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: 0 |
Silverman et al. | no | yes: 0 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 12, no: 0 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0020022 | acidocalcisome | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 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 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEU2
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0006885 | regulation of pH | 8 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 1 |
GO:0030641 | regulation of cellular pH | 7 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051452 | intracellular pH reduction | 9 | 1 |
GO:0051453 | regulation of intracellular pH | 8 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004427 | inorganic diphosphate phosphatase activity | 6 | 13 |
GO:0005215 | transporter activity | 1 | 13 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 13 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 13 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 13 |
GO:0015078 | proton transmembrane transporter activity | 5 | 13 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 13 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0022804 | active transmembrane transporter activity | 3 | 13 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 13 |
GO:0022857 | transmembrane transporter activity | 2 | 13 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.540 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.391 |
CLV_Separin_Metazoa | 105 | 109 | PF03568 | 0.540 |
DEG_MDM2_SWIB_1 | 76 | 84 | PF02201 | 0.434 |
DEG_SCF_FBW7_1 | 27 | 34 | PF00400 | 0.512 |
DOC_CKS1_1 | 28 | 33 | PF01111 | 0.586 |
DOC_CYCLIN_RxL_1 | 400 | 409 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 6 | 12 | PF00134 | 0.556 |
DOC_MAPK_DCC_7 | 4 | 12 | PF00069 | 0.561 |
DOC_MAPK_DCC_7 | 598 | 606 | PF00069 | 0.374 |
DOC_MAPK_HePTP_8 | 772 | 784 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 4 | 12 | PF00069 | 0.673 |
DOC_MAPK_MEF2A_6 | 598 | 606 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 610 | 617 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 763 | 772 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 775 | 784 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 791 | 799 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 216 | 222 | PF00149 | 0.646 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.540 |
DOC_PP4_MxPP_1 | 677 | 680 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.392 |
DOC_USP7_UBL2_3 | 740 | 744 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 116 | 124 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 54 | 64 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 82 | 100 | PF00022 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.732 |
LIG_BIR_III_4 | 536 | 540 | PF00653 | 0.392 |
LIG_BIR_III_4 | 566 | 570 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 780 | 784 | PF00533 | 0.392 |
LIG_eIF4E_1 | 698 | 704 | PF01652 | 0.313 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.607 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.540 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.369 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.405 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.350 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.540 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.443 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.392 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.540 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.540 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.333 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.435 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.616 |
LIG_FHA_2 | 755 | 761 | PF00498 | 0.540 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 171 | 180 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 358 | 369 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 85 | 91 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 781 | 787 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.595 |
LIG_LYPXL_S_1 | 365 | 369 | PF13949 | 0.540 |
LIG_LYPXL_yS_3 | 366 | 369 | PF13949 | 0.340 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.392 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.526 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.405 |
LIG_Pex14_2 | 784 | 788 | PF04695 | 0.439 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.610 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.265 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.540 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.540 |
LIG_SH2_GRB2like | 195 | 198 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 114 | 118 | PF00017 | 0.631 |
LIG_SH2_NCK_1 | 265 | 269 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 698 | 702 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.641 |
LIG_SH2_STAT3 | 731 | 734 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.532 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.400 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.599 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.631 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.431 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.392 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.374 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.540 |
LIG_SH3_3 | 780 | 786 | PF00018 | 0.392 |
LIG_Sin3_3 | 11 | 18 | PF02671 | 0.648 |
LIG_SUMO_SIM_anti_2 | 413 | 418 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 366 | 371 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 682 | 687 | PF11976 | 0.434 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.423 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.523 |
LIG_TYR_ITIM | 112 | 117 | PF00017 | 0.625 |
LIG_TYR_ITIM | 490 | 495 | PF00017 | 0.540 |
LIG_UBA3_1 | 240 | 248 | PF00899 | 0.369 |
LIG_Vh1_VBS_1 | 369 | 387 | PF01044 | 0.424 |
LIG_WRC_WIRS_1 | 337 | 342 | PF05994 | 0.392 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.615 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.404 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.393 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.449 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.392 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.423 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.430 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.392 |
MOD_Cter_Amidation | 655 | 658 | PF01082 | 0.431 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.546 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.390 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.268 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.588 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.330 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.551 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.348 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.385 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.623 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.392 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.400 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.392 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.392 |
