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. | 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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q842
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 12 |
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006090 | pyruvate metabolic process | 7 | 12 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 12 |
GO:0006096 | glycolytic process | 5 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006163 | purine nucleotide metabolic process | 5 | 12 |
GO:0006165 | obsolete nucleoside diphosphate phosphorylation | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 12 |
GO:0006757 | obsolete ATP generation from ADP | 4 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009117 | nucleotide metabolic process | 5 | 12 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 12 |
GO:0009135 | purine nucleoside diphosphate metabolic process | 6 | 12 |
GO:0009141 | nucleoside triphosphate metabolic process | 5 | 12 |
GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 12 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 12 |
GO:0009179 | purine ribonucleoside diphosphate metabolic process | 7 | 12 |
GO:0009185 | ribonucleoside diphosphate metabolic process | 6 | 12 |
GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 12 |
GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 12 |
GO:0009259 | ribonucleotide metabolic process | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016052 | carbohydrate catabolic process | 4 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0019693 | ribose phosphate metabolic process | 4 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound 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:0046031 | ADP metabolic process | 7 | 12 |
GO:0046034 | ATP metabolic process | 7 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 12 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072521 | purine-containing compound metabolic process | 4 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004619 | phosphoglycerate mutase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0016868 | intramolecular transferase activity, phosphotransferases | 4 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046537 | 2,3-bisphosphoglycerate-independent phosphoglycerate mutase activity | 6 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.346 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 782 | 784 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 824 | 826 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.187 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.332 |
CLV_Separin_Metazoa | 733 | 737 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 277 | 285 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 589 | 597 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 613 | 621 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 668 | 676 | PF00400 | 0.546 |
DEG_COP1_1 | 96 | 106 | PF00400 | 0.410 |
DEG_ODPH_VHL_1 | 622 | 633 | PF01847 | 0.546 |
DEG_SCF_FBW7_1 | 159 | 164 | PF00400 | 0.569 |
DEG_SPOP_SBC_1 | 161 | 165 | PF00917 | 0.501 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 588 | 597 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 128 | 134 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 351 | PF00134 | 0.546 |
DOC_MAPK_FxFP_2 | 365 | 368 | PF00069 | 0.463 |
DOC_MAPK_FxFP_2 | 466 | 469 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 590 | 598 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 813 | 822 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 84 | 91 | PF00069 | 0.426 |
DOC_MAPK_JIP1_4 | 257 | 263 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 726 | 734 | PF00069 | 0.515 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.248 |
DOC_PP2B_PxIxI_1 | 331 | 337 | PF00149 | 0.481 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.552 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.463 |
DOC_PP4_FxxP_1 | 466 | 469 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 759 | 763 | PF00917 | 0.483 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 120 | 130 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 783 | 790 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 825 | 831 | PF00244 | 0.332 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.475 |
LIG_APCC_ABBA_1 | 177 | 182 | PF00400 | 0.551 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.576 |
LIG_Clathr_ClatBox_1 | 261 | 265 | PF01394 | 0.457 |
LIG_EH1_1 | 339 | 347 | PF00400 | 0.546 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.521 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.446 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.460 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.536 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.446 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.453 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.446 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.520 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.403 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.554 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.449 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.431 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.462 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.449 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.515 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.546 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.460 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.505 |
LIG_FHA_2 | 782 | 788 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 363 | 368 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 269 | 280 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 3 | 14 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 706 | 716 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 799 | 807 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 829 | 833 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 706 | 712 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 743 | 749 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 799 | 804 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 829 | 833 | PF02991 | 0.364 |
LIG_NRBOX | 592 | 598 | PF00104 | 0.475 |
LIG_OCRL_FandH_1 | 610 | 622 | PF00620 | 0.546 |
LIG_Pex14_1 | 607 | 611 | PF04695 | 0.471 |
LIG_Pex14_2 | 395 | 399 | PF04695 | 0.446 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.606 |
LIG_SH2_CRK | 709 | 713 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 224 | 228 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 535 | 539 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 540 | 544 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.370 |
LIG_SH3_1 | 250 | 256 | PF00018 | 0.501 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.567 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.414 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.512 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.435 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.426 |
LIG_SUMO_SIM_anti_2 | 279 | 285 | PF11976 | 0.471 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.243 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.495 |
LIG_UBA3_1 | 501 | 508 | PF00899 | 0.475 |
LIG_UBA3_1 | 819 | 824 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 399 | 404 | PF05994 | 0.546 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.493 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.574 |
MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.560 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.591 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.594 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.533 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.483 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.513 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.384 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.463 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.464 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.471 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.475 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.555 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.353 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.495 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.481 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.475 |
MOD_DYRK1A_RPxSP_1 | 293 | 297 | PF00069 | 0.395 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.463 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.392 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.649 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.374 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.254 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.295 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.346 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.320 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.346 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.334 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.600 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.468 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.391 |
MOD_GlcNHglycan | 93 | 98 | PF01048 | 0.201 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.623 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.519 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.535 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.579 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.489 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.527 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.555 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.490 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.535 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.535 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.526 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.221 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.346 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.379 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.493 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.430 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.561 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.465 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.556 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.327 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.514 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.513 |
MOD_NEK2_2 | 538 | 543 | PF00069 | 0.546 |
MOD_NEK2_2 | 649 | 654 | PF00069 | 0.546 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.557 |
MOD_PKA_1 | 782 | 788 | PF00069 | 0.515 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.454 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.583 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.546 |
MOD_PKA_2 | 782 | 788 | PF00069 | 0.554 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.617 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.383 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.457 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.421 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.365 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.475 |
MOD_Plk_1 | 724 | 730 | PF00069 | 0.444 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.489 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.537 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.557 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.489 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.489 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.477 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.678 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.446 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.552 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.505 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.457 |
MOD_SUMO_for_1 | 730 | 733 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 799 | 807 | PF00179 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 709 | 712 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 801 | 804 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 830 | 833 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 554 | 556 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 735 | 737 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4B9 | Leptomonas seymouri | 69% | 100% |
A0A0S4J9H6 | Bodo saltans | 37% | 100% |
A0A1X0NQP8 | Trypanosomatidae | 41% | 100% |
A0A3S7X1Q9 | Leishmania donovani | 95% | 100% |
A0A422MUW5 | Trypanosoma rangeli | 47% | 100% |
A4HGS6 | Leishmania braziliensis | 84% | 100% |
A4I3V2 | Leishmania infantum | 95% | 100% |
D0A920 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B043 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D5P0 | Trypanosoma cruzi | 44% | 100% |