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. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A0A3S7WPW0
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0005215 | transporter activity | 1 | 14 |
GO:0005388 | P-type calcium transporter activity | 4 | 14 |
GO:0005488 | binding | 1 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 14 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 14 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 14 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 14 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 14 |
GO:0015662 | P-type ion transporter activity | 4 | 14 |
GO:0016462 | pyrophosphatase activity | 5 | 18 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 18 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 18 |
GO:0016887 | ATP hydrolysis activity | 7 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 18 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 14 |
GO:0022804 | active transmembrane transporter activity | 3 | 14 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 14 |
GO:0022857 | transmembrane transporter activity | 2 | 14 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 14 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 663 | 667 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 1077 | 1079 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 1105 | 1107 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 821 | 823 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 889 | 891 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 897 | 899 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 954 | 956 | PF00675 | 0.250 |
CLV_PCSK_FUR_1 | 1103 | 1107 | PF00082 | 0.415 |
CLV_PCSK_FUR_1 | 218 | 222 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 1077 | 1079 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 1103 | 1105 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 884 | 886 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 897 | 899 | PF00082 | 0.197 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 884 | 886 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 1047 | 1051 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 822 | 826 | PF00082 | 0.259 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.773 |
DEG_SCF_FBW7_2 | 320 | 327 | PF00400 | 0.467 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.584 |
DOC_CYCLIN_RxL_1 | 820 | 830 | PF00134 | 0.458 |
DOC_CYCLIN_yCln2_LP_2 | 460 | 466 | PF00134 | 0.600 |
DOC_MAPK_DCC_7 | 456 | 466 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 218 | 228 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 822 | 829 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 897 | 903 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 955 | 963 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 221 | 230 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 748 | 755 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 822 | 831 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 970 | 977 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 748 | 756 | PF00069 | 0.478 |
DOC_MAPK_NFAT4_5 | 822 | 830 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 807 | 814 | PF00149 | 0.466 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.402 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.450 |
DOC_PP2B_PxIxI_1 | 972 | 978 | PF00149 | 0.204 |
DOC_USP7_MATH_1 | 1000 | 1004 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 893 | 897 | PF00917 | 0.467 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 848 | 853 | PF00397 | 0.294 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 470 | 475 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.669 |
LIG_Actin_WH2_2 | 89 | 107 | PF00022 | 0.533 |
LIG_AP2alpha_1 | 371 | 375 | PF02296 | 0.467 |
LIG_APCC_ABBAyCdc20_2 | 1068 | 1074 | PF00400 | 0.462 |
LIG_BIR_III_4 | 719 | 723 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 978 | 982 | PF00533 | 0.323 |
LIG_DLG_GKlike_1 | 470 | 477 | PF00625 | 0.535 |
LIG_EVH1_2 | 129 | 133 | PF00568 | 0.473 |
LIG_FHA_1 | 1012 | 1018 | PF00498 | 0.371 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.244 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.443 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.580 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.460 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.486 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.480 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.494 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.535 |
LIG_FHA_1 | 853 | 859 | PF00498 | 0.263 |
LIG_FHA_1 | 912 | 918 | PF00498 | 0.295 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.500 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.423 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.448 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.668 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.529 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.488 |
