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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
GO:0016020 | membrane | 2 | 3 |
GO:0005739 | mitochondrion | 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:0031019 | mitochondrial mRNA editing complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045293 | mRNA editing complex | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HEP5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 24 |
GO:0006396 | RNA processing | 6 | 24 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 24 |
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0016070 | RNA metabolic process | 5 | 24 |
GO:0031123 | RNA 3'-end processing | 7 | 24 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0044237 | cellular metabolic process | 2 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0046483 | heterocycle metabolic process | 3 | 24 |
GO:0071076 | RNA 3' uridylation | 8 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:0090304 | nucleic acid metabolic process | 4 | 24 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 24 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0016740 | transferase activity | 2 | 24 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 24 |
GO:0016779 | nucleotidyltransferase activity | 4 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043169 | cation binding | 3 | 24 |
GO:0046872 | metal ion binding | 4 | 24 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 24 |
GO:0070569 | uridylyltransferase activity | 5 | 24 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 24 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 24 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 4 |
GO:0070566 | adenylyltransferase activity | 5 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.338 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.245 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.286 |
DEG_COP1_1 | 273 | 283 | PF00400 | 0.286 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.564 |
DOC_ANK_TNKS_1 | 221 | 228 | PF00023 | 0.206 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.367 |
DOC_MAPK_MEF2A_6 | 278 | 285 | PF00069 | 0.299 |
DOC_PP1_RVXF_1 | 353 | 360 | PF00149 | 0.382 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.173 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.463 |
DOC_USP7_UBL2_3 | 322 | 326 | PF12436 | 0.314 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 194 | 203 | PF00244 | 0.227 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 473 | 479 | PF00244 | 0.460 |
LIG_AP2alpha_2 | 361 | 363 | PF02296 | 0.337 |
LIG_CaMK_CASK_1 | 226 | 232 | PF00069 | 0.302 |
LIG_Clathr_ClatBox_1 | 438 | 442 | PF01394 | 0.255 |
LIG_deltaCOP1_diTrp_1 | 422 | 427 | PF00928 | 0.286 |
LIG_eIF4E_1 | 103 | 109 | PF01652 | 0.529 |
LIG_eIF4E_1 | 154 | 160 | PF01652 | 0.249 |
LIG_eIF4E_1 | 341 | 347 | PF01652 | 0.439 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.632 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.459 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.356 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.208 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.467 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.374 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.310 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.354 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.425 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.348 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.388 |
LIG_HP1_1 | 415 | 419 | PF01393 | 0.173 |
LIG_LIR_Apic_2 | 422 | 428 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 434 | 441 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 442 | 453 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.264 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.302 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.297 |
LIG_Pex14_2 | 284 | 288 | PF04695 | 0.305 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.421 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.419 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 10 | 14 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.302 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.233 |
LIG_SH2_SRC | 445 | 448 | PF00017 | 0.302 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.257 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.500 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.339 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.321 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.286 |
LIG_TYR_ITIM | 17 | 22 | PF00017 | 0.442 |
MOD_CDK_SPxxK_3 | 164 | 171 | PF00069 | 0.345 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.445 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.445 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.635 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.678 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.311 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.593 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.286 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.307 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.718 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.345 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.670 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.641 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.349 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.387 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.375 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.661 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.608 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.332 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.406 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.662 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.335 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.352 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.345 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.419 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.465 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.544 |
MOD_PKA_1 | 495 | 501 | PF00069 | 0.416 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.480 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.344 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.275 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.303 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.623 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.587 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.330 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.296 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.348 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.436 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.469 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.521 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.254 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.336 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.406 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.345 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.679 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.722 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.372 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.445 |
MOD_SUMO_for_1 | 467 | 470 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 190 | 196 | PF00179 | 0.289 |
MOD_SUMO_rev_2 | 94 | 102 | PF00179 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.733 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P857 | Leptomonas seymouri | 24% | 98% |
A0A0N1IJQ4 | Leptomonas seymouri | 76% | 100% |
A0A0S4JJR1 | Bodo saltans | 72% | 100% |
A0A0S4JJT6 | Bodo saltans | 27% | 88% |
A0A1X0NSS0 | Trypanosomatidae | 76% | 100% |
A0A1X0NZU6 | Trypanosomatidae | 28% | 98% |
A0A3Q8IC11 | Leishmania donovani | 88% | 100% |
A0A3Q8IHZ8 | Leishmania donovani | 25% | 100% |
A0A3R7K3P5 | Trypanosoma rangeli | 28% | 97% |
A0A3R7KH85 | Trypanosoma rangeli | 25% | 71% |
A0A422NVH7 | Trypanosoma rangeli | 74% | 100% |
A4HGC0 | Leishmania braziliensis | 25% | 100% |
A4I1X5 | Leishmania infantum | 88% | 100% |
A4I3F3 | Leishmania infantum | 25% | 100% |
C9ZS45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 100% |
D0A7Y7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 97% |
E9AY21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AZP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q8J1 | Leishmania major | 26% | 100% |
Q4Q9F2 | Leishmania major | 88% | 99% |
Q86MV5 | Trypanosoma brucei brucei | 76% | 100% |
V5BG78 | Trypanosoma cruzi | 28% | 97% |
V5BQ07 | Trypanosoma cruzi | 75% | 100% |