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: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 |
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 | 537 | 541 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.334 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 316 | 322 | PF00134 | 0.350 |
DOC_MAPK_gen_1 | 118 | 125 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 142 | 151 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 336 | 346 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 339 | 348 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 482 | 490 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 554 | 562 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 84 | 91 | PF00149 | 0.527 |
DOC_PP2B_LxvP_1 | 405 | 408 | PF13499 | 0.502 |
DOC_PP2B_LxvP_1 | 681 | 684 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.502 |
DOC_PP4_FxxP_1 | 44 | 47 | PF00568 | 0.484 |
DOC_PP4_FxxP_1 | 460 | 463 | PF00568 | 0.502 |
DOC_PP4_FxxP_1 | 685 | 688 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.502 |
DOC_USP7_MATH_2 | 92 | 98 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 699 | 703 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 119 | 124 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 411 | 420 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 502 | 512 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 582 | 586 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 618 | 628 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 117 | 132 | PF00022 | 0.566 |
LIG_APCC_ABBA_1 | 488 | 493 | PF00400 | 0.431 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.642 |
LIG_Clathr_ClatBox_1 | 148 | 152 | PF01394 | 0.498 |
LIG_deltaCOP1_diTrp_1 | 370 | 380 | PF00928 | 0.514 |
LIG_deltaCOP1_diTrp_1 | 623 | 627 | PF00928 | 0.386 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.570 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.514 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.502 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.524 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.502 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.476 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.461 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.544 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.594 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.557 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.378 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.514 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.517 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.499 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.509 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.503 |
LIG_FHA_2 | 665 | 671 | PF00498 | 0.535 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.594 |
LIG_LIR_Apic_2 | 358 | 362 | PF02991 | 0.502 |
LIG_LIR_Apic_2 | 457 | 463 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 622 | 631 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 706 | 715 | PF02991 | 0.567 |
LIG_LIR_LC3C_4 | 146 | 150 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 622 | 627 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 706 | 711 | PF02991 | 0.567 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.502 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.514 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.447 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.502 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.484 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.514 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 389 | 395 | PF11976 | 0.566 |
LIG_SUMO_SIM_anti_2 | 505 | 512 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 62 | 67 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 97 | 104 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 121 | 126 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 389 | 395 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.486 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.542 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.546 |
LIG_TRAF2_1 | 655 | 658 | PF00917 | 0.507 |
LIG_TRFH_1 | 136 | 140 | PF08558 | 0.498 |
LIG_TYR_ITIM | 242 | 247 | PF00017 | 0.419 |
LIG_UBA3_1 | 112 | 118 | PF00899 | 0.561 |
LIG_UBA3_1 | 12 | 17 | PF00899 | 0.536 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.614 |
LIG_WW_3 | 499 | 503 | PF00397 | 0.407 |
MOD_CDK_SPxxK_3 | 360 | 367 | PF00069 | 0.514 |
MOD_CDK_SPxxK_3 | 540 | 547 | PF00069 | 0.502 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.676 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.514 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.384 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.484 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.508 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.492 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.590 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.444 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.509 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.503 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.502 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.314 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.491 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.613 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.686 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.315 |
MOD_GlcNHglycan | 246 | 250 | PF01048 | 0.280 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.386 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.302 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.525 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.502 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.527 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.520 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.502 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.594 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.347 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.492 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.302 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.493 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.613 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.519 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.569 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.528 |
MOD_PKA_1 | 652 | 658 | PF00069 | 0.502 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.502 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.594 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.527 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.554 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.572 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.507 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.469 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.544 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.614 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.527 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.573 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.520 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.514 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.569 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.527 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.516 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.529 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.594 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.514 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.543 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.514 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.503 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.502 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.602 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.436 |
MOD_SUMO_for_1 | 381 | 384 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 210 | 218 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 654 | 662 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_2 | 622 | 628 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.594 |
TRG_NES_CRM1_1 | 11 | 22 | PF08389 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY85 | Leptomonas seymouri | 83% | 100% |
A0A0S4JN58 | Bodo saltans | 59% | 87% |
A0A1X0P793 | Trypanosomatidae | 67% | 88% |
A0A3R7KPX0 | Trypanosoma rangeli | 67% | 84% |
A0A3S7WV15 | Leishmania donovani | 94% | 99% |
A0A3S7WV32 | Leishmania donovani | 85% | 99% |
A0M4Z3 | Gramella forsetii (strain KT0803) | 35% | 100% |
A0Q2I3 | Clostridium novyi (strain NT) | 42% | 100% |
A1RSR6 | Pyrobaculum islandicum (strain DSM 4184 / JCM 9189 / GEO3) | 28% | 100% |
A1RYD8 | Thermofilum pendens (strain DSM 2475 / Hrk 5) | 34% | 100% |
A2ST96 | Methanocorpusculum labreanum (strain ATCC 43576 / DSM 4855 / Z) | 33% | 100% |
A3MV50 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 30% | 100% |
A4H9N1 | Leishmania braziliensis | 80% | 99% |
A4HXZ5 | Leishmania infantum | 84% | 88% |
A4HY00 | Leishmania infantum | 94% | 99% |
A4WJ22 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 28% | 100% |
A4YI09 | Metallosphaera sedula (strain ATCC 51363 / DSM 5348 / JCM 9185 / NBRC 15509 / TH2) | 31% | 100% |
A5FA31 | Flavobacterium johnsoniae (strain ATCC 17061 / DSM 2064 / JCM 8514 / NBRC 14942 / NCIMB 11054 / UW101) | 35% | 100% |
A5I768 | Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A) | 40% | 100% |
A5UU62 | Roseiflexus sp. (strain RS-1) | 41% | 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) | 36% | 100% |
A7FYU0 | Clostridium botulinum (strain ATCC 19397 / Type A) | 40% | 100% |
A7GIT0 | Clostridium botulinum (strain Langeland / NCTC 10281 / Type F) | 40% | 100% |
A7I9R7 | Methanoregula boonei (strain DSM 21154 / JCM 14090 / 6A8) | 31% | 100% |
A7NKX0 | Roseiflexus castenholzii (strain DSM 13941 / HLO8) | 42% | 100% |
A8A9E3 | Ignicoccus hospitalis (strain KIN4/I / DSM 18386 / JCM 14125) | 31% | 100% |
A8MC04 | Caldivirga maquilingensis (strain ATCC 700844 / DSM 13496 / JCM 10307 / IC-167) | 31% | 100% |
A8MLB3 | Alkaliphilus oremlandii (strain OhILAs) | 42% | 100% |
A9KL35 | Lachnoclostridium phytofermentans (strain ATCC 700394 / DSM 18823 / ISDg) | 42% | 100% |
A9W9Q2 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 39% | 100% |
B0R3A3 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 39% | 100% |
B1IFI2 | Clostridium botulinum (strain Okra / Type B1) | 40% | 100% |
B1L224 | Clostridium botulinum (strain Loch Maree / Type A3) | 39% | 100% |
B1Y963 | Pyrobaculum neutrophilum (strain DSM 2338 / JCM 9278 / NBRC 100436 / V24Sta) | 28% | 100% |
