Homologous to other eukaryotic P-type Ca2+ ATPases.. For some reason, this group has heavily expanded in Kinetoplastida.. Localization: Endosomal (by homology) / 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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0005886 | plasma membrane | 3 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
Related structures:
AlphaFold database: E9AL76
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0003824 | catalytic activity | 1 | 21 |
GO:0005215 | transporter activity | 1 | 16 |
GO:0005388 | P-type calcium transporter activity | 4 | 16 |
GO:0005488 | binding | 1 | 21 |
GO:0005524 | ATP binding | 5 | 21 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 16 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 16 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 16 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 16 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 16 |
GO:0015662 | P-type ion transporter activity | 4 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 21 |
GO:0016787 | hydrolase activity | 2 | 21 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 21 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 21 |
GO:0016887 | ATP hydrolysis activity | 7 | 21 |
GO:0017076 | purine nucleotide binding | 4 | 21 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 21 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 16 |
GO:0022804 | active transmembrane transporter activity | 3 | 16 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 21 |
GO:0032553 | ribonucleotide binding | 3 | 21 |
GO:0032555 | purine ribonucleotide binding | 4 | 21 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 21 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 16 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043168 | anion binding | 3 | 21 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:0097367 | carbohydrate derivative binding | 2 | 21 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 1076 | 1078 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 797 | 799 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 860 | 862 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 865 | 867 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 929 | 931 | PF00675 | 0.267 |
CLV_PCSK_FUR_1 | 194 | 198 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 1050 | 1052 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 1076 | 1078 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 860 | 862 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 873 | 875 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 1050 | 1052 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 539 | 541 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 1021 | 1025 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 1026 | 1030 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 1082 | 1086 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.265 |
DEG_APCC_DBOX_1 | 1020 | 1028 | PF00400 | 0.466 |
DEG_MDM2_SWIB_1 | 896 | 903 | PF02201 | 0.319 |
DEG_SCF_FBW7_2 | 296 | 303 | PF00400 | 0.483 |
DEG_SPOP_SBC_1 | 466 | 470 | PF00917 | 0.588 |
DOC_CYCLIN_RxL_1 | 796 | 806 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 436 | 442 | PF00134 | 0.596 |
DOC_MAPK_DCC_7 | 432 | 442 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 1048 | 1057 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 194 | 204 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 451 | 459 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 798 | 805 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 873 | 881 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 905 | 915 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 930 | 938 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 944 | 951 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 197 | 206 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 724 | 731 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 798 | 807 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 873 | 881 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 944 | 951 | PF00069 | 0.428 |
DOC_MAPK_NFAT4_5 | 724 | 732 | PF00069 | 0.497 |
DOC_MAPK_NFAT4_5 | 798 | 806 | PF00069 | 0.470 |
DOC_PP1_RVXF_1 | 783 | 790 | PF00149 | 0.488 |
DOC_PP1_RVXF_1 | 972 | 978 | PF00149 | 0.205 |
DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.438 |
DOC_PP2B_LxvP_1 | 221 | 224 | PF13499 | 0.467 |
DOC_PP2B_PxIxI_1 | 946 | 952 | PF00149 | 0.206 |
DOC_PP4_FxxP_1 | 1099 | 1102 | PF00568 | 0.527 |
DOC_USP7_MATH_1 | 1039 | 1043 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 869 | 873 | PF00917 | 0.494 |
