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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGS6
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_C14_Caspase3-7 | 785 | 789 | PF00656 | 0.428 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 783 | 785 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 825 | 827 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 783 | 785 | PF00082 | 0.278 |
CLV_PCSK_PC1ET2_1 | 825 | 827 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.178 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.279 |
CLV_Separin_Metazoa | 734 | 738 | PF03568 | 0.478 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 614 | 622 | PF00400 | 0.535 |
DEG_APCC_DBOX_1 | 669 | 677 | PF00400 | 0.535 |
DEG_ODPH_VHL_1 | 623 | 634 | PF01847 | 0.535 |
DEG_SCF_FBW7_1 | 159 | 164 | PF00400 | 0.655 |
DEG_SPOP_SBC_1 | 161 | 165 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.435 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.189 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 727 | 733 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 346 | 352 | PF00134 | 0.535 |
DOC_MAPK_FxFP_2 | 366 | 369 | PF00069 | 0.448 |
DOC_MAPK_FxFP_2 | 467 | 470 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 591 | 599 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 814 | 823 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 84 | 91 | PF00069 | 0.425 |
DOC_MAPK_JIP1_4 | 256 | 262 | PF00069 | 0.281 |
DOC_MAPK_MEF2A_6 | 727 | 735 | PF00069 | 0.478 |
DOC_PP2B_PxIxI_1 | 332 | 338 | PF00149 | 0.466 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.564 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 467 | 470 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.468 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 120 | 130 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 162 | 171 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 784 | 791 | PF00244 | 0.478 |
LIG_APCC_ABBA_1 | 177 | 182 | PF00400 | 0.678 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.587 |
LIG_CaM_IQ_9 | 192 | 207 | PF13499 | 0.395 |
LIG_Clathr_ClatBox_1 | 260 | 264 | PF01394 | 0.442 |
LIG_EH1_1 | 170 | 178 | PF00400 | 0.398 |
LIG_EH1_1 | 340 | 348 | PF00400 | 0.542 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.335 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.475 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.528 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.431 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.451 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.417 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.450 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.431 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.491 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.378 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.570 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.434 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.337 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.447 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.435 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.478 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.540 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.442 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.442 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.462 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.558 |
LIG_Integrin_RGD_1 | 816 | 818 | PF01839 | 0.367 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 213 | 218 | PF02991 | 0.462 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 707 | 717 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 744 | 754 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 800 | 807 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 744 | 750 | PF02991 | 0.498 |
LIG_OCRL_FandH_1 | 611 | 623 | PF00620 | 0.535 |
LIG_PCNA_PIPBox_1 | 824 | 833 | PF02747 | 0.491 |
LIG_Pex14_1 | 608 | 612 | PF04695 | 0.456 |
LIG_Pex14_2 | 396 | 400 | PF04695 | 0.431 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.227 |
LIG_SH2_CRK | 710 | 714 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 536 | 540 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 536 | 540 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 802 | 806 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.189 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.571 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.422 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.428 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.433 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.484 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.713 |
LIG_TRAF2_1 | 649 | 652 | PF00917 | 0.462 |
LIG_UBA3_1 | 820 | 825 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 400 | 405 | PF05994 | 0.535 |
LIG_WRC_WIRS_1 | 609 | 614 | PF05994 | 0.478 |
MOD_CDC14_SPxK_1 | 295 | 298 | PF00782 | 0.376 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.665 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.376 |
MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.680 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.354 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.739 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.600 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.520 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.470 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.472 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.369 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.447 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.435 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.345 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.547 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.351 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.452 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.513 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.465 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.288 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.523 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.297 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.369 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.251 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.343 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.339 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.320 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.334 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.468 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.348 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.357 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.546 |
MOD_GlcNHglycan | 808 | 811 | PF01048 | 0.559 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.443 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.624 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.614 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.437 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.501 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.413 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.513 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.476 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.515 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.530 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.537 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.335 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.320 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.268 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.693 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.422 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.460 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.421 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.508 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.235 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.481 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.532 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.547 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.447 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.482 |
MOD_NEK2_2 | 361 | 366 | PF00069 | 0.501 |
MOD_NEK2_2 | 539 | 544 | PF00069 | 0.535 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.535 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.416 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.417 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.376 |
MOD_PKA_1 | 783 | 789 | PF00069 | 0.478 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.542 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.601 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.495 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.557 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.542 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.618 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.331 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.477 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.599 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.476 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.573 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.396 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.281 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.608 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.709 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.466 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.466 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.491 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.442 |
MOD_SUMO_for_1 | 731 | 734 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 413 | 423 | PF00179 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 802 | 805 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 831 | 834 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 736 | 738 | PF00400 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4B9 | Leptomonas seymouri | 69% | 100% |
A0A0S4J9H6 | Bodo saltans | 35% | 100% |
A0A1X0NQP8 | Trypanosomatidae | 41% | 100% |
A0A3S7X1Q9 | Leishmania donovani | 84% | 100% |
A0A422MUW5 | Trypanosoma rangeli | 46% | 100% |
A4I3V2 | Leishmania infantum | 84% | 100% |
D0A920 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B043 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q842 | Leishmania major | 84% | 100% |
V5D5P0 | Trypanosoma cruzi | 44% | 100% |