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: 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:0017101 | aminoacyl-tRNA synthetase multienzyme complex | 3 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0140535 | intracellular protein-containing complex | 2 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:0016020 | membrane | 2 | 1 |
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 | 552 | 556 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.341 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.766 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.319 |
DEG_COP1_1 | 637 | 646 | PF00400 | 0.401 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.690 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 142 | 151 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 486 | 494 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 569 | 577 | PF00069 | 0.488 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 84 | 91 | PF00149 | 0.513 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 696 | 699 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.488 |
DOC_PP4_FxxP_1 | 44 | 47 | PF00568 | 0.470 |
DOC_PP4_FxxP_1 | 464 | 467 | PF00568 | 0.488 |
DOC_PP4_FxxP_1 | 700 | 703 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.488 |
DOC_USP7_MATH_2 | 92 | 98 | PF00917 | 0.456 |
DOC_USP7_UBL2_3 | 715 | 719 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 415 | 424 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 506 | 516 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 597 | 601 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 633 | 643 | PF00244 | 0.532 |
LIG_Actin_WH2_2 | 117 | 132 | PF00022 | 0.549 |
LIG_APCC_ABBA_1 | 492 | 497 | PF00400 | 0.421 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_Clathr_ClatBox_1 | 148 | 152 | PF01394 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 374 | 384 | PF00928 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 638 | 642 | PF00928 | 0.373 |
LIG_EH1_1 | 118 | 126 | PF00400 | 0.403 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.554 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.500 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.488 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.510 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.481 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.462 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.456 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.323 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.529 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.575 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.546 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.368 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.500 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.725 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.485 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.495 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.489 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.770 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 362 | 366 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 461 | 467 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 637 | 646 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 722 | 731 | PF02991 | 0.551 |
LIG_LIR_LC3C_4 | 146 | 150 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 637 | 642 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 722 | 727 | PF02991 | 0.551 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.358 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.488 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 401 | 405 | PF00017 | 0.500 |
LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.438 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.488 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.470 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.500 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.399 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 11 | 18 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 393 | 399 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 509 | 516 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 62 | 67 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 97 | 104 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 121 | 126 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 393 | 399 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.472 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.528 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.531 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.521 |
LIG_TRAF2_1 | 670 | 673 | PF00917 | 0.493 |
LIG_TRFH_1 | 136 | 140 | PF08558 | 0.474 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.411 |
LIG_UBA3_1 | 112 | 118 | PF00899 | 0.538 |
LIG_UBA3_1 | 12 | 17 | PF00899 | 0.519 |
LIG_WRC_WIRS_1 | 433 | 438 | PF05994 | 0.590 |
LIG_WW_3 | 503 | 507 | PF00397 | 0.398 |
MOD_CDK_SPxxK_3 | 364 | 371 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 555 | 562 | PF00069 | 0.488 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.678 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.500 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.374 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.482 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.667 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.706 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.563 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.428 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.495 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.489 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.488 |
MOD_Cter_Amidation | 415 | 418 | PF01082 | 0.300 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.509 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.587 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.704 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.276 |
MOD_GlcNHglycan | 250 | 254 | PF01048 | 0.261 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.367 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.288 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.511 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.479 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.512 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.503 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.488 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.575 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.332 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.484 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.282 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.677 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.592 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.505 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.546 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.504 |
MOD_PKA_1 | 667 | 673 | PF00069 | 0.488 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.488 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.552 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.503 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.511 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.555 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.537 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.461 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.529 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.590 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.513 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.556 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.503 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.494 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.546 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.500 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.505 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.575 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.500 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.542 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.500 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.476 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.479 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 226 | 229 | PF00179 | 0.428 |
MOD_SUMO_for_1 | 385 | 388 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 214 | 222 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 669 | 677 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 11 | 16 | PF01217 | 0.505 |
TRG_DiLeu_BaEn_2 | 637 | 643 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 633 | 636 | PF00400 | 0.574 |
TRG_NES_CRM1_1 | 11 | 22 | PF08389 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.203 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY85 | Leptomonas seymouri | 82% | 100% |
A0A0S4JN58 | Bodo saltans | 59% | 89% |
A0A1X0P793 | Trypanosomatidae | 67% | 90% |
A0A3R7KPX0 | Trypanosoma rangeli | 68% | 85% |
A0A3S7WV15 | Leishmania donovani | 96% | 100% |
A0A3S7WV32 | Leishmania donovani | 87% | 100% |
A0M4Z3 | Gramella forsetii (strain KT0803) | 35% | 100% |
A4H9N1 | Leishmania braziliensis | 80% | 100% |
A4HXZ5 | Leishmania infantum | 87% | 90% |
A4HY00 | Leishmania infantum | 96% | 100% |
A5FA31 | Flavobacterium johnsoniae (strain ATCC 17061 / DSM 2064 / JCM 8514 / NBRC 14942 / NCIMB 11054 / UW101) | 35% | 100% |
A6L5I2 | Phocaeicola vulgatus (strain ATCC 8482 / DSM 1447 / JCM 5826 / CCUG 4940 / NBRC 14291 / NCTC 11154) | 37% | 100% |
A6LAP3 | Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / CIP 104284 / JCM 5825 / NCTC 11152) | 35% | 100% |
B0R3A3 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 39% | 100% |
B2RJG1 | Porphyromonas gingivalis (strain ATCC 33277 / DSM 20709 / CIP 103683 / JCM 12257 / NCTC 11834 / 2561) | 37% | 100% |
B3ER64 | Amoebophilus asiaticus (strain 5a2) | 37% | 100% |
B7J1X2 | Borreliella burgdorferi (strain ZS7) | 37% | 100% |
B9LUM0 | Halorubrum lacusprofundi (strain ATCC 49239 / DSM 5036 / JCM 8891 / ACAM 34) | 41% | 100% |
D0A5B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 90% |
E9ARQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9ARQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O51363 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 37% | 100% |
O60155 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 45% | 100% |
P38708 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
Q0SNA5 | Borreliella afzelii (strain PKo) | 36% | 100% |
Q11Q45 | Cytophaga hutchinsonii (strain ATCC 33406 / DSM 1761 / CIP 103989 / NBRC 15051 / NCIMB 9469 / D465) | 34% | 100% |
Q18JG3 | Haloquadratum walsbyi (strain DSM 16790 / HBSQ001) | 40% | 100% |
Q1GTS7 | Sphingopyxis alaskensis (strain DSM 13593 / LMG 18877 / RB2256) | 36% | 100% |
Q1J0W2 | Deinococcus geothermalis (strain DSM 11300 / AG-3a) | 35% | 100% |
Q2ILX2 | Anaeromyxobacter dehalogenans (strain 2CP-C) | 39% | 100% |
Q2RZJ2 | Salinibacter ruber (strain DSM 13855 / M31) | 35% | 100% |
Q2W136 | Magnetospirillum magneticum (strain AMB-1 / ATCC 700264) | 36% | 100% |
Q4QDS1 | Leishmania major | 89% | 100% |
Q5LCF0 | Bacteroides fragilis (strain ATCC 25285 / DSM 2151 / CCUG 4856 / JCM 11019 / NCTC 9343 / Onslow) | 37% | 100% |
Q64TJ6 | Bacteroides fragilis (strain YCH46) | 37% | 100% |
Q661L6 | Borrelia garinii subsp. bavariensis (strain ATCC BAA-2496 / DSM 23469 / PBi) | 37% | 100% |
Q67PA6 | Symbiobacterium thermophilum (strain T / IAM 14863) | 41% | 100% |
Q6MIW2 | Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIMB 9529 / HD100) | 36% | 100% |
Q7MVS7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 37% | 100% |
Q7UGJ7 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 35% | 100% |
Q7X2P1 | Sphingomonas elodea | 35% | 100% |
Q81Z76 | Bacillus anthracis | 41% | 100% |
Q8A988 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 37% | 100% |
Q8I5R7 | Plasmodium falciparum (isolate 3D7) | 40% | 98% |
Q8SSD7 | Encephalitozoon cuniculi (strain GB-M1) | 49% | 100% |
Q9FYR6 | Arabidopsis thaliana | 37% | 100% |
Q9HS52 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 39% | 100% |
Q9M1R2 | Arabidopsis thaliana | 54% | 100% |
Q9RUW4 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 36% | 100% |
V5AZ66 | Trypanosoma cruzi | 67% | 90% |