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 | 2 |
GO:0005681 | spliceosomal complex | 3 | 4 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 4 |
GO:1990904 | ribonucleoprotein complex | 2 | 4 |
GO:0071011 | precatalytic spliceosome | 4 | 2 |
Related structures:
AlphaFold database: Q4Q9W3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
GO:0006396 | RNA processing | 6 | 4 |
GO:0006397 | mRNA processing | 7 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008380 | RNA splicing | 7 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016070 | RNA metabolic process | 5 | 4 |
GO:0016071 | mRNA metabolic process | 6 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090304 | nucleic acid metabolic process | 4 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
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 | 0.400 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.644 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 610 | 612 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.525 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.433 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.580 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.688 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.550 |
DOC_ANK_TNKS_1 | 493 | 500 | PF00023 | 0.604 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.366 |
DOC_CYCLIN_RxL_1 | 259 | 267 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 413 | 424 | PF00134 | 0.400 |
DOC_CYCLIN_yClb1_LxF_4 | 601 | 606 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 435 | 443 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 618 | 625 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 629 | 640 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 633 | 642 | PF00069 | 0.601 |
DOC_MAPK_NFAT4_5 | 633 | 641 | PF00069 | 0.599 |
DOC_MAPK_RevD_3 | 522 | 538 | PF00069 | 0.591 |
DOC_PP1_RVXF_1 | 601 | 607 | PF00149 | 0.609 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.348 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.284 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.638 |
DOC_USP7_MATH_2 | 164 | 170 | PF00917 | 0.429 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.366 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 645 | 649 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 215 | 230 | PF00022 | 0.409 |
LIG_APCC_ABBA_1 | 572 | 577 | PF00400 | 0.678 |
LIG_BIR_III_4 | 586 | 590 | PF00653 | 0.667 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.643 |
LIG_Clathr_ClatBox_1 | 573 | 577 | PF01394 | 0.637 |
LIG_CSL_BTD_1 | 428 | 431 | PF09270 | 0.284 |
LIG_CtBP_PxDLS_1 | 116 | 122 | PF00389 | 0.401 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.641 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.430 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.483 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.284 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.545 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.555 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.395 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.536 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.284 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.400 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.770 |
LIG_GBD_Chelix_1 | 342 | 350 | PF00786 | 0.400 |
LIG_GBD_Chelix_1 | 368 | 376 | PF00786 | 0.312 |
LIG_LIR_Gen_1 | 150 | 158 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 207 | 213 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 653 | 659 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.648 |
LIG_PAM2_1 | 267 | 279 | PF00658 | 0.407 |
LIG_PCNA_PIPBox_1 | 354 | 363 | PF02747 | 0.400 |
LIG_PDZ_Class_2 | 654 | 659 | PF00595 | 0.534 |
LIG_PTAP_UEV_1 | 196 | 201 | PF05743 | 0.600 |
LIG_PTAP_UEV_1 | 41 | 46 | PF05743 | 0.527 |
LIG_PTB_Apo_2 | 566 | 573 | PF02174 | 0.466 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.439 |
LIG_PTB_Phospho_1 | 82 | 88 | PF10480 | 0.433 |
LIG_Rb_LxCxE_1 | 396 | 416 | PF01857 | 0.346 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.400 |
LIG_SH2_GRB2like | 567 | 570 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 379 | 383 | PF00017 | 0.284 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 320 | 323 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.570 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.480 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.586 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.549 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.497 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.476 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.515 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.583 |
LIG_Sin3_3 | 31 | 38 | PF02671 | 0.486 |
LIG_SUMO_SIM_anti_2 | 557 | 566 | PF11976 | 0.629 |
LIG_SUMO_SIM_anti_2 | 639 | 644 | PF11976 | 0.548 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.506 |
LIG_TRFH_1 | 379 | 383 | PF08558 | 0.400 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.308 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.564 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.609 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.479 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.494 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.767 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.549 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.620 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.600 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.508 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.755 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.638 |
MOD_Cter_Amidation | 643 | 646 | PF01082 | 0.617 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.683 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.571 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.577 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.505 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.386 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.605 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.477 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.654 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.778 |
MOD_GlcNHglycan | 588 | 592 | PF01048 | 0.741 |
MOD_GlcNHglycan | 619 | 623 | PF01048 | 0.670 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.648 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.515 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.652 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.505 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.599 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.702 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.215 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.739 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.614 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.633 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.679 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.735 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.461 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.617 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.420 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.434 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.540 |
MOD_NEK2_2 | 644 | 649 | PF00069 | 0.519 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.500 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.607 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.576 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.413 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.334 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.624 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.594 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.508 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.542 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.547 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.656 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.284 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.366 |
TRG_DiLeu_BaEn_3 | 335 | 341 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.662 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 629 | 631 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.445 |
TRG_NLS_MonoCore_2 | 534 | 539 | PF00514 | 0.635 |
TRG_NLS_MonoExtC_3 | 609 | 615 | PF00514 | 0.573 |
TRG_NLS_MonoExtN_4 | 607 | 614 | PF00514 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 523 | 528 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 538 | 542 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBP9 | Leptomonas seymouri | 62% | 100% |
A0A1X0NM33 | Trypanosomatidae | 34% | 100% |
A0A3Q8IDC3 | Leishmania donovani | 93% | 100% |
A0A422P1Y9 | Trypanosoma rangeli | 33% | 100% |
A4HE72 | Leishmania braziliensis | 83% | 99% |
A4I1H4 | Leishmania infantum | 93% | 100% |
C9ZJZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AXK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |