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 | 541 | 545 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.256 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 27 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 309 | 315 | PF00134 | 0.362 |
DOC_MAPK_gen_1 | 329 | 339 | PF00069 | 0.510 |
DOC_MAPK_JIP1_4 | 120 | 126 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 332 | 341 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.510 |
DOC_MAPK_RevD_3 | 45 | 61 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 165 | 172 | PF00149 | 0.494 |
DOC_PP1_RVXF_1 | 85 | 92 | PF00149 | 0.535 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.510 |
DOC_PP2B_LxvP_1 | 685 | 688 | PF13499 | 0.501 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 689 | 692 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 703 | 707 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 120 | 125 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 316 | 325 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 404 | 413 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 495 | 505 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 581 | 589 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 622 | 632 | PF00244 | 0.548 |
LIG_Actin_WH2_2 | 63 | 80 | PF00022 | 0.551 |
LIG_APCC_ABBA_1 | 155 | 160 | PF00400 | 0.254 |
LIG_APCC_ABBA_1 | 481 | 486 | PF00400 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.604 |
LIG_deltaCOP1_diTrp_1 | 363 | 373 | PF00928 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 627 | 631 | PF00928 | 0.397 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.576 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.497 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.542 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.521 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.510 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.510 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.481 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.525 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.475 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.542 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.595 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.563 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.389 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.522 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.521 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.507 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.517 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.511 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.597 |
LIG_LIR_Apic_2 | 351 | 355 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 626 | 635 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 710 | 719 | PF02991 | 0.572 |
LIG_LIR_LC3C_4 | 573 | 578 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 626 | 631 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 710 | 715 | PF02991 | 0.572 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.510 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.521 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.458 |
LIG_SH2_SRC | 225 | 228 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 390 | 394 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.510 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.510 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.423 |
LIG_SUMO_SIM_anti_2 | 35 | 43 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 382 | 388 | PF11976 | 0.571 |
LIG_SUMO_SIM_anti_2 | 498 | 505 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 99 | 105 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 122 | 129 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 382 | 388 | PF11976 | 0.571 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.549 |
LIG_TRAF2_1 | 512 | 515 | PF00917 | 0.553 |
LIG_TRAF2_1 | 659 | 662 | PF00917 | 0.509 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.432 |
LIG_WRC_WIRS_1 | 422 | 427 | PF05994 | 0.612 |
LIG_WW_3 | 492 | 496 | PF00397 | 0.421 |
MOD_CDK_SPxxK_3 | 353 | 360 | PF00069 | 0.521 |
MOD_CDK_SPxxK_3 | 544 | 551 | PF00069 | 0.510 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.621 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.515 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.425 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.563 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.395 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.522 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.528 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.503 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.449 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.517 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.511 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.510 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.425 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.514 |
MOD_Cter_Amidation | 404 | 407 | PF01082 | 0.321 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.610 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.681 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.322 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.282 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.305 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.597 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.395 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.537 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.462 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.510 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.535 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.524 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.510 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.597 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.325 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.498 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.310 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.207 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.505 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.496 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.525 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.614 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.515 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.493 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.496 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.614 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.531 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.425 |