LIG_FHA_2 | 755 | 761 | PF00498 | 0.572 |
LIG_GBD_Chelix_1 | 96 | 104 | PF00786 | 0.233 |
LIG_IBAR_NPY_1 | 700 | 702 | PF08397 | 0.463 |
LIG_KLC1_Yacidic_2 | 1069 | 1074 | PF13176 | 0.455 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 202 | 211 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 34 | 43 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 647 | 656 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 830 | 841 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 937 | 948 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 979 | 988 | PF02991 | 0.336 |
LIG_LIR_LC3C_4 | 242 | 247 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 647 | 653 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 712 | 716 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 801 | 807 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 830 | 836 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 937 | 943 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 979 | 983 | PF02991 | 0.296 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.485 |
LIG_PCNA_TLS_4 | 369 | 376 | PF02747 | 0.479 |
LIG_PCNA_yPIPBox_3 | 815 | 825 | PF02747 | 0.447 |
LIG_Pex14_1 | 177 | 181 | PF04695 | 0.317 |
LIG_Pex14_2 | 1033 | 1037 | PF04695 | 0.629 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.467 |
LIG_Pex14_2 | 980 | 984 | PF04695 | 0.323 |
LIG_PTB_Apo_2 | 697 | 704 | PF02174 | 0.451 |
LIG_PTB_Apo_2 | 712 | 719 | PF02174 | 0.544 |
LIG_PTB_Apo_2 | 776 | 783 | PF02174 | 0.490 |
LIG_PTB_Phospho_1 | 697 | 703 | PF10480 | 0.453 |
LIG_PTB_Phospho_1 | 712 | 718 | PF10480 | 0.545 |
LIG_REV1ctd_RIR_1 | 117 | 125 | PF16727 | 0.473 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.605 |
LIG_SH2_GRB2like | 594 | 597 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 833 | 836 | PF00017 | 0.338 |
LIG_SH2_SRC | 920 | 923 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 920 | 924 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 1072 | 1075 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.338 |
LIG_SH3_3 | 1025 | 1031 | PF00018 | 0.504 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.579 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.439 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.424 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.541 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.499 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.269 |
LIG_SUMO_SIM_anti_2 | 796 | 802 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 186 | 192 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 225 | 232 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 279 | 284 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 382 | 388 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 390 | 395 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 751 | 757 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 760 | 765 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 796 | 802 | PF11976 | 0.464 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.451 |
LIG_TRAF2_1 | 874 | 877 | PF00917 | 0.346 |
LIG_TRAF2_1 | 878 | 881 | PF00917 | 0.485 |
LIG_TYR_ITIM | 372 | 377 | PF00017 | 0.346 |
LIG_TYR_ITIM | 629 | 634 | PF00017 | 0.406 |
LIG_TYR_ITIM | 831 | 836 | PF00017 | 0.338 |
LIG_WRC_WIRS_1 | 977 | 982 | PF05994 | 0.328 |
MOD_CK1_1 | 1055 | 1061 | PF00069 | 0.431 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.624 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.570 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.277 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.419 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.372 |
MOD_CK1_1 | 851 | 857 | PF00069 | 0.325 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.509 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.390 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.286 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.422 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.498 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.465 |
MOD_GlcNHglycan | 1054 | 1057 | PF01048 | 0.441 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.654 |
MOD_GlcNHglycan | 210 | 215 | PF01048 | 0.529 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.426 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.528 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.336 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.390 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.358 |
MOD_GlcNHglycan | 970 | 973 | PF01048 | 0.212 |
MOD_GSK3_1 | 1016 | 1023 | PF00069 | 0.181 |
