Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
GO:0005829 | cytosol | 2 | 2 |
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 |
Related structures:
AlphaFold database: E9AV72
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 23 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 23 |
GO:0006399 | tRNA metabolic process | 7 | 23 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 23 |
GO:0006422 | aspartyl-tRNA aminoacylation | 7 | 23 |
GO:0006520 | amino acid metabolic process | 3 | 23 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 23 |
GO:0006807 | nitrogen compound metabolic process | 2 | 23 |
GO:0008152 | metabolic process | 1 | 23 |
GO:0009987 | cellular process | 1 | 23 |
GO:0016070 | RNA metabolic process | 5 | 23 |
GO:0019752 | carboxylic acid metabolic process | 5 | 23 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 23 |
GO:0034660 | ncRNA metabolic process | 6 | 23 |
GO:0043038 | amino acid activation | 4 | 23 |
GO:0043039 | tRNA aminoacylation | 5 | 23 |
GO:0043170 | macromolecule metabolic process | 3 | 23 |
GO:0043436 | oxoacid metabolic process | 4 | 23 |
GO:0044237 | cellular metabolic process | 2 | 23 |
GO:0044238 | primary metabolic process | 2 | 23 |
GO:0044281 | small molecule metabolic process | 2 | 23 |
GO:0046483 | heterocycle metabolic process | 3 | 23 |
GO:0071704 | organic substance metabolic process | 2 | 23 |
GO:0090304 | nucleic acid metabolic process | 4 | 23 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 23 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 23 |
GO:0003676 | nucleic acid binding | 3 | 21 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 23 |
GO:0004815 | aspartate-tRNA ligase activity | 5 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0005524 | ATP binding | 5 | 23 |
GO:0016874 | ligase activity | 2 | 23 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 23 |
GO:0017076 | purine nucleotide binding | 4 | 23 |
GO:0030554 | adenyl nucleotide binding | 5 | 23 |
GO:0032553 | ribonucleotide binding | 3 | 23 |
GO:0032555 | purine ribonucleotide binding | 4 | 23 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 23 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 23 |
GO:0036094 | small molecule binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043168 | anion binding | 3 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0097367 | carbohydrate derivative binding | 2 | 23 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 23 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 23 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 23 |
GO:1901265 | nucleoside phosphate binding | 3 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
GO:0003723 | RNA binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 547 | 551 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.321 |
CLV_PCSK_FUR_1 | 13 | 17 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.768 |
CLV_PCSK_PC1ET2_1 | 637 | 639 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.342 |
CLV_Separin_Metazoa | 413 | 417 | PF03568 | 0.463 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.512 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.500 |
DEG_APCC_DBOX_1 | 614 | 622 | PF00400 | 0.494 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.651 |
DEG_SPOP_SBC_1 | 200 | 204 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.720 |
DOC_ANK_TNKS_1 | 464 | 471 | PF00023 | 0.463 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.489 |
DOC_CKS1_1 | 79 | 84 | PF01111 | 0.565 |
DOC_MAPK_gen_1 | 145 | 154 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 519 | 528 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 585 | 592 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.503 |
DOC_PP1_RVXF_1 | 149 | 155 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 506 | 509 | PF00568 | 0.567 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.746 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.576 |
DOC_USP7_UBL2_3 | 585 | 589 | PF12436 | 0.442 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 104 | 114 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 257 | 266 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 435 | 440 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 477 | 481 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 581 | 587 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 627 | 632 | PF00244 | 0.478 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.485 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.541 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.513 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.535 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.482 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.461 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.514 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.553 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.553 |
LIG_LIR_Apic_2 | 504 | 509 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.488 |
LIG_PCNA_PIPBox_1 | 370 | 379 | PF02747 | 0.442 |
LIG_SH2_CRK | 540 | 544 | PF00017 | 0.449 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 556 | 560 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 305 | 308 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.489 |
