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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
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: A4H514
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 20 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0005215 | transporter activity | 1 | 16 |
GO:0005388 | P-type calcium transporter activity | 4 | 16 |
GO:0005488 | binding | 1 | 20 |
GO:0005524 | ATP binding | 5 | 20 |
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 | 20 |
GO:0016787 | hydrolase activity | 2 | 20 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 20 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 20 |
GO:0016887 | ATP hydrolysis activity | 7 | 20 |
GO:0017076 | purine nucleotide binding | 4 | 20 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 20 |
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 | 20 |
GO:0032553 | ribonucleotide binding | 3 | 20 |
GO:0032555 | purine ribonucleotide binding | 4 | 20 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 20 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
GO:0036094 | small molecule binding | 2 | 20 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 16 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043168 | anion binding | 3 | 20 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0097367 | carbohydrate derivative binding | 2 | 20 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 527 | 531 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 661 | 665 | PF00656 | 0.558 |
CLV_MEL_PAP_1 | 45 | 51 | PF00089 | 0.322 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 887 | 889 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 895 | 897 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.266 |
CLV_PCSK_FUR_1 | 1028 | 1032 | PF00082 | 0.404 |
CLV_PCSK_FUR_1 | 216 | 220 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 1030 | 1032 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 1072 | 1074 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 882 | 884 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 895 | 897 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 926 | 928 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 1030 | 1032 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 1072 | 1074 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 882 | 884 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 926 | 928 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 1048 | 1052 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 1104 | 1108 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 1116 | 1120 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 968 | 972 | PF00082 | 0.238 |
CLV_Separin_Metazoa | 353 | 357 | PF03568 | 0.418 |
DEG_APCC_DBOX_1 | 967 | 975 | PF00400 | 0.409 |
DEG_SCF_FBW7_2 | 318 | 325 | PF00400 | 0.482 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.501 |
DEG_SPOP_SBC_1 | 488 | 492 | PF00917 | 0.589 |
DOC_CYCLIN_RxL_1 | 818 | 828 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 458 | 464 | PF00134 | 0.584 |
DOC_MAPK_DCC_7 | 454 | 464 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 1070 | 1079 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 473 | 481 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 820 | 827 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 895 | 903 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 926 | 937 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 952 | 960 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 966 | 974 | PF00069 | 0.405 |
DOC_MAPK_JIP1_4 | 968 | 974 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 746 | 753 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 820 | 829 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 895 | 903 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 966 | 973 | PF00069 | 0.427 |
DOC_MAPK_NFAT4_5 | 746 | 754 | PF00069 | 0.498 |
DOC_MAPK_NFAT4_5 | 820 | 828 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 805 | 812 | PF00149 | 0.488 |
DOC_PP1_RVXF_1 | 994 | 1000 | PF00149 | 0.204 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.438 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.466 |
DOC_USP7_MATH_1 | 1061 | 1065 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 789 | 793 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 891 | 895 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 846 | 851 | PF00397 | 0.331 |
LIG_14-3-3_CanoR_1 | 1075 | 1080 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 468 | 473 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 474 | 481 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 509 | 518 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 996 | 1006 | PF00244 | 0.204 |
LIG_Actin_WH2_2 | 1107 | 1122 | PF00022 | 0.492 |
LIG_Actin_WH2_2 | 985 | 1000 | PF00022 | 0.476 |
LIG_AP2alpha_1 | 369 | 373 | PF02296 | 0.482 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BIR_III_4 | 717 | 721 | PF00653 | 0.625 |
LIG_BRCT_BRCA1_1 | 966 | 970 | PF00533 | 0.483 |
LIG_CNOT1_NIM_1 | 366 | 375 | PF04054 | 0.424 |
LIG_DLG_GKlike_1 | 468 | 475 | PF00625 | 0.536 |
LIG_EVH1_2 | 127 | 131 | PF00568 | 0.476 |
LIG_FHA_1 | 1003 | 1009 | PF00498 | 0.390 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.365 |
LIG_FHA_1 | 1010 | 1016 | PF00498 | 0.389 |
