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: A0A451EJB4
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_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.365 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.378 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.279 |
DOC_CDC14_PxL_1 | 216 | 224 | PF14671 | 0.411 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.325 |
DOC_MAPK_gen_1 | 260 | 269 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 293 | 302 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 346 | 354 | PF00069 | 0.427 |
DOC_PP1_RVXF_1 | 381 | 388 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.342 |
DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.490 |
DOC_USP7_UBL2_3 | 360 | 364 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.325 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 403 | 411 | PF00244 | 0.506 |
LIG_APCC_ABBA_1 | 107 | 112 | PF00400 | 0.447 |
LIG_APCC_ABBA_1 | 177 | 182 | PF00400 | 0.315 |
LIG_APCC_ABBAyCdc20_2 | 106 | 112 | PF00400 | 0.447 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 373 | 377 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.277 |
LIG_BRCT_BRCA1_2 | 373 | 379 | PF00533 | 0.479 |
LIG_Clathr_ClatBox_1 | 177 | 181 | PF01394 | 0.447 |
LIG_DLG_GKlike_1 | 262 | 269 | PF00625 | 0.403 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.566 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.545 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.365 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.506 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.382 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.490 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.505 |
LIG_Integrin_RGD_1 | 245 | 247 | PF01839 | 0.340 |
LIG_LIR_Apic_2 | 213 | 218 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 11 | 19 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 126 | 133 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 264 | 272 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 396 | 400 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.437 |
LIG_MLH1_MIPbox_1 | 383 | 387 | PF16413 | 0.392 |
LIG_MYND_3 | 308 | 312 | PF01753 | 0.543 |
LIG_NRBOX | 89 | 95 | PF00104 | 0.340 |
LIG_PCNA_PIPBox_1 | 356 | 365 | PF02747 | 0.498 |
LIG_PCNA_yPIPBox_3 | 356 | 364 | PF02747 | 0.490 |
LIG_PTB_Apo_2 | 189 | 196 | PF02174 | 0.338 |
LIG_PTB_Phospho_1 | 189 | 195 | PF10480 | 0.338 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.411 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.471 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.314 |
LIG_SH3_1 | 118 | 124 | PF00018 | 0.329 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.323 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.315 |
LIG_SUMO_SIM_anti_2 | 172 | 179 | PF11976 | 0.276 |
LIG_SUMO_SIM_anti_2 | 348 | 354 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 365 | 374 | PF11976 | 0.574 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.487 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.500 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.572 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.447 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.483 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.355 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.389 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.397 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.420 |
MOD_Cter_Amidation | 296 | 299 | PF01082 | 0.660 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.296 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.325 |
MOD_GlcNHglycan | 251 | 255 | PF01048 | 0.447 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.317 |
MOD_GlcNHglycan | 8 | 13 | PF01048 | 0.561 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.326 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.416 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.439 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.479 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.483 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.396 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.409 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.408 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.467 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.276 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.388 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.494 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.581 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.434 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.355 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.519 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.296 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.497 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.579 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.620 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.325 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.385 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.518 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.386 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.484 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.445 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.514 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.327 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.390 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.470 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.529 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.458 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.273 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.325 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.595 |
MOD_SUMO_for_1 | 345 | 348 | PF00179 | 0.357 |
MOD_SUMO_rev_2 | 264 | 272 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 390 | 400 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_1 | 348 | 353 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 336 | 341 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.533 |
TRG_NLS_MonoExtC_3 | 134 | 139 | PF00514 | 0.315 |
TRG_NLS_MonoExtC_3 | 294 | 299 | PF00514 | 0.393 |
TRG_NLS_MonoExtN_4 | 133 | 139 | PF00514 | 0.476 |
TRG_NLS_MonoExtN_4 | 293 | 299 | PF00514 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTX0 | Leptomonas seymouri | 39% | 100% |
A0A0N1IKD9 | Leptomonas seymouri | 82% | 83% |
A0A0S4IH84 | Bodo saltans | 71% | 86% |
A0A0S4JRM1 | Bodo saltans | 40% | 83% |
A0A1X0NW43 | Trypanosomatidae | 43% | 100% |
A0A1X0P2V9 | Trypanosomatidae | 75% | 91% |
A0A3R7NWI2 | Trypanosoma rangeli | 42% | 100% |
A0A3S5H791 | Leishmania donovani | 39% | 100% |
A0A422NFE4 | Trypanosoma rangeli | 76% | 92% |
A4H382 | Leishmania braziliensis | 92% | 100% |
A4HRI2 | Leishmania infantum | 100% | 100% |
A4HZ02 | Leishmania infantum | 39% | 100% |
C9ZIM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZXL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 75% | 90% |
E9AC50 | Leishmania major | 98% | 100% |
E9AIM1 | Leishmania braziliensis | 38% | 100% |
E9AJE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9AUV4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
P86924 | Trypanosoma brucei brucei | 43% | 100% |
P86925 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 42% | 100% |
P86926 | Trypanosoma brucei brucei | 75% | 90% |
P86927 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 75% | 90% |
Q6T452 | Leishmania major | 39% | 100% |
V5ASZ3 | Trypanosoma cruzi | 40% | 100% |
V5DD75 | Trypanosoma cruzi | 75% | 85% |