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. | yes | yes: 3 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
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 | 2 |
Related structures:
AlphaFold database: Q4Q3R1
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.622 |
CLV_PCSK_FUR_1 | 340 | 344 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 610 | 612 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 620 | 622 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 809 | 813 | PF00082 | 0.477 |
DEG_MDM2_SWIB_1 | 382 | 389 | PF02201 | 0.571 |
DEG_SCF_FBW7_2 | 295 | 302 | PF00400 | 0.491 |
DEG_SPOP_SBC_1 | 578 | 582 | PF00917 | 0.491 |
DOC_CKS1_1 | 296 | 301 | PF01111 | 0.491 |
DOC_CKS1_1 | 499 | 504 | PF01111 | 0.491 |
DOC_CKS1_1 | 715 | 720 | PF01111 | 0.443 |
DOC_CKS1_1 | 747 | 752 | PF01111 | 0.571 |
DOC_CYCLIN_RxL_1 | 494 | 501 | PF00134 | 0.491 |
DOC_MAPK_DCC_7 | 285 | 295 | PF00069 | 0.532 |
DOC_MAPK_DCC_7 | 680 | 689 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 25 | 32 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 282 | 290 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 407 | 415 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 518 | 528 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 620 | 632 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 645 | 651 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 676 | 684 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 723 | 732 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.712 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 625 | 632 | PF00069 | 0.479 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.491 |
DOC_PP2B_LxvP_1 | 811 | 814 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 568 | 571 | PF00568 | 0.561 |
DOC_PP4_FxxP_1 | 632 | 635 | PF00568 | 0.571 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 444 | 448 | PF12436 | 0.449 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.675 |
DOC_USP7_UBL2_3 | 793 | 797 | PF12436 | 0.558 |
DOC_USP7_UBL2_3 | 812 | 816 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 88 | 92 | PF12436 | 0.635 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 410 | 416 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 678 | 683 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 734 | 739 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 783 | 787 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 675 | 692 | PF00022 | 0.575 |
LIG_Actin_WH2_2 | 701 | 716 | PF00022 | 0.502 |
LIG_Clathr_ClatBox_1 | 293 | 297 | PF01394 | 0.491 |
LIG_Clathr_ClatBox_1 | 429 | 433 | PF01394 | 0.491 |
LIG_CtBP_PxDLS_1 | 751 | 757 | PF00389 | 0.591 |
LIG_EH1_1 | 465 | 473 | PF00400 | 0.543 |
LIG_FAT_LD_1 | 586 | 594 | PF03623 | 0.491 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.491 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.358 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.491 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.556 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.569 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.486 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.518 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.717 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.708 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.444 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.404 |
LIG_GBD_Chelix_1 | 320 | 328 | PF00786 | 0.291 |
LIG_LIR_Apic_2 | 532 | 538 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 567 | 571 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 623 | 634 | PF02991 | 0.571 |
LIG_LIR_LC3C_4 | 540 | 545 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 662 | 667 | PF02991 | 0.544 |
LIG_NRBOX | 585 | 591 | PF00104 | 0.491 |
LIG_Pex14_2 | 382 | 386 | PF04695 | 0.571 |
LIG_Rb_pABgroove_1 | 351 | 359 | PF01858 | 0.521 |
LIG_Rb_pABgroove_1 | 655 | 663 | PF01858 | 0.491 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.521 |
LIG_SH2_GRB2like | 403 | 406 | PF00017 | 0.545 |
LIG_SH2_GRB2like | 667 | 670 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 535 | 538 | PF00017 | 0.543 |
LIG_SH2_SRC | 514 | 517 | PF00017 | 0.491 |
LIG_SH2_SRC | 535 | 538 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.347 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.457 |
LIG_SH3_4 | 128 | 135 | PF00018 | 0.721 |
LIG_Sin3_3 | 318 | 325 | PF02671 | 0.491 |
LIG_SUMO_SIM_anti_2 | 316 | 321 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 428 | 433 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 467 | 472 | PF11976 | 0.571 |
LIG_SUMO_SIM_anti_2 | 540 | 546 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 726 | 733 | PF11976 | 0.538 |
LIG_SUMO_SIM_anti_2 | 799 | 806 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 318 | 323 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 428 | 433 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 704 | 709 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 743 | 749 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 799 | 806 | PF11976 | 0.570 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.736 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.766 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.552 |
LIG_UBA3_1 | 22 | 29 | PF00899 | 0.564 |
LIG_UBA3_1 | 589 | 597 | PF00899 | 0.491 |
LIG_UBA3_1 | 656 | 663 | PF00899 | 0.539 |