MOD_PKA_1 | 656 | 662 | PF00069 | 0.510 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.510 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.597 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.535 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.558 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.550 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.476 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.551 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.612 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.535 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.521 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.535 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.524 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.496 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.588 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.521 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.626 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.521 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.510 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 374 | 377 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 5 | 15 | PF00179 | 0.359 |
MOD_SUMO_rev_2 | 72 | 80 | PF00179 | 0.571 |
TRG_DiLeu_BaEn_1 | 36 | 41 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_2 | 626 | 632 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 109 | 114 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 525 | 530 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 569 | 573 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY85 | Leptomonas seymouri | 82% | 100% |
A0A0S4JN58 | Bodo saltans | 56% | 88% |
A0A1X0P793 | Trypanosomatidae | 62% | 89% |
A0A3R7KPX0 | Trypanosoma rangeli | 64% | 84% |
A0A3S7WV15 | Leishmania donovani | 81% | 99% |
A0A3S7WV32 | Leishmania donovani | 89% | 99% |
A0M4Z3 | Gramella forsetii (strain KT0803) | 35% | 100% |
A3MV50 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 30% | 100% |
A4HXZ5 | Leishmania infantum | 89% | 89% |
A4HY00 | Leishmania infantum | 81% | 100% |
A4YI09 | Metallosphaera sedula (strain ATCC 51363 / DSM 5348 / JCM 9185 / NBRC 15509 / TH2) | 30% | 100% |
A5FA31 | Flavobacterium johnsoniae (strain ATCC 17061 / DSM 2064 / JCM 8514 / NBRC 14942 / NCIMB 11054 / UW101) | 35% | 100% |
A5UU62 | Roseiflexus sp. (strain RS-1) | 40% | 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% |
A7NKX0 | Roseiflexus castenholzii (strain DSM 13941 / HLO8) | 41% | 100% |
A8MC04 | Caldivirga maquilingensis (strain ATCC 700844 / DSM 13496 / JCM 10307 / IC-167) | 31% | 100% |
A8MLB3 | Alkaliphilus oremlandii (strain OhILAs) | 41% | 100% |
A9W9Q2 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 40% | 100% |
B0R3A3 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 39% | 100% |
B2A5T8 | Natranaerobius thermophilus (strain ATCC BAA-1301 / DSM 18059 / JW/NM-WN-LF) | 42% | 100% |
B2RJG1 | Porphyromonas gingivalis (strain ATCC 33277 / DSM 20709 / CIP 103683 / JCM 12257 / NCTC 11834 / 2561) | 37% | 100% |
B2UL92 | Akkermansia muciniphila (strain ATCC BAA-835 / DSM 22959 / JCM 33894 / BCRC 81048 / CCUG 64013 / CIP 107961 / Muc) | 36% | 100% |
B3EP23 | Chlorobium phaeobacteroides (strain BS1) | 40% | 100% |
B3ER64 | Amoebophilus asiaticus (strain 5a2) | 37% | 100% |
B3QPX3 | Chlorobaculum parvum (strain DSM 263 / NCIMB 8327) | 39% | 100% |
B4S9D5 | Prosthecochloris aestuarii (strain DSM 271 / SK 413) | 39% | 100% |
B4SG51 | Pelodictyon phaeoclathratiforme (strain DSM 5477 / BU-1) | 38% | 100% |
B7J1X2 | Borreliella burgdorferi (strain ZS7) | 36% | 100% |
B8G3V5 | Chloroflexus aggregans (strain MD-66 / DSM 9485) | 39% | 100% |
B8ZRT2 | Mycobacterium leprae (strain Br4923) | 40% | 100% |
B9LC55 | Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) | 40% | 100% |
B9LUM0 | Halorubrum lacusprofundi (strain ATCC 49239 / DSM 5036 / JCM 8891 / ACAM 34) | 39% | 100% |
D0A5B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 89% |
E9ARQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9ARQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O51363 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 36% | 100% |
O58734 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 34% | 100% |
O60155 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 44% | 100% |
P38708 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
Q0SNA5 | Borreliella afzelii (strain PKo) | 35% | 100% |
Q18CD7 | Clostridioides difficile (strain 630) | 41% | 100% |
Q1J0W2 | Deinococcus geothermalis (strain DSM 11300 / AG-3a) | 36% | 100% |
Q2ILX2 | Anaeromyxobacter dehalogenans (strain 2CP-C) | 40% | 100% |
Q2W136 | Magnetospirillum magneticum (strain AMB-1 / ATCC 700264) | 36% | 100% |
Q3ASP3 | Chlorobium chlorochromatii (strain CaD3) | 38% | 100% |
Q3IS99 | Natronomonas pharaonis (strain ATCC 35678 / DSM 2160 / CIP 103997 / JCM 8858 / NBRC 14720 / NCIMB 2260 / Gabara) | 39% | 100% |
Q46G28 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 33% | 100% |
Q4A5S0 | Mycoplasmopsis synoviae (strain 53) | 34% | 100% |
Q4J8L4 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 30% | 100% |
Q4QDS0 | Leishmania major | 80% | 100% |
Q4QDS1 | Leishmania major | 87% | 100% |
Q5JF49 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 32% | 100% |
Q5LCF0 | Bacteroides fragilis (strain ATCC 25285 / DSM 2151 / CCUG 4856 / JCM 11019 / NCTC 9343 / Onslow) | 36% | 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) | 36% | 100% |
Q67PA6 | Symbiobacterium thermophilum (strain T / IAM 14863) | 41% | 100% |
Q6MIW2 | Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIMB 9529 / HD100) | 35% | 100% |
Q7MVS7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 36% | 100% |
Q81Z76 | Bacillus anthracis | 40% | 100% |
Q8A988 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 36% | 100% |
Q8I5R7 | Plasmodium falciparum (isolate 3D7) | 39% | 96% |
Q8KCD1 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 39% | 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% |
Q8TJA2 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 34% | 100% |
Q971B5 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 29% | 100% |
Q9FYR6 | Arabidopsis thaliana | 38% | 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) | 40% | 100% |
Q9M1R2 | Arabidopsis thaliana | 53% | 100% |
Q9RUW4 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 35% | 100% |
Q9V022 | Pyrococcus abyssi (strain GE5 / Orsay) | 33% | 100% |
Q9Y9G0 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 32% | 100% |
Q9Z5I7 | Mycobacterium leprae (strain TN) | 40% | 100% |
V5AZ66 | Trypanosoma cruzi | 64% | 89% |