 173 | 177 | PF01753 | 0.281 |
LIG_NRBOX | 122 | 128 | PF00104 | 0.411 |
LIG_PCNA_yPIPBox_3 | 281 | 294 | PF02747 | 0.331 |
LIG_PDZ_Class_2 | 446 | 451 | PF00595 | 0.426 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.374 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.331 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 19 | 23 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 448 | 451 | PF00017 | 0.462 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.393 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.447 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.459 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.354 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.387 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.406 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.494 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.349 |
LIG_SUMO_SIM_anti_2 | 104 | 110 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 267 | 274 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 267 | 274 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 58 | 64 | PF11976 | 0.391 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.358 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.575 |
LIG_TRAF2_1 | 444 | 447 | PF00917 | 0.432 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.424 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.331 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.300 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.334 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.465 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.413 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.395 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.516 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.331 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.454 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.283 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.322 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.346 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.506 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.610 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.411 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.483 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.548 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.394 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.509 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.324 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.357 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.383 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.320 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.489 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.449 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.504 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.180 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.276 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.486 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.411 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.298 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.491 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.489 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.492 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.314 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.385 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.326 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.497 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.360 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.375 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.292 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.227 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.278 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.307 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.501 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.496 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.392 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.284 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.287 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.383 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_1 | 407 | 412 | PF01217 | 0.345 |
TRG_DiLeu_BaLyEn_6 | 415 | 420 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.536 |
TRG_NLS_MonoExtN_4 | 2 | 8 | PF00514 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 315 | 320 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJZ5 | Leptomonas seymouri | 76% | 100% |
A0A0S4JES6 | Bodo saltans | 30% | 100% |
A0A1X0P3J8 | Trypanosomatidae | 45% | 100% |
A0A3Q8IL58 | Leishmania donovani | 96% | 100% |
A0A422N1N1 | Trypanosoma rangeli | 46% | 100% |
A4HPN9 | Leishmania braziliensis | 93% | 100% |
A4ID25 | Leishmania infantum | 96% | 100% |
D0A8H5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
Q4Q144 | Leishmania major | 96% | 100% |
V5AU86 | Trypanosoma cruzi | 46% | 100% |