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:0031019 | mitochondrial mRNA editing complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0045293 | mRNA editing complex | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 21 |
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
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 |
Related structures:
AlphaFold database: Q4Q9F2
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_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.533 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.363 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.352 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.291 |
DEG_COP1_1 | 273 | 283 | PF00400 | 0.291 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.694 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 450 | 459 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.374 |
DOC_PP1_RVXF_1 | 353 | 360 | PF00149 | 0.385 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.635 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.460 |
DOC_USP7_UBL2_3 | 322 | 326 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 194 | 203 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 473 | 479 | PF00244 | 0.473 |
LIG_AP2alpha_2 | 361 | 363 | PF02296 | 0.342 |
LIG_CaMK_CASK_1 | 226 | 232 | PF00069 | 0.307 |
LIG_Clathr_ClatBox_1 | 438 | 442 | PF01394 | 0.262 |
LIG_deltaCOP1_diTrp_1 | 422 | 427 | PF00928 | 0.291 |
LIG_eIF4E_1 | 103 | 109 | PF01652 | 0.533 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.633 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.471 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.366 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.376 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.428 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.392 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.365 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.460 |
LIG_LIR_Apic_2 | 422 | 428 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 434 | 441 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 442 | 453 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 5 | 13 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.487 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.307 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.303 |
LIG_Pex14_2 | 284 | 288 | PF04695 | 0.311 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.426 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 10 | 13 | PF00017 | 0.477 |
LIG_SH2_SRC | 445 | 448 | PF00017 | 0.307 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.530 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.262 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.495 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.360 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 408 | 413 | PF11976 | 0.326 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.291 |
MOD_CDK_SPxxK_3 | 164 | 171 | PF00069 | 0.355 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.291 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.291 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.436 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.637 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.594 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.306 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.629 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.291 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.325 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.723 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.403 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.662 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.633 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.355 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.535 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.379 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.674 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.337 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.375 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.639 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.341 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.346 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.384 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.394 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.491 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.486 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.349 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.281 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.327 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.262 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.354 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.302 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.359 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.278 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.347 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.535 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.467 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.258 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.314 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.444 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.354 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.679 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.721 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.408 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.291 |
MOD_SUMO_for_1 | 467 | 470 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 190 | 196 | PF00179 | 0.317 |
MOD_SUMO_rev_2 | 94 | 102 | PF00179 | 0.291 |
TRG_DiLeu_BaEn_1 | 387 | 392 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P857 | Leptomonas seymouri | 25% | 97% |
A0A0N1IJQ4 | Leptomonas seymouri | 76% | 100% |
A0A0S4JJR1 | Bodo saltans | 69% | 100% |
A0A0S4JJT6 | Bodo saltans | 27% | 87% |
A0A1X0NSS0 | Trypanosomatidae | 76% | 100% |
A0A1X0NZU6 | Trypanosomatidae | 29% | 97% |
A0A3Q8IC11 | Leishmania donovani | 97% | 100% |
A0A3Q8IHZ8 | Leishmania donovani | 25% | 100% |
A0A3R7K3P5 | Trypanosoma rangeli | 29% | 97% |
A0A3R7KH85 | Trypanosoma rangeli | 26% | 71% |
A0A422NVH7 | Trypanosoma rangeli | 74% | 100% |
A4HEP5 | Leishmania braziliensis | 88% | 99% |
A4HGC0 | Leishmania braziliensis | 25% | 100% |
A4I1X5 | Leishmania infantum | 97% | 100% |
A4I3F3 | Leishmania infantum | 25% | 100% |
C9ZS45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 74% | 100% |
D0A7Y7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 97% |
E9AY21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AZP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q8J1 | Leishmania major | 25% | 100% |
Q86MV5 | Trypanosoma brucei brucei | 72% | 100% |
V5BG78 | Trypanosoma cruzi | 29% | 97% |
V5BQ07 | Trypanosoma cruzi | 74% | 100% |