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: 9 |
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 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
Related structures:
AlphaFold database: A4H5F6
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 12 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 12 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008380 | RNA splicing | 7 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000386 | second spliceosomal transesterification activity | 4 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0030628 | pre-mRNA 3'-splice site binding | 6 | 12 |
GO:0036002 | pre-mRNA binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.364 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.301 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.725 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.731 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.671 |
DOC_AGCK_PIF_2 | 272 | 277 | PF00069 | 0.534 |
DOC_ANK_TNKS_1 | 70 | 77 | PF00023 | 0.379 |
DOC_CYCLIN_yClb3_PxF_3 | 47 | 55 | PF00134 | 0.514 |
DOC_MAPK_DCC_7 | 28 | 37 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 151 | 161 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 133 | 141 | PF00069 | 0.287 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 89 | 95 | PF00149 | 0.298 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.437 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.432 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.379 |
LIG_14-3-3_CanoR_1 | 379 | 389 | PF00244 | 0.447 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.467 |
LIG_BIR_III_4 | 408 | 412 | PF00653 | 0.383 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.426 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.465 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.707 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.469 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.519 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.389 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.477 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.486 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.311 |
LIG_LIR_Apic_2 | 218 | 224 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 253 | 259 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 269 | 280 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 388 | 395 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.402 |
LIG_PDZ_Class_1 | 412 | 417 | PF00595 | 0.552 |
LIG_SH2_GRB2like | 130 | 133 | PF00017 | 0.533 |
LIG_SH2_GRB2like | 254 | 257 | PF00017 | 0.441 |
LIG_SH2_SRC | 257 | 260 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.336 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.605 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.373 |
LIG_SUMO_SIM_par_1 | 33 | 41 | PF11976 | 0.383 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.383 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.431 |
LIG_TRFH_1 | 30 | 34 | PF08558 | 0.387 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.505 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.525 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.635 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.455 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.553 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.441 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.434 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.277 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.565 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.660 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.494 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.569 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.518 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.492 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.569 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.404 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.460 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.464 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.263 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.595 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.493 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.376 |
MOD_PK_1 | 10 | 16 | PF00069 | 0.591 |
MOD_PK_1 | 125 | 131 | PF00069 | 0.493 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.687 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.517 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.539 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.503 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.463 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.529 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.625 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.603 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.280 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.448 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.571 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.376 |
MOD_SUMO_rev_2 | 138 | 147 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 218 | 226 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 335 | 343 | PF00179 | 0.613 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 15 | 20 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 263 | 268 | PF00026 | 0.364 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD09 | Leptomonas seymouri | 66% | 98% |
A0A0S4IP46 | Bodo saltans | 35% | 97% |
A0A1X0NEY6 | Trypanosomatidae | 47% | 92% |
A0A3R7NLB9 | Trypanosoma rangeli | 45% | 98% |
A0A3S5H692 | Leishmania donovani | 82% | 100% |
A4HTQ1 | Leishmania infantum | 82% | 100% |
C9ZPF5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 87% |
E9AMI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O23174 | Arabidopsis thaliana | 27% | 78% |
O95391 | Homo sapiens | 27% | 71% |
Q3ZBE5 | Bos taurus | 27% | 71% |
Q4QI51 | Leishmania major | 84% | 100% |
Q4R4P2 | Macaca fascicularis | 27% | 71% |
Q4WWR2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 88% |
Q51LA6 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 88% |
Q54TA0 | Dictyostelium discoideum | 26% | 75% |
Q5B3U2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 89% |
Q5U3F2 | Danio rerio | 27% | 73% |
Q5ZIG2 | Gallus gallus | 27% | 74% |
Q7SDY6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
Q80ZG5 | Rattus norvegicus | 27% | 71% |
Q8BHJ9 | Mus musculus | 27% | 71% |
Q9SHY8 | Arabidopsis thaliana | 29% | 78% |
Q9VAQ7 | Drosophila melanogaster | 29% | 73% |
V5DAD7 | Trypanosoma cruzi | 46% | 90% |