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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031019 | mitochondrial mRNA editing complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045293 | mRNA editing complex | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AIM1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0003972 | RNA ligase (ATP) activity | 5 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0005524 | ATP binding | 5 | 23 |
GO:0008452 | RNA ligase activity | 4 | 23 |
GO:0016874 | ligase activity | 2 | 23 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 23 |
GO:0017076 | purine nucleotide binding | 4 | 23 |
GO:0030554 | adenyl nucleotide binding | 5 | 23 |
GO:0032553 | ribonucleotide binding | 3 | 23 |
GO:0032555 | purine ribonucleotide binding | 4 | 23 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 23 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 23 |
GO:0036094 | small molecule binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043168 | anion binding | 3 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0097367 | carbohydrate derivative binding | 2 | 23 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 23 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 23 |
GO:1901265 | nucleoside phosphate binding | 3 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.388 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.692 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DOC_CDC14_PxL_1 | 198 | 206 | PF14671 | 0.197 |
DOC_CDC14_PxL_1 | 377 | 385 | PF14671 | 0.395 |
DOC_CYCLIN_RxL_1 | 102 | 113 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 12 | 18 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 140 | 147 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 296 | 302 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 388 | 395 | PF00149 | 0.392 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.324 |
DOC_USP7_MATH_2 | 346 | 352 | PF00917 | 0.277 |
DOC_USP7_UBL2_3 | 363 | 367 | PF12436 | 0.292 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.311 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.216 |
LIG_14-3-3_CanoR_1 | 179 | 186 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 320 | 327 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 334 | 339 | PF00244 | 0.332 |
LIG_AP2alpha_2 | 345 | 347 | PF02296 | 0.245 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.297 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.411 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.340 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.295 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.411 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.341 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.373 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.321 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 27 | 35 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 389 | 399 | PF02991 | 0.278 |
LIG_LIR_LC3C_4 | 246 | 251 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.297 |
LIG_NRBOX | 356 | 362 | PF00104 | 0.283 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.311 |
LIG_PTB_Apo_2 | 156 | 163 | PF02174 | 0.382 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 29 | 33 | PF00017 | 0.439 |
LIG_SH2_SRC | 133 | 136 | PF00017 | 0.311 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.145 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.145 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.368 |
LIG_SH3_1 | 133 | 139 | PF00018 | 0.306 |
LIG_SH3_2 | 136 | 141 | PF14604 | 0.432 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.316 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.428 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.432 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.420 |
LIG_UBA3_1 | 268 | 272 | PF00899 | 0.326 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.389 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.388 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.334 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.298 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.429 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.432 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.635 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.425 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.301 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.192 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.449 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.295 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.295 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.326 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.309 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.374 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.326 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.375 |
MOD_PK_1 | 141 | 147 | PF00069 | 0.290 |
MOD_PK_1 | 296 | 302 | PF00069 | 0.410 |
MOD_PK_1 | 334 | 340 | PF00069 | 0.388 |
MOD_PKA_1 | 141 | 147 | PF00069 | 0.326 |
MOD_PKA_1 | 296 | 302 | PF00069 | 0.459 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.206 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.324 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.404 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.416 |
MOD_PKB_1 | 150 | 158 | PF00069 | 0.277 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.342 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.341 |
MOD_Plk_2-3 | 27 | 33 | PF00069 | 0.405 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.311 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.197 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.306 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.416 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.388 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.270 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.488 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.388 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.311 |
MOD_SUMO_rev_2 | 258 | 266 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 368 | 378 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 356 | 361 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.266 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.455 |
TRG_NLS_MonoExtN_4 | 139 | 144 | PF00514 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 4 | 9 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTX0 | Leptomonas seymouri | 76% | 100% |
A0A0N1IKD9 | Leptomonas seymouri | 41% | 81% |
A0A0S4IH84 | Bodo saltans | 40% | 85% |
A0A0S4JRM1 | Bodo saltans | 59% | 82% |
A0A1X0NW43 | Trypanosomatidae | 68% | 100% |
A0A1X0P2V9 | Trypanosomatidae | 42% | 90% |
A0A3R7NWI2 | Trypanosoma rangeli | 69% | 100% |
A0A3S5H791 | Leishmania donovani | 89% | 100% |
A0A422NFE4 | Trypanosoma rangeli | 42% | 91% |
A0A451EJB4 | Leishmania donovani | 38% | 99% |
A4H382 | Leishmania braziliensis | 39% | 100% |
A4HRI2 | Leishmania infantum | 38% | 99% |
A4HZ02 | Leishmania infantum | 89% | 100% |
C9ZIM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
C9ZXL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 89% |
E9AC50 | Leishmania major | 38% | 100% |
E9AJE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AUV4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P86924 | Trypanosoma brucei brucei | 67% | 100% |
P86925 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 67% | 100% |
P86926 | Trypanosoma brucei brucei | 41% | 89% |
P86927 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 41% | 89% |
Q6T452 | Leishmania major | 88% | 100% |
V5ASZ3 | Trypanosoma cruzi | 68% | 100% |
V5DD75 | Trypanosoma cruzi | 42% | 84% |