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. | no | 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: A4HJA5
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 | 561 | 565 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.254 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.454 |
DEG_MDM2_SWIB_1 | 77 | 85 | PF02201 | 0.334 |
DOC_CYCLIN_RxL_1 | 401 | 410 | PF00134 | 0.488 |
DOC_MAPK_DCC_7 | 599 | 607 | PF00069 | 0.288 |
DOC_MAPK_gen_1 | 599 | 607 | PF00069 | 0.231 |
DOC_MAPK_HePTP_8 | 773 | 785 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 599 | 607 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 764 | 773 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 776 | 785 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 792 | 800 | PF00069 | 0.313 |
DOC_PP1_RVXF_1 | 217 | 223 | PF00149 | 0.513 |
DOC_PP4_FxxP_1 | 649 | 652 | PF00568 | 0.454 |
DOC_PP4_MxPP_1 | 678 | 681 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.254 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 741 | 745 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 744 | 749 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 117 | 125 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 393 | 400 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 786 | 801 | PF00022 | 0.275 |
LIG_BIR_III_4 | 537 | 541 | PF00653 | 0.291 |
LIG_BIR_III_4 | 567 | 571 | PF00653 | 0.454 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.291 |
LIG_BRCT_BRCA1_1 | 583 | 587 | PF00533 | 0.204 |
LIG_BRCT_BRCA1_1 | 781 | 785 | PF00533 | 0.291 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.512 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.454 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.597 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.319 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.274 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.374 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.454 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.364 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.331 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.479 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.475 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.286 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.454 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 264 | 274 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 359 | 370 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 584 | 595 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 782 | 788 | PF02991 | 0.291 |
LIG_LYPXL_S_1 | 366 | 370 | PF13949 | 0.454 |
LIG_LYPXL_yS_3 | 367 | 370 | PF13949 | 0.254 |
LIG_Pex14_2 | 136 | 140 | PF04695 | 0.291 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.441 |
LIG_Pex14_2 | 77 | 81 | PF04695 | 0.310 |
LIG_Pex14_2 | 785 | 789 | PF04695 | 0.339 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.533 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.193 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.454 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 196 | 199 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.563 |
LIG_SH2_NCK_1 | 266 | 270 | PF00017 | 0.274 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 699 | 703 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 732 | 735 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 732 | 735 | PF00017 | 0.454 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.335 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.570 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.363 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.291 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.288 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.454 |
LIG_SH3_3 | 781 | 787 | PF00018 | 0.291 |
LIG_SUMO_SIM_anti_2 | 413 | 419 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 61 | 67 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 367 | 372 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 683 | 688 | PF11976 | 0.334 |
LIG_TYR_ITIM | 113 | 118 | PF00017 | 0.563 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.454 |
LIG_WRC_WIRS_1 | 338 | 343 | PF05994 | 0.291 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.533 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.303 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.254 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.347 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.304 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.291 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.362 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.291 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.254 |
MOD_Cter_Amidation | 656 | 659 | PF01082 | 0.363 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.363 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.325 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.344 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.245 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.482 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.262 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.300 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.552 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.303 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.299 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.272 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.291 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.291 |
MOD_GlcNHglycan | 765 | 769 | PF01048 | 0.257 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.463 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.285 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.480 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.704 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.327 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.347 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.256 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.443 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.292 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.196 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.291 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.454 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.293 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.304 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.333 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.529 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.508 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.254 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.626 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.363 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.576 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.328 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.336 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.308 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.291 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.285 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.245 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.291 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.292 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.369 |
MOD_NEK2_1 | 715 | 720 | PF00069 | 0.397 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.473 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.274 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.230 |
MOD_NEK2_2 | 84 | 89 | PF00069 | 0.431 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.410 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.454 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.485 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.308 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.551 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.323 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.530 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.196 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.319 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.264 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.353 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.323 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.329 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.301 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.375 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.224 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.296 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.261 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.256 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.472 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.319 |
MOD_ProDKin_1 | 744 | 750 | PF00069 | 0.462 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.533 |
MOD_SUMO_rev_2 | 128 | 133 | PF00179 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.211 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 645 | 647 | PF00400 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 471 | 475 | PF00026 | 0.196 |
TRG_Pf-PMV_PEXEL_1 | 560 | 564 | PF00026 | 0.263 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5A1 | Leptomonas seymouri | 88% | 100% |
A0A0S4J2L1 | Bodo saltans | 77% | 100% |
A0A1X0NPP6 | Trypanosomatidae | 79% | 95% |
A0A3Q8IEU2 | Leishmania donovani | 90% | 100% |
A0A422NED3 | Trypanosoma rangeli | 77% | 99% |
A4I6P8 | Leishmania infantum | 90% | 100% |
C9ZM75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 97% |
C9ZWU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 75% | 97% |
E9B1S0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O68460 | Rhodospirillum rubrum (strain ATCC 11170 / ATH 1.1.1 / DSM 467 / LMG 4362 / NCIMB 8255 / S1) | 40% | 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 | 54% | 100% |
Q2RIS7 | Moorella thermoacetica (strain ATCC 39073 / JCM 9320) | 47% | 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 | 88% | 100% |
Q56ZN6 | Arabidopsis thaliana | 38% | 100% |
Q72Q29 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar copenhageni (strain Fiocruz L1-130) | 49% | 100% |
Q82EJ8 | Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) | 38% | 100% |
Q82TF3 | Nitrosomonas europaea (strain ATCC 19718 / CIP 103999 / KCTC 2705 / NBRC 14298) | 41% | 100% |
Q898Q9 | Clostridium tetani (strain Massachusetts / E88) | 47% | 100% |
Q89K83 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 39% | 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) | 49% | 100% |
Q8G1E6 | Brucella suis biovar 1 (strain 1330) | 37% | 100% |
Q8KDT8 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 29% | 100% |
Q8KY01 | Rhodopseudomonas palustris | 39% | 100% |
Q8P5M6 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 40% | 100% |
Q8PH20 | Xanthomonas axonopodis pv. citri (strain 306) | 41% | 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) | 43% | 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) | 43% | 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) | 37% | 100% |
Q8VRZ2 | Brucella anthropi (strain ATCC 49188 / DSM 6882 / CCUG 24695 / JCM 21032 / LMG 3331 / NBRC 15819 / NCTC 12168 / Alc 37) | 36% | 100% |
Q8VRZ3 | Rhizobium meliloti (strain 1021) | 38% | 100% |
Q8YGH4 | Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094) | 37% | 100% |
Q8ZWI8 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 37% | 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 | 38% | 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 | 80% | 99% |