LIG_SH3_1 | 540 | 546 | PF00018 | 0.463 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.469 |
LIG_SH3_2 | 549 | 554 | PF14604 | 0.550 |
LIG_SH3_2 | 633 | 638 | PF14604 | 0.543 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.651 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.544 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.712 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.581 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.546 |
LIG_SH3_3 | 630 | 636 | PF00018 | 0.483 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.753 |
LIG_SUMO_SIM_anti_2 | 360 | 367 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.698 |
LIG_SUMO_SIM_par_1 | 360 | 367 | PF11976 | 0.508 |
LIG_UBA3_1 | 384 | 390 | PF00899 | 0.382 |
LIG_WRC_WIRS_1 | 596 | 601 | PF05994 | 0.377 |
LIG_WW_3 | 413 | 417 | PF00397 | 0.299 |
MOD_CDK_SPK_2 | 277 | 282 | PF00069 | 0.320 |
MOD_CDK_SPxK_1 | 448 | 454 | PF00069 | 0.299 |
MOD_CDK_SPxxK_3 | 443 | 450 | PF00069 | 0.270 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.559 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.678 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.467 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.538 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.679 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.761 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.481 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.340 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.296 |
MOD_DYRK1A_RPxSP_1 | 195 | 199 | PF00069 | 0.410 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.669 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.411 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.437 |
MOD_GlcNHglycan | 469 | 473 | PF01048 | 0.330 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.691 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.320 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.690 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.320 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.663 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.628 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.772 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.620 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.559 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.412 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.486 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.395 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.324 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.622 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.441 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.695 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.695 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.714 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.755 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.438 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.536 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.653 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.333 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.394 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.421 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.262 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.393 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.798 |
MOD_NEK2_2 | 595 | 600 | PF00069 | 0.367 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.512 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.469 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.457 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.637 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.569 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.699 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.571 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.537 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.405 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.469 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.366 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.335 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.270 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.365 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.442 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.337 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.335 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.323 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.402 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.434 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.320 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.333 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.626 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.437 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.783 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 298 | 304 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 630 | 639 | PF00179 | 0.355 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.380 |
TRG_NES_CRM1_1 | 315 | 327 | PF08389 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 512 | 516 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P9 | Leptomonas seymouri | 60% | 98% |
A0A0N1HZP3 | Leptomonas seymouri | 43% | 100% |
A0A0N1IMR3 | Leptomonas seymouri | 26% | 72% |
