Homologous to animal ER-localized Ca2+ ATPases. Localization: ER (by homology)
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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005783 | endoplasmic reticulum | 5 | 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 |
Related structures:
AlphaFold database: E9AJY3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006816 | calcium ion transport | 7 | 1 |
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:0009987 | cellular process | 1 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055065 | obsolete metal ion 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:0055085 | transmembrane transport | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0070588 | calcium ion transmembrane transport | 6 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005388 | P-type calcium transporter activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0015662 | P-type ion transporter activity | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.296 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 969 | 973 | PF00082 | 0.380 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.428 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.469 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.561 |
DOC_CKS1_1 | 649 | 654 | PF01111 | 0.561 |
DOC_CYCLIN_RxL_1 | 463 | 477 | PF00134 | 0.561 |
DOC_CYCLIN_RxL_1 | 635 | 646 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 568 | 574 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 974 | 980 | PF00134 | 0.428 |
DOC_MAPK_DCC_7 | 937 | 946 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 465 | 473 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 474 | 480 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 513 | 520 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 603 | 611 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 701 | 707 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 233 | 240 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 291 | 298 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 605 | 613 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 701 | 709 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 825 | 833 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 879 | 887 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 969 | 978 | PF00069 | 0.416 |
DOC_MAPK_NFAT4_5 | 969 | 977 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 549 | 556 | PF00149 | 0.456 |
DOC_PP1_RVXF_1 | 636 | 643 | PF00149 | 0.523 |
DOC_PP1_RVXF_1 | 818 | 825 | PF00149 | 0.352 |
DOC_PP2B_LxvP_1 | 590 | 593 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 974 | 977 | PF13499 | 0.416 |
DOC_PP4_FxxP_1 | 770 | 773 | PF00568 | 0.328 |
DOC_SPAK_OSR1_1 | 378 | 382 | PF12202 | 0.481 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 918 | 922 | PF00917 | 0.412 |
DOC_USP7_UBL2_3 | 470 | 474 | PF12436 | 0.352 |
DOC_USP7_UBL2_3 | 717 | 721 | PF12436 | 0.521 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.262 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 648 | 653 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 939 | 944 | PF00397 | 0.372 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 212 | 222 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 463 | 468 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 482 | 488 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 498 | 503 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 656 | 665 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 751 | 761 | PF00244 | 0.308 |
LIG_Actin_WH2_2 | 276 | 293 | PF00022 | 0.316 |
LIG_Actin_WH2_2 | 536 | 553 | PF00022 | 0.456 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 935 | 939 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_2 | 39 | 45 | PF00533 | 0.504 |
LIG_Clathr_ClatBox_1 | 154 | 158 | PF01394 | 0.561 |
LIG_Clathr_ClatBox_1 | 886 | 890 | PF01394 | 0.308 |
LIG_deltaCOP1_diTrp_1 | 819 | 824 | PF00928 | 0.542 |
LIG_EH1_1 | 3 | 11 | PF00400 | 0.505 |
LIG_EH1_1 | 82 | 90 | PF00400 | 0.324 |
LIG_EH1_1 | 849 | 857 | PF00400 | 0.152 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.469 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.463 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.504 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.456 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.308 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.456 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.512 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.449 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.450 |
LIG_FHA_1 | 786 | 792 | PF00498 | 0.307 |
LIG_FHA_1 | 968 | 974 | PF00498 | 0.426 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.530 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.218 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.434 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.461 |
LIG_FHA_2 | 849 | 855 | PF00498 | 0.307 |
LIG_FHA_2 | 858 | 864 | PF00498 | 0.286 |
LIG_GBD_Chelix_1 | 761 | 769 | PF00786 | 0.308 |
LIG_Integrin_RGD_1 | 812 | 814 | PF01839 | 0.305 |
LIG_LIR_Apic_2 | 280 | 285 | PF02991 | 0.256 |
LIG_LIR_Apic_2 | 767 | 773 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 376 | 386 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 726 | 736 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 819 | 829 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 956 | 965 | PF02991 | 0.301 |
LIG_LIR_LC3C_4 | 884 | 888 | PF02991 | 0.343 |
LIG_LIR_LC3C_4 | 903 | 906 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 641 | 645 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 726 | 732 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 819 | 824 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 928 | 934 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 956 | 960 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 966 | 971 | PF02991 | 0.227 |
LIG_NRBOX | 675 | 681 | PF00104 | 0.456 |
LIG_NRBOX | 980 | 986 | PF00104 | 0.375 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.280 |
LIG_Pex14_2 | 841 | 845 | PF04695 | 0.256 |
LIG_Pex14_2 | 935 | 939 | PF04695 | 0.304 |
LIG_REV1ctd_RIR_1 | 821 | 829 | PF16727 | 0.424 |
LIG_REV1ctd_RIR_1 | 932 | 941 | PF16727 | 0.342 |
LIG_SH2_CRK | 826 | 830 | PF00017 | 0.311 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.277 |
LIG_SH2_PTP2 | 282 | 285 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 832 | 835 | PF00017 | 0.308 |
LIG_SH2_SRC | 752 | 755 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 752 | 755 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 931 | 934 | PF00017 | 0.294 |
LIG_SH3_1 | 524 | 530 | PF00018 | 0.408 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.464 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.508 |
LIG_SH3_3 | 903 | 909 | PF00018 | 0.516 |
LIG_SH3_3 | 956 | 962 | PF00018 | 0.316 |
LIG_SUMO_SIM_anti_2 | 884 | 890 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 903 | 908 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 970 | 975 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 153 | 161 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 610 | 615 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 884 | 890 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 969 | 975 | PF11976 | 0.403 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.361 |
LIG_TRAF2_1 | 507 | 510 | PF00917 | 0.467 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.277 |
LIG_UBA3_1 | 438 | 444 | PF00899 | 0.456 |
LIG_UBA3_1 | 5 | 13 | PF00899 | 0.539 |
LIG_WRC_WIRS_1 | 64 | 69 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 855 | 860 | PF05994 | 0.342 |
LIG_WW_3 | 591 | 595 | PF00397 | 0.456 |
MOD_CDK_SPK_2 | 526 | 531 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 38 | 45 | PF00069 | 0.467 |
MOD_CDK_SPxxK_3 | 648 | 655 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 694 | 701 | PF00069 | 0.542 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.489 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.456 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.552 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.506 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.563 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.452 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.403 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.301 |