MOD_GSK3_1 | 1033 | 1040 | PF00069 | 0.490 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.405 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.263 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.466 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.189 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.292 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.324 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.338 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.316 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.369 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.261 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.421 |
MOD_GSK3_1 | 996 | 1003 | PF00069 | 0.380 |
MOD_LATS_1 | 579 | 585 | PF00433 | 0.321 |
MOD_N-GLC_1 | 1093 | 1098 | PF02516 | 0.366 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.449 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.393 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.380 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.272 |
MOD_N-GLC_1 | 623 | 628 | PF02516 | 0.362 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.378 |
MOD_NEK2_1 | 1037 | 1042 | PF00069 | 0.580 |
MOD_NEK2_1 | 1093 | 1098 | PF00069 | 0.534 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.406 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.403 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.276 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.321 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.316 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.276 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.513 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.557 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.395 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.360 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.331 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.272 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.272 |
MOD_NEK2_1 | 899 | 904 | PF00069 | 0.289 |
MOD_NEK2_1 | 911 | 916 | PF00069 | 0.259 |
MOD_NEK2_1 | 996 | 1001 | PF00069 | 0.261 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.436 |
MOD_NEK2_2 | 674 | 679 | PF00069 | 0.352 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.334 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.357 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.356 |
MOD_PIKK_1 | 740 | 746 | PF00454 | 0.378 |
MOD_PKA_1 | 563 | 569 | PF00069 | 0.321 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.741 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.590 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.641 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.377 |
MOD_PKB_1 | 549 | 557 | PF00069 | 0.453 |
MOD_Plk_1 | 1033 | 1039 | PF00069 | 0.345 |
MOD_Plk_1 | 1093 | 1099 | PF00069 | 0.516 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.364 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.333 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.286 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.321 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.382 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.352 |
MOD_Plk_1 | 933 | 939 | PF00069 | 0.302 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.377 |
MOD_Plk_2-3 | 876 | 882 | PF00069 | 0.321 |
MOD_Plk_4 | 1037 | 1043 | PF00069 | 0.535 |
MOD_Plk_4 | 1111 | 1117 | PF00069 | 0.406 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.269 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.269 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.243 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.273 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.304 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.292 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.315 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.362 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.703 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.395 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.472 |
MOD_Plk_4 | 735 | 741 | PF00069 | 0.483 |
MOD_Plk_4 | 836 | 842 | PF00069 | 0.286 |
MOD_Plk_4 | 899 | 905 | PF00069 | 0.231 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.267 |
MOD_Plk_4 | 944 | 950 | PF00069 | 0.252 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.374 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.257 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.352 |
MOD_ProDKin_1 | 848 | 854 | PF00069 | 0.263 |
MOD_SUMO_rev_2 | 1040 | 1049 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 560 | 565 | PF00179 | 0.327 |
TRG_DiLeu_BaEn_1 | 1111 | 1116 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_1 | 572 | 577 | PF01217 | 0.338 |
TRG_DiLeu_BaEn_4 | 1111 | 1117 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 1021 | 1026 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 703 | 706 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 920 | 923 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 958 | 961 | PF00928 | 0.325 |
