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:0030532 | small nuclear ribonucleoprotein complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 12 |
GO:0097525 | spliceosomal snRNP complex | 4 | 12 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 12 |
GO:0120114 | Sm-like protein family complex | 2 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005687 | U4 snRNP | 5 | 1 |
GO:0071011 | precatalytic spliceosome | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HL50
Term | Name | Level | Count |
---|---|---|---|
GO:0000244 | spliceosomal tri-snRNP complex assembly | 8 | 12 |
GO:0000387 | spliceosomal snRNP assembly | 7 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
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: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 | 244 | 246 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.514 |
CLV_PCSK_FUR_1 | 304 | 308 | PF00082 | 0.339 |
CLV_PCSK_FUR_1 | 335 | 339 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.550 |
CLV_PCSK_PC7_1 | 240 | 246 | PF00082 | 0.358 |
CLV_PCSK_PC7_1 | 332 | 338 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.248 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.645 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.495 |
DOC_CYCLIN_RxL_1 | 272 | 282 | PF00134 | 0.465 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 203 | 212 | PF00134 | 0.453 |
DOC_MAPK_gen_1 | 275 | 285 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 96 | 103 | PF00069 | 0.468 |
DOC_MAPK_JIP1_4 | 273 | 279 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 278 | 287 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.539 |
DOC_MAPK_RevD_3 | 230 | 245 | PF00069 | 0.558 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.480 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.453 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 306 | 313 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 56 | 65 | PF00244 | 0.549 |
LIG_14-3-3_CterR_2 | 337 | 341 | PF00244 | 0.627 |
LIG_Actin_WH2_2 | 310 | 325 | PF00022 | 0.520 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.453 |
LIG_CtBP_PxDLS_1 | 170 | 174 | PF00389 | 0.558 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.453 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.463 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.487 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.392 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.660 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.378 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.447 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.539 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.240 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 136 | 144 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 76 | 84 | PF02991 | 0.429 |
LIG_LIR_LC3C_4 | 150 | 155 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.423 |
LIG_MYND_1 | 270 | 274 | PF01753 | 0.478 |
LIG_RPA_C_Fungi | 284 | 296 | PF08784 | 0.391 |
LIG_RPA_C_Fungi | 93 | 105 | PF08784 | 0.426 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.306 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.469 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.532 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.485 |
LIG_SUMO_SIM_anti_2 | 150 | 156 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 24 | 32 | PF11976 | 0.625 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.693 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.340 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.292 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.654 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.306 |
LIG_TYR_ITIM | 34 | 39 | PF00017 | 0.483 |
LIG_TYR_ITSM | 296 | 303 | PF00017 | 0.426 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.265 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.357 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.413 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.451 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.513 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.471 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.690 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.324 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.306 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.306 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.439 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.456 |
MOD_Cter_Amidation | 333 | 336 | PF01082 | 0.596 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.459 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.435 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.327 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.401 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.449 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.306 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.352 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.352 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.384 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.487 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.391 |
MOD_N-GLC_2 | 207 | 209 | PF02516 | 0.306 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.338 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.302 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.306 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.347 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.400 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.453 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.301 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.291 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.306 |
MOD_PK_1 | 35 | 41 | PF00069 | 0.439 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.261 |
MOD_PKA_1 | 306 | 312 | PF00069 | 0.408 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.532 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.396 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.277 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.408 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.507 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.532 |
MOD_PKB_1 | 304 | 312 | PF00069 | 0.305 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.340 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.391 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.521 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.505 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.391 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.316 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.353 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.243 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.306 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.426 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.590 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.409 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.443 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.422 |
TRG_DiLeu_BaEn_1 | 41 | 46 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_4 | 181 | 187 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.527 |
TRG_NLS_MonoCore_2 | 334 | 339 | PF00514 | 0.597 |
TRG_NLS_MonoExtC_3 | 334 | 339 | PF00514 | 0.575 |
TRG_NLS_MonoExtN_4 | 332 | 339 | PF00514 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKZ4 | Leptomonas seymouri | 89% | 100% |
A0A0N1PD49 | Leptomonas seymouri | 23% | 80% |
A0A0S4J686 | Bodo saltans | 55% | 96% |
A0A0S4JJS5 | Bodo saltans | 24% | 81% |
A0A1X0NUB3 | Trypanosomatidae | 25% | 78% |
A0A1X0P0H6 | Trypanosomatidae | 69% | 96% |
A0A3Q8IDJ5 | Leishmania donovani | 95% | 100% |
A0A3R7KY21 | Trypanosoma rangeli | 66% | 96% |
A0A3S5H6V9 | Leishmania donovani | 24% | 77% |
A4H8A6 | Leishmania braziliensis | 24% | 77% |
A4HWM6 | Leishmania infantum | 24% | 77% |
A4I8M9 | Leishmania infantum | 95% | 100% |
A6ZPE5 | Saccharomyces cerevisiae (strain YJM789) | 23% | 67% |
A7TIF5 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 23% | 66% |
D0A4K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 96% |
E9AQD3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 76% |
E9B3J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O04656 | Arabidopsis thaliana | 24% | 76% |
Q12499 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 67% |
Q4Q4L0 | Leishmania major | 95% | 100% |
Q5U5C5 | Xenopus laevis | 29% | 68% |
Q6CKR8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 67% |
Q6NVP6 | Xenopus tropicalis | 31% | 68% |
Q753I4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 66% |
Q7SXM7 | Danio rerio | 32% | 67% |
Q8CCF0 | Mus musculus | 30% | 68% |
Q8RXN6 | Arabidopsis thaliana | 32% | 70% |
Q8WWY3 | Homo sapiens | 30% | 68% |
V5BFW3 | Trypanosoma cruzi | 68% | 96% |