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. | no | 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. | no | 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:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HPQ1
Term | Name | Level | Count |
---|---|---|---|
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: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 |
GO:0000959 | mitochondrial RNA metabolic process | 6 | 1 |
GO:0070127 | tRNA aminoacylation for mitochondrial protein translation | 7 | 1 |
GO:0070150 | mitochondrial glycyl-tRNA aminoacylation | 8 | 1 |
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_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.297 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.254 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.497 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.626 |
DEG_ODPH_VHL_1 | 508 | 520 | PF01847 | 0.454 |
DOC_CYCLIN_RxL_1 | 382 | 392 | PF00134 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 561 | 567 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 602 | 608 | PF00134 | 0.575 |
DOC_MAPK_DCC_7 | 512 | 520 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 23 | 32 | PF00069 | 0.288 |
DOC_MAPK_gen_1 | 553 | 563 | PF00069 | 0.444 |
DOC_MAPK_JIP1_4 | 521 | 527 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 557 | 565 | PF00069 | 0.444 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 561 | 564 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.357 |
DOC_PP4_FxxP_1 | 248 | 251 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.382 |
DOC_USP7_UBL2_3 | 254 | 258 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.301 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 499 | 505 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 538 | 543 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 589 | 599 | PF00244 | 0.446 |
LIG_AP2alpha_1 | 165 | 169 | PF02296 | 0.357 |
LIG_AP2alpha_2 | 167 | 169 | PF02296 | 0.423 |
LIG_APCC_ABBA_1 | 307 | 312 | PF00400 | 0.481 |
LIG_APCC_ABBAyCdc20_2 | 306 | 312 | PF00400 | 0.427 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.467 |
LIG_BIR_III_4 | 139 | 143 | PF00653 | 0.436 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.275 |
LIG_deltaCOP1_diTrp_1 | 266 | 270 | PF00928 | 0.490 |
LIG_EH1_1 | 471 | 479 | PF00400 | 0.469 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.361 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.611 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.580 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.586 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.463 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.538 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.329 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.211 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.471 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.444 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.299 |
LIG_LIR_Apic_2 | 164 | 168 | PF02991 | 0.203 |
LIG_LIR_Apic_2 | 246 | 251 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 376 | 381 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 610 | 619 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 90 | 97 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.370 |
LIG_MYND_1 | 506 | 510 | PF01753 | 0.559 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.461 |
LIG_Pex14_1 | 59 | 63 | PF04695 | 0.268 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.401 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.290 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.491 |
LIG_SH2_GRB2like | 410 | 413 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 555 | 559 | PF00017 | 0.444 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.621 |
LIG_SH2_STAT3 | 618 | 621 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.430 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.508 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.444 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.508 |
LIG_SUMO_SIM_anti_2 | 523 | 530 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 432 | 438 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 523 | 530 | PF11976 | 0.470 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.531 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.652 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.623 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.323 |
LIG_TRFH_1 | 42 | 46 | PF08558 | 0.335 |
LIG_TYR_ITIM | 477 | 482 | PF00017 | 0.450 |
LIG_TYR_ITSM | 341 | 348 | PF00017 | 0.473 |
LIG_UBA3_1 | 387 | 393 | PF00899 | 0.627 |
LIG_UBA3_1 | 515 | 521 | PF00899 | 0.510 |
LIG_WRC_WIRS_1 | 448 | 453 | PF05994 | 0.612 |
LIG_WRC_WIRS_1 | 501 | 506 | PF05994 | 0.586 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.275 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.348 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.535 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.462 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.440 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.334 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.473 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.610 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.579 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.472 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.444 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.314 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.284 |
MOD_Cter_Amidation | 400 | 403 | PF01082 | 0.424 |
MOD_Cter_Amidation | 551 | 554 | PF01082 | 0.244 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.708 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.346 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.342 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.291 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.429 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.489 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.561 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.609 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.304 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.303 |
MOD_LATS_1 | 256 | 262 | PF00433 | 0.524 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.342 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.267 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.400 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.509 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.297 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.518 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.519 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.489 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.464 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.281 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.365 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.444 |
MOD_OFUCOSY | 70 | 76 | PF10250 | 0.511 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.508 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.548 |
MOD_PK_1 | 258 | 264 | PF00069 | 0.522 |
MOD_PK_1 | 538 | 544 | PF00069 | 0.548 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.461 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.444 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.317 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.478 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.473 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.465 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.488 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.617 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.467 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.480 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.556 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.318 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.316 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.472 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.467 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.583 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.313 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.617 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.548 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.304 |
MOD_SUMO_for_1 | 520 | 523 | PF00179 | 0.444 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.354 |
MOD_SUMO_rev_2 | 288 | 295 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 450 | 456 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 132 | 137 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_2 | 243 | 249 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 503 | 508 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.513 |
TRG_NES_CRM1_1 | 298 | 312 | PF08389 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 385 | 390 | PF00026 | 0.364 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZB0 | Leptomonas seymouri | 84% | 95% |
A0A0S4JJA5 | Bodo saltans | 66% | 100% |
A0A1X0P3R2 | Trypanosomatidae | 73% | 100% |
A0A3Q8IPA6 | Leishmania donovani | 94% | 100% |
A0A422MT81 | Trypanosoma rangeli | 70% | 100% |
A0B5U4 | Methanothrix thermoacetophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) | 38% | 100% |
A4FZX1 | Methanococcus maripaludis (strain C5 / ATCC BAA-1333) | 37% | 100% |
A4ID12 | Leishmania infantum | 94% | 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) | 36% | 100% |
D0A8G2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9ATG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O23627 | Arabidopsis thaliana | 47% | 86% |
O27874 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 39% | 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 | 45% | 85% |
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) | 42% | 96% |
Q4Q131 | Leishmania major | 93% | 100% |
Q57681 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 39% | 100% |
Q5I0G4 | Rattus norvegicus | 46% | 86% |
Q5JID8 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 37% | 100% |
Q5RBL1 | Pongo abelii | 45% | 85% |
Q6M0Q7 | Methanococcus maripaludis (strain S2 / LL) | 37% | 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 | 46% | 86% |
Q9RSR5 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 30% | 100% |
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) | 35% | 100% |
V5AU76 | Trypanosoma cruzi | 72% | 100% |