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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 2 |
GO:0097525 | spliceosomal snRNP complex | 4 | 2 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120114 | Sm-like protein family complex | 2 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
GO:0005840 | ribosome | 5 | 4 |
GO:0043228 | non-membrane-bounded organelle | 3 | 4 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: Q4QC84
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 2 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0017069 | snRNA binding | 5 | 2 |
GO:0017070 | U6 snRNA binding | 6 | 2 |
GO:0030621 | U4 snRNA binding | 6 | 2 |
GO:0030627 | pre-mRNA 5'-splice site binding | 6 | 2 |
GO:0036002 | pre-mRNA binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 556 | 560 | PF00656 | 0.764 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.680 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 608 | 612 | PF03568 | 0.612 |
DEG_APCC_DBOX_1 | 472 | 480 | PF00400 | 0.538 |
DEG_SCF_TRCP1_1 | 122 | 127 | PF00400 | 0.540 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.656 |
DOC_CYCLIN_yClb3_PxF_3 | 477 | 483 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 198 | 207 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 78 | 88 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.462 |
DOC_SPAK_OSR1_1 | 540 | 544 | PF12202 | 0.500 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 482 | 492 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.549 |
LIG_APCC_ABBA_1 | 391 | 396 | PF00400 | 0.609 |
LIG_BIR_III_4 | 244 | 248 | PF00653 | 0.378 |
LIG_BIR_III_4 | 327 | 331 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.698 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.568 |
LIG_CSL_BTD_1 | 361 | 364 | PF09270 | 0.480 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.543 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.390 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.575 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.391 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.464 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.468 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.393 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.478 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.462 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.437 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.701 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 194 | 202 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 538 | 548 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.668 |
LIG_MYND_1 | 474 | 478 | PF01753 | 0.543 |
LIG_PCNA_yPIPBox_3 | 30 | 43 | PF02747 | 0.518 |
LIG_Rb_pABgroove_1 | 375 | 383 | PF01858 | 0.539 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.488 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.486 |
LIG_SH2_GRB2like | 419 | 422 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.574 |
LIG_SH2_PTP2 | 8 | 11 | PF00017 | 0.716 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.474 |
LIG_SH2_SRC | 419 | 422 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.697 |
LIG_SH3_1 | 573 | 579 | PF00018 | 0.604 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.476 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.414 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.453 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.630 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 485 | 493 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 139 | 146 | PF11976 | 0.377 |
LIG_UBA3_1 | 569 | 575 | PF00899 | 0.651 |
MOD_CDC14_SPxK_1 | 229 | 232 | PF00782 | 0.398 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.693 |
MOD_CDK_SPK_2 | 477 | 482 | PF00069 | 0.365 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.394 |
MOD_CDK_SPxK_1 | 226 | 232 | PF00069 | 0.404 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.683 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.624 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.600 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.428 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.497 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.675 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.637 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.633 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.382 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.709 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.581 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.615 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.515 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.709 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.646 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.439 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.640 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.684 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.444 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.690 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.723 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.434 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.306 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.509 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.320 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.682 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.454 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.465 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.643 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.743 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.694 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.644 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.449 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.461 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.616 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.586 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.657 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.633 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.508 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.419 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.472 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.645 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.444 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.517 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.647 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.366 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.690 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.433 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.658 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.329 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.396 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.577 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.450 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.500 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.607 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.655 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.513 |
MOD_OFUCOSY | 103 | 109 | PF10250 | 0.375 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.476 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.626 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.579 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.526 |
MOD_PK_1 | 167 | 173 | PF00069 | 0.456 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.592 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.415 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.549 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.567 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.539 |
MOD_Plk_2-3 | 599 | 605 | PF00069 | 0.766 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.347 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.474 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.403 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.356 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.713 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.496 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.646 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.661 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.622 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.533 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.552 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.445 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.645 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.448 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.625 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.716 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.400 |
TRG_NLS_MonoExtC_3 | 572 | 577 | PF00514 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3A5 | Leptomonas seymouri | 60% | 95% |
A0A0S4JGF5 | Bodo saltans | 30% | 100% |
A0A1X0NYH8 | Trypanosomatidae | 35% | 94% |
A0A3S7WWM8 | Leishmania donovani | 93% | 100% |
A0A422NAK4 | Trypanosoma rangeli | 40% | 100% |
A4HBX0 | Leishmania braziliensis | 81% | 100% |
D0A183 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AGY0 | Leishmania infantum | 93% | 100% |
E9AV96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5B548 | Trypanosoma cruzi | 36% | 100% |