RNA Processing, spliceosome-associated
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:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0005686 | U2 snRNP | 5 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071011 | precatalytic spliceosome | 4 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H7M4
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.561 |
CLV_Separin_Metazoa | 331 | 335 | PF03568 | 0.551 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.566 |
DEG_COP1_1 | 369 | 377 | PF00400 | 0.526 |
DEG_SIAH_1 | 425 | 433 | PF03145 | 0.673 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.406 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.686 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.583 |
DOC_CYCLIN_RxL_1 | 25 | 34 | PF00134 | 0.459 |
DOC_CYCLIN_yCln2_LP_2 | 312 | 318 | PF00134 | 0.402 |
DOC_MAPK_DCC_7 | 406 | 414 | PF00069 | 0.558 |
DOC_MAPK_FxFP_2 | 340 | 343 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 242 | 249 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 274 | 282 | PF00069 | 0.419 |
DOC_PP2B_LxvP_1 | 307 | 310 | PF13499 | 0.285 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.267 |
DOC_PP4_FxxP_1 | 340 | 343 | PF00568 | 0.437 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.673 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 242 | 246 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 42 | 59 | PF00022 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.557 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.577 |
LIG_EVH1_1 | 49 | 53 | PF00568 | 0.586 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.385 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.316 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.529 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.355 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.555 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.558 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.586 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.457 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.627 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.650 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 134 | 143 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 434 | 440 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.548 |
LIG_LYPXL_yS_3 | 304 | 307 | PF13949 | 0.277 |
LIG_Pex14_2 | 230 | 234 | PF04695 | 0.443 |
LIG_PTAP_UEV_1 | 283 | 288 | PF05743 | 0.399 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.668 |
LIG_SH2_PTP2 | 435 | 438 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.277 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.539 |
LIG_SH3_1 | 299 | 305 | PF00018 | 0.295 |
LIG_SH3_1 | 47 | 53 | PF00018 | 0.596 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.572 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.277 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.283 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.255 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.634 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.596 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.482 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.644 |
LIG_TRAF2_1 | 431 | 434 | PF00917 | 0.563 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.560 |
LIG_TRFH_1 | 47 | 51 | PF08558 | 0.668 |
LIG_WW_1 | 301 | 304 | PF00397 | 0.277 |
LIG_WW_3 | 331 | 335 | PF00397 | 0.419 |
MOD_CDK_SPxxK_3 | 235 | 242 | PF00069 | 0.428 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.642 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.349 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.606 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.577 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.561 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.475 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.624 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.602 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.638 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.685 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.727 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.727 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.586 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.714 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.442 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.680 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.525 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.655 |
MOD_LATS_1 | 18 | 24 | PF00433 | 0.368 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.692 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.651 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.364 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.320 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.454 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.548 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.595 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.732 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.467 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.590 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.379 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.325 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.566 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.530 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.610 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.469 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.412 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.477 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.525 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.678 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.686 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.577 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.635 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.650 |
MOD_SUMO_for_1 | 170 | 173 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 136 | 140 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 4 | 11 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 149 | 154 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_2 | 335 | 341 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_3 | 197 | 203 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.698 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.295 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T1 | Leptomonas seymouri | 71% | 98% |
A0A1X0P248 | Trypanosomatidae | 48% | 100% |
A0A3R7MML5 | Trypanosoma rangeli | 49% | 100% |
A4HI08 | Leishmania braziliensis | 86% | 100% |
A4I585 | Leishmania infantum | 100% | 100% |
C9ZQL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 99% |
E9B0I2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q7P9 | Leishmania major | 95% | 100% |
V5B7R6 | Trypanosoma cruzi | 48% | 100% |