A0A0S4IKL4 | Bodo saltans | 45% | 100% |
A0A0S4INT6 | Bodo saltans | 34% | 100% |
A0A0S4ISB0 | Bodo saltans | 49% | 100% |
A0A0S4JDH2 | Bodo saltans | 26% | 76% |
A0A1X0NXR0 | Trypanosomatidae | 53% | 100% |
A0A1X0P268 | Trypanosomatidae | 43% | 100% |
A0A1X0P9Y4 | Trypanosomatidae | 25% | 86% |
A0A3Q8IHQ2 | Leishmania donovani | 44% | 100% |
A0A3R7KLC9 | Trypanosoma rangeli | 54% | 100% |
A0A3R7LNW3 | Trypanosoma rangeli | 44% | 100% |
A0A3R7P1H1 | Trypanosoma rangeli | 25% | 85% |
A0A3S7WWM6 | Leishmania donovani | 90% | 99% |
A0A3S7X7X7 | Leishmania donovani | 25% | 72% |
A0PZX0 | Clostridium novyi (strain NT) | 22% | 100% |
A1JRL1 | Yersinia enterocolitica serotype O:8 / biotype 1B (strain NCTC 13174 / 8081) | 24% | 100% |
A2SPG1 | Methanocorpusculum labreanum (strain ATCC 43576 / DSM 4855 / Z) | 31% | 100% |
A4HBV0 | Leishmania braziliensis | 79% | 100% |
A4HHZ7 | Leishmania braziliensis | 44% | 100% |
A4I574 | Leishmania infantum | 44% | 100% |
A4IA13 | Leishmania infantum | 25% | 72% |
A4TJK5 | Yersinia pestis (strain Pestoides F) | 24% | 100% |
A5VMP9 | Limosilactobacillus reuteri (strain DSM 20016) | 25% | 100% |
A6LBU6 | Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / CIP 104284 / JCM 5825 / NCTC 11152) | 24% | 100% |
A6LNG3 | Thermosipho melanesiensis (strain DSM 12029 / CIP 104789 / BI429) | 24% | 100% |
A6LTP1 | Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) | 24% | 100% |
A6TB35 | Klebsiella pneumoniae subsp. pneumoniae (strain ATCC 700721 / MGH 78578) | 23% | 100% |
A7FID0 | Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) | 24% | 100% |
A7HME4 | Fervidobacterium nodosum (strain ATCC 35602 / DSM 5306 / Rt17-B1) | 25% | 100% |
A8ESW7 | Aliarcobacter butzleri (strain RM4018) | 22% | 100% |
A8F7R7 | Pseudothermotoga lettingae (strain ATCC BAA-301 / DSM 14385 / NBRC 107922 / TMO) | 24% | 100% |
A9KIA6 | Lachnoclostridium phytofermentans (strain ATCC 700394 / DSM 18823 / ISDg) | 25% | 100% |
A9QYX8 | Yersinia pestis bv. Antiqua (strain Angola) | 24% | 100% |
B0B8B6 | Chlamydia trachomatis serovar L2 (strain 434/Bu / ATCC VR-902B) | 26% | 100% |
B0B9Z5 | Chlamydia trachomatis serovar L2b (strain UCH-1/proctitis) | 26% | 100% |
B1HV71 | Lysinibacillus sphaericus (strain C3-41) | 25% | 100% |
B1JLL5 | Yersinia pseudotuberculosis serotype O:3 (strain YPIII) | 24% | 100% |
B2GA02 | Limosilactobacillus reuteri (strain JCM 1112) | 25% | 100% |
B2J116 | Nostoc punctiforme (strain ATCC 29133 / PCC 73102) | 26% | 100% |
B2K319 | Yersinia pseudotuberculosis serotype IB (strain PB1/+) | 24% | 100% |
B2RHE0 | Porphyromonas gingivalis (strain ATCC 33277 / DSM 20709 / CIP 103683 / JCM 12257 / NCTC 11834 / 2561) | 25% | 100% |
B2S3J9 | Treponema pallidum subsp. pallidum (strain SS14) | 26% | 100% |
B2TN05 | Clostridium botulinum (strain Eklund 17B / Type B) | 24% | 100% |
B2V351 | Clostridium botulinum (strain Alaska E43 / Type E3) | 24% | 100% |
B6JLK1 | Helicobacter pylori (strain P12) | 23% | 100% |
B7IE30 | Thermosipho africanus (strain TCF52B) | 24% | 100% |
C4ZI12 | Agathobacter rectalis (strain ATCC 33656 / DSM 3377 / JCM 17463 / KCTC 5835 / VPI 0990) | 25% | 100% |
C9ZMM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 86% |
C9ZQK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A1C3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AGV6 | Leishmania infantum | 92% | 100% |
E9B0H1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9B520 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 73% |
O83618 | Treponema pallidum (strain Nichols) | 26% | 100% |
O84546 | Chlamydia trachomatis (strain D/UW-3/Cx) | 26% | 100% |
P54263 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 27% | 100% |
Q17XK9 | Helicobacter acinonychis (strain Sheeba) | 22% | 100% |
Q1C820 | Yersinia pestis bv. Antiqua (strain Antiqua) | 24% | 100% |
Q1CJH0 | Yersinia pestis bv. Antiqua (strain Nepal516) | 24% | 100% |
Q1CTQ7 | Helicobacter pylori (strain HPAG1) | 24% | 100% |
Q2SR42 | Mycoplasma capricolum subsp. capricolum (strain California kid / ATCC 27343 / NCTC 10154) | 22% | 100% |
Q3KLF5 | Chlamydia trachomatis serovar A (strain ATCC VR-571B / DSM 19440 / HAR-13) | 26% | 100% |
Q46175 | Chlamydia caviae (strain ATCC VR-813 / DSM 19441 / 03DC25 / GPIC) | 25% | 100% |
Q4FMP8 | Pelagibacter ubique (strain HTCC1062) | 22% | 100% |
Q4Q7R2 | Leishmania major | 43% | 100% |
Q4QCA9 | Leishmania major | 91% | 100% |
Q5L734 | Chlamydia abortus (strain DSM 27085 / S26/3) | 26% | 100% |
Q66AU4 | Yersinia pseudotuberculosis serotype I (strain IP32953) | 24% | 100% |
Q6F1A0 | Mesoplasma florum (strain ATCC 33453 / NBRC 100688 / NCTC 11704 / L1) | 23% | 100% |
Q6FEH6 | Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) | 24% | 100% |
Q6LUN2 | Photobacterium profundum (strain SS9) | 22% | 100% |
Q7MXM0 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 25% | 100% |
Q831X4 | Enterococcus faecalis (strain ATCC 700802 / V583) | 29% | 100% |
Q892B2 | Clostridium tetani (strain Massachusetts / E88) | 22% | 100% |
Q8RGJ4 | Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / DSM 15643 / BCRC 10681 / CIP 101130 / JCM 8532 / KCTC 2640 / LMG 13131 / VPI 4355) | 24% | 100% |
Q8ZEV0 | Yersinia pestis | 24% | 100% |
Q980V3 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 30% | 100% |
V5AS93 | Trypanosoma cruzi | 44% | 100% |
V5DGS5 | Trypanosoma cruzi | 26% | 86% |