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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071011 | precatalytic spliceosome | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H7H4
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 11 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 11 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008380 | RNA splicing | 7 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 471 | 475 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.413 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.735 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.740 |
CLV_PCSK_PC7_1 | 381 | 387 | PF00082 | 0.370 |
CLV_PCSK_PC7_1 | 481 | 487 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.516 |
CLV_Separin_Metazoa | 497 | 501 | PF03568 | 0.544 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.434 |
DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.619 |
DOC_CYCLIN_yCln2_LP_2 | 280 | 286 | PF00134 | 0.603 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 557 | 566 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 560 | 568 | PF00069 | 0.446 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 167 | 174 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 565 | 575 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 579 | 595 | PF00022 | 0.480 |
LIG_APCC_ABBA_1 | 99 | 104 | PF00400 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.561 |
LIG_BIR_III_2 | 516 | 520 | PF00653 | 0.536 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.561 |
LIG_Clathr_ClatBox_1 | 451 | 455 | PF01394 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 272 | 279 | PF00928 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 627 | 636 | PF00928 | 0.507 |
LIG_eIF4E_1 | 102 | 108 | PF01652 | 0.388 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.630 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.528 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.386 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.389 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.481 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.355 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.434 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.580 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.560 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.587 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 520 | 526 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 326 | 332 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 360 | 368 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 370 | 378 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 633 | 643 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 594 | 599 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.396 |
LIG_LRP6_Inhibitor_1 | 45 | 51 | PF00058 | 0.427 |
LIG_PCNA_yPIPBox_3 | 135 | 147 | PF02747 | 0.509 |
LIG_Pex14_1 | 275 | 279 | PF04695 | 0.680 |
LIG_Pex14_1 | 372 | 376 | PF04695 | 0.380 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.450 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.523 |
LIG_SH2_CRK | 523 | 527 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 523 | 527 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 155 | 158 | PF00017 | 0.518 |
LIG_SH2_SRC | 102 | 105 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 685 | 689 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.474 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.671 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.664 |
LIG_SUMO_SIM_anti_2 | 312 | 319 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 494 | 500 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 652 | 658 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 652 | 658 | PF11976 | 0.422 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.593 |
LIG_TYR_ITIM | 45 | 50 | PF00017 | 0.452 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.435 |
LIG_TYR_ITSM | 113 | 120 | PF00017 | 0.471 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.544 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.512 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.580 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.714 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.686 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.473 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.598 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.548 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.567 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.474 |
MOD_Cter_Amidation | 69 | 72 | PF01082 | 0.733 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.751 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.565 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.422 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.529 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.382 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.704 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.482 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.581 |
MOD_GlcNHglycan | 650 | 654 | PF01048 | 0.499 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.298 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.699 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.483 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.706 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.681 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.718 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.694 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.565 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.345 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.424 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.630 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.391 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.720 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.497 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.428 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.425 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.417 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.415 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.430 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.547 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.431 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.492 |
MOD_NEK2_2 | 608 | 613 | PF00069 | 0.347 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.471 |
MOD_NEK2_2 | 659 | 664 | PF00069 | 0.342 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.521 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.570 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.728 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.558 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.384 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.669 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.521 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.581 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.443 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.450 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.505 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.698 |
MOD_PKB_1 | 263 | 271 | PF00069 | 0.510 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.614 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.637 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.637 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.430 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.444 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.614 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.493 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.607 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.485 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.471 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.273 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.437 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.436 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.564 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.376 |
MOD_SUMO_rev_2 | 110 | 115 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 228 | 234 | PF00179 | 0.721 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 605 | 610 | PF01217 | 0.401 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.401 |
TRG_NES_CRM1_1 | 97 | 111 | PF08389 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 37 | 42 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYM3 | Leptomonas seymouri | 63% | 100% |
A0A1X0P521 | Trypanosomatidae | 31% | 100% |
A0A3R7KHV4 | Trypanosoma rangeli | 33% | 100% |
A4HFI4 | Leishmania braziliensis | 78% | 100% |
D0A5R0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AD35 | Leishmania major | 93% | 100% |
E9AHC8 | Leishmania infantum | 99% | 100% |
E9AYV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q2TAY7 | Homo sapiens | 24% | 100% |
Q2TBS9 | Bos taurus | 24% | 100% |
Q3UKJ7 | Mus musculus | 24% | 100% |
Q5ZME8 | Gallus gallus | 25% | 100% |
Q6NRT3 | Xenopus laevis | 24% | 100% |
Q6P4J8 | Xenopus tropicalis | 24% | 100% |
Q76B40 | Cricetulus griseus | 24% | 100% |
Q7ZVA0 | Danio rerio | 23% | 100% |
Q99M63 | Rattus norvegicus | 24% | 100% |
V5B9I2 | Trypanosoma cruzi | 33% | 100% |