LIG_FHA_1 | 1088 | 1094 | PF00498 | 0.675 |
LIG_FHA_1 | 1105 | 1111 | PF00498 | 0.594 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.272 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.466 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.482 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.396 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.454 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.499 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.514 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.538 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.550 |
LIG_FHA_1 | 851 | 857 | PF00498 | 0.286 |
LIG_FHA_1 | 898 | 904 | PF00498 | 0.503 |
LIG_FHA_1 | 910 | 916 | PF00498 | 0.342 |
LIG_FHA_2 | 1054 | 1060 | PF00498 | 0.591 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.468 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.497 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.677 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.483 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.675 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.490 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.594 |
LIG_FHA_2 | 705 | 711 | PF00498 | 0.520 |
LIG_FHA_2 | 753 | 759 | PF00498 | 0.587 |
LIG_FHA_2 | 985 | 991 | PF00498 | 0.341 |
LIG_Integrin_RGD_1 | 701 | 703 | PF01839 | 0.311 |
LIG_LIR_Gen_1 | 1007 | 1017 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 32 | 41 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 828 | 839 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 934 | 945 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 967 | 978 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 990 | 999 | PF02991 | 0.236 |
LIG_LIR_LC3C_4 | 240 | 245 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 1007 | 1013 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 1078 | 1084 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.763 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 710 | 714 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 799 | 805 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 828 | 834 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 934 | 940 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 959 | 964 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 967 | 973 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 987 | 991 | PF02991 | 0.256 |
LIG_NRBOX | 344 | 350 | PF00104 | 0.499 |
LIG_PCNA_yPIPBox_3 | 813 | 823 | PF02747 | 0.470 |
LIG_PDZ_Class_1 | 1121 | 1126 | PF00595 | 0.510 |
LIG_Pex14_1 | 1080 | 1084 | PF04695 | 0.522 |
LIG_Pex14_1 | 175 | 179 | PF04695 | 0.339 |
LIG_Pex14_2 | 1029 | 1033 | PF04695 | 0.656 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.482 |
LIG_Pex14_2 | 918 | 922 | PF04695 | 0.276 |
LIG_Pex14_2 | 942 | 946 | PF04695 | 0.401 |
LIG_Pex14_2 | 976 | 980 | PF04695 | 0.344 |
LIG_PTB_Apo_2 | 710 | 717 | PF02174 | 0.583 |
LIG_PTB_Apo_2 | 774 | 781 | PF02174 | 0.509 |
LIG_PTB_Phospho_1 | 710 | 716 | PF10480 | 0.579 |
LIG_REV1ctd_RIR_1 | 115 | 123 | PF16727 | 0.476 |
LIG_SH2_CRK | 629 | 633 | PF00017 | 0.618 |
LIG_SH2_CRK | 907 | 911 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 592 | 595 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 955 | 959 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 831 | 834 | PF00017 | 0.344 |
LIG_SH2_SRC | 955 | 958 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 1084 | 1088 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 831 | 834 | PF00017 | 0.344 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.476 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.454 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.385 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.458 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.561 |
LIG_SH3_3 | 654 | 660 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 184 | 190 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 378 | 383 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 794 | 800 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 900 | 905 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 1004 | 1009 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 222 | 230 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 749 | 755 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 758 | 763 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 794 | 800 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 981 | 987 | PF11976 | 0.313 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.474 |
LIG_TRAF2_1 | 872 | 875 | PF00917 | 0.366 |
LIG_TRAF2_1 | 876 | 879 | PF00917 | 0.499 |
LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.499 |
LIG_TYR_ITIM | 627 | 632 | PF00017 | 0.546 |
LIG_TYR_ITIM | 829 | 834 | PF00017 | 0.344 |
LIG_UBA3_1 | 945 | 953 | PF00899 | 0.280 |
LIG_WRC_WIRS_1 | 985 | 990 | PF05994 | 0.347 |
MOD_CK1_1 | 1108 | 1114 | PF00069 | 0.680 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.678 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.645 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.469 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.458 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.514 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.651 |
MOD_CK1_1 | 849 | 855 | PF00069 | 0.273 |