DOC_WW_Pin1_4 | 1098 | 1103 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.330 |
LIG_14-3-3_CanoR_1 | 1053 | 1058 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.260 |
LIG_14-3-3_CanoR_1 | 250 | 258 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 974 | 984 | PF00244 | 0.205 |
LIG_Actin_WH2_2 | 438 | 456 | PF00022 | 0.444 |
LIG_Actin_WH2_2 | 65 | 83 | PF00022 | 0.544 |
LIG_Actin_WH2_2 | 963 | 978 | PF00022 | 0.479 |
LIG_AP2alpha_1 | 347 | 351 | PF02296 | 0.483 |
LIG_APCC_ABBA_1 | 9 | 14 | PF00400 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.642 |
LIG_BIR_III_4 | 695 | 699 | PF00653 | 0.612 |
LIG_BRCT_BRCA1_1 | 944 | 948 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 952 | 956 | PF00533 | 0.347 |
LIG_Clathr_ClatBox_1 | 999 | 1003 | PF01394 | 0.594 |
LIG_CNOT1_NIM_1 | 344 | 353 | PF04054 | 0.424 |
LIG_EH1_1 | 885 | 893 | PF00400 | 0.188 |
LIG_EVH1_2 | 105 | 109 | PF00568 | 0.476 |
LIG_FHA_1 | 1066 | 1072 | PF00498 | 0.634 |
LIG_FHA_1 | 1083 | 1089 | PF00498 | 0.566 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.275 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.468 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.485 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.458 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.500 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.516 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.538 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.554 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.287 |
LIG_FHA_1 | 876 | 882 | PF00498 | 0.373 |
LIG_FHA_1 | 979 | 985 | PF00498 | 0.314 |
LIG_FHA_1 | 988 | 994 | PF00498 | 0.390 |
LIG_FHA_2 | 1032 | 1038 | PF00498 | 0.649 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.492 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.459 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.493 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.636 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.678 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.482 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.518 |
LIG_FHA_2 | 731 | 737 | PF00498 | 0.590 |
LIG_FHA_2 | 963 | 969 | PF00498 | 0.341 |
LIG_GBD_Chelix_1 | 72 | 80 | PF00786 | 0.267 |
LIG_Integrin_RGD_1 | 679 | 681 | PF01839 | 0.307 |
LIG_LIR_Apic_2 | 1098 | 1102 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 623 | 632 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 806 | 817 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 912 | 923 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 953 | 962 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 968 | 977 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 987 | 996 | PF02991 | 0.321 |
LIG_LIR_LC3C_4 | 218 | 223 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 1056 | 1062 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 688 | 692 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 806 | 812 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 912 | 918 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 937 | 942 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 945 | 951 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 953 | 957 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 965 | 969 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 987 | 991 | PF02991 | 0.347 |
LIG_NRBOX | 322 | 328 | PF00104 | 0.500 |
LIG_PCNA_TLS_4 | 345 | 352 | PF02747 | 0.495 |
LIG_PCNA_yPIPBox_3 | 791 | 801 | PF02747 | 0.472 |
LIG_PCNA_yPIPBox_3 | 905 | 918 | PF02747 | 0.147 |
LIG_Pex14_1 | 1058 | 1062 | PF04695 | 0.488 |
LIG_Pex14_1 | 153 | 157 | PF04695 | 0.339 |
LIG_Pex14_2 | 1007 | 1011 | PF04695 | 0.653 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.483 |
LIG_Pex14_2 | 896 | 900 | PF04695 | 0.277 |
LIG_Pex14_2 | 920 | 924 | PF04695 | 0.402 |
LIG_Pex14_2 | 938 | 942 | PF04695 | 0.386 |
LIG_Pex14_2 | 954 | 958 | PF04695 | 0.345 |
LIG_PTB_Apo_2 | 688 | 695 | PF02174 | 0.568 |
LIG_PTB_Apo_2 | 752 | 759 | PF02174 | 0.509 |
LIG_PTB_Phospho_1 | 688 | 694 | PF10480 | 0.567 |
LIG_REV1ctd_RIR_1 | 93 | 101 | PF16727 | 0.476 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.619 |
LIG_SH2_CRK | 885 | 889 | PF00017 | 0.331 |
LIG_SH2_GRB2like | 570 | 573 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 933 | 937 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 809 | 812 | PF00017 | 0.341 |
LIG_SH2_SRC | 1062 | 1065 | PF00017 | 0.478 |
