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: E9ANG5
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 | 255 | 257 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.575 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.209 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.624 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.310 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.565 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.578 |
DOC_ANK_TNKS_1 | 400 | 407 | PF00023 | 0.530 |
DOC_ANK_TNKS_1 | 539 | 546 | PF00023 | 0.543 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.420 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.457 |
DOC_CYCLIN_RxL_1 | 184 | 194 | PF00134 | 0.338 |
DOC_CYCLIN_RxL_1 | 351 | 362 | PF00134 | 0.429 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 281 | 290 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.469 |
DOC_MAPK_DCC_7 | 8 | 18 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 253 | 263 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 6 | 18 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 157 | 165 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 357 | 365 | PF00069 | 0.318 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.349 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.277 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.483 |
DOC_USP7_UBL2_3 | 253 | 257 | PF12436 | 0.404 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 574 | 582 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 588 | 596 | PF00244 | 0.668 |
LIG_APCC_ABBA_1 | 375 | 380 | PF00400 | 0.396 |
LIG_APCC_ABBAyCdc20_2 | 374 | 380 | PF00400 | 0.401 |
LIG_BIR_III_2 | 59 | 63 | PF00653 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 194 | 200 | PF00928 | 0.409 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.448 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.412 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.432 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.394 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.507 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.409 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.549 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.363 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.394 |
LIG_LIR_LC3C_4 | 495 | 500 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.288 |
LIG_NBox_RRM_1 | 159 | 169 | PF00076 | 0.409 |
LIG_PCNA_yPIPBox_3 | 168 | 182 | PF02747 | 0.409 |
LIG_Pex14_1 | 196 | 200 | PF04695 | 0.409 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.416 |
LIG_SH2_SRC | 467 | 470 | PF00017 | 0.686 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 276 | 279 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 31 | 34 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.488 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.513 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.420 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.781 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.347 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 546 | 551 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 180 | 186 | PF11976 | 0.420 |
LIG_WRC_WIRS_1 | 502 | 507 | PF05994 | 0.500 |
MOD_CDC14_SPxK_1 | 409 | 412 | PF00782 | 0.496 |
MOD_CDK_SPK_2 | 105 | 110 | PF00069 | 0.392 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.420 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.491 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.607 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.492 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.364 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.414 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.651 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.644 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.344 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.384 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.367 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.355 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.524 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.376 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.512 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.227 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.209 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.450 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.605 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.734 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.682 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.311 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.377 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.412 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.491 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.578 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.709 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.732 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.513 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.437 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.306 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.425 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.465 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.428 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.460 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.527 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.666 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.252 |
MOD_N-GLC_1 | 597 | 602 | PF02516 | 0.515 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.518 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.344 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.394 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.257 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.426 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.440 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.552 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.477 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.667 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.559 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.432 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.474 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.444 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.582 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.551 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.496 |
MOD_PKA_1 | 460 | 466 | PF00069 | 0.455 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.248 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.562 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.431 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.372 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.735 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.488 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.659 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.441 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.308 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.410 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.409 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.409 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.478 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.417 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.496 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.422 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.420 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.420 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.412 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.538 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.445 |
MOD_SUMO_rev_2 | 489 | 499 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 356 | 361 | PF01217 | 0.357 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_1 | 544 | 549 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.570 |
TRG_NES_CRM1_1 | 172 | 188 | PF08389 | 0.420 |
TRG_NES_CRM1_1 | 252 | 267 | PF08389 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.220 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJV4 | Leptomonas seymouri | 75% | 100% |
A0A0S4JYL8 | Bodo saltans | 49% | 92% |
A0A1X0NSB4 | Trypanosomatidae | 21% | 100% |
A0A1X0NV90 | Trypanosomatidae | 60% | 100% |
A0A3Q8ICA8 | Leishmania donovani | 94% | 100% |
A0A3R7MZZ8 | Trypanosoma rangeli | 60% | 100% |
A4H9T9 | Leishmania braziliensis | 88% | 100% |
A4HUT1 | Leishmania infantum | 94% | 100% |
D0A7N1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
D0AAP5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
Q09719 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 72% |
Q4P7M1 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 89% |
Q4QH61 | Leishmania major | 93% | 100% |
Q6FU81 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 23% | 91% |
Q8W4E1 | Arabidopsis thaliana | 23% | 100% |
V5C100 | Trypanosoma cruzi | 60% | 99% |