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 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0005686 | U2 snRNP | 5 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0071004 | U2-type prespliceosome | 5 | 1 |
GO:0071010 | prespliceosome | 4 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AXL9
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:0045292 | mRNA cis splicing, via spliceosome | 9 | 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:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 380 | 382 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.333 |
CLV_Separin_Metazoa | 126 | 130 | PF03568 | 0.552 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.705 |
DEG_SCF_FBW7_2 | 10 | 16 | PF00400 | 0.467 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.538 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.688 |
DOC_CKS1_1 | 10 | 15 | PF01111 | 0.467 |
DOC_CYCLIN_RxL_1 | 213 | 224 | PF00134 | 0.583 |
DOC_MAPK_gen_1 | 151 | 158 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 280 | 289 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 48 | 55 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 268 | 274 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.570 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.731 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.616 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.436 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 323 | 330 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.607 |
LIG_AP2alpha_2 | 141 | 143 | PF02296 | 0.434 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.706 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.486 |
LIG_CtBP_PxDLS_1 | 14 | 20 | PF00389 | 0.441 |
LIG_eIF4E_1 | 366 | 372 | PF01652 | 0.695 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.528 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.547 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.510 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.743 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.527 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.584 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.281 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.417 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.666 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.384 |
LIG_LYPXL_S_1 | 61 | 65 | PF13949 | 0.330 |
LIG_MYND_1 | 76 | 80 | PF01753 | 0.511 |
LIG_PCNA_yPIPBox_3 | 268 | 279 | PF02747 | 0.551 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.352 |
LIG_PTB_Apo_2 | 188 | 195 | PF02174 | 0.486 |
LIG_RPA_C_Fungi | 22 | 34 | PF08784 | 0.465 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 249 | 253 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.382 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.610 |
LIG_SUMO_SIM_par_1 | 154 | 159 | PF11976 | 0.519 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.448 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.345 |
LIG_WRC_WIRS_1 | 279 | 284 | PF05994 | 0.512 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.512 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.489 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.474 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.274 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.431 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.694 |
MOD_Cter_Amidation | 378 | 381 | PF01082 | 0.739 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.447 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.609 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.663 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.592 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.464 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.502 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.658 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.677 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.708 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.290 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.326 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.536 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.667 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.569 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.481 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.327 |
MOD_NEK2_2 | 99 | 104 | PF00069 | 0.558 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.475 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.538 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.562 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.546 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.537 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.380 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.494 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.670 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.587 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.652 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.719 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.683 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.574 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.491 |
MOD_SUMO_rev_2 | 148 | 153 | PF00179 | 0.658 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXM6 | Leptomonas seymouri | 71% | 100% |
A0A0S4IPX0 | Bodo saltans | 34% | 86% |
A0A1X0NNP0 | Trypanosomatidae | 43% | 80% |
A0A3R7KXN8 | Trypanosoma rangeli | 47% | 88% |
A0A3S7WZ46 | Leishmania donovani | 94% | 100% |
A4HEF0 | Leishmania braziliensis | 88% | 100% |
A4I1I4 | Leishmania infantum | 94% | 100% |
C9ZJY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4Q9V3 | Leishmania major | 94% | 100% |
V5BCN7 | Trypanosoma cruzi | 47% | 81% |