tRNA synthetase, prolyl-tRNA synthetase
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) | yes | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 28 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0017101 | aminoacyl-tRNA synthetase multienzyme complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0016020 | membrane | 2 | 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
|
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 16 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 16 |
GO:0006399 | tRNA metabolic process | 7 | 16 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 16 |
GO:0006433 | prolyl-tRNA aminoacylation | 7 | 16 |
GO:0006520 | amino acid metabolic process | 3 | 16 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016070 | RNA metabolic process | 5 | 16 |
GO:0019752 | carboxylic acid metabolic process | 5 | 16 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 16 |
GO:0034660 | ncRNA metabolic process | 6 | 16 |
GO:0043038 | amino acid activation | 4 | 16 |
GO:0043039 | tRNA aminoacylation | 5 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043436 | oxoacid metabolic process | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0044281 | small molecule metabolic process | 2 | 16 |
GO:0046483 | heterocycle metabolic process | 3 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0090304 | nucleic acid metabolic process | 4 | 16 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 15 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 16 |
GO:0004827 | proline-tRNA ligase activity | 5 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 15 |
GO:0016874 | ligase activity | 2 | 16 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 16 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.410 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.204 |
CLV_NRD_NRD_1 | 726 | 728 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.250 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.230 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.451 |
DEG_SCF_FBW7_1 | 49 | 55 | PF00400 | 0.419 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.423 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.307 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.237 |
DOC_MAPK_gen_1 | 205 | 212 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 419 | 429 | PF00069 | 0.399 |
DOC_MAPK_JIP1_4 | 206 | 212 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 205 | 212 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 422 | 431 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 565 | 573 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 648 | 656 | PF00069 | 0.399 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.372 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 488 | 491 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 775 | 778 | PF13499 | 0.399 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 543 | 546 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 779 | 782 | PF00568 | 0.399 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.348 |
DOC_USP7_UBL2_3 | 164 | 168 | PF12436 | 0.356 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.411 |
DOC_USP7_UBL2_3 | 794 | 798 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 176 | 183 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 494 | 503 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 585 | 595 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 676 | 680 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 712 | 722 | PF00244 | 0.440 |
LIG_Actin_WH2_2 | 162 | 178 | PF00022 | 0.385 |
LIG_APCC_ABBA_1 | 571 | 576 | PF00400 | 0.321 |
LIG_deltaCOP1_diTrp_1 | 453 | 463 | PF00928 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 717 | 721 | PF00928 | 0.272 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.209 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.439 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.471 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.387 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.431 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.503 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.428 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.399 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.426 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.399 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.376 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.350 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.442 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.500 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.410 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.513 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.439 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.264 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.403 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.396 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.405 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.409 |
LIG_FHA_2 | 759 | 765 | PF00498 | 0.431 |
LIG_LIR_Apic_2 | 441 | 445 | PF02991 | 0.399 |
LIG_LIR_Apic_2 | 540 | 546 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 195 | 203 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 231 | 238 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 312 | 322 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 478 | 488 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 716 | 725 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 801 | 810 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 716 | 721 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 801 | 806 | PF02991 | 0.467 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.399 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.537 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 480 | 484 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 315 | 318 | PF00017 | 0.336 |
LIG_SH2_SRC | 315 | 318 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 480 | 484 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.424 |
LIG_SH3_2 | 61 | 66 | PF14604 | 0.415 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.410 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.447 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.459 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.298 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.404 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 472 | 478 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 588 | 595 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 208 | 213 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.466 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.440 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.363 |
LIG_TRAF2_1 | 602 | 605 | PF00917 | 0.444 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.439 |
LIG_TRAF2_1 | 749 | 752 | PF00917 | 0.403 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.306 |
LIG_UBA3_1 | 199 | 205 | PF00899 | 0.444 |
LIG_WRC_WIRS_1 | 235 | 240 | PF05994 | 0.363 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.458 |
LIG_WW_3 | 582 | 586 | PF00397 | 0.295 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.419 |
MOD_CDK_SPxK_1 | 60 | 66 | PF00069 | 0.414 |
MOD_CDK_SPxxK_3 | 443 | 450 | PF00069 | 0.410 |
MOD_CDK_SPxxK_3 | 634 | 641 | PF00069 | 0.399 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.420 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.466 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.389 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.563 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.425 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.410 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.411 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.438 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.418 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.450 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.277 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.408 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.503 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.330 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.423 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.399 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.399 |
MOD_Cter_Amidation | 494 | 497 | PF01082 | 0.210 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.460 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.565 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.222 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.336 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.291 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.580 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.199 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.404 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.416 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.500 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.639 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.315 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.577 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.444 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.460 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.403 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.449 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.458 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.535 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.402 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.500 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.383 |
MOD_N-GLC_1 | 634 | 639 | PF02516 | 0.199 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.586 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.420 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.395 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.388 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.396 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.405 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.527 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.381 |
MOD_NEK2_2 | 479 | 484 | PF00069 | 0.428 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.433 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.534 |
MOD_PKA_1 | 746 | 752 | PF00069 | 0.399 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.654 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.399 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.500 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.424 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.453 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.441 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.404 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.357 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.455 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.458 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.424 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.423 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.410 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.428 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.441 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.421 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.425 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.500 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.363 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.410 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.410 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.421 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.529 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.399 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.488 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 305 | 308 | PF00179 | 0.319 |
MOD_SUMO_for_1 | 464 | 467 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 293 | 301 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 748 | 756 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 92 | 102 | PF00179 | 0.348 |
TRG_DiLeu_BaEn_1 | 123 | 128 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_1 | 98 | 103 | PF01217 | 0.392 |
TRG_DiLeu_BaEn_2 | 716 | 722 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 2 | 7 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 449 | 452 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 493 | 496 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 615 | 617 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 712 | 715 | PF00400 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 615 | 620 | PF00026 | 0.244 |
TRG_Pf-PMV_PEXEL_1 | 659 | 663 | PF00026 | 0.306 |
TRG_PTS2 | 1 | 44 | PF00400 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY85 | Leptomonas seymouri | 84% | 100% |
A0A0S4JN58 | Bodo saltans | 58% | 99% |
A0A1X0P793 | Trypanosomatidae | 62% | 100% |
A0A3R7KPX0 | Trypanosoma rangeli | 65% | 95% |
A0A3S7WV15 | Leishmania donovani | 89% | 100% |
A0A3S7WV32 | Leishmania donovani | 100% | 100% |
A4H9N1 | Leishmania braziliensis | 89% | 99% |
A4HY00 | Leishmania infantum | 88% | 100% |
D0A5B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ARQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9ARQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
O60155 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 45% | 100% |
P38708 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 100% |
Q4QDS0 | Leishmania major | 87% | 100% |
Q4QDS1 | Leishmania major | 96% | 100% |
Q8I5R7 | Plasmodium falciparum (isolate 3D7) | 39% | 100% |
Q9FYR6 | Arabidopsis thaliana | 37% | 100% |
V5AZ66 | Trypanosoma cruzi | 63% | 100% |