LIG_UBA3_1 | 803 | 812 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 589 | 594 | PF05994 | 0.521 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.539 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.491 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.491 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.561 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.571 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.521 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.480 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.323 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.703 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.709 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.404 |
MOD_DYRK1A_RPxSP_1 | 714 | 718 | PF00069 | 0.562 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.394 |
MOD_GlcNHglycan | 392 | 396 | PF01048 | 0.394 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.291 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.394 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.491 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.480 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.531 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.443 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.491 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.521 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.491 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.561 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.529 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.603 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.404 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.563 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.422 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.491 |
MOD_PIKK_1 | 491 | 497 | PF00454 | 0.491 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.566 |
MOD_PK_1 | 678 | 684 | PF00069 | 0.599 |
MOD_PK_1 | 725 | 731 | PF00069 | 0.579 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.716 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.682 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.672 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.491 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.538 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.491 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.491 |
MOD_PKA_2 | 782 | 788 | PF00069 | 0.431 |
MOD_PKB_1 | 308 | 316 | PF00069 | 0.491 |
MOD_Plk_1 | 725 | 731 | PF00069 | 0.613 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.491 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.491 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.491 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.404 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.521 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.616 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.441 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.418 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.482 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.491 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.440 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.579 |
MOD_SUMO_for_1 | 28 | 31 | PF00179 | 0.652 |
MOD_SUMO_for_1 | 389 | 392 | PF00179 | 0.505 |
MOD_SUMO_for_1 | 792 | 795 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 192 | 199 | PF00179 | 0.718 |
MOD_SUMO_rev_2 | 794 | 798 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 80 | 90 | PF00179 | 0.679 |
TRG_DiLeu_BaEn_1 | 334 | 339 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_4 | 37 | 43 | PF01217 | 0.554 |
TRG_DiLeu_LyEn_5 | 334 | 339 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.491 |
TRG_NES_CRM1_1 | 677 | 688 | PF08389 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P688 | Leptomonas seymouri | 77% | 99% |
A0A1X0NR88 | Trypanosomatidae | 69% | 98% |
A0A3Q8IHQ5 | Leishmania donovani | 98% | 100% |
A0A3R7NFT4 | Trypanosoma rangeli | 69% | 98% |
A0B8Q6 | Methanothrix thermoacetophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) | 35% | 100% |
A1RUX2 | Pyrobaculum islandicum (strain DSM 4184 / JCM 9189 / GEO3) | 32% | 100% |
A1RXH6 | Thermofilum pendens (strain DSM 2475 / Hrk 5) | 36% | 100% |
A1TSK3 | Acidovorax citrulli (strain AAC00-1) | 27% | 87% |
A1VXL9 | Campylobacter jejuni subsp. jejuni serotype O:23/36 (strain 81-176) | 27% | 94% |
A1W8Z4 | Acidovorax sp. (strain JS42) | 26% | 87% |
A2BJZ8 | Hyperthermus butylicus (strain DSM 5456 / JCM 9403 / PLM1-5) | 36% | 100% |
A2STM8 | Methanocorpusculum labreanum (strain ATCC 43576 / DSM 4855 / Z) | 36% | 100% |
A3CSP4 | Methanoculleus marisnigri (strain ATCC 35101 / DSM 1498 / JR1) | 35% | 100% |
A3DMS0 | Staphylothermus marinus (strain ATCC 43588 / DSM 3639 / JCM 9404 / F1) | 37% | 100% |
A3MTU7 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 34% | 100% |
A4FZQ3 | Methanococcus maripaludis (strain C5 / ATCC BAA-1333) | 35% | 100% |
A4G7S7 | Herminiimonas arsenicoxydans | 28% | 87% |
A4HLY5 | Leishmania braziliensis | 92% | 100% |
A4I9B4 | Leishmania infantum | 98% | 100% |
A4WIK2 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 33% | 100% |
A4YCQ5 | Metallosphaera sedula (strain ATCC 51363 / DSM 5348 / JCM 9185 / NBRC 15509 / TH2) | 36% | 100% |
A5UJM9 | Methanobrevibacter smithii (strain ATCC 35061 / DSM 861 / OCM 144 / PS) | 31% | 100% |