MOD_CK1_1 | 989 | 995 | PF00069 | 0.653 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.530 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.260 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.493 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.480 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.496 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.473 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.542 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.240 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.163 |
MOD_GlcNHglycan | 364 | 368 | PF01048 | 0.361 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.295 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.348 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.267 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.304 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.338 |
MOD_GlcNHglycan | 999 | 1002 | PF01048 | 0.523 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.561 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.496 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.259 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.487 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.465 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.456 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.456 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.456 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.426 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.460 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.465 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.437 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.403 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.285 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.279 |
MOD_GSK3_1 | 963 | 970 | PF00069 | 0.340 |
MOD_N-GLC_1 | 694 | 699 | PF02516 | 0.342 |
MOD_N-GLC_1 | 743 | 748 | PF02516 | 0.285 |
MOD_N-GLC_1 | 900 | 905 | PF02516 | 0.256 |
MOD_N-GLC_1 | 997 | 1002 | PF02516 | 0.389 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.456 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.516 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.561 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.467 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.531 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.316 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.540 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.488 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.490 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.265 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.381 |
MOD_NEK2_1 | 925 | 930 | PF00069 | 0.373 |
MOD_NEK2_1 | 972 | 977 | PF00069 | 0.365 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.561 |
MOD_PK_1 | 485 | 491 | PF00069 | 0.467 |
MOD_PKA_1 | 474 | 480 | PF00069 | 0.517 |
MOD_PKA_1 | 513 | 519 | PF00069 | 0.496 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.467 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.542 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.487 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.456 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.481 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.525 |
MOD_PKA_2 | 907 | 913 | PF00069 | 0.456 |
MOD_PKA_2 | 989 | 995 | PF00069 | 0.634 |
MOD_PKB_1 | 187 | 195 | PF00069 | 0.477 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.482 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.452 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.326 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.408 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.456 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.324 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.467 |
MOD_Plk_1 | 900 | 906 | PF00069 | 0.456 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.518 |