LIG_SH2_SRC | 933 | 936 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 1062 | 1066 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.341 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.443 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.461 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.585 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.552 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.476 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.320 |
LIG_SUMO_SIM_anti_2 | 356 | 361 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 772 | 778 | PF11976 | 0.506 |
LIG_SUMO_SIM_anti_2 | 878 | 883 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 981 | 987 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 162 | 168 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 201 | 208 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 358 | 364 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 366 | 371 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 727 | 733 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 736 | 741 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 772 | 778 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 959 | 965 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 981 | 987 | PF11976 | 0.426 |
LIG_TRAF2_1 | 1001 | 1004 | PF00917 | 0.598 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.476 |
LIG_TRAF2_1 | 850 | 853 | PF00917 | 0.366 |
LIG_TRAF2_1 | 854 | 857 | PF00917 | 0.500 |
LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.500 |
LIG_TYR_ITIM | 605 | 610 | PF00017 | 0.547 |
LIG_TYR_ITIM | 807 | 812 | PF00017 | 0.341 |
LIG_UBA3_1 | 923 | 931 | PF00899 | 0.280 |
LIG_WRC_WIRS_1 | 951 | 956 | PF05994 | 0.349 |
LIG_WRC_WIRS_1 | 963 | 968 | PF05994 | 0.348 |
LIG_WRC_WIRS_1 | 985 | 990 | PF05994 | 0.479 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.515 |
MOD_CK1_1 | 1086 | 1092 | PF00069 | 0.657 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.472 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.516 |
MOD_CK1_1 | 827 | 833 | PF00069 | 0.274 |
MOD_CK1_1 | 978 | 984 | PF00069 | 0.325 |
MOD_CK2_1 | 1031 | 1037 | PF00069 | 0.661 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.529 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.670 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.477 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.555 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.609 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.567 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.588 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.455 |
MOD_GlcNHglycan | 1041 | 1044 | PF01048 | 0.444 |
MOD_GlcNHglycan | 186 | 191 | PF01048 | 0.443 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.283 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.341 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.424 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.286 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.362 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.337 |
MOD_GSK3_1 | 1082 | 1089 | PF00069 | 0.683 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.522 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.314 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.603 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.486 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.456 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.728 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.504 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.559 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.512 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.327 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.296 |
MOD_GSK3_1 | 848 | 855 | PF00069 | 0.313 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.436 |
MOD_LATS_1 | 555 | 561 | PF00433 | 0.482 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.366 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.320 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.241 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.316 |
MOD_N-GLC_1 | 675 | 680 | PF02516 | 0.301 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.435 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.552 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.443 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.483 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.419 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.476 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.455 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.601 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.609 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.561 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.517 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.494 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.525 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.322 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.322 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.461 |
MOD_NEK2_1 | 942 | 947 | PF00069 | 0.488 |
MOD_NEK2_2 | 446 | 451 | PF00069 | 0.595 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.507 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.466 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.512 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.542 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.530 |
MOD_PKA_1 | 249 | 255 | PF00069 | 0.530 |
MOD_PKA_1 | 539 | 545 | PF00069 | 0.470 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.467 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.483 |
MOD_PKA_2 | 904 | 910 | PF00069 | 0.297 |
MOD_PKA_2 | 975 | 981 | PF00069 | 0.205 |
MOD_PKB_1 | 1051 | 1059 | PF00069 | 0.492 |
MOD_PKB_1 | 519 | 527 | PF00069 | 0.431 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.515 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.492 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.458 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.477 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.515 |
MOD_Plk_1 | 978 | 984 | PF00069 | 0.182 |
MOD_Plk_2-3 | 852 | 858 | PF00069 | 0.509 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.460 |
MOD_Plk_4 | 1053 | 1059 | PF00069 | 0.630 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.457 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.297 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.323 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.472 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.468 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.487 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.514 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.532 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.597 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.596 |
MOD_Plk_4 | 812 | 818 | PF00069 | 0.319 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.265 |
MOD_Plk_4 | 980 | 986 | PF00069 | 0.333 |
MOD_ProDKin_1 | 1098 | 1104 | PF00069 | 0.578 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.519 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.459 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.611 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.262 |
MOD_SUMO_rev_2 | 536 | 541 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_1 | 307 | 312 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_1 | 548 | 553 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 120 | 125 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 995 | 1000 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 1093 | 1096 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 809 | 812 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 885 | 888 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 898 | 901 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 933 | 936 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 1051 | 1054 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 1075 | 1077 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 859 | 861 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 873 | 875 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 974 | 977 | PF00400 | 0.329 |
TRG_NES_CRM1_1 | 622 | 634 | PF08389 | 0.556 |
TRG_NES_CRM1_1 | 720 | 736 | PF08389 | 0.520 |
TRG_NLS_MonoExtN_4 | 1048 | 1054 | PF00514 | 0.506 |
TRG_NLS_MonoExtN_4 | 248 | 253 | PF00514 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 690 | 695 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 930 | 934 | PF00026 | 0.266 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 29% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 41% | 99% |
A0A0N1PFH3 | Leptomonas seymouri | 26% | 91% |
A0A0S4J1M1 | Bodo saltans | 27% | 100% |
A0A0S4J5A1 | Bodo saltans | 27% | 100% |
A0A0S4J6U4 | Bodo saltans | 38% | 100% |
A0A0S4JA92 | Bodo saltans | 42% | 100% |
A0A0S4JDQ9 | Bodo saltans | 22% | 99% |
A0A0S4JRV4 | Bodo saltans | 40% | 100% |
A0A0S4KIG5 | Bodo saltans | 29% | 100% |
A0A0S4KNQ6 | Bodo saltans | 63% | 99% |
A0A1X0NNY6 | Trypanosomatidae | 29% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 66% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 41% | 97% |
A0A1X0P0Y8 | Trypanosomatidae | 36% | 100% |
A0A1X0P689 | Trypanosomatidae | 28% | 100% |
A0A1X0P720 | Trypanosomatidae | 24% | 100% |
A0A1X0P7A1 | Trypanosomatidae | 24% | 100% |
A0A1X0P842 | Trypanosomatidae | 23% | 100% |
A0A381MFJ0 | Leishmania infantum | 23% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 67% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 95% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WPW0 | Leishmania donovani | 86% | 99% |
A0A3S7WUG2 | Leishmania donovani | 40% | 97% |
A0A3S7WV61 | Leishmania donovani | 23% | 100% |
A0A3S7WV68 | Leishmania donovani | 23% | 100% |
A0A3S7X978 | Leishmania donovani | 27% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 29% | 100% |
A0A451EJU6 | Leishmania donovani | 28% | 100% |
A2VDL6 | Bos taurus | 28% | 100% |
A4H3S2 | Leishmania braziliensis | 27% | 100% |
A4H514 | Leishmania braziliensis | 89% | 100% |
A4H903 | Leishmania braziliensis | 40% | 100% |
A4H9Q5 | Leishmania braziliensis | 24% | 100% |
A4HMM8 | Leishmania braziliensis | 27% | 100% |
A4HRZ6 | Leishmania infantum | 28% | 100% |
A4HT82 | Leishmania infantum | 85% | 100% |
A4HTF0 | Leishmania infantum | 95% | 100% |
A4HXD4 | Leishmania infantum | 40% | 97% |
A4HY23 | Leishmania infantum | 23% | 100% |
A4IBA6 | Leishmania infantum | 26% | 100% |
A7L9Z8 | Mus musculus | 28% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 24% | 100% |
D2WKD8 | Sus scrofa | 28% | 100% |
D3K0R6 | Bos taurus | 36% | 91% |
E9AF31 | Leishmania major | 27% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 97% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 90% |
G5E829 | Mus musculus | 38% | 90% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 38% | 78% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
O14983 | Homo sapiens | 29% | 100% |
O22218 | Arabidopsis thaliana | 37% | 100% |
O23087 | Arabidopsis thaliana | 27% | 100% |
O34431 | Bacillus subtilis (strain 168) | 30% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
O46674 | Canis lupus familiaris | 27% | 100% |
O55143 | Mus musculus | 28% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
O64806 | Arabidopsis thaliana | 38% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 84% |
O75185 | Homo sapiens | 28% | 100% |
O77696 | Sus scrofa | 28% | 100% |
O81108 | Arabidopsis thaliana | 38% | 100% |
P04074 | Ovis aries | 26% | 100% |
P04191 | Oryctolagus cuniculus | 29% | 100% |
P05023 | Homo sapiens | 27% | 100% |
P05024 | Sus scrofa | 27% | 100% |
P05025 | Tetronarce californica | 28% | 100% |
P06685 | Rattus norvegicus | 27% | 100% |
P06686 | Rattus norvegicus | 28% | 100% |
P06687 | Rattus norvegicus | 27% | 100% |
P09572 | Gallus gallus | 28% | 100% |
P09626 | Rattus norvegicus | 25% | 100% |
P09627 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 25% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 25% | 100% |
P11505 | Rattus norvegicus | 38% | 90% |
P11506 | Rattus norvegicus | 39% | 89% |
P11507 | Rattus norvegicus | 27% | 100% |
P11607 | Sus scrofa | 27% | 100% |
P11718 | Leishmania donovani | 23% | 100% |
P12522 | Leishmania donovani | 23% | 100% |
P13585 | Gallus gallus | 28% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P13607 | Drosophila melanogaster | 27% | 100% |
P13637 | Homo sapiens | 27% | 100% |
P16615 | Homo sapiens | 28% | 100% |
P17326 | Artemia franciscana | 28% | 100% |
P18596 | Rattus norvegicus | 28% | 100% |
P18907 | Equus caballus | 27% | 100% |
P19156 | Sus scrofa | 26% | 100% |
P20020 | Homo sapiens | 38% | 90% |
P20431 | Arabidopsis thaliana | 22% | 100% |
P20647 | Oryctolagus cuniculus | 27% | 100% |
P20648 | Homo sapiens | 25% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 24% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
P22700 | Drosophila melanogaster | 27% | 100% |
P23220 | Sus scrofa | 38% | 90% |
P23634 | Homo sapiens | 37% | 89% |
P24797 | Gallus gallus | 28% | 100% |
P24798 | Gallus gallus | 27% | 100% |
P25489 | Catostomus commersonii | 28% | 100% |
P27112 | Oryctolagus cuniculus | 25% | 100% |
P28774 | Artemia franciscana | 28% | 100% |
P30714 | Rhinella marina | 27% | 100% |
P35315 | Trypanosoma brucei brucei | 30% | 100% |
P35316 | Artemia franciscana | 25% | 100% |
P35317 | Hydra vulgaris | 28% | 100% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 24% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 31% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 28% | 100% |
P38929 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 94% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 27% | 100% |
P50993 | Homo sapiens | 28% | 100% |
P50996 | Canis lupus familiaris | 26% | 100% |
P50997 | Canis lupus familiaris | 27% | 100% |
P54209 | Dunaliella bioculata | 28% | 100% |
P54211 | Dunaliella bioculata | 23% | 98% |
P54678 | Dictyostelium discoideum | 40% | 99% |
P54679 | Dictyostelium discoideum | 23% | 100% |
P54707 | Homo sapiens | 28% | 100% |
P54708 | Rattus norvegicus | 27% | 100% |
P57709 | Bos taurus | 28% | 100% |
P58165 | Oreochromis mossambicus | 40% | 99% |
P58312 | Oreochromis mossambicus | 26% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70083 | Makaira nigricans | 27% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 28% | 100% |
P92939 | Arabidopsis thaliana | 28% | 100% |
P98194 | Homo sapiens | 28% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q00779 | Felis catus | 27% | 100% |
Q00804 | Oryctolagus cuniculus | 38% | 90% |
Q01814 | Homo sapiens | 39% | 89% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q03669 | Gallus gallus | 27% | 100% |
Q07421 | Ajellomyces capsulatus | 24% | 100% |
Q08435 | Nicotiana plumbaginifolia | 23% | 100% |
Q08436 | Nicotiana plumbaginifolia | 22% | 100% |
Q08DA1 | Bos taurus | 26% | 100% |
Q0VCY0 | Bos taurus | 29% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q13733 | Homo sapiens | 29% | 100% |
Q16720 | Homo sapiens | 35% | 90% |
Q21286 | Caenorhabditis elegans | 22% | 92% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 27% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 37% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 37% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 37% | 100% |
Q37145 | Arabidopsis thaliana | 37% | 100% |
Q42883 | Solanum lycopersicum | 27% | 100% |
Q43128 | Arabidopsis thaliana | 24% | 100% |
Q4QDN7 | Leishmania major | 23% | 100% |
Q4QDN8 | Leishmania major | 23% | 100% |
Q4QED4 | Leishmania major | 40% | 100% |
Q4QIM6 | Leishmania major | 85% | 100% |
Q4QIM8 | Leishmania major | 94% | 100% |
Q4VNC1 | Homo sapiens | 22% | 92% |
Q58623 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 25% | 100% |
Q5R5K5 | Pongo abelii | 28% | 100% |
Q5RCD8 | Pongo abelii | 28% | 100% |
Q5RDR3 | Pongo abelii | 27% | 100% |
Q5XF89 | Mus musculus | 20% | 91% |
Q5XF90 | Mus musculus | 21% | 93% |
Q5ZKB7 | Gallus gallus | 22% | 92% |
Q64392 | Cavia porcellus | 28% | 100% |
Q64436 | Mus musculus | 26% | 100% |
Q64518 | Mus musculus | 28% | 100% |
Q64541 | Rattus norvegicus | 26% | 100% |
Q64542 | Rattus norvegicus | 38% | 92% |
Q64566 | Rattus norvegicus | 27% | 100% |
Q64568 | Rattus norvegicus | 35% | 88% |
Q64578 | Rattus norvegicus | 28% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 36% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6PIC6 | Mus musculus | 27% | 100% |
Q6PIE5 | Mus musculus | 28% | 100% |
Q6Q477 | Mus musculus | 36% | 92% |
Q6RWA9 | Taenia solium | 28% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 29% | 100% |
Q7PPA5 | Anopheles gambiae | 28% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 37% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 36% | 100% |
Q80XR2 | Mus musculus | 27% | 100% |
Q8R429 | Mus musculus | 28% | 100% |
Q8R4C1 | Rattus norvegicus | 29% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 37% | 100% |
Q8VDN2 | Mus musculus | 27% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 30% | 100% |
Q92030 | Anguilla anguilla | 28% | 100% |
Q92036 | Rhinella marina | 27% | 100% |
Q92105 | Pelophylax lessonae | 29% | 100% |
Q92123 | Xenopus laevis | 28% | 100% |
Q92126 | Xenopus laevis | 27% | 100% |
Q93084 | Homo sapiens | 28% | 100% |
Q95Z93 | Leishmania major | 28% | 100% |
Q98SH2 | Gallus gallus | 36% | 92% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 28% | 100% |
Q9CTG6 | Mus musculus | 24% | 94% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 85% |
Q9LF79 | Arabidopsis thaliana | 38% | 100% |
Q9LIK7 | Arabidopsis thaliana | 35% | 100% |
Q9LU41 | Arabidopsis thaliana | 36% | 100% |
Q9LV11 | Arabidopsis thaliana | 23% | 100% |
Q9LY77 | Arabidopsis thaliana | 36% | 100% |
Q9M2A0 | Arabidopsis thaliana | 22% | 100% |
Q9M2L4 | Arabidopsis thaliana | 38% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 27% | 100% |
Q9NQ11 | Homo sapiens | 23% | 94% |
Q9R0K7 | Mus musculus | 36% | 92% |
Q9SJB3 | Arabidopsis thaliana | 22% | 100% |
Q9SY55 | Arabidopsis thaliana | 27% | 100% |
Q9SZR1 | Arabidopsis thaliana | 37% | 100% |
Q9TV52 | Oryctolagus cuniculus | 29% | 100% |
Q9WV27 | Mus musculus | 27% | 100% |
Q9XES1 | Arabidopsis thaliana | 28% | 100% |
Q9Y2G3 | Homo sapiens | 21% | 94% |
Q9YGL9 | Gallus gallus | 28% | 100% |
Q9YH26 | Oreochromis mossambicus | 28% | 100% |
Q9Z1W8 | Mus musculus | 27% | 100% |
V5B873 | Trypanosoma cruzi | 65% | 100% |
V5BHZ2 | Trypanosoma cruzi | 26% | 100% |
V5BLM1 | Trypanosoma cruzi | 30% | 100% |
V5BPC6 | Trypanosoma cruzi | 35% | 100% |