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:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ACY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006400 | tRNA modification | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 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:0101030 | tRNA-guanine transglycosylation | 7 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 9 |
GO:0008479 | queuine tRNA-ribosyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016757 | glycosyltransferase activity | 3 | 12 |
GO:0016763 | pentosyltransferase activity | 4 | 12 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.540 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.254 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.244 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.278 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.528 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.642 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.426 |
DOC_MAPK_gen_1 | 111 | 121 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 198 | 204 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 96 | 103 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.515 |
DOC_PP2B_LxvP_1 | 237 | 240 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.457 |
DOC_PP2B_PxIxI_1 | 205 | 211 | PF00149 | 0.396 |
DOC_PP4_FxxP_1 | 46 | 49 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 318 | 323 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 34 | 44 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 73 | 77 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.465 |
LIG_BIR_III_2 | 175 | 179 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.564 |
LIG_Clathr_ClatBox_1 | 238 | 242 | PF01394 | 0.499 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.536 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.483 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.504 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.472 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.509 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 45 | 49 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 38 | 49 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.499 |
LIG_MYND_1 | 18 | 22 | PF01753 | 0.465 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.528 |
LIG_PDZ_Class_1 | 331 | 336 | PF00595 | 0.514 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.547 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.532 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.558 |
LIG_SH2_SRC | 286 | 289 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.557 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 298 | 305 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 289 | 295 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 68 | 75 | PF11976 | 0.455 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.499 |
LIG_TRAF2_1 | 292 | 295 | PF00917 | 0.444 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.558 |
MOD_CDC14_SPxK_1 | 196 | 199 | PF00782 | 0.558 |
MOD_CDK_SPK_2 | 193 | 198 | PF00069 | 0.558 |
MOD_CDK_SPxK_1 | 193 | 199 | PF00069 | 0.558 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.530 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.503 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.528 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.536 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.487 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.478 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.519 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.444 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.553 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.331 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.348 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.555 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.352 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.214 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.507 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.472 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.438 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.521 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.483 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.382 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.340 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.567 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.538 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.515 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.506 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.471 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.434 |
MOD_OFUCOSY | 274 | 279 | PF10250 | 0.254 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.558 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.536 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.540 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.461 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.540 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.562 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.524 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.467 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.445 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.478 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.461 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.550 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.460 |
TRG_DiLeu_BaEn_2 | 41 | 47 | PF01217 | 0.558 |
TRG_DiLeu_BaEn_4 | 150 | 156 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.497 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.478 |
TRG_NLS_MonoCore_2 | 132 | 137 | PF00514 | 0.454 |
TRG_NLS_MonoExtN_4 | 130 | 137 | PF00514 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWE8 | Leptomonas seymouri | 67% | 100% |
A0A0S4IR14 | Bodo saltans | 36% | 96% |
A0A1X0NPI6 | Trypanosomatidae | 38% | 100% |
A0A3R7K861 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X0A8 | Leishmania donovani | 93% | 100% |
A4HFC2 | Leishmania braziliensis | 83% | 100% |
A4I2J9 | Leishmania infantum | 93% | 100% |
B0WAN0 | Culex quinquefasciatus | 24% | 78% |
B3NCH1 | Drosophila erecta | 22% | 80% |
B3RNT0 | Trichoplax adhaerens | 23% | 91% |
B4H1X9 | Drosophila persimilis | 23% | 81% |
B4HL48 | Drosophila sechellia | 24% | 80% |
B4IXD3 | Drosophila grimshawi | 24% | 80% |
B4KXI8 | Drosophila mojavensis | 23% | 81% |
B4LFW2 | Drosophila virilis | 23% | 81% |
B4N549 | Drosophila willistoni | 23% | 79% |
B4PEV9 | Drosophila yakuba | 23% | 80% |
C9ZPM4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AYQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q16RF5 | Aedes aegypti | 22% | 80% |
Q29EE9 | Drosophila pseudoobscura pseudoobscura | 25% | 81% |
Q7Q727 | Anopheles gambiae | 23% | 78% |
Q9VSZ6 | Drosophila melanogaster | 23% | 80% |
V5BCL2 | Trypanosoma cruzi | 40% | 100% |