MOD_CK2_1 | 1053 | 1059 | PF00069 | 0.591 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.474 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.551 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.609 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.706 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.473 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.614 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.478 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.586 |
MOD_GlcNHglycan | 1063 | 1066 | PF01048 | 0.438 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.536 |
MOD_GlcNHglycan | 208 | 213 | PF01048 | 0.438 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.213 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.229 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.285 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.435 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.356 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.333 |
MOD_GSK3_1 | 1002 | 1009 | PF00069 | 0.433 |
MOD_GSK3_1 | 1104 | 1111 | PF00069 | 0.709 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.519 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.607 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.311 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.598 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.481 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.455 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.504 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.508 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.327 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.298 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.310 |
MOD_GSK3_1 | 926 | 933 | PF00069 | 0.339 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.556 |
MOD_LATS_1 | 577 | 583 | PF00433 | 0.481 |
MOD_LATS_1 | 928 | 934 | PF00433 | 0.145 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.338 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.314 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.240 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.273 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.318 |
MOD_N-GLC_1 | 697 | 702 | PF02516 | 0.301 |
MOD_NEK2_1 | 1015 | 1020 | PF00069 | 0.203 |
MOD_NEK2_1 | 1110 | 1115 | PF00069 | 0.527 |
MOD_NEK2_1 | 1119 | 1124 | PF00069 | 0.557 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.442 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.549 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.437 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.482 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.416 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.473 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.453 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.607 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.562 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.516 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.492 |
MOD_NEK2_1 | 825 | 830 | PF00069 | 0.319 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.319 |
MOD_NEK2_1 | 897 | 902 | PF00069 | 0.459 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.280 |
MOD_NEK2_1 | 964 | 969 | PF00069 | 0.485 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.524 |
MOD_NEK2_1 | 992 | 997 | PF00069 | 0.235 |
MOD_NEK2_2 | 672 | 677 | PF00069 | 0.505 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.464 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.513 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.540 |
MOD_PIKK_1 | 738 | 744 | PF00454 | 0.531 |
MOD_PK_1 | 271 | 277 | PF00069 | 0.474 |
MOD_PKA_1 | 271 | 277 | PF00069 | 0.528 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.403 |
MOD_PKA_1 | 561 | 567 | PF00069 | 0.469 |
MOD_PKA_1 | 926 | 932 | PF00069 | 0.145 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.715 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.429 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.482 |
MOD_PKA_2 | 926 | 932 | PF00069 | 0.292 |
MOD_PKA_2 | 997 | 1003 | PF00069 | 0.204 |
MOD_PKB_1 | 1073 | 1081 | PF00069 | 0.521 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.513 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.490 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.457 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.476 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.533 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.518 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.519 |
MOD_Plk_1 | 930 | 936 | PF00069 | 0.257 |
MOD_Plk_1 | 992 | 998 | PF00069 | 0.178 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.345 |
MOD_Plk_2-3 | 874 | 880 | PF00069 | 0.506 |
MOD_Plk_4 | 1075 | 1081 | PF00069 | 0.660 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.457 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.454 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.296 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.320 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.470 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.466 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.485 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.419 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.413 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.509 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.729 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.531 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.670 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.559 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.594 |
