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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 3 |
GO:1990904 | ribonucleoprotein complex | 2 | 3 |
GO:0071011 | precatalytic spliceosome | 4 | 2 |
Related structures:
AlphaFold database: A0A3Q8IDC3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006397 | mRNA processing | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008380 | RNA splicing | 7 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.798 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.538 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.434 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.593 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.723 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.541 |
DOC_ANK_TNKS_1 | 493 | 500 | PF00023 | 0.610 |
DOC_CDC14_PxL_1 | 388 | 396 | PF14671 | 0.265 |
DOC_CYCLIN_RxL_1 | 259 | 267 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 413 | 424 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 629 | 640 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 633 | 642 | PF00069 | 0.603 |
DOC_MAPK_NFAT4_5 | 633 | 641 | PF00069 | 0.600 |
DOC_MAPK_RevD_3 | 522 | 538 | PF00069 | 0.599 |
DOC_PP1_RVXF_1 | 601 | 607 | PF00149 | 0.613 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.347 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.322 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.668 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 645 | 649 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 215 | 230 | PF00022 | 0.410 |
LIG_APCC_ABBA_1 | 572 | 577 | PF00400 | 0.680 |
LIG_BIR_III_4 | 586 | 590 | PF00653 | 0.665 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.622 |
LIG_Clathr_ClatBox_1 | 573 | 577 | PF01394 | 0.639 |
LIG_CSL_BTD_1 | 428 | 431 | PF09270 | 0.353 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.529 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.436 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.499 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.573 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.433 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.539 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.356 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.469 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.753 |
LIG_GBD_Chelix_1 | 342 | 350 | PF00786 | 0.432 |
LIG_GBD_Chelix_1 | 368 | 376 | PF00786 | 0.334 |
LIG_LIR_Apic_2 | 41 | 45 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 150 | 161 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 207 | 213 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 653 | 659 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.639 |
LIG_PAM2_1 | 267 | 279 | PF00658 | 0.409 |
LIG_PCNA_PIPBox_1 | 354 | 363 | PF02747 | 0.463 |
LIG_PCNA_yPIPBox_3 | 417 | 430 | PF02747 | 0.483 |
LIG_PDZ_Class_2 | 654 | 659 | PF00595 | 0.522 |
LIG_PTAP_UEV_1 | 196 | 201 | PF05743 | 0.595 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.436 |
LIG_PTB_Phospho_1 | 82 | 88 | PF10480 | 0.430 |
LIG_Rb_LxCxE_1 | 396 | 416 | PF01857 | 0.419 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 379 | 383 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.439 |
LIG_SH2_STAT3 | 320 | 323 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.572 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.516 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.592 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.482 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.522 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 555 | 566 | PF11976 | 0.630 |
LIG_SUMO_SIM_anti_2 | 639 | 644 | PF11976 | 0.548 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.448 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.504 |
LIG_TRFH_1 | 379 | 383 | PF08558 | 0.434 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.355 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.519 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.744 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.604 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.476 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.493 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.733 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.559 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.754 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.649 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.400 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.599 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.512 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.634 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.737 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.681 |
MOD_Cter_Amidation | 643 | 646 | PF01082 | 0.612 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.686 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.690 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.690 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.558 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.404 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.625 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.495 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.685 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.754 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.616 |
MOD_GlcNHglycan | 619 | 623 | PF01048 | 0.730 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.711 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.521 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.692 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.495 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.488 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.697 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.639 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.730 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.618 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.768 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.767 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.627 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.423 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.529 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.542 |
MOD_NEK2_2 | 644 | 649 | PF00069 | 0.511 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.501 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.721 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.577 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.543 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.427 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.549 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.616 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.393 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.413 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.413 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.505 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.552 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.547 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.651 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.345 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.565 |
MOD_SUMO_rev_2 | 274 | 284 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 615 | 620 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_3 | 335 | 341 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.661 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 629 | 631 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.451 |
TRG_NLS_MonoCore_2 | 534 | 539 | PF00514 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 523 | 528 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 538 | 542 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBP9 | Leptomonas seymouri | 62% | 100% |
A0A1X0NM33 | Trypanosomatidae | 32% | 100% |
A0A422P1Y9 | Trypanosoma rangeli | 33% | 100% |
A4HE72 | Leishmania braziliensis | 83% | 100% |
A4I1H4 | Leishmania infantum | 100% | 100% |
C9ZJZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AXK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q9W3 | Leishmania major | 93% | 100% |