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:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 12 |
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 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q95Z93
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0006816 | calcium ion transport | 7 | 2 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 2 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 2 |
GO:0055074 | calcium ion homeostasis | 8 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0070588 | calcium ion transmembrane transport | 6 | 2 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 2 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 2 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
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 | 608 | 612 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.296 |
CLV_PCSK_FUR_1 | 196 | 200 | PF00082 | 0.193 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 480 | 482 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 981 | 985 | PF00082 | 0.392 |
DOC_ANK_TNKS_1 | 462 | 469 | PF00023 | 0.557 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.468 |
DOC_CKS1_1 | 539 | 544 | PF01111 | 0.560 |
DOC_CKS1_1 | 661 | 666 | PF01111 | 0.560 |
DOC_CYCLIN_RxL_1 | 475 | 489 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 91 | 97 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 986 | 992 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 224 | 233 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 477 | 485 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 486 | 492 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 494 | 501 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 525 | 532 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 615 | 623 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 713 | 719 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 303 | 310 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 617 | 625 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 713 | 721 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 837 | 845 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 891 | 899 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 981 | 990 | PF00069 | 0.392 |
DOC_MAPK_NFAT4_5 | 981 | 989 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 527 | 533 | PF00149 | 0.504 |
DOC_PP1_RVXF_1 | 561 | 568 | PF00149 | 0.445 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 602 | 605 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 986 | 989 | PF13499 | 0.390 |
DOC_PP4_FxxP_1 | 782 | 785 | PF00568 | 0.346 |
DOC_SPAK_OSR1_1 | 390 | 394 | PF12202 | 0.481 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 930 | 934 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.266 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 224 | 234 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 494 | 500 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 668 | 677 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 763 | 773 | PF00244 | 0.307 |
LIG_Actin_WH2_2 | 288 | 305 | PF00022 | 0.316 |
LIG_Actin_WH2_2 | 548 | 565 | PF00022 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 947 | 951 | PF00533 | 0.326 |
LIG_BRCT_BRCA1_2 | 51 | 57 | PF00533 | 0.503 |
LIG_Clathr_ClatBox_1 | 166 | 170 | PF01394 | 0.560 |
LIG_Clathr_ClatBox_1 | 898 | 902 | PF01394 | 0.307 |
LIG_deltaCOP1_diTrp_1 | 831 | 836 | PF00928 | 0.541 |
LIG_EH1_1 | 15 | 23 | PF00400 | 0.504 |
LIG_EH1_1 | 94 | 102 | PF00400 | 0.323 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.469 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.462 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.503 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.455 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.307 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.455 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.455 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.511 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.449 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.449 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.307 |
LIG_FHA_1 | 980 | 986 | PF00498 | 0.388 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.515 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.460 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.289 |
LIG_FHA_2 | 870 | 876 | PF00498 | 0.269 |
LIG_GBD_Chelix_1 | 773 | 781 | PF00786 | 0.307 |
LIG_Integrin_RGD_1 | 824 | 826 | PF01839 | 0.304 |
LIG_LIR_Apic_2 | 292 | 297 | PF02991 | 0.255 |
LIG_LIR_Apic_2 | 779 | 785 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 738 | 748 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 831 | 841 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.330 |
