Homologous to animal ER-localized Ca2+ ATPases. Localization: ER (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H3S2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006816 | calcium ion transport | 7 | 1 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0070588 | calcium ion transmembrane transport | 6 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005388 | P-type calcium transporter activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0015662 | P-type ion transporter activity | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.380 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.407 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.180 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.281 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.306 |
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 | 0.360 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 667 | 669 | PF00082 | 0.175 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 981 | 985 | PF00082 | 0.379 |
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_CKS1_1 | 986 | 991 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 475 | 489 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 986 | 992 | PF00134 | 0.428 |
DOC_MAPK_DCC_7 | 949 | 958 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 244 | 252 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 477 | 485 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 494 | 501 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 713 | 719 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 746 | 755 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 303 | 310 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 713 | 721 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 837 | 845 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 891 | 899 | PF00069 | 0.255 |
DOC_PP1_RVXF_1 | 479 | 486 | PF00149 | 0.380 |
DOC_PP1_RVXF_1 | 561 | 568 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 750 | 756 | PF00149 | 0.406 |
DOC_PP1_RVXF_1 | 86 | 92 | PF00149 | 0.454 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 602 | 605 | PF13499 | 0.480 |
DOC_PP2B_PxIxI_1 | 988 | 994 | PF00149 | 0.222 |
DOC_PP4_FxxP_1 | 782 | 785 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.196 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 930 | 934 | PF00917 | 0.396 |
DOC_USP7_MATH_2 | 648 | 654 | PF00917 | 0.380 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.262 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.524 |
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 |
DOC_WW_Pin1_4 | 951 | 956 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 985 | 990 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.546 |
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 | 0.484 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 494 | 500 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 763 | 773 | PF00244 | 0.308 |
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 | 0.675 |
LIG_Clathr_ClatBox_1 | 166 | 170 | PF01394 | 0.560 |
LIG_Clathr_ClatBox_1 | 898 | 902 | PF01394 | 0.308 |
LIG_deltaCOP1_diTrp_1 | 831 | 836 | PF00928 | 0.541 |
LIG_EH1_1 | 94 | 102 | PF00400 | 0.323 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.469 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.463 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.455 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.308 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.448 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.488 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.511 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.464 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.449 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.308 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.282 |
LIG_FHA_1 | 980 | 986 | PF00498 | 0.426 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.530 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.218 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.513 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.460 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.306 |
LIG_GBD_Chelix_1 | 773 | 781 | PF00786 | 0.308 |
LIG_GBD_Chelix_1 | 850 | 858 | PF00786 | 0.202 |
LIG_LIR_Apic_2 | 292 | 297 | PF02991 | 0.255 |
LIG_LIR_Apic_2 | 779 | 785 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 90 | 94 | PF02991 | 0.183 |
LIG_LIR_Gen_1 | 262 | 273 | PF02991 | 0.202 |
LIG_LIR_Gen_1 | 738 | 748 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 831 | 841 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 923 | 931 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 967 | 977 | 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 | 0.455 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.465 |
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 | 0.488 |
LIG_LIR_Nem_3 | 758 | 764 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 831 | 836 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 923 | 929 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 940 | 946 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 967 | 972 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 978 | 983 | PF02991 | 0.231 |
LIG_NRBOX | 687 | 693 | PF00104 | 0.455 |
LIG_Pex14_1 | 290 | 294 | PF04695 | 0.280 |
LIG_Pex14_2 | 853 | 857 | PF04695 | 0.255 |
LIG_Pex14_2 | 91 | 95 | PF04695 | 0.207 |
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_REV1ctd_RIR_1 | 997 | 1006 | PF16727 | 0.290 |
LIG_SH2_CRK | 838 | 842 | PF00017 | 0.311 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 844 | 847 | PF00017 | 0.308 |
LIG_SH2_SRC | 764 | 767 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 764 | 767 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 844 | 847 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 943 | 946 | PF00017 | 0.308 |
LIG_SH3_1 | 536 | 542 | PF00018 | 0.407 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.529 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.464 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.451 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.507 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.532 |
LIG_SH3_3 | 822 | 828 | PF00018 | 0.403 |
LIG_SH3_3 | 915 | 921 | PF00018 | 0.516 |
LIG_SH3_3 | 968 | 974 | PF00018 | 0.316 |
LIG_SUMO_SIM_anti_2 | 896 | 902 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 915 | 920 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 982 | 988 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 165 | 172 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 20 | 26 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 622 | 627 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 891 | 896 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 897 | 902 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 927 | 934 | PF11976 | 0.222 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 981 | 988 | PF11976 | 0.402 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.360 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.466 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.268 |
LIG_UBA3_1 | 17 | 25 | PF00899 | 0.538 |
LIG_UBA3_1 | 450 | 456 | PF00899 | 0.455 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 867 | 872 | PF05994 | 0.341 |
LIG_WW_3 | 603 | 607 | PF00397 | 0.455 |
MOD_CDK_SPK_2 | 538 | 543 | PF00069 | 0.560 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.466 |
MOD_CDK_SPxxK_3 | 660 | 667 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 706 | 713 | PF00069 | 0.541 |
MOD_CK1_1 | 1001 | 1007 | PF00069 | 0.646 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.566 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.483 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.455 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.479 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.502 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.554 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.301 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.606 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.479 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.530 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.530 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.205 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.492 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.433 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.489 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.473 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.539 |
MOD_GlcNHglycan | 1011 | 1014 | PF01048 | 0.511 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.365 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.293 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.347 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.267 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.335 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.429 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.560 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.485 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.259 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.480 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.455 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.455 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.466 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.459 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.465 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.528 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.489 |
MOD_GSK3_1 | 856 | 863 | PF00069 | 0.284 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.291 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.286 |
MOD_GSK3_1 | 975 | 982 | PF00069 | 0.339 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.341 |
MOD_N-GLC_1 | 755 | 760 | PF02516 | 0.284 |
MOD_N-GLC_1 | 874 | 879 | PF02516 | 0.443 |
MOD_N-GLC_1 | 912 | 917 | PF02516 | 0.255 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.455 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.530 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.386 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.508 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.516 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.563 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.466 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.315 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.487 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.495 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.282 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.378 |
MOD_NEK2_1 | 984 | 989 | PF00069 | 0.365 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.381 |
MOD_NEK2_2 | 118 | 123 | PF00069 | 0.536 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.560 |
MOD_PK_1 | 382 | 388 | PF00069 | 0.380 |
MOD_PK_1 | 497 | 503 | PF00069 | 0.466 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.496 |
MOD_PKA_1 | 630 | 636 | PF00069 | 0.466 |
MOD_PKA_2 | 1001 | 1007 | PF00069 | 0.627 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.541 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.484 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.447 