MOD_GlcNHglycan | 764 | 768 | PF01048 | 0.340 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.550 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.487 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.560 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.420 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.604 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.340 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.519 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.391 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.392 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.534 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.394 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.405 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.405 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.646 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.340 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.431 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.631 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.398 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.380 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.384 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.392 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.370 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.338 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.392 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.386 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.428 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.386 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.487 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.540 |
MOD_NEK2_2 | 168 | 173 | PF00069 | 0.360 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.540 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.446 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.403 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.608 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.421 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.351 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.403 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.382 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.422 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.402 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.381 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.628 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.348 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.312 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.634 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.421 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.540 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 127 | 132 | PF00179 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 644 | 646 | PF00400 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 559 | 563 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5A1 | Leptomonas seymouri | 87% | 100% |
A0A0S4J2L1 | Bodo saltans | 76% | 100% |
A0A1X0NPP6 | Trypanosomatidae | 76% | 95% |
A0A422NED3 | Trypanosoma rangeli | 77% | 99% |
A4HJA5 | Leishmania braziliensis | 90% | 100% |
A4I6P8 | Leishmania infantum | 100% | 100% |
C9ZM75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 97% |
C9ZWU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 97% |
E9B1S0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O68460 | Rhodospirillum rubrum (strain ATCC 11170 / ATH 1.1.1 / DSM 467 / LMG 4362 / NCIMB 8255 / S1) | 41% | 100% |
P21616 | Vigna radiata var. radiata | 54% | 100% |
P31414 | Arabidopsis thaliana | 54% | 100% |
P60363 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 38% | 100% |
Q06572 | Hordeum vulgare | 55% | 100% |
Q2RIS7 | Moorella thermoacetica (strain ATCC 39073 / JCM 9320) | 48% | 100% |
Q2RLE0 | Moorella thermoacetica (strain ATCC 39073 / JCM 9320) | 41% | 100% |
Q3AFC6 | Carboxydothermus hydrogenoformans (strain ATCC BAA-161 / DSM 6008 / Z-2901) | 44% | 100% |
Q4Q6E1 | Leishmania major | 97% | 100% |
Q56ZN6 | Arabidopsis thaliana | 39% | 100% |
Q72Q29 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar copenhageni (strain Fiocruz L1-130) | 52% | 100% |
Q82EJ8 | Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) | 37% | 100% |
Q82TF3 | Nitrosomonas europaea (strain ATCC 19718 / CIP 103999 / KCTC 2705 / NBRC 14298) | 41% | 100% |
Q898Q9 | Clostridium tetani (strain Massachusetts / E88) | 46% | 100% |
Q89K83 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 40% | 100% |
Q8A294 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 39% | 100% |
Q8F641 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar Lai (strain 56601) | 52% | 100% |
Q8G1E6 | Brucella suis biovar 1 (strain 1330) | 38% | 100% |
Q8KDT8 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 31% | 100% |
Q8KY01 | Rhodopseudomonas palustris | 40% | 100% |
Q8P5M6 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 41% | 100% |
Q8PH20 | Xanthomonas axonopodis pv. citri (strain 306) | 42% | 100% |
Q8PYZ7 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 43% | 100% |
Q8PYZ8 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 44% | 100% |
Q8RCX1 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 40% | 100% |
Q8RHJ2 | Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / DSM 15643 / BCRC 10681 / CIP 101130 / JCM 8532 / KCTC 2640 / LMG 13131 / VPI 4355) | 44% | 100% |
Q8TJA8 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 44% | 100% |
Q8TJA9 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 44% | 100% |
Q8UG67 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 37% | 100% |
Q8VNW3 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 36% | 100% |
Q8VRZ2 | Brucella anthropi (strain ATCC 49188 / DSM 6882 / CCUG 24695 / JCM 21032 / LMG 3331 / NBRC 15819 / NCTC 12168 / Alc 37) | 38% | 100% |
Q8VRZ3 | Rhizobium meliloti (strain 1021) | 39% | 100% |
Q8YGH4 | Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094) | 38% | 100% |
Q8ZWI8 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 39% | 100% |
Q983A3 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 40% | 100% |
Q9A8J0 | Caulobacter vibrioides (strain ATCC 19089 / CB15) | 38% | 100% |
Q9FWR2 | Arabidopsis thaliana | 39% | 100% |
Q9S5X0 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 40% | 100% |
Q9X913 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 37% | 100% |
V5BFF6 | Trypanosoma cruzi | 78% | 98% |