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:0005737 | cytoplasm | 2 | 12 |
GO:0031499 | TRAMP complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0005730 | nucleolus | 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: A4HEQ5
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:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043631 | RNA polyadenylation | 6 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071076 | RNA 3' uridylation | 8 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 8 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 12 |
GO:0070566 | adenylyltransferase activity | 5 | 12 |
GO:0070569 | uridylyltransferase activity | 5 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.704 |
CLV_MEL_PAP_1 | 374 | 380 | PF00089 | 0.551 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.717 |
CLV_PCSK_FUR_1 | 274 | 278 | PF00082 | 0.394 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.509 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.686 |
CLV_PCSK_PC7_1 | 490 | 496 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.791 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.350 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.555 |
DOC_CYCLIN_RxL_1 | 146 | 156 | PF00134 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 154 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 258 | 268 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 375 | 382 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 300 | 308 | PF00069 | 0.433 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.612 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.389 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.352 |
DOC_PP4_FxxP_1 | 416 | 419 | PF00568 | 0.449 |
DOC_SPAK_OSR1_1 | 377 | 381 | PF12202 | 0.307 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.736 |
DOC_USP7_UBL2_3 | 414 | 418 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 142 | 151 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 274 | 284 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.695 |
LIG_BH_BH3_1 | 260 | 276 | PF00452 | 0.300 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.508 |
LIG_EH_1 | 131 | 135 | PF12763 | 0.456 |
LIG_EH1_1 | 359 | 367 | PF00400 | 0.357 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.760 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.547 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.320 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.427 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.482 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.360 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.378 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.340 |
LIG_LIR_Apic_2 | 415 | 419 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.640 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.388 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.474 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 410 | 413 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.427 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.421 |
LIG_SUMO_SIM_anti_2 | 363 | 368 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 125 | 131 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 159 | 165 | PF11976 | 0.285 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.466 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.568 |
LIG_TRFH_1 | 173 | 177 | PF08558 | 0.497 |
LIG_UBA3_1 | 161 | 167 | PF00899 | 0.263 |
LIG_UBA3_1 | 336 | 341 | PF00899 | 0.358 |
MOD_CDK_SPxxK_3 | 16 | 23 | PF00069 | 0.568 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.548 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.460 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.359 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.523 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.673 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.545 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.621 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.808 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.366 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.523 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.403 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.316 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.707 |
MOD_Cter_Amidation | 90 | 93 | PF01082 | 0.701 |
MOD_DYRK1A_RPxSP_1 | 16 | 20 | PF00069 | 0.567 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.740 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.765 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.405 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.536 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.468 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.595 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.489 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.521 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.496 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.454 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.204 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.388 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.465 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.665 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.363 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.609 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.406 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.423 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.764 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.740 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.714 |
MOD_LATS_1 | 117 | 123 | PF00433 | 0.536 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.567 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.311 |
MOD_N-GLC_2 | 345 | 347 | PF02516 | 0.486 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.422 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.445 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.451 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.383 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.318 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.433 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.532 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.649 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.804 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.781 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.793 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.683 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.538 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.505 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.424 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.428 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.491 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.794 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.781 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.662 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.532 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.386 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.525 |
MOD_Plk_2-3 | 108 | 114 | PF00069 | 0.697 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.584 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.424 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.386 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.418 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.749 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.664 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.449 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.733 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.709 |
MOD_SUMO_rev_2 | 302 | 306 | PF00179 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.750 |
TRG_NES_CRM1_1 | 204 | 219 | PF08389 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 404 | 409 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD64 | Leptomonas seymouri | 56% | 92% |
A0A0S4IQ72 | Bodo saltans | 31% | 94% |
A0A1X0NU61 | Trypanosomatidae | 38% | 100% |
A0A3Q8IDQ5 | Leishmania donovani | 70% | 87% |
A0A3S5IS02 | Trypanosoma rangeli | 38% | 100% |
A4I1Y4 | Leishmania infantum | 70% | 87% |
C9ZS34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AY31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q9E2 | Leishmania major | 71% | 100% |
V5B9F7 | Trypanosoma cruzi | 39% | 100% |