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: A4HE72
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 | 0.525 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.573 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.488 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.650 |
DEG_SPOP_SBC_1 | 177 | 181 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.566 |
DOC_ANK_TNKS_1 | 460 | 467 | PF00023 | 0.660 |
DOC_ANK_TNKS_1 | 552 | 559 | PF00023 | 0.515 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 259 | 267 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 413 | 424 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 634 | 645 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 638 | 647 | PF00069 | 0.634 |
DOC_MAPK_NFAT4_5 | 638 | 646 | PF00069 | 0.630 |
DOC_MAPK_RevD_3 | 524 | 540 | PF00069 | 0.722 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.396 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.384 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.625 |
DOC_USP7_MATH_2 | 164 | 170 | PF00917 | 0.497 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 215 | 230 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 574 | 579 | PF00400 | 0.719 |
LIG_BIR_III_4 | 588 | 592 | PF00653 | 0.766 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.754 |
LIG_Clathr_ClatBox_1 | 575 | 579 | PF01394 | 0.760 |
LIG_CSL_BTD_1 | 428 | 431 | PF09270 | 0.417 |
LIG_CtBP_PxDLS_1 | 116 | 122 | PF00389 | 0.458 |
LIG_eIF4E_1 | 259 | 265 | PF01652 | 0.331 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.630 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.478 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.525 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.379 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.555 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.600 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.446 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.575 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.399 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.718 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.519 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.777 |
LIG_GBD_Chelix_1 | 342 | 350 | PF00786 | 0.475 |
LIG_LIR_Apic_2 | 5 | 9 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 207 | 213 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 658 | 664 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 658 | 664 | PF02991 | 0.683 |
LIG_PAM2_1 | 267 | 279 | PF00658 | 0.520 |
LIG_PCNA_PIPBox_1 | 354 | 363 | PF02747 | 0.498 |
LIG_PCNA_yPIPBox_3 | 417 | 430 | PF02747 | 0.503 |
LIG_PDZ_Class_2 | 659 | 664 | PF00595 | 0.566 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.560 |
LIG_PTB_Phospho_1 | 82 | 88 | PF10480 | 0.555 |
LIG_Rb_LxCxE_1 | 396 | 416 | PF01857 | 0.479 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 379 | 383 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.593 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.529 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.518 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.595 |
LIG_SUMO_SIM_anti_2 | 559 | 568 | PF11976 | 0.739 |
LIG_SUMO_SIM_anti_2 | 644 | 649 | PF11976 | 0.593 |
LIG_TRFH_1 | 379 | 383 | PF08558 | 0.476 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.405 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.649 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.677 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.658 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.522 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.493 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.563 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.740 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.542 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.697 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.688 |
MOD_Cter_Amidation | 648 | 651 | PF01082 | 0.646 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.706 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.685 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.537 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.412 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.584 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.635 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.706 |
MOD_GlcNHglycan | 487 | 491 | PF01048 | 0.700 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.597 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.737 |
MOD_GlcNHglycan | 621 | 625 | PF01048 | 0.794 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.551 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.680 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.541 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.413 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.751 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.598 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.680 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.604 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.752 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.644 |
MOD_N-GLC_2 | 324 | 326 | PF02516 | 0.292 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.508 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.727 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.629 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.479 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.535 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.668 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.585 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.541 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.405 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.604 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.514 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.506 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.437 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.544 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.592 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.772 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.391 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.645 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.452 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.774 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.611 |
TRG_DiLeu_BaEn_3 | 335 | 341 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.693 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.493 |
TRG_NLS_MonoCore_2 | 536 | 541 | PF00514 | 0.661 |
TRG_NLS_MonoExtN_4 | 609 | 616 | PF00514 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 525 | 530 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 540 | 544 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBP9 | Leptomonas seymouri | 61% | 100% |
A0A1X0NM33 | Trypanosomatidae | 32% | 100% |
A0A3Q8IDC3 | Leishmania donovani | 83% | 100% |
A0A422P1Y9 | Trypanosoma rangeli | 34% | 100% |
A4I1H4 | Leishmania infantum | 83% | 100% |
C9ZJZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AXK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q9W3 | Leishmania major | 83% | 99% |