MOD_Plk_4 | 834 | 840 | PF00069 | 0.315 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.290 |
MOD_Plk_4 | 931 | 937 | PF00069 | 0.262 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.518 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.376 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.456 |
MOD_ProDKin_1 | 846 | 852 | PF00069 | 0.259 |
MOD_SUMO_for_1 | 1029 | 1032 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 196 | 203 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 528 | 536 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 558 | 563 | PF00179 | 0.465 |
TRG_AP2beta_CARGO_1 | 959 | 968 | PF09066 | 0.345 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 570 | 575 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 1017 | 1022 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 1115 | 1118 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 831 | 834 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 907 | 910 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 955 | 958 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 1073 | 1076 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 215 | 218 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 895 | 897 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 966 | 969 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 996 | 999 | PF00400 | 0.328 |
TRG_NES_CRM1_1 | 644 | 656 | PF08389 | 0.553 |
TRG_NES_CRM1_1 | 742 | 758 | PF08389 | 0.521 |
TRG_NLS_MonoExtC_3 | 270 | 276 | PF00514 | 0.418 |
TRG_NLS_MonoExtN_4 | 1070 | 1076 | PF00514 | 0.527 |
TRG_NLS_MonoExtN_4 | 270 | 275 | PF00514 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 473 | 477 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 712 | 717 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 952 | 956 | PF00026 | 0.265 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 29% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 40% | 100% |
A0A0N1PFH3 | Leptomonas seymouri | 27% | 93% |
A0A0S4J5A1 | Bodo saltans | 30% | 100% |
A0A0S4J6U4 | Bodo saltans | 39% | 100% |
A0A0S4JA92 | Bodo saltans | 42% | 100% |
A0A0S4JDQ9 | Bodo saltans | 22% | 100% |
A0A0S4JRV4 | Bodo saltans | 41% | 100% |
A0A0S4KIG5 | Bodo saltans | 29% | 100% |
A0A0S4KNQ6 | Bodo saltans | 62% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 28% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 64% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 40% | 99% |
A0A1X0P0Y8 | Trypanosomatidae | 36% | 100% |
A0A1X0P689 | Trypanosomatidae | 27% | 100% |
A0A381MFJ0 | Leishmania infantum | 24% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 67% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 89% | 100% |
A0A3S5IRL5 | Trypanosoma rangeli | 24% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WPW0 | Leishmania donovani | 82% | 100% |
A0A3S7WUG2 | Leishmania donovani | 39% | 99% |
A0A3S7WV61 | Leishmania donovani | 24% | 100% |
A0A3S7WV68 | Leishmania donovani | 24% | 100% |
A0A3S7X978 | Leishmania donovani | 26% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 30% | 100% |
A0A451EJU6 | Leishmania donovani | 28% | 100% |
A2VDL6 | Bos taurus | 28% | 100% |
A4H3S2 | Leishmania braziliensis | 28% | 100% |
A4H903 | Leishmania braziliensis | 39% | 100% |
A4H9Q5 | Leishmania braziliensis | 24% | 100% |
A4HMM8 | Leishmania braziliensis | 28% | 100% |
A4HRZ6 | Leishmania infantum | 28% | 100% |
A4HT82 | Leishmania infantum | 82% | 100% |
A4HTF0 | Leishmania infantum | 91% | 100% |
A4HXD4 | Leishmania infantum | 39% | 99% |
A4HY23 | Leishmania infantum | 24% | 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) | 35% | 100% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 25% | 100% |
D2WKD8 | Sus scrofa | 28% | 100% |
D3K0R6 | Bos taurus | 36% | 93% |
E9AF31 | Leishmania major | 26% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 99% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 92% |
G5E829 | Mus musculus | 39% | 92% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 38% | 80% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 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) | 29% | 100% |
O46674 | Canis lupus familiaris | 27% | 100% |
O55143 | Mus musculus | 27% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
O64806 | Arabidopsis thaliana | 38% | 100% |
O75185 | Homo sapiens | 27% | 100% |
O77696 | Sus scrofa | 29% | 100% |
O81108 | Arabidopsis thaliana | 38% | 100% |
P04074 | Ovis aries | 27% | 100% |
P04191 | Oryctolagus cuniculus | 28% | 100% |
P05023 | Homo sapiens | 27% | 100% |
P05024 | Sus scrofa | 27% | 100% |
P05025 | Tetronarce californica | 28% | 100% |
P06685 | Rattus norvegicus | 28% | 100% |
P06686 | Rattus norvegicus | 29% | 100% |
P06687 | Rattus norvegicus | 28% | 100% |
P09572 | Gallus gallus | 28% | 100% |
P09626 | Rattus norvegicus | 26% | 100% |
P09627 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 25% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 25% | 100% |
P11505 | Rattus norvegicus | 39% | 92% |