A6MVX8 | Rhodomonas salina | 27% | 100% |
A6T0Y8 | Janthinobacterium sp. (strain Marseille) | 28% | 87% |
A6URS1 | Methanococcus vannielii (strain ATCC 35089 / DSM 1224 / JCM 13029 / OCM 148 / SB) | 34% | 100% |
A6UVG0 | Methanococcus aeolicus (strain ATCC BAA-1280 / DSM 17508 / OCM 812 / Nankai-3) | 36% | 100% |
A6VIS4 | Methanococcus maripaludis (strain C7 / ATCC BAA-1331) | 36% | 100% |
A7GZZ3 | Campylobacter curvus (strain 525.92) | 28% | 90% |
A7H1L5 | Campylobacter jejuni subsp. doylei (strain ATCC BAA-1458 / RM4099 / 269.97) | 27% | 96% |
A7IAP7 | Methanoregula boonei (strain DSM 21154 / JCM 14090 / 6A8) | 35% | 100% |
A8A8D3 | Ignicoccus hospitalis (strain KIN4/I / DSM 18386 / JCM 14125) | 36% | 100% |
A8FJU1 | Campylobacter jejuni subsp. jejuni serotype O:6 (strain 81116 / NCTC 11828) | 27% | 94% |
A8MBV9 | Caldivirga maquilingensis (strain ATCC 700844 / DSM 13496 / JCM 10307 / IC-167) | 36% | 100% |
A9A813 | Methanococcus maripaludis (strain C6 / ATCC BAA-1332) | 36% | 100% |
B0R6U5 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 37% | 100% |
B1MZH4 | Leuconostoc citreum (strain KM20) | 27% | 97% |
B1YCQ7 | Pyrobaculum neutrophilum (strain DSM 2338 / JCM 9278 / NBRC 100436 / V24Sta) | 33% | 100% |
B2GUV7 | Rattus norvegicus | 47% | 67% |
B4RXT8 | Alteromonas mediterranea (strain DSM 17117 / CIP 110805 / LMG 28347 / Deep ecotype) | 26% | 94% |
B6YWH3 | Thermococcus onnurineus (strain NA1) | 36% | 100% |
B8GP02 | Thioalkalivibrio sulfidiphilus (strain HL-EbGR7) | 25% | 96% |
B9KEV0 | Campylobacter lari (strain RM2100 / D67 / ATCC BAA-1060) | 27% | 93% |
B9LQL7 | Halorubrum lacusprofundi (strain ATCC 49239 / DSM 5036 / JCM 8891 / ACAM 34) | 33% | 100% |
C1DFK9 | Azotobacter vinelandii (strain DJ / ATCC BAA-1303) | 27% | 98% |
C4L8X4 | Tolumonas auensis (strain DSM 9187 / TA4) | 26% | 90% |
C6A1V3 | Thermococcus sibiricus (strain DSM 12597 / MM 739) | 35% | 100% |
C9ZJA9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 98% |
E9B4B4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
G0S8G9 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 51% | 73% |
O26359 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 35% | 100% |
O29490 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 37% | 100% |
O58822 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 34% | 78% |
O60841 | Homo sapiens | 47% | 67% |
O67825 | Aquifex aeolicus (strain VF5) | 27% | 100% |
P39730 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 45% | 81% |
P95691 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 34% | 100% |
Q05D44 | Mus musculus | 47% | 67% |
Q0VSS1 | Alcanivorax borkumensis (strain ATCC 700651 / DSM 11573 / NCIMB 13689 / SK2) | 26% | 91% |
Q0W8X2 | Methanocella arvoryzae (strain DSM 22066 / NBRC 105507 / MRE50) | 37% | 100% |
Q12Z93 | Methanococcoides burtonii (strain DSM 6242 / NBRC 107633 / OCM 468 / ACE-M) | 34% | 100% |
Q18FT0 | Haloquadratum walsbyi (strain DSM 16790 / HBSQ001) | 34% | 100% |
Q2FU48 | Methanospirillum hungatei JF-1 (strain ATCC 27890 / DSM 864 / NBRC 100397 / JF-1) | 36% | 100% |
Q2NGM6 | Methanosphaera stadtmanae (strain ATCC 43021 / DSM 3091 / JCM 11832 / MCB-3) | 33% | 100% |
Q30WJ0 | Oleidesulfovibrio alaskensis (strain ATCC BAA-1058 / DSM 17464 / G20) | 25% | 83% |
Q38W81 | Latilactobacillus sakei subsp. sakei (strain 23K) | 27% | 87% |
Q3IMS5 | Natronomonas pharaonis (strain ATCC 35678 / DSM 2160 / CIP 103997 / JCM 8858 / NBRC 14720 / NCIMB 2260 / Gabara) | 32% | 100% |
Q466D5 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 34% | 100% |
Q54XP6 | Dictyostelium discoideum | 46% | 78% |
Q57710 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 35% | 71% |
Q5HX30 | Campylobacter jejuni (strain RM1221) | 27% | 94% |
Q5JGR9 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 35% | 71% |
Q5QTY8 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 26% | 91% |
Q5RDE1 | Pongo abelii | 46% | 67% |
Q5UXU6 | Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) | 35% | 100% |
Q609C0 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 26% | 94% |
Q6FF40 | Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) | 28% | 91% |
Q6M0I6 | Methanococcus maripaludis (strain S2 / LL) | 35% | 100% |
Q8PU78 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 34% | 100% |
Q8TQL5 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 34% | 100% |
Q8TV06 | Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) | 35% | 100% |
Q8U1R8 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 34% | 83% |
Q8ZX20 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 34% | 100% |
Q976A1 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 35% | 100% |
Q97BK4 | Thermoplasma volcanium (strain ATCC 51530 / DSM 4299 / JCM 9571 / NBRC 15438 / GSS1) | 31% | 100% |
Q980Q8 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 35% | 100% |
Q98R05 | Mycoplasmopsis pulmonis (strain UAB CTIP) | 25% | 100% |
Q9HJ60 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 31% | 100% |
Q9HNQ2 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 37% | 100% |
Q9PIZ1 | Campylobacter jejuni subsp. jejuni serotype O:2 (strain ATCC 700819 / NCTC 11168) | 27% | 94% |
Q9UZK7 | Pyrococcus abyssi (strain GE5 / Orsay) | 35% | 82% |
Q9Y9B3 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 35% | 100% |
V5AV36 | Trypanosoma cruzi | 70% | 92% |