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:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9T9
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.638 |
CLV_PCSK_FUR_1 | 296 | 300 | PF00082 | 0.156 |
CLV_PCSK_FUR_1 | 335 | 339 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.796 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 22 | 28 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.410 |
DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.698 |
DOC_ANK_TNKS_1 | 443 | 450 | PF00023 | 0.617 |
DOC_ANK_TNKS_1 | 582 | 589 | PF00023 | 0.555 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.425 |
DOC_CYCLIN_RxL_1 | 397 | 405 | PF00134 | 0.355 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 324 | 333 | PF00134 | 0.457 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 51 | 61 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 296 | 306 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 51 | 61 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 153 | 161 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 400 | 408 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 54 | 61 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 415 | 422 | PF00149 | 0.348 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 593 | 596 | PF13499 | 0.360 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 609 | 612 | PF13499 | 0.341 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.396 |
LIG_14-3-3_CanoR_1 | 172 | 180 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 488 | 498 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 617 | 625 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 631 | 640 | PF00244 | 0.636 |
LIG_APCC_ABBA_1 | 418 | 423 | PF00400 | 0.415 |
LIG_APCC_ABBAyCdc20_2 | 417 | 423 | PF00400 | 0.421 |
LIG_APCC_ABBAyCdc20_2 | 506 | 512 | PF00400 | 0.486 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.418 |
LIG_CaM_IQ_9 | 41 | 56 | PF13499 | 0.368 |
LIG_deltaCOP1_diTrp_1 | 237 | 243 | PF00928 | 0.414 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.468 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.417 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.437 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.425 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.414 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.404 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.556 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.378 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.441 |
LIG_LIR_Gen_1 | 508 | 518 | PF02991 | 0.664 |
LIG_LIR_LC3C_4 | 538 | 543 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.650 |
LIG_NBox_RRM_1 | 202 | 212 | PF00076 | 0.414 |
LIG_PCNA_yPIPBox_3 | 211 | 225 | PF02747 | 0.414 |
LIG_Pex14_1 | 239 | 243 | PF04695 | 0.414 |
LIG_SH2_SRC | 510 | 513 | PF00017 | 0.707 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.489 |
LIG_SH2_STAT3 | 319 | 322 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.455 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.516 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.425 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.801 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.454 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.360 |
LIG_SUMO_SIM_anti_2 | 223 | 231 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 589 | 594 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 223 | 231 | PF11976 | 0.425 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.407 |
LIG_TRAF2_1 | 259 | 262 | PF00917 | 0.356 |
LIG_TRAF2_1 | 494 | 497 | PF00917 | 0.522 |
LIG_TRFH_1 | 4 | 8 | PF08558 | 0.402 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.392 |
MOD_CDC14_SPxK_1 | 7 | 10 | PF00782 | 0.390 |
MOD_CDK_SPK_2 | 148 | 153 | PF00069 | 0.386 |
MOD_CDK_SPxK_1 | 275 | 281 | PF00069 | 0.425 |
MOD_CDK_SPxK_1 | 4 | 10 | PF00069 | 0.399 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.610 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.674 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.642 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.497 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.367 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.420 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.381 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.394 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.558 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.492 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.358 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.685 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.232 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.214 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.511 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.601 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.304 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.406 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.356 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.419 |
MOD_GlcNHglycan | 62 | 66 | PF01048 | 0.519 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.462 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.428 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.664 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.566 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.667 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.531 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.465 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.335 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.399 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.457 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.529 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.434 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.570 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.445 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.543 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.555 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.312 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.122 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.563 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.425 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.267 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.455 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.549 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.602 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.473 |
MOD_NEK2_2 | 505 | 510 | PF00069 | 0.558 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.488 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.377 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.438 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.414 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.414 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.256 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.734 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.437 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.400 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.733 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.501 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.629 |
MOD_PKB_1 | 486 | 494 | PF00069 | 0.516 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.463 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.341 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.253 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.414 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.414 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.453 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.523 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.558 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.454 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.417 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.425 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.425 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.399 |
MOD_SUMO_for_1 | 494 | 497 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 532 | 542 | PF00179 | 0.516 |
TRG_DiLeu_BaEn_1 | 399 | 404 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 429 | 434 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 587 | 592 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.707 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.657 |
TRG_NES_CRM1_1 | 215 | 231 | PF08389 | 0.425 |
TRG_NES_CRM1_1 | 295 | 310 | PF08389 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.225 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJV4 | Leptomonas seymouri | 74% | 100% |
A0A0S4JYL8 | Bodo saltans | 48% | 98% |
A0A1X0NV90 | Trypanosomatidae | 59% | 100% |
A0A3Q8ICA8 | Leishmania donovani | 87% | 100% |
A0A3R7MZZ8 | Trypanosoma rangeli | 59% | 100% |
A0A3R7N587 | Trypanosoma rangeli | 23% | 79% |
A4HUT1 | Leishmania infantum | 87% | 100% |
A5DPU0 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 23% | 86% |
A7EM78 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 23% | 100% |
D0A7N1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ANG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q09719 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 77% |
Q4P7M1 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 95% |
Q4QH61 | Leishmania major | 87% | 100% |
Q6C7X8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 70% |
Q8W4E1 | Arabidopsis thaliana | 23% | 100% |
V5BG99 | Trypanosoma cruzi | 24% | 79% |
V5C100 | Trypanosoma cruzi | 61% | 100% |