tRNA synthetase, Uncharacterized
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AGV9
Term | Name | Level | Count |
---|---|---|---|
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 193 | 197 | PF00082 | 0.393 |
CLV_PCSK_FUR_1 | 56 | 60 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.406 |
DEG_APCC_DBOX_1 | 67 | 75 | PF00400 | 0.425 |
DEG_SCF_TRCP1_1 | 200 | 206 | PF00400 | 0.377 |
DOC_ANK_TNKS_1 | 146 | 153 | PF00023 | 0.531 |
DOC_CYCLIN_yCln2_LP_2 | 17 | 23 | PF00134 | 0.402 |
DOC_CYCLIN_yCln2_LP_2 | 295 | 301 | PF00134 | 0.511 |
DOC_MAPK_DCC_7 | 68 | 76 | PF00069 | 0.427 |
DOC_MAPK_DCC_7 | 90 | 99 | PF00069 | 0.476 |
DOC_MAPK_FxFP_2 | 75 | 78 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 68 | 76 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.427 |
DOC_MAPK_NFAT4_5 | 68 | 76 | PF00069 | 0.427 |
DOC_PP2B_LxvP_1 | 17 | 20 | PF13499 | 0.408 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.319 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.465 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.455 |
DOC_PP4_FxxP_1 | 75 | 78 | PF00568 | 0.431 |
DOC_SPAK_OSR1_1 | 131 | 135 | PF12202 | 0.434 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 167 | 175 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 7 | 17 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 132 | 149 | PF00022 | 0.497 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.338 |
LIG_CSL_BTD_1 | 209 | 212 | PF09270 | 0.435 |
LIG_EVH1_1 | 106 | 110 | PF00568 | 0.435 |
LIG_EVH1_1 | 23 | 27 | PF00568 | 0.384 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.497 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.531 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.424 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.483 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.441 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.474 |
LIG_MYND_1 | 179 | 183 | PF01753 | 0.454 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.530 |
LIG_SH3_1 | 90 | 96 | PF00018 | 0.479 |
LIG_SH3_2 | 32 | 37 | PF14604 | 0.375 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.437 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.460 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.442 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.439 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.506 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.463 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.455 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.467 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.396 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.530 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.711 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.422 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.428 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.422 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.420 |
MOD_Cter_Amidation | 286 | 289 | PF01082 | 0.247 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.470 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.440 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.419 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.349 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.696 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.317 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.517 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.490 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.404 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.506 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.425 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.340 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.436 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.448 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.450 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.389 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.565 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.568 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.435 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.674 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.449 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.453 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.450 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.442 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 66 | 71 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.420 |
TRG_NES_CRM1_1 | 123 | 136 | PF08389 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.295 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I030 | Leptomonas seymouri | 73% | 100% |
A0A1X0NXR2 | Trypanosomatidae | 48% | 100% |
A0A3Q8IDY4 | Leishmania donovani | 97% | 100% |
A4HK97 | Leishmania braziliensis | 79% | 100% |
D0A1C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AV75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QCA6 | Leishmania major | 91% | 100% |
V5B6I0 | Trypanosoma cruzi | 49% | 100% |