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 | 2 |
GO:0005684 | U2-type spliceosomal complex | 4 | 2 |
GO:0005686 | U2 snRNP | 5 | 2 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0071011 | precatalytic spliceosome | 4 | 2 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 2 |
GO:0097525 | spliceosomal snRNP complex | 4 | 2 |
GO:0120114 | Sm-like protein family complex | 2 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4Q7P9
Term | Name | Level | Count |
---|---|---|---|
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 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.575 |
CLV_Separin_Metazoa | 329 | 333 | PF03568 | 0.588 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.634 |
DEG_SIAH_1 | 423 | 431 | PF03145 | 0.699 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.704 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.683 |
DOC_CYCLIN_RxL_1 | 25 | 34 | PF00134 | 0.561 |
DOC_CYCLIN_yCln2_LP_2 | 310 | 316 | PF00134 | 0.457 |
DOC_MAPK_DCC_7 | 404 | 412 | PF00069 | 0.606 |
DOC_MAPK_FxFP_2 | 338 | 341 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.449 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.324 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.732 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.450 |
DOC_USP7_UBL2_3 | 258 | 262 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.598 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 130 | 134 | PF00244 | 0.443 |
LIG_Actin_WH2_2 | 42 | 59 | PF00022 | 0.646 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.613 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.608 |
LIG_EVH1_1 | 49 | 53 | PF00568 | 0.689 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.411 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.362 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.621 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.408 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.595 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.588 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.715 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.524 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.674 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.656 |
LIG_LIR_Apic_2 | 325 | 330 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 335 | 341 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 464 | 469 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 132 | 141 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 432 | 438 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.609 |
LIG_LYPXL_yS_3 | 302 | 305 | PF13949 | 0.335 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.490 |
LIG_PTAP_UEV_1 | 281 | 286 | PF05743 | 0.440 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.713 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.681 |
LIG_SH2_PTP2 | 433 | 436 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 417 | 420 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.580 |
LIG_SH3_1 | 297 | 303 | PF00018 | 0.354 |
LIG_SH3_1 | 47 | 53 | PF00018 | 0.703 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.335 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.329 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.331 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.670 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.703 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.619 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.613 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.773 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.618 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.679 |
LIG_TRFH_1 | 47 | 51 | PF08558 | 0.681 |
LIG_WW_1 | 299 | 302 | PF00397 | 0.335 |
LIG_WW_3 | 329 | 333 | PF00397 | 0.476 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.696 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.479 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.634 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.608 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.677 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.552 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.668 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.624 |
MOD_Cter_Amidation | 115 | 118 | PF01082 | 0.777 |
MOD_Cter_Amidation | 124 | 127 | PF01082 | 0.671 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.720 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.713 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.661 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.754 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.489 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.711 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.583 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.674 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.699 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.675 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.415 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.378 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.501 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.583 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.724 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.798 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.534 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.732 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.577 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.654 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.433 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.383 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.576 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.617 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.593 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.523 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.483 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.567 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.697 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.725 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.568 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.675 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 168 | 171 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 134 | 138 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 4 | 11 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 147 | 152 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 333 | 339 | PF01217 | 0.505 |
TRG_DiLeu_BaEn_3 | 195 | 201 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T1 | Leptomonas seymouri | 70% | 98% |
A0A1X0P248 | Trypanosomatidae | 47% | 100% |
A0A3R7MML5 | Trypanosoma rangeli | 49% | 100% |
A0A3S5H7M4 | Leishmania donovani | 95% | 100% |
A4HI08 | Leishmania braziliensis | 86% | 99% |
A4I585 | Leishmania infantum | 95% | 100% |
C9ZQL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 99% |
E9B0I2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5B7R6 | Trypanosoma cruzi | 47% | 100% |