TRG_ER_diArg_1 | 1077 | 1080 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 1102 | 1105 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 609 | 612 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 897 | 899 | PF00400 | 0.293 |
TRG_NES_CRM1_1 | 646 | 658 | PF08389 | 0.422 |
TRG_NES_CRM1_1 | 744 | 760 | PF08389 | 0.368 |
TRG_NLS_MonoExtN_4 | 272 | 277 | PF00514 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 1082 | 1087 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 309 | 313 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 358 | 363 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 714 | 719 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 955 | 959 | PF00026 | 0.282 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 30% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 41% | 100% |
A0A0N1PFH3 | Leptomonas seymouri | 26% | 92% |
A0A0S4J1M1 | Bodo saltans | 27% | 100% |
A0A0S4J5A1 | Bodo saltans | 28% | 100% |
A0A0S4J6U4 | Bodo saltans | 38% | 100% |
A0A0S4JA92 | Bodo saltans | 42% | 100% |
A0A0S4JRV4 | Bodo saltans | 41% | 100% |
A0A0S4KIG5 | Bodo saltans | 28% | 100% |
A0A0S4KNQ6 | Bodo saltans | 63% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 28% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 66% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 40% | 99% |
A0A1X0P0Y8 | Trypanosomatidae | 36% | 100% |
A0A1X0P689 | Trypanosomatidae | 26% | 100% |
A0A381MFJ0 | Leishmania infantum | 24% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 67% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 89% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WUG2 | Leishmania donovani | 39% | 99% |
A0A3S7WV61 | Leishmania donovani | 24% | 100% |
A0A3S7WV68 | Leishmania donovani | 24% | 100% |
A0A3S7X978 | Leishmania donovani | 25% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 29% | 100% |
A0A451EJU6 | Leishmania donovani | 29% | 100% |
A2VDL6 | Bos taurus | 28% | 100% |
A4H3S2 | Leishmania braziliensis | 27% | 100% |
A4H514 | Leishmania braziliensis | 82% | 100% |
A4H903 | Leishmania braziliensis | 38% | 100% |
A4H9Q5 | Leishmania braziliensis | 24% | 100% |
A4HMM8 | Leishmania braziliensis | 26% | 100% |
A4HRZ6 | Leishmania infantum | 29% | 100% |
A4HT82 | Leishmania infantum | 100% | 100% |
A4HTF0 | Leishmania infantum | 96% | 100% |
A4HXD4 | Leishmania infantum | 39% | 100% |
A4HY23 | Leishmania infantum | 24% | 100% |
A4IBA6 | Leishmania infantum | 25% | 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) | 59% | 100% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A564 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 25% | 100% |
D2WKD8 | Sus scrofa | 28% | 100% |
D3K0R6 | Bos taurus | 36% | 93% |
E9AF31 | Leishmania major | 25% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
G5E829 | Mus musculus | 39% | 92% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 37% | 79% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
O14983 | Homo sapiens | 27% | 100% |
O22218 | Arabidopsis thaliana | 37% | 100% |
O23087 | Arabidopsis thaliana | 26% | 100% |
O34431 | Bacillus subtilis (strain 168) | 29% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
O46674 | Canis lupus familiaris | 27% | 100% |
O55143 | Mus musculus | 27% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
O64806 | Arabidopsis thaliana | 37% | 100% |
O75185 | Homo sapiens | 27% | 100% |
O77696 | Sus scrofa | 29% | 100% |
O81108 | Arabidopsis thaliana | 38% | 100% |
P04074 | Ovis aries | 26% | 100% |
P04191 | Oryctolagus cuniculus | 27% | 100% |
P05023 | Homo sapiens | 26% | 100% |
P05024 | Sus scrofa | 26% | 100% |
P05025 | Tetronarce californica | 27% | 100% |
P05030 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P06685 | Rattus norvegicus | 26% | 100% |
P06686 | Rattus norvegicus | 29% | 100% |
P06687 | Rattus norvegicus | 27% | 100% |
P09572 | Gallus gallus | 27% | 100% |
P09626 | Rattus norvegicus | 27% | 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 | 39% | 92% |
P11506 | Rattus norvegicus | 38% | 90% |
P11507 | Rattus norvegicus | 27% | 100% |
P11607 | Sus scrofa | 27% | 100% |
P11718 | Leishmania donovani | 24% | 100% |
P12522 | Leishmania donovani | 24% | 100% |
P13585 | Gallus gallus | 28% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P13607 | Drosophila melanogaster | 26% | 100% |
P13637 | Homo sapiens | 27% | 100% |
P16615 | Homo sapiens | 27% | 100% |
P17326 | Artemia franciscana | 28% | 100% |
P18596 | Rattus norvegicus | 29% | 100% |
P18907 | Equus caballus | 27% | 100% |
P19156 | Sus scrofa | 27% | 100% |
P20020 | Homo sapiens | 38% | 92% |
P20431 | Arabidopsis thaliana | 23% | 100% |
P20647 | Oryctolagus cuniculus | 27% | 100% |
P20648 | Homo sapiens | 27% | 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% | 92% |
P23634 | Homo sapiens | 38% | 90% |
P24545 | Zygosaccharomyces rouxii | 24% | 100% |
P24797 | Gallus gallus | 27% | 100% |
P24798 | Gallus gallus | 27% | 100% |
P25489 | Catostomus commersonii | 27% | 100% |