MOD_Plk_2-3 | 359 | 365 | PF00069 | 0.561 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.500 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.480 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.477 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.342 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.487 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.562 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.480 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.546 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.324 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.467 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.489 |
MOD_Plk_4 | 881 | 887 | PF00069 | 0.298 |
MOD_Plk_4 | 900 | 906 | PF00069 | 0.409 |
MOD_Plk_4 | 925 | 931 | PF00069 | 0.351 |
MOD_Plk_4 | 967 | 973 | PF00069 | 0.327 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.456 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.262 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.457 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.518 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.550 |
MOD_ProDKin_1 | 648 | 654 | PF00069 | 0.516 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.542 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.267 |
MOD_ProDKin_1 | 939 | 945 | PF00069 | 0.372 |
MOD_SUMO_for_1 | 572 | 575 | PF00179 | 0.542 |
MOD_SUMO_rev_2 | 225 | 235 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 964 | 971 | PF00179 | 0.237 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 435 | 440 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_1 | 900 | 905 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 826 | 829 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 832 | 835 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 931 | 934 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 627 | 629 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 810 | 812 | PF00400 | 0.497 |
TRG_ER_FFAT_2 | 854 | 863 | PF00635 | 0.334 |
TRG_NLS_MonoExtN_4 | 465 | 472 | PF00514 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 76% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 30% | 91% |
A0A0N1HZI4 | Leptomonas seymouri | 21% | 81% |
A0A0N1I8I8 | Leptomonas seymouri | 28% | 83% |
A0A0N1PFH3 | Leptomonas seymouri | 31% | 83% |
A0A0S4INU6 | Bodo saltans | 21% | 83% |
A0A0S4J1M1 | Bodo saltans | 30% | 93% |
A0A0S4J5A1 | Bodo saltans | 31% | 95% |
A0A0S4J6U4 | Bodo saltans | 27% | 93% |
A0A0S4JA92 | Bodo saltans | 28% | 100% |
A0A0S4JRV4 | Bodo saltans | 30% | 100% |
A0A0S4KIG5 | Bodo saltans | 63% | 100% |
A0A0S4KNQ6 | Bodo saltans | 27% | 91% |
A0A1X0NNY6 | Trypanosomatidae | 68% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 28% | 92% |
A0A1X0NTI6 | Trypanosomatidae | 27% | 89% |
A0A1X0P0Y8 | Trypanosomatidae | 25% | 92% |
A0A1X0P689 | Trypanosomatidae | 31% | 97% |
A0A3R7KM63 | Trypanosoma rangeli | 28% | 97% |
A0A3R7MRX8 | Trypanosoma rangeli | 31% | 97% |
A0A3S5H5Y9 | Leishmania donovani | 28% | 92% |
A0A3S5ISK9 | Trypanosoma rangeli | 27% | 95% |
A0A3S7WPW0 | Leishmania donovani | 28% | 91% |
A0A3S7WUG2 | Leishmania donovani | 30% | 89% |
A0A3S7X978 | Leishmania donovani | 31% | 91% |
A0A422NTS7 | Trypanosoma rangeli | 67% | 100% |
A0A451EJU6 | Leishmania donovani | 95% | 99% |
A2VDL6 | Bos taurus | 31% | 99% |
A4H3S2 | Leishmania braziliensis | 86% | 100% |
A4H514 | Leishmania braziliensis | 28% | 100% |
A4H903 | Leishmania braziliensis | 29% | 100% |
A4HLF4 | Leishmania braziliensis | 26% | 85% |
A4HMM8 | Leishmania braziliensis | 31% | 100% |
A4HRZ6 | Leishmania infantum | 95% | 99% |
A4HT82 | Leishmania infantum | 30% | 100% |
A4HTF0 | Leishmania infantum | 29% | 100% |
A4HXD4 | Leishmania infantum | 30% | 89% |
A4IBA6 | Leishmania infantum | 31% | 91% |
A7L9Z8 | Mus musculus | 33% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
C9ZUI4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 80% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 97% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 92% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 27% | 100% |
D2WKD8 | Sus scrofa | 31% | 99% |
D3K0R6 | Bos taurus | 27% | 84% |
E9AF31 | Leishmania major | 30% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 92% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 89% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 83% |
G5E829 | Mus musculus | 29% | 83% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 29% | 72% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 92% |
O14983 | Homo sapiens | 49% | 100% |
O22218 | Arabidopsis thaliana | 29% | 98% |
O23087 | Arabidopsis thaliana | 43% | 96% |
O34431 | Bacillus subtilis (strain 168) | 35% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 35% | 100% |
O46674 | Canis lupus familiaris | 48% | 100% |
O55143 | Mus musculus | 47% | 97% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
O64806 | Arabidopsis thaliana | 28% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 77% |
O75185 | Homo sapiens | 32% | 100% |
O77696 | Sus scrofa | 48% | 100% |
O81108 | Arabidopsis thaliana | 28% | 100% |
P04074 | Ovis aries | 32% | 99% |
P04191 | Oryctolagus cuniculus | 49% | 100% |
P05023 | Homo sapiens | 32% | 99% |
P05024 | Sus scrofa | 32% | 99% |
P05025 | Tetronarce californica | 32% | 99% |
P06685 | Rattus norvegicus | 32% | 99% |
P06686 | Rattus norvegicus | 31% | 99% |
P06687 | Rattus norvegicus | 32% | 100% |
P09572 | Gallus gallus | 33% | 99% |
P09626 | Rattus norvegicus | 32% | 98% |
P0ABB8 | Escherichia coli (strain K12) | 27% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 27% | 100% |
P11505 | Rattus norvegicus | 29% | 83% |
P11506 | Rattus norvegicus | 29% | 81% |
P11507 | Rattus norvegicus | 47% | 97% |
P11607 | Sus scrofa | 48% | 97% |
P13585 | Gallus gallus | 49% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 93% |
P13607 | Drosophila melanogaster | 33% | 97% |
P13637 | Homo sapiens | 32% | 100% |
P16615 | Homo sapiens | 47% | 97% |
P17326 | Artemia franciscana | 31% | 100% |
P18596 | Rattus norvegicus | 49% | 100% |
P18907 | Equus caballus | 32% | 99% |
P19156 | Sus scrofa | 31% | 98% |
P19456 | Arabidopsis thaliana | 27% | 100% |
P20020 | Homo sapiens | 29% | 83% |
P20431 | Arabidopsis thaliana | 29% | 100% |
P20647 | Oryctolagus cuniculus | 48% | 97% |
P20648 | Homo sapiens | 32% | 98% |
P20649 | Arabidopsis thaliana | 27% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 29% | 100% |
P22180 | Solanum lycopersicum | 26% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 98% |
P22700 | Drosophila melanogaster | 48% | 99% |
P23220 | Sus scrofa | 29% | 83% |
P23634 | Homo sapiens | 27% | 82% |
P24797 | Gallus gallus | 34% | 100% |
P24798 | Gallus gallus | 33% | 100% |
P25489 | Catostomus commersonii | 32% | 99% |
P27112 | Oryctolagus cuniculus | 32% | 98% |
P28774 | Artemia franciscana | 31% | 100% |
P30714 | Rhinella marina | 32% | 99% |
P35315 | Trypanosoma brucei brucei | 68% | 100% |
P35316 | Artemia franciscana | 48% | 100% |
P35317 | Hydra vulgaris | 30% | 98% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 34% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 34% | 100% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 31% | 100% |
P50993 | Homo sapiens | 31% | 99% |
P50996 | Canis lupus familiaris | 31% | 98% |
P50997 | Canis lupus familiaris | 31% | 99% |
P54209 | Dunaliella bioculata | 46% | 98% |
P54210 | Dunaliella acidophila | 25% | 92% |
P54211 | Dunaliella bioculata | 25% | 90% |
P54678 | Dictyostelium discoideum | 30% | 91% |
P54707 | Homo sapiens | 31% | 97% |
P54708 | Rattus norvegicus | 32% | 98% |
P57709 | Bos taurus | 33% | 100% |
P58165 | Oreochromis mossambicus | 29% | 91% |
P58312 | Oreochromis mossambicus | 31% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 34% | 100% |
P70083 | Makaira nigricans | 49% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 30% | 100% |
P83970 | Triticum aestivum | 25% | 100% |
P90747 | Caenorhabditis elegans | 23% | 86% |
P92939 | Arabidopsis thaliana | 44% | 95% |
P98194 | Homo sapiens | 33% | 100% |
P98197 | Mus musculus | 23% | 85% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 34% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 34% | 100% |
Q00779 | Felis catus | 48% | 100% |
Q00804 | Oryctolagus cuniculus | 30% | 83% |
Q01814 | Homo sapiens | 29% | 81% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 93% |
Q03194 | Nicotiana plumbaginifolia | 26% | 100% |
Q03669 | Gallus gallus | 48% | 97% |
Q08435 | Nicotiana plumbaginifolia | 26% | 100% |
Q08436 | Nicotiana plumbaginifolia | 26% | 100% |
Q08DA1 | Bos taurus | 32% | 99% |
Q0VCY0 | Bos taurus | 49% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 93% |
Q13733 | Homo sapiens | 31% | 98% |
Q16720 | Homo sapiens | 28% | 83% |
Q21286 | Caenorhabditis elegans | 23% | 84% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 48% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 27% | 99% |
Q2QY12 | Oryza sativa subsp. japonica | 29% | 97% |
Q2RAS0 | Oryza sativa subsp. japonica | 29% | 100% |
Q37145 | Arabidopsis thaliana | 30% | 99% |
Q3TYU2 | Mus musculus | 22% | 83% |
Q42556 | Arabidopsis thaliana | 25% | 100% |
Q42883 | Solanum lycopersicum | 43% | 97% |
Q43128 | Arabidopsis thaliana | 26% | 100% |
Q4QED4 | Leishmania major | 31% | 96% |
Q4QIM6 | Leishmania major | 27% | 100% |
Q4QIM8 | Leishmania major | 28% | 100% |
Q4VNC0 | Homo sapiens | 22% | 83% |
Q4VNC1 | Homo sapiens | 22% | 85% |
Q5R5K5 | Pongo abelii | 33% | 100% |
Q5RCD8 | Pongo abelii | 31% | 99% |
Q5RDR3 | Pongo abelii | 32% | 99% |
Q5XF89 | Mus musculus | 20% | 83% |
Q5XF90 | Mus musculus | 21% | 85% |
Q5ZKB7 | Gallus gallus | 22% | 84% |
Q64392 | Cavia porcellus | 31% | 98% |
Q64436 | Mus musculus | 33% | 98% |
Q64518 | Mus musculus | 49% | 100% |
Q64541 | Rattus norvegicus | 30% | 99% |
Q64542 | Rattus norvegicus | 27% | 84% |
Q64566 | Rattus norvegicus | 33% | 100% |
Q64568 | Rattus norvegicus | 28% | 81% |
Q64578 | Rattus norvegicus | 50% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 30% | 99% |
Q6ATV4 | Oryza sativa subsp. japonica | 31% | 98% |
Q6DFW5 | Mus musculus | 22% | 86% |
Q6PIC6 | Mus musculus | 32% | 100% |
Q6PIE5 | Mus musculus | 31% | 99% |
Q6Q477 | Mus musculus | 28% | 84% |
Q6RWA9 | Taenia solium | 32% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 34% | 100% |
Q7PPA5 | Anopheles gambiae | 48% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 28% | 93% |
Q7XEK4 | Oryza sativa subsp. japonica | 31% | 98% |
Q7XPY2 | Oryza sativa subsp. japonica | 28% | 100% |
Q80XR2 | Mus musculus | 33% | 100% |
Q8R429 | Mus musculus | 50% | 100% |
Q8R4C1 | Rattus norvegicus | 32% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 29% | 97% |
Q8VDN2 | Mus musculus | 32% | 99% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 33% | 100% |
Q92030 | Anguilla anguilla | 33% | 99% |
Q92036 | Rhinella marina | 29% | 97% |
Q92105 | Pelophylax lessonae | 49% | 100% |
Q92123 | Xenopus laevis | 32% | 99% |
Q92126 | Xenopus laevis | 32% | 98% |
Q93084 | Homo sapiens | 48% | 100% |
Q95050 | Tetrahymena thermophila | 21% | 89% |
Q95JN5 | Macaca fascicularis | 21% | 83% |
Q95Z93 | Leishmania major | 94% | 100% |
Q98SH2 | Gallus gallus | 28% | 84% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 35% | 100% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 78% |
Q9LF79 | Arabidopsis thaliana | 29% | 94% |
Q9LIK7 | Arabidopsis thaliana | 30% | 100% |
Q9LU41 | Arabidopsis thaliana | 30% | 93% |
Q9LV11 | Arabidopsis thaliana | 26% | 100% |
Q9LY32 | Arabidopsis thaliana | 27% | 100% |
Q9LY77 | Arabidopsis thaliana | 29% | 98% |
Q9M2A0 | Arabidopsis thaliana | 26% | 100% |
Q9M2L4 | Arabidopsis thaliana | 26% | 99% |
Q9N0Z4 | Oryctolagus cuniculus | 21% | 87% |
Q9N0Z6 | Oryctolagus cuniculus | 32% | 99% |
Q9NQ11 | Homo sapiens | 22% | 86% |
Q9R0K7 | Mus musculus | 27% | 85% |
Q9SH76 | Arabidopsis thaliana | 25% | 100% |
Q9SJB3 | Arabidopsis thaliana | 26% | 100% |
Q9SU58 | Arabidopsis thaliana | 26% | 100% |
Q9SY55 | Arabidopsis thaliana | 46% | 100% |
Q9SZR1 | Arabidopsis thaliana | 30% | 95% |
Q9TV52 | Oryctolagus cuniculus | 31% | 93% |
Q9WV27 | Mus musculus | 30% | 98% |
Q9XES1 | Arabidopsis thaliana | 45% | 95% |
Q9Y2G3 | Homo sapiens | 21% | 86% |
Q9YGL9 | Gallus gallus | 48% | 100% |
Q9YH26 | Oreochromis mossambicus | 32% | 99% |
Q9Z1W8 | Mus musculus | 32% | 98% |
V5B873 | Trypanosoma cruzi | 28% | 92% |
V5BHZ2 | Trypanosoma cruzi | 31% | 97% |
V5BLM1 | Trypanosoma cruzi | 67% | 100% |
V5BPC6 | Trypanosoma cruzi | 25% | 96% |