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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3S7WQS5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006412 | translation | 4 | 9 |
GO:0006518 | peptide metabolic process | 4 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 12 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0032774 | RNA biosynthetic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 10 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043043 | peptide biosynthetic process | 5 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043603 | amide metabolic process | 3 | 9 |
GO:0043604 | amide biosynthetic process | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 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:0097056 | obsolete selenocysteinyl-tRNA(Sec) biosynthetic process | 6 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0001514 | selenocysteine incorporation | 7 | 1 |
GO:0006414 | translational elongation | 5 | 1 |
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006451 | translational readthrough | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016785 | selenotransferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0098621 | phosphoseryl-selenocysteinyl-tRNA selenium transferase activity | 4 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.289 |
CLV_PCSK_FUR_1 | 444 | 448 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.288 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.447 |
DEG_SCF_FBW7_1 | 273 | 279 | PF00400 | 0.586 |
DEG_SCF_FBW7_1 | 535 | 541 | PF00400 | 0.548 |
DEG_SPOP_SBC_1 | 276 | 280 | PF00917 | 0.637 |
DEG_SPOP_SBC_1 | 307 | 311 | PF00917 | 0.454 |
DOC_CKS1_1 | 210 | 215 | PF01111 | 0.493 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.603 |
DOC_CKS1_1 | 535 | 540 | PF01111 | 0.548 |
DOC_CYCLIN_RxL_1 | 53 | 63 | PF00134 | 0.469 |
DOC_CYCLIN_yCln2_LP_2 | 207 | 213 | PF00134 | 0.552 |
DOC_MAPK_DCC_7 | 560 | 568 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 432 | 441 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 444 | 452 | PF00069 | 0.461 |
DOC_MAPK_HePTP_8 | 113 | 125 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 560 | 569 | PF00069 | 0.493 |
DOC_MAPK_RevD_3 | 332 | 348 | PF00069 | 0.548 |
DOC_MIT_MIM_1 | 581 | 590 | PF04212 | 0.521 |
DOC_PP1_RVXF_1 | 212 | 219 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 359 | 365 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.599 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.366 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.493 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 78 | 86 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 139 | 155 | PF00022 | 0.484 |
LIG_BIR_III_4 | 231 | 235 | PF00653 | 0.498 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.543 |
LIG_FAT_LD_1 | 580 | 588 | PF03623 | 0.477 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.511 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.462 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.499 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.529 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.415 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.504 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.611 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.548 |
LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.460 |
LIG_PCNA_PIPBox_1 | 403 | 412 | PF02747 | 0.548 |
LIG_PCNA_PIPBox_1 | 584 | 593 | PF02747 | 0.515 |
LIG_PCNA_yPIPBox_3 | 116 | 126 | PF02747 | 0.487 |
LIG_PDZ_Class_2 | 590 | 595 | PF00595 | 0.433 |
LIG_Pex14_1 | 425 | 429 | PF04695 | 0.454 |
LIG_PTB_Apo_2 | 336 | 343 | PF02174 | 0.446 |
LIG_PTB_Phospho_1 | 336 | 342 | PF10480 | 0.446 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.548 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 342 | 345 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.443 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.468 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.561 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.576 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.431 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.513 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.632 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.465 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.366 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.454 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.447 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.474 |
LIG_Sin3_3 | 135 | 142 | PF02671 | 0.548 |
LIG_SUMO_SIM_anti_2 | 147 | 152 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 448 | 458 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 118 | 124 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 448 | 458 | PF11976 | 0.529 |
LIG_TRAF2_1 | 188 | 191 | PF00917 | 0.694 |
MOD_CDK_SPK_2 | 209 | 214 | PF00069 | 0.520 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.699 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.728 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.542 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.468 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.493 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.484 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.484 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.472 |
MOD_Cter_Amidation | 416 | 419 | PF01082 | 0.329 |
MOD_DYRK1A_RPxSP_1 | 534 | 538 | PF00069 | 0.548 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.474 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.699 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.697 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.268 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.254 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.293 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.262 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.329 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.166 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.616 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.450 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.711 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.651 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.526 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.511 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.452 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.490 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.428 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.591 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.712 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.459 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.443 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.448 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.478 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.320 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.501 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.490 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.459 |
MOD_OFUCOSY | 306 | 313 | PF10250 | 0.243 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.548 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.493 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.641 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.508 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.629 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.447 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.498 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.452 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.473 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.657 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.529 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.543 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.443 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.443 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.542 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.506 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.522 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.444 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.510 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.761 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.454 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.538 |
MOD_SUMO_rev_2 | 453 | 460 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 579 | 584 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 431 | 436 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.484 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 519 | 524 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGI4 | Leptomonas seymouri | 65% | 100% |
A0A0S4KH93 | Bodo saltans | 41% | 100% |
A0A1X0NN47 | Trypanosomatidae | 48% | 88% |
A0A3R7N0G5 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WQS5 | Leishmania donovani | 100% | 100% |
A4H5S3 | Leishmania braziliensis | 84% | 100% |
A4HU16 | Leishmania infantum | 100% | 100% |
D0A9I4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AMU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q28EN2 | Xenopus tropicalis | 34% | 100% |
Q4QHS9 | Leishmania major | 96% | 100% |
Q54VQ6 | Dictyostelium discoideum | 33% | 100% |
Q5RAK7 | Pongo abelii | 34% | 100% |
Q6P6M7 | Mus musculus | 34% | 100% |
Q803A7 | Danio rerio | 34% | 100% |
Q9HD40 | Homo sapiens | 34% | 100% |
V5BBE8 | Trypanosoma cruzi | 52% | 100% |