LIG_LIR_LC3C_4 | 896 | 900 | PF02991 | 0.342 |
LIG_LIR_LC3C_4 | 915 | 918 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 738 | 744 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 758 | 764 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 831 | 836 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 940 | 946 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 978 | 983 | PF02991 | 0.231 |
LIG_MAD2 | 140 | 148 | PF02301 | 0.477 |
LIG_NRBOX | 687 | 693 | PF00104 | 0.455 |
LIG_NRBOX | 992 | 998 | PF00104 | 0.374 |
LIG_Pex14_1 | 290 | 294 | PF04695 | 0.280 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.221 |
LIG_Pex14_2 | 853 | 857 | PF04695 | 0.255 |
LIG_Pex14_2 | 947 | 951 | PF04695 | 0.311 |
LIG_REV1ctd_RIR_1 | 833 | 841 | PF16727 | 0.428 |
LIG_REV1ctd_RIR_1 | 944 | 953 | PF16727 | 0.341 |
LIG_RPA_C_Fungi | 385 | 397 | PF08784 | 0.221 |
LIG_SH2_CRK | 838 | 842 | PF00017 | 0.311 |
LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 844 | 847 | PF00017 | 0.307 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.355 |
LIG_SH2_SRC | 764 | 767 | PF00017 | 0.307 |
LIG_SH2_STAP1 | 1011 | 1015 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 764 | 767 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 844 | 847 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 943 | 946 | PF00017 | 0.306 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.406 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.327 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.380 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.415 |
LIG_SH3_3 | 915 | 921 | PF00018 | 0.392 |
LIG_SH3_3 | 968 | 974 | PF00018 | 0.371 |
LIG_SUMO_SIM_anti_2 | 896 | 902 | PF11976 | 0.307 |
LIG_SUMO_SIM_anti_2 | 915 | 920 | PF11976 | 0.307 |
LIG_SUMO_SIM_anti_2 | 982 | 987 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 165 | 173 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 20 | 26 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 622 | 627 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 896 | 902 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 981 | 987 | PF11976 | 0.414 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.454 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.323 |
LIG_UBA3_1 | 17 | 25 | PF00899 | 0.424 |
LIG_UBA3_1 | 450 | 456 | PF00899 | 0.307 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 867 | 872 | PF05994 | 0.428 |
LIG_WW_3 | 603 | 607 | PF00397 | 0.307 |
MOD_CDK_SPK_2 | 538 | 543 | PF00069 | 0.454 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.323 |
MOD_CDK_SPxxK_3 | 660 | 667 | PF00069 | 0.392 |
MOD_CDK_SPxxK_3 | 706 | 713 | PF00069 | 0.428 |
MOD_CK1_1 | 1001 | 1007 | PF00069 | 0.578 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.351 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.307 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.442 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.378 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.457 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.318 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.354 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.341 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.338 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.359 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.391 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.364 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.332 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.430 |
MOD_GlcNHglycan | 1011 | 1014 | PF01048 | 0.659 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.454 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.362 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.436 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.324 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.374 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.425 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.454 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.364 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.348 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.307 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.307 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.307 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.266 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.322 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.313 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.321 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.288 |
MOD_GSK3_1 | 856 | 863 | PF00069 | 0.336 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.285 |
MOD_GSK3_1 | 975 | 982 | PF00069 | 0.425 |
MOD_N-GLC_1 | 1009 | 1014 | PF02516 | 0.470 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.338 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.428 |
