Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | yes | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q131
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 2 |
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
GO:0006426 | glycyl-tRNA aminoacylation | 7 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043038 | amino acid activation | 4 | 12 |
GO:0043039 | tRNA aminoacylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0070127 | tRNA aminoacylation for mitochondrial protein translation | 7 | 2 |
GO:0070150 | mitochondrial glycyl-tRNA aminoacylation | 8 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
GO:0004820 | glycine-tRNA ligase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 499 | 501 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.602 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.706 |
DEG_ODPH_VHL_1 | 509 | 521 | PF01847 | 0.560 |
DOC_CYCLIN_RxL_1 | 383 | 393 | PF00134 | 0.708 |
DOC_CYCLIN_yCln2_LP_2 | 562 | 568 | PF00134 | 0.549 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.674 |
DOC_MAPK_DCC_7 | 513 | 521 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 24 | 33 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 259 | 268 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 554 | 564 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 513 | 521 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.549 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.587 |
DOC_PP2B_LxvP_1 | 562 | 565 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 166 | 169 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.599 |
DOC_PP4_MxPP_1 | 144 | 147 | PF00568 | 0.363 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.469 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.616 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 323 | 333 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 500 | 506 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.635 |
LIG_AP2alpha_1 | 166 | 170 | PF02296 | 0.478 |
LIG_AP2alpha_2 | 168 | 170 | PF02296 | 0.553 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.528 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.401 |
LIG_deltaCOP1_diTrp_1 | 267 | 275 | PF00928 | 0.605 |
LIG_EH_1 | 163 | 167 | PF12763 | 0.456 |
LIG_EH1_1 | 472 | 480 | PF00400 | 0.574 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.462 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.694 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.671 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.673 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.410 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.449 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.575 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.610 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.603 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.549 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.405 |
LIG_LIR_Apic_2 | 247 | 252 | PF02991 | 0.593 |
LIG_LIR_Apic_2 | 267 | 272 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 377 | 382 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 258 | 268 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 611 | 620 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 91 | 98 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 611 | 615 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.476 |
LIG_MYND_1 | 507 | 511 | PF01753 | 0.649 |
LIG_MYND_3 | 591 | 595 | PF01753 | 0.487 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.566 |
LIG_Pex14_1 | 271 | 275 | PF04695 | 0.540 |
LIG_Pex14_1 | 60 | 64 | PF04695 | 0.375 |
LIG_Pex14_2 | 112 | 116 | PF04695 | 0.491 |
LIG_Pex14_2 | 166 | 170 | PF04695 | 0.417 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.596 |
LIG_SH2_GRB2like | 411 | 414 | PF00017 | 0.634 |
LIG_SH2_NCK_1 | 556 | 560 | PF00017 | 0.549 |
LIG_SH2_SRC | 379 | 382 | PF00017 | 0.721 |
LIG_SH2_SRC | 411 | 414 | PF00017 | 0.659 |
LIG_SH2_STAT3 | 619 | 622 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.530 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.706 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.573 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.549 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.613 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.719 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.634 |
LIG_TRAF2_1 | 439 | 442 | PF00917 | 0.738 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.705 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.431 |
LIG_TRFH_1 | 43 | 47 | PF08558 | 0.442 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.555 |
LIG_TYR_ITSM | 342 | 349 | PF00017 | 0.577 |
LIG_UBA3_1 | 388 | 394 | PF00899 | 0.700 |
LIG_UBA3_1 | 516 | 522 | PF00899 | 0.610 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.695 |
LIG_WRC_WIRS_1 | 502 | 507 | PF05994 | 0.670 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.401 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.638 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.569 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.440 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.574 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.684 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.708 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.639 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.497 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.626 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.549 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.421 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.386 |
MOD_Cter_Amidation | 401 | 404 | PF01082 | 0.505 |
MOD_Cter_Amidation | 552 | 555 | PF01082 | 0.349 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.470 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.517 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.396 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.467 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.490 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.596 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.662 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.410 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.409 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.376 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.497 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.614 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.391 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.642 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.610 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.566 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.567 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.617 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.422 |
MOD_NEK2_2 | 576 | 581 | PF00069 | 0.549 |
MOD_OFUCOSY | 71 | 77 | PF10250 | 0.620 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.613 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.635 |
MOD_PK_1 | 539 | 545 | PF00069 | 0.635 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.655 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.549 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.413 |
MOD_PKB_1 | 237 | 245 | PF00069 | 0.581 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.578 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.573 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.593 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.704 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.571 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.654 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.419 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.391 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.577 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.571 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.653 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.441 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.681 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.641 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.549 |
MOD_SUMO_for_1 | 592 | 595 | PF00179 | 0.598 |
MOD_SUMO_for_1 | 9 | 12 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 289 | 296 | PF00179 | 0.677 |
MOD_SUMO_rev_2 | 451 | 460 | PF00179 | 0.648 |
TRG_DiLeu_BaEn_1 | 133 | 138 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_2 | 244 | 250 | PF01217 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZB0 | Leptomonas seymouri | 85% | 95% |
A0A0S4JJA5 | Bodo saltans | 66% | 100% |
A0A1X0P3R2 | Trypanosomatidae | 72% | 100% |
A0A3Q8IPA6 | Leishmania donovani | 97% | 100% |
A0A422MT81 | Trypanosoma rangeli | 70% | 100% |
A0B5U4 | Methanothrix thermoacetophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) | 37% | 100% |
A4FZX1 | Methanococcus maripaludis (strain C5 / ATCC BAA-1333) | 37% | 100% |
A4HPQ1 | Leishmania braziliensis | 93% | 100% |
A4ID12 | Leishmania infantum | 98% | 100% |
A6URK3 | Methanococcus vannielii (strain ATCC 35089 / DSM 1224 / JCM 13029 / OCM 148 / SB) | 37% | 100% |
A6VIK1 | Methanococcus maripaludis (strain C7 / ATCC BAA-1331) | 38% | 100% |
A9A885 | Methanococcus maripaludis (strain C6 / ATCC BAA-1332) | 38% | 100% |
C5A1H0 | Thermococcus gammatolerans (strain DSM 15229 / JCM 11827 / EJ3) | 37% | 100% |
C6A317 | Thermococcus sibiricus (strain DSM 12597 / MM 739) | 37% | 100% |
D0A8G2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9ATG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O23627 | Arabidopsis thaliana | 48% | 86% |
O27874 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 40% | 100% |
O29346 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 39% | 100% |
O59235 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 36% | 100% |
P38088 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 44% | 91% |
P41250 | Homo sapiens | 44% | 85% |
P56206 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 29% | 100% |
Q04451 | Bombyx mori | 44% | 86% |
Q06817 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 42% | 100% |
Q10039 | Caenorhabditis elegans | 44% | 85% |
Q10179 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 96% |
Q57681 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 40% | 100% |
Q5I0G4 | Rattus norvegicus | 45% | 86% |
Q5JID8 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 36% | 100% |
Q5RBL1 | Pongo abelii | 45% | 85% |
Q6M0Q7 | Methanococcus maripaludis (strain S2 / LL) | 37% | 100% |
Q72L85 | Thermus thermophilus (strain ATCC BAA-163 / DSM 7039 / HB27) | 28% | 100% |
Q7UEU9 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 27% | 100% |
Q8SQZ6 | Encephalitozoon cuniculi (strain GB-M1) | 41% | 100% |
Q8TYY9 | Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) | 37% | 100% |
Q8U0G2 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 36% | 100% |
Q9CZD3 | Mus musculus | 45% | 86% |
Q9V176 | Pyrococcus abyssi (strain GE5 / Orsay) | 36% | 100% |
Q9VUK8 | Drosophila melanogaster | 45% | 82% |
Q9YBF8 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 34% | 100% |
V5AU76 | Trypanosoma cruzi | 70% | 100% |