P11506 | Rattus norvegicus | 38% | 91% |
P11507 | Rattus norvegicus | 27% | 100% |
P11607 | Sus scrofa | 27% | 100% |
P13585 | Gallus gallus | 28% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P13637 | Homo sapiens | 28% | 100% |
P16615 | Homo sapiens | 27% | 100% |
P17326 | Artemia franciscana | 28% | 100% |
P18596 | Rattus norvegicus | 29% | 100% |
P18907 | Equus caballus | 27% | 100% |
P19156 | Sus scrofa | 26% | 100% |
P20020 | Homo sapiens | 38% | 92% |
P20647 | Oryctolagus cuniculus | 27% | 100% |
P20648 | Homo sapiens | 26% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
P22700 | Drosophila melanogaster | 27% | 100% |
P23220 | Sus scrofa | 38% | 92% |
P23634 | Homo sapiens | 40% | 91% |
P24797 | Gallus gallus | 29% | 100% |
P24798 | Gallus gallus | 28% | 100% |
P25489 | Catostomus commersonii | 28% | 100% |
P27112 | Oryctolagus cuniculus | 26% | 100% |
P28774 | Artemia franciscana | 29% | 100% |
P30714 | Rhinella marina | 27% | 100% |
P35315 | Trypanosoma brucei brucei | 30% | 100% |
P35316 | Artemia franciscana | 27% | 100% |
P35317 | Hydra vulgaris | 29% | 100% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 30% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 28% | 100% |
P38929 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 96% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 27% | 100% |
P49380 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 100% |
P50993 | Homo sapiens | 29% | 100% |
P50996 | Canis lupus familiaris | 26% | 100% |
P50997 | Canis lupus familiaris | 27% | 100% |
P54209 | Dunaliella bioculata | 29% | 100% |
P54211 | Dunaliella bioculata | 24% | 100% |
P54678 | Dictyostelium discoideum | 39% | 100% |
P54707 | Homo sapiens | 27% | 100% |
P54708 | Rattus norvegicus | 27% | 100% |
P57709 | Bos taurus | 28% | 100% |
P58312 | Oreochromis mossambicus | 27% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70083 | Makaira nigricans | 29% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 28% | 100% |
P92939 | Arabidopsis thaliana | 28% | 100% |
P98194 | Homo sapiens | 27% | 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% | 92% |
Q01814 | Homo sapiens | 38% | 91% |
Q03669 | Gallus gallus | 27% | 100% |
Q07421 | Ajellomyces capsulatus | 24% | 100% |
Q08DA1 | Bos taurus | 27% | 100% |
Q0VCY0 | Bos taurus | 29% | 100% |
Q16720 | Homo sapiens | 36% | 92% |
Q21286 | Caenorhabditis elegans | 22% | 94% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 28% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 37% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 38% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 38% | 100% |
Q37145 | Arabidopsis thaliana | 37% | 100% |
Q4QDN7 | Leishmania major | 24% | 100% |
Q4QDN8 | Leishmania major | 24% | 100% |
Q4QED4 | Leishmania major | 40% | 100% |
Q4QIM6 | Leishmania major | 81% | 100% |
Q4QIM8 | Leishmania major | 88% | 100% |
Q4VNC1 | Homo sapiens | 22% | 94% |
Q5R5K5 | Pongo abelii | 28% | 100% |
Q5RCD8 | Pongo abelii | 29% | 100% |
Q5RDR3 | Pongo abelii | 28% | 100% |
Q5XF90 | Mus musculus | 23% | 94% |
Q5ZKB7 | Gallus gallus | 21% | 94% |
Q64392 | Cavia porcellus | 26% | 100% |
Q64518 | Mus musculus | 29% | 100% |
Q64541 | Rattus norvegicus | 28% | 100% |
Q64542 | Rattus norvegicus | 36% | 94% |
Q64566 | Rattus norvegicus | 27% | 100% |
Q64568 | Rattus norvegicus | 37% | 90% |
Q64578 | Rattus norvegicus | 28% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 36% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6PIC6 | Mus musculus | 28% | 100% |
Q6PIE5 | Mus musculus | 29% | 100% |
Q6Q477 | Mus musculus | 36% | 93% |
Q6RWA9 | Taenia solium | 29% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 29% | 100% |
Q7PPA5 | Anopheles gambiae | 28% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 36% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 37% | 100% |
Q80XR2 | Mus musculus | 27% | 100% |
Q8R429 | Mus musculus | 28% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 38% | 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 | 26% | 100% |
Q92105 | Pelophylax lessonae | 29% | 100% |
Q92123 | Xenopus laevis | 28% | 100% |
Q92126 | Xenopus laevis | 27% | 100% |
Q93084 | Homo sapiens | 29% | 100% |
Q95Z93 | Leishmania major | 28% | 100% |
Q98SH2 | Gallus gallus | 37% | 93% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 28% | 100% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 87% |
Q9LF79 | Arabidopsis thaliana | 36% | 100% |
Q9LIK7 | Arabidopsis thaliana | 35% | 100% |
Q9LU41 | Arabidopsis thaliana | 36% | 100% |
Q9LY77 | Arabidopsis thaliana | 37% | 100% |
Q9M2A0 | Arabidopsis thaliana | 23% | 100% |
Q9M2L4 | Arabidopsis thaliana | 38% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 28% | 100% |
Q9NQ11 | Homo sapiens | 24% | 95% |
Q9R0K7 | Mus musculus | 36% | 94% |
Q9SH76 | Arabidopsis thaliana | 22% | 100% |
Q9SY55 | Arabidopsis thaliana | 27% | 100% |
Q9SZR1 | Arabidopsis thaliana | 37% | 100% |
Q9TV52 | Oryctolagus cuniculus | 27% | 100% |
Q9WV27 | Mus musculus | 28% | 100% |
Q9XES1 | Arabidopsis thaliana | 28% | 100% |
Q9YGL9 | Gallus gallus | 29% | 100% |
Q9YH26 | Oreochromis mossambicus | 28% | 100% |
Q9Z1W8 | Mus musculus | 27% | 100% |
V5B873 | Trypanosoma cruzi | 63% | 100% |
V5BHZ2 | Trypanosoma cruzi | 27% | 100% |
V5BLM1 | Trypanosoma cruzi | 30% | 100% |
V5BPC6 | Trypanosoma cruzi | 35% | 100% |