P27112 | Oryctolagus cuniculus | 26% | 100% |
P28774 | Artemia franciscana | 28% | 100% |
P30714 | Rhinella marina | 26% | 100% |
P35315 | Trypanosoma brucei brucei | 30% | 100% |
P35316 | Artemia franciscana | 26% | 100% |
P35317 | Hydra vulgaris | 28% | 100% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 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) | 35% | 95% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 26% | 100% |
P49380 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
P50993 | Homo sapiens | 28% | 100% |
P50996 | Canis lupus familiaris | 27% | 100% |
P50997 | Canis lupus familiaris | 26% | 100% |
P54209 | Dunaliella bioculata | 30% | 100% |
P54211 | Dunaliella bioculata | 24% | 99% |
P54678 | Dictyostelium discoideum | 40% | 100% |
P54707 | Homo sapiens | 28% | 100% |
P54708 | Rattus norvegicus | 27% | 100% |
P57709 | Bos taurus | 28% | 100% |
P58165 | Oreochromis mossambicus | 40% | 100% |
P58312 | Oreochromis mossambicus | 26% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 29% | 100% |
P70083 | Makaira nigricans | 29% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 28% | 100% |
P92939 | Arabidopsis thaliana | 27% | 100% |
P98194 | Homo sapiens | 28% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 29% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 29% | 100% |
Q00779 | Felis catus | 26% | 100% |
Q00804 | Oryctolagus cuniculus | 38% | 92% |
Q01814 | Homo sapiens | 38% | 90% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q03669 | Gallus gallus | 26% | 100% |
Q07421 | Ajellomyces capsulatus | 24% | 100% |
Q08435 | Nicotiana plumbaginifolia | 23% | 100% |
Q08436 | Nicotiana plumbaginifolia | 23% | 100% |
Q08DA1 | Bos taurus | 26% | 100% |
Q0VCY0 | Bos taurus | 29% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q16720 | Homo sapiens | 37% | 92% |
Q21286 | Caenorhabditis elegans | 22% | 93% |
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 | 36% | 100% |
Q42883 | Solanum lycopersicum | 27% | 100% |
Q4QDN7 | Leishmania major | 24% | 100% |
Q4QDN8 | Leishmania major | 24% | 100% |
Q4QED4 | Leishmania major | 40% | 100% |
Q4QIM6 | Leishmania major | 96% | 100% |
Q4QIM8 | Leishmania major | 87% | 100% |
Q4VNC1 | Homo sapiens | 21% | 94% |
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 | 26% | 100% |
Q64392 | Cavia porcellus | 28% | 100% |
Q64436 | Mus musculus | 27% | 100% |
Q64518 | Mus musculus | 28% | 100% |
Q64541 | Rattus norvegicus | 27% | 100% |
Q64542 | Rattus norvegicus | 38% | 93% |
Q64566 | Rattus norvegicus | 27% | 100% |
Q64568 | Rattus norvegicus | 36% | 89% |
Q64578 | Rattus norvegicus | 27% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 36% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6DFW5 | Mus musculus | 21% | 95% |
Q6PIC6 | Mus musculus | 27% | 100% |
Q6PIE5 | Mus musculus | 29% | 100% |
Q6Q477 | Mus musculus | 38% | 93% |
Q6RWA9 | Taenia solium | 28% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 29% | 100% |
Q7PPA5 | Anopheles gambiae | 27% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 36% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 35% | 100% |
Q80XR2 | Mus musculus | 28% | 100% |
Q8R429 | Mus musculus | 27% | 100% |
Q8R4C1 | Rattus norvegicus | 28% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 37% | 100% |
Q8VDN2 | Mus musculus | 26% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 30% | 100% |
Q92030 | Anguilla anguilla | 27% | 100% |
Q92036 | Rhinella marina | 26% | 100% |
Q92105 | Pelophylax lessonae | 27% | 100% |
Q92123 | Xenopus laevis | 27% | 100% |
Q92126 | Xenopus laevis | 27% | 100% |
Q93084 | Homo sapiens | 29% | 100% |
Q95Z93 | Leishmania major | 27% | 100% |
Q98SH2 | Gallus gallus | 37% | 93% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CTG6 | Mus musculus | 23% | 96% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 87% |
Q9LF79 | Arabidopsis thaliana | 36% | 100% |
Q9LIK7 | Arabidopsis thaliana | 35% | 100% |
Q9LU41 | Arabidopsis thaliana | 36% | 100% |
Q9LY32 | Arabidopsis thaliana | 22% | 100% |
Q9LY77 | Arabidopsis thaliana | 37% | 100% |
Q9M2A0 | Arabidopsis thaliana | 23% | 100% |
Q9M2L4 | Arabidopsis thaliana | 38% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 26% | 100% |
Q9NQ11 | Homo sapiens | 23% | 95% |
Q9R0K7 | Mus musculus | 36% | 93% |
Q9SJB3 | Arabidopsis thaliana | 22% | 100% |
Q9SU58 | Arabidopsis thaliana | 23% | 100% |
Q9SY55 | Arabidopsis thaliana | 29% | 100% |
Q9SZR1 | Arabidopsis thaliana | 36% | 100% |
Q9TV52 | Oryctolagus cuniculus | 29% | 100% |
Q9WV27 | Mus musculus | 27% | 100% |
Q9XES1 | Arabidopsis thaliana | 27% | 100% |
Q9Y2G3 | Homo sapiens | 21% | 95% |
Q9YGL9 | Gallus gallus | 28% | 100% |
Q9YH26 | Oreochromis mossambicus | 28% | 100% |
Q9Z1W8 | Mus musculus | 27% | 100% |
V5B873 | Trypanosoma cruzi | 64% | 100% |
V5BHZ2 | Trypanosoma cruzi | 27% | 100% |
V5BLM1 | Trypanosoma cruzi | 30% | 100% |
V5BPC6 | Trypanosoma cruzi | 36% | 100% |