B2A5T8 | Natranaerobius thermophilus (strain ATCC BAA-1301 / DSM 18059 / JW/NM-WN-LF) | 41% | 100% |
B2RJG1 | Porphyromonas gingivalis (strain ATCC 33277 / DSM 20709 / CIP 103683 / JCM 12257 / NCTC 11834 / 2561) | 38% | 100% |
B2UL92 | Akkermansia muciniphila (strain ATCC BAA-835 / DSM 22959 / JCM 33894 / BCRC 81048 / CCUG 64013 / CIP 107961 / Muc) | 35% | 100% |
B3EP23 | Chlorobium phaeobacteroides (strain BS1) | 40% | 100% |
B3ER64 | Amoebophilus asiaticus (strain 5a2) | 37% | 100% |
B3QPX3 | Chlorobaculum parvum (strain DSM 263 / NCIMB 8327) | 41% | 100% |
B4S9D5 | Prosthecochloris aestuarii (strain DSM 271 / SK 413) | 40% | 100% |
B4SG51 | Pelodictyon phaeoclathratiforme (strain DSM 5477 / BU-1) | 39% | 100% |
B7J1X2 | Borreliella burgdorferi (strain ZS7) | 37% | 100% |
B8G3V5 | Chloroflexus aggregans (strain MD-66 / DSM 9485) | 39% | 100% |
B8I5R4 | Ruminiclostridium cellulolyticum (strain ATCC 35319 / DSM 5812 / JCM 6584 / H10) | 42% | 100% |
B8ZRT2 | Mycobacterium leprae (strain Br4923) | 39% | 100% |
B9LC55 | Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) | 39% | 100% |
B9LUM0 | Halorubrum lacusprofundi (strain ATCC 49239 / DSM 5036 / JCM 8891 / ACAM 34) | 42% | 100% |
C1FM10 | Clostridium botulinum (strain Kyoto / Type A2) | 40% | 100% |
C3KUV8 | Clostridium botulinum (strain 657 / Type Ba4) | 39% | 100% |
C4Z1D7 | Lachnospira eligens (strain ATCC 27750 / DSM 3376 / VPI C15-48 / C15-B4) | 41% | 100% |
C4ZC24 | Agathobacter rectalis (strain ATCC 33656 / DSM 3377 / JCM 17463 / KCTC 5835 / VPI 0990) | 40% | 100% |
D0A5B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 88% |
E9ARQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O51363 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 37% | 100% |
O58734 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 33% | 100% |
O60155 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
P38708 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
Q0SAY4 | Rhodococcus jostii (strain RHA1) | 38% | 100% |
Q0SNA5 | Borreliella afzelii (strain PKo) | 37% | 100% |
Q11Q45 | Cytophaga hutchinsonii (strain ATCC 33406 / DSM 1761 / CIP 103989 / NBRC 15051 / NCIMB 9469 / D465) | 35% | 100% |
Q12ZC6 | Methanococcoides burtonii (strain DSM 6242 / NBRC 107633 / OCM 468 / ACE-M) | 32% | 100% |
Q18CD7 | Clostridioides difficile (strain 630) | 41% | 100% |
Q18JG3 | Haloquadratum walsbyi (strain DSM 16790 / HBSQ001) | 39% | 100% |
Q1CXV1 | Myxococcus xanthus (strain DK1622) | 37% | 100% |
Q1J0W2 | Deinococcus geothermalis (strain DSM 11300 / AG-3a) | 35% | 100% |
Q2FLY5 | Methanospirillum hungatei JF-1 (strain ATCC 27890 / DSM 864 / NBRC 100397 / JF-1) | 35% | 100% |
Q2ILX2 | Anaeromyxobacter dehalogenans (strain 2CP-C) | 38% | 100% |
Q2RZJ2 | Salinibacter ruber (strain DSM 13855 / M31) | 36% | 100% |
Q2W136 | Magnetospirillum magneticum (strain AMB-1 / ATCC 700264) | 36% | 100% |
Q3ASP3 | Chlorobium chlorochromatii (strain CaD3) | 39% | 100% |
Q3IS99 | Natronomonas pharaonis (strain ATCC 35678 / DSM 2160 / CIP 103997 / JCM 8858 / NBRC 14720 / NCIMB 2260 / Gabara) | 38% | 100% |
Q46G28 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 32% | 100% |
Q4A5S0 | Mycoplasmopsis synoviae (strain 53) | 35% | 100% |
Q4J8L4 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 30% | 100% |
Q4QDS0 | Leishmania major | 94% | 100% |
Q4QDS1 | Leishmania major | 84% | 100% |
Q5JF49 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 33% | 100% |
Q5LCF0 | Bacteroides fragilis (strain ATCC 25285 / DSM 2151 / CCUG 4856 / JCM 11019 / NCTC 9343 / Onslow) | 36% | 100% |
Q5SM28 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 42% | 100% |
Q5V5H0 | Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) | 37% | 100% |
Q64TJ6 | Bacteroides fragilis (strain YCH46) | 36% | 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% |
Q72GF9 | Thermus thermophilus (strain ATCC BAA-163 / DSM 7039 / HB27) | 42% | 100% |
Q7MVS7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 38% | 100% |
Q7X2P1 | Sphingomonas elodea | 36% | 100% |
Q81Z76 | Bacillus anthracis | 42% | 100% |
Q8A988 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 36% | 100% |
Q8ESQ5 | Oceanobacillus iheyensis (strain DSM 14371 / CIP 107618 / JCM 11309 / KCTC 3954 / HTE831) | 39% | 100% |
Q8I5R7 | Plasmodium falciparum (isolate 3D7) | 39% | 96% |
Q8KCD1 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 40% | 100% |
Q8PYZ1 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 32% | 100% |
Q8SSD7 | Encephalitozoon cuniculi (strain GB-M1) | 48% | 100% |
Q8U1C4 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 34% | 100% |
Q8ZVQ9 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 28% | 100% |
Q971B5 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 29% | 100% |
Q9FYR6 | Arabidopsis thaliana | 37% | 100% |
Q9HS52 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 39% | 100% |
Q9L4Q8 | Acetoanaerobium sticklandii (strain ATCC 12662 / DSM 519 / JCM 1433 / CCUG 9281 / NCIMB 10654 / HF) | 41% | 100% |
Q9M1R2 | Arabidopsis thaliana | 52% | 100% |
Q9RUW4 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 36% | 100% |
Q9V022 | Pyrococcus abyssi (strain GE5 / Orsay) | 32% | 100% |
Q9Y9G0 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 32% | 100% |
Q9Z5I7 | Mycobacterium leprae (strain TN) | 39% | 100% |
V5AZ66 | Trypanosoma cruzi | 67% | 88% |