MOD_N-GLC_1 | 755 | 760 | PF02516 | 0.352 |
MOD_N-GLC_1 | 912 | 917 | PF02516 | 0.307 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.307 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.413 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.386 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.381 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.392 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.454 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.323 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.426 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.315 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.352 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.363 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.266 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.410 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.379 |
MOD_NEK2_1 | 951 | 956 | PF00069 | 0.284 |
MOD_NEK2_1 | 984 | 989 | PF00069 | 0.364 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.380 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.454 |
MOD_PK_1 | 497 | 503 | PF00069 | 0.323 |
MOD_PKA_1 | 486 | 492 | PF00069 | 0.394 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.364 |
MOD_PKA_1 | 630 | 636 | PF00069 | 0.323 |
MOD_PKA_2 | 1001 | 1007 | PF00069 | 0.551 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.428 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.348 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.307 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.343 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.404 |
MOD_PKA_2 | 919 | 925 | PF00069 | 0.302 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.338 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.362 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.313 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.406 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.307 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.323 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.323 |
MOD_Plk_1 | 912 | 918 | PF00069 | 0.307 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.395 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.454 |
MOD_Plk_2-3 | 9 | 15 | PF00069 | 0.477 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.434 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.342 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.337 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.378 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.428 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.348 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.456 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.342 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.323 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.323 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.355 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.307 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.307 |
MOD_Plk_4 | 937 | 943 | PF00069 | 0.372 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.307 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.394 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.309 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.439 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.392 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.428 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.323 |
MOD_SUMO_for_1 | 197 | 200 | PF00179 | 0.221 |
MOD_SUMO_for_1 | 584 | 587 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 20 | 27 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 237 | 247 | PF00179 | 0.309 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.307 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_1 | 912 | 917 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 838 | 841 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 844 | 847 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 943 | 946 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 639 | 641 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 822 | 824 | PF00400 | 0.366 |
TRG_ER_FFAT_2 | 866 | 875 | PF00635 | 0.417 |
TRG_NES_CRM1_1 | 187 | 200 | PF08389 | 0.221 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 28 | 32 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 477 | 482 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 570 | 574 | PF00026 | 0.428 |
TRG_PTS1 | 1020 | 1023 | PF00515 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 76% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 30% | 92% |
A0A0N1I8I8 | Leptomonas seymouri | 27% | 84% |
A0A0N1PFH3 | Leptomonas seymouri | 30% | 84% |
A0A0S4J1M1 | Bodo saltans | 29% | 93% |
A0A0S4J5A1 | Bodo saltans | 32% | 96% |
A0A0S4J6U4 | Bodo saltans | 29% | 94% |
A0A0S4JA92 | Bodo saltans | 28% | 100% |
A0A0S4JRV4 | Bodo saltans | 31% | 100% |
A0A0S4KIG5 | Bodo saltans | 63% | 100% |
A0A0S4KNQ6 | Bodo saltans | 28% | 92% |
A0A1X0NNY6 | Trypanosomatidae | 69% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 28% | 93% |
A0A1X0NTI6 | Trypanosomatidae | 29% | 90% |
A0A1X0P0Y8 | Trypanosomatidae | 26% | 93% |
A0A1X0P689 | Trypanosomatidae | 31% | 98% |
A0A3R7KM63 | Trypanosoma rangeli | 29% | 98% |
A0A3R7MRX8 | Trypanosoma rangeli | 31% | 98% |
A0A3S5H5Y9 | Leishmania donovani | 29% | 93% |
A0A3S5ISK9 | Trypanosoma rangeli | 26% | 96% |
A0A3S7WPW0 | Leishmania donovani | 27% | 91% |
A0A3S7WUG2 | Leishmania donovani | 30% | 90% |
A0A3S7X6H3 | Leishmania donovani | 24% | 85% |
A0A3S7X978 | Leishmania donovani | 31% | 92% |
A0A422NTS7 | Trypanosoma rangeli | 66% | 100% |
A0A451EJU6 | Leishmania donovani | 95% | 100% |
A2VDL6 | Bos taurus | 31% | 100% |
A4H3S2 | Leishmania braziliensis | 86% | 100% |
A4H514 | Leishmania braziliensis | 28% | 91% |
A4H553 | Leishmania braziliensis | 21% | 82% |
A4H903 | Leishmania braziliensis | 29% | 92% |
A4HLF4 | Leishmania braziliensis | 26% | 86% |
A4HMM8 | Leishmania braziliensis | 31% | 93% |
A4HRZ6 | Leishmania infantum | 95% | 100% |
A4HT82 | Leishmania infantum | 31% | 100% |
A4HTF0 | Leishmania infantum | 28% | 100% |
A4HXD4 | Leishmania infantum | 30% | 90% |
A4I8W5 | Leishmania infantum | 24% | 85% |
A4IBA6 | Leishmania infantum | 31% | 92% |
A7L9Z8 | Mus musculus | 32% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 95% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 93% |
D2WKD8 | Sus scrofa | 31% | 100% |
D3K0R6 | Bos taurus | 27% | 85% |
E9AF31 | Leishmania major | 31% | 92% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 93% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 90% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 84% |
G5E829 | Mus musculus | 30% | 84% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 27% | 72% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 93% |
O14983 | Homo sapiens | 49% | 100% |
O22218 | Arabidopsis thaliana | 29% | 99% |
O23087 | Arabidopsis thaliana | 43% | 97% |
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 | 48% | 98% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
O64806 | Arabidopsis thaliana | 29% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 78% |
O75185 | Homo sapiens | 32% | 100% |
O77696 | Sus scrofa | 48% | 100% |
O81108 | Arabidopsis thaliana | 30% | 100% |
P04074 | Ovis aries | 32% | 100% |
P04191 | Oryctolagus cuniculus | 49% | 100% |
P05023 | Homo sapiens | 32% | 100% |
P05024 | Sus scrofa | 32% | 100% |
P05025 | Tetronarce californica | 31% | 100% |
P06685 | Rattus norvegicus | 32% | 100% |
P06686 | Rattus norvegicus | 31% | 100% |
P06687 | Rattus norvegicus | 31% | 100% |
P09572 | Gallus gallus | 32% | 100% |
P09626 | Rattus norvegicus | 32% | 99% |
P11505 | Rattus norvegicus | 30% | 84% |
P11506 | Rattus norvegicus | 29% | 82% |
P11507 | Rattus norvegicus | 48% | 98% |
P11607 | Sus scrofa | 48% | 98% |
P13585 | Gallus gallus | 49% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
P13607 | Drosophila melanogaster | 32% | 98% |
P13637 | Homo sapiens | 31% | 100% |
P16615 | Homo sapiens | 48% | 98% |
P17326 | Artemia franciscana | 31% | 100% |
P18596 | Rattus norvegicus | 48% | 100% |
P18907 | Equus caballus | 32% | 100% |
P19156 | Sus scrofa | 31% | 99% |
P19456 | Arabidopsis thaliana | 28% | 100% |
P20020 | Homo sapiens | 30% | 84% |
P20431 | Arabidopsis thaliana | 28% | 100% |
P20647 | Oryctolagus cuniculus | 48% | 98% |
P20648 | Homo sapiens | 29% | 99% |
P20649 | Arabidopsis thaliana | 28% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 29% | 100% |
P22180 | Solanum lycopersicum | 27% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 99% |
P22700 | Drosophila melanogaster | 48% | 100% |
P23220 | Sus scrofa | 30% | 84% |
P23634 | Homo sapiens | 26% | 82% |
P24797 | Gallus gallus | 31% | 100% |
P24798 | Gallus gallus | 31% | 100% |
P25489 | Catostomus commersonii | 32% | 100% |
P27112 | Oryctolagus cuniculus | 31% | 99% |
P28774 | Artemia franciscana | 31% | 100% |
P30714 | Rhinella marina | 32% | 100% |
P35315 | Trypanosoma brucei brucei | 67% | 100% |
P35316 | Artemia franciscana | 48% | 100% |
P35317 | Hydra vulgaris | 30% | 99% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 35% | 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% | 100% |
P50996 | Canis lupus familiaris | 31% | 99% |
P50997 | Canis lupus familiaris | 32% | 100% |
P54209 | Dunaliella bioculata | 46% | 99% |
P54211 | Dunaliella bioculata | 25% | 90% |
P54678 | Dictyostelium discoideum | 30% | 92% |
P54707 | Homo sapiens | 31% | 98% |
P54708 | Rattus norvegicus | 31% | 99% |
P57709 | Bos taurus | 33% | 100% |
P58165 | Oreochromis mossambicus | 28% | 92% |
P58312 | Oreochromis mossambicus | 29% | 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 | 27% | 100% |
P90747 | Caenorhabditis elegans | 23% | 87% |
P92939 | Arabidopsis thaliana | 44% | 96% |
P98194 | Homo sapiens | 33% | 100% |
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 | 29% | 84% |
Q01814 | Homo sapiens | 30% | 82% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q03194 | Nicotiana plumbaginifolia | 27% | 100% |
Q03669 | Gallus gallus | 48% | 98% |
Q08435 | Nicotiana plumbaginifolia | 27% | 100% |
Q08436 | Nicotiana plumbaginifolia | 27% | 100% |
Q08DA1 | Bos taurus | 32% | 100% |
Q0VCY0 | Bos taurus | 49% | 100% |
Q10309 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 99% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q13733 | Homo sapiens | 31% | 99% |
Q16720 | Homo sapiens | 28% | 84% |
Q21286 | Caenorhabditis elegans | 22% | 85% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 49% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 29% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 29% | 98% |
Q2RAS0 | Oryza sativa subsp. japonica | 29% | 100% |
Q37145 | Arabidopsis thaliana | 30% | 100% |
Q3TYU2 | Mus musculus | 22% | 84% |
Q42556 | Arabidopsis thaliana | 27% | 100% |
Q42883 | Solanum lycopersicum | 44% | 98% |
Q43128 | Arabidopsis thaliana | 27% | 100% |
Q4Q490 | Leishmania major | 25% | 86% |
Q4QED4 | Leishmania major | 31% | 97% |
Q4QG01 | Leishmania major | 22% | 93% |
Q4QIM6 | Leishmania major | 27% | 91% |
Q4QIM8 | Leishmania major | 28% | 93% |
Q4VNC0 | Homo sapiens | 21% | 84% |
Q4VNC1 | Homo sapiens | 23% | 86% |
Q5R5K5 | Pongo abelii | 34% | 100% |
Q5RCD8 | Pongo abelii | 31% | 100% |
Q5RDR3 | Pongo abelii | 32% | 100% |
Q5ZKB7 | Gallus gallus | 22% | 85% |
Q64392 | Cavia porcellus | 32% | 99% |
Q64436 | Mus musculus | 29% | 99% |
Q64518 | Mus musculus | 49% | 100% |
Q64541 | Rattus norvegicus | 30% | 100% |
Q64542 | Rattus norvegicus | 27% | 85% |
Q64566 | Rattus norvegicus | 33% | 100% |
Q64568 | Rattus norvegicus | 28% | 81% |
Q64578 | Rattus norvegicus | 50% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 31% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 30% | 99% |
Q6DFW5 | Mus musculus | 21% | 87% |
Q6PIC6 | Mus musculus | 31% | 100% |
Q6PIE5 | Mus musculus | 31% | 100% |
Q6Q477 | Mus musculus | 27% | 85% |
Q6RWA9 | Taenia solium | 30% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 34% | 100% |
Q7PPA5 | Anopheles gambiae | 48% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 28% | 94% |
Q7XEK4 | Oryza sativa subsp. japonica | 30% | 99% |
Q7XPY2 | Oryza sativa subsp. japonica | 27% | 100% |
Q80XR2 | Mus musculus | 33% | 100% |
Q8R429 | Mus musculus | 50% | 100% |
Q8R4C1 | Rattus norvegicus | 32% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 29% | 98% |
Q8VDN2 | Mus musculus | 32% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 34% | 100% |
Q92030 | Anguilla anguilla | 33% | 100% |
Q92036 | Rhinella marina | 30% | 98% |
Q92105 | Pelophylax lessonae | 49% | 100% |
Q92123 | Xenopus laevis | 32% | 100% |
Q92126 | Xenopus laevis | 30% | 99% |
Q93084 | Homo sapiens | 48% | 100% |
Q95JN5 | Macaca fascicularis | 22% | 83% |
Q98SH2 | Gallus gallus | 28% | 85% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 35% | 100% |
Q9CTG6 | Mus musculus | 22% | 88% |
Q9HD20 | Homo sapiens | 24% | 85% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 79% |
Q9LF79 | Arabidopsis thaliana | 29% | 95% |
Q9LIK7 | Arabidopsis thaliana | 30% | 100% |
Q9LU41 | Arabidopsis thaliana | 28% | 94% |
Q9LV11 | Arabidopsis thaliana | 28% | 100% |
Q9LY32 | Arabidopsis thaliana | 27% | 100% |
Q9LY77 | Arabidopsis thaliana | 29% | 99% |
Q9M2A0 | Arabidopsis thaliana | 27% | 100% |
Q9M2L4 | Arabidopsis thaliana | 28% | 100% |
Q9N0Z4 | Oryctolagus cuniculus | 22% | 88% |
Q9N0Z6 | Oryctolagus cuniculus | 32% | 100% |
Q9NQ11 | Homo sapiens | 23% | 87% |
Q9R0K7 | Mus musculus | 28% | 85% |
Q9SH76 | Arabidopsis thaliana | 26% | 100% |
Q9SJB3 | Arabidopsis thaliana | 25% | 100% |
Q9SU58 | Arabidopsis thaliana | 27% | 100% |
Q9SY55 | Arabidopsis thaliana | 46% | 100% |
Q9SZR1 | Arabidopsis thaliana | 29% | 96% |
Q9TV52 | Oryctolagus cuniculus | 31% | 94% |
Q9WV27 | Mus musculus | 30% | 99% |
Q9XES1 | Arabidopsis thaliana | 44% | 96% |
Q9Y2G3 | Homo sapiens | 21% | 87% |
Q9YGL9 | Gallus gallus | 47% | 100% |
Q9YH26 | Oreochromis mossambicus | 32% | 100% |
Q9Z1W8 | Mus musculus | 31% | 99% |
V5B873 | Trypanosoma cruzi | 29% | 93% |
V5BHI7 | Trypanosoma cruzi | 22% | 100% |
V5BHZ2 | Trypanosoma cruzi | 31% | 98% |
V5BLM1 | Trypanosoma cruzi | 67% | 100% |
V5BPC6 | Trypanosoma cruzi | 26% | 97% |