tRNA synthetase, arginyl-tRNA synthetase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | yes | yes: 1 |
Forrest at al. (metacyclic) | yes | yes: 1 |
Forrest at al. (procyclic) | yes | yes: 1 |
Silverman et al. | no | yes: 1 |
Pissara et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 3 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 3 |
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 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I2T4
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
GO:0006420 | arginyl-tRNA aminoacylation | 7 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043038 | amino acid activation | 4 | 12 |
GO:0043039 | tRNA aminoacylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule 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:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
GO:0004814 | arginine-tRNA ligase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.335 |
CLV_C14_Caspase3-7 | 485 | 489 | PF00656 | 0.464 |
CLV_MEL_PAP_1 | 407 | 413 | PF00089 | 0.341 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 588 | 590 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.264 |
DEG_APCC_DBOX_1 | 368 | 376 | PF00400 | 0.496 |
DEG_APCC_DBOX_1 | 665 | 673 | PF00400 | 0.475 |
DEG_CRL4_CDT2_1 | 199 | 211 | PF00400 | 0.361 |
DEG_CRL4_CDT2_2 | 199 | 211 | PF00400 | 0.361 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.631 |
DEG_ODPH_VHL_1 | 379 | 392 | PF01847 | 0.437 |
DOC_CKS1_1 | 606 | 611 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 152 | 163 | PF00134 | 0.550 |
DOC_CYCLIN_RxL_1 | 273 | 283 | PF00134 | 0.489 |
DOC_CYCLIN_RxL_1 | 674 | 687 | PF00134 | 0.569 |
DOC_MAPK_DCC_7 | 384 | 392 | PF00069 | 0.550 |
DOC_MAPK_FxFP_2 | 411 | 414 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 123 | 130 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 219 | 226 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 493 | 502 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 678 | 686 | PF00069 | 0.489 |
DOC_MAPK_HePTP_8 | 382 | 394 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 123 | 130 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 365 | 372 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 385 | 394 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 92 | 99 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 153 | 160 | PF00149 | 0.550 |
DOC_PP4_FxxP_1 | 130 | 133 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.464 |
DOC_SPAK_OSR1_1 | 437 | 441 | PF12202 | 0.569 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 109 | 113 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 299 | 303 | PF12436 | 0.439 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 410 | 414 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 620 | 625 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 674 | 678 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 132 | 147 | PF00022 | 0.475 |
LIG_Actin_WH2_2 | 536 | 554 | PF00022 | 0.477 |
LIG_Actin_WH2_2 | 612 | 629 | PF00022 | 0.505 |
LIG_Actin_WH2_2 | 663 | 680 | PF00022 | 0.475 |
LIG_BRCT_BRCA1_1 | 648 | 652 | PF00533 | 0.470 |
LIG_Clathr_ClatBox_1 | 683 | 687 | PF01394 | 0.569 |
LIG_deltaCOP1_diTrp_1 | 172 | 177 | PF00928 | 0.455 |
LIG_deltaCOP1_diTrp_1 | 467 | 476 | PF00928 | 0.465 |
LIG_FAT_LD_1 | 372 | 380 | PF03623 | 0.485 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.507 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.475 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.526 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.541 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.550 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.507 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.505 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.550 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.475 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.472 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.447 |
LIG_LIR_Apic_2 | 129 | 133 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 267 | 272 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 562 | 569 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 639 | 648 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.495 |
LIG_MAD2 | 125 | 133 | PF02301 | 0.489 |
LIG_MAD2 | 54 | 62 | PF02301 | 0.513 |
LIG_MLH1_MIPbox_1 | 648 | 652 | PF16413 | 0.475 |
LIG_PDZ_Class_3 | 687 | 692 | PF00595 | 0.475 |
LIG_Pex14_1 | 173 | 177 | PF04695 | 0.454 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.489 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.475 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.505 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.464 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.475 |
LIG_SH2_SRC | 579 | 582 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 383 | 386 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.459 |
LIG_SH3_1 | 24 | 30 | PF00018 | 0.550 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.508 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.467 |
LIG_SH3_4 | 361 | 368 | PF00018 | 0.407 |
LIG_SUMO_SIM_anti_2 | 513 | 519 | PF11976 | 0.489 |
LIG_SUMO_SIM_anti_2 | 680 | 685 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 276 | 283 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 595 | 603 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 622 | 628 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 668 | 673 | PF11976 | 0.475 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.489 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.489 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.457 |
LIG_TRAF2_1 | 30 | 33 | PF00917 | 0.569 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.453 |
LIG_TRAF2_1 | 594 | 597 | PF00917 | 0.485 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.431 |
LIG_TRFH_1 | 26 | 30 | PF08558 | 0.569 |
LIG_TYR_ITAM | 252 | 273 | PF00017 | 0.508 |
LIG_TYR_ITIM | 546 | 551 | PF00017 | 0.466 |
LIG_UBA3_1 | 179 | 185 | PF00899 | 0.464 |
LIG_UBA3_1 | 334 | 340 | PF00899 | 0.453 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.454 |
LIG_UBA3_1 | 375 | 384 | PF00899 | 0.434 |
LIG_UBA3_1 | 540 | 547 | PF00899 | 0.505 |
MOD_CDK_SPK_2 | 87 | 92 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 605 | 612 | PF00069 | 0.475 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.525 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.464 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.371 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.550 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.473 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.464 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.498 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.444 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.453 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.501 |
MOD_Cter_Amidation | 488 | 491 | PF01082 | 0.264 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.373 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.274 |
MOD_GlcNHglycan | 568 | 572 | PF01048 | 0.403 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.491 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.443 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.464 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.499 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.550 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.369 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.289 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.475 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.473 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.336 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.489 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.507 |
MOD_PIKK_1 | 523 | 529 | PF00454 | 0.505 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.550 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.541 |
MOD_PK_1 | 583 | 589 | PF00069 | 0.464 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.475 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.475 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.475 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.464 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.472 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.475 |
MOD_Plk_1 | 602 | 608 | PF00069 | 0.534 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.511 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.475 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.489 |
MOD_Plk_2-3 | 472 | 478 | PF00069 | 0.525 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.474 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.463 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.541 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.460 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.470 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.492 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 356 | 362 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_4 | 350 | 356 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_4 | 532 | 538 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 152 | 157 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.475 |
TRG_NES_CRM1_1 | 504 | 519 | PF08389 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 656 | 660 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S4 | Leptomonas seymouri | 85% | 100% |
A0A0S4JSY3 | Bodo saltans | 60% | 100% |
A0A1X0P461 | Trypanosomatidae | 69% | 100% |
A0A3Q8IED7 | Leishmania donovani | 100% | 100% |
A0A3R7MEE6 | Trypanosoma rangeli | 71% | 100% |
A4HFQ8 | Leishmania braziliensis | 91% | 100% |
D0A5Z9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E9ADB2 | Leishmania major | 97% | 100% |
E9AZ37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q7URC7 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 32% | 100% |
Q8ZTA8 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 23% | 100% |
Q971X1 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 24% | 100% |
V5BQK5 | Trypanosoma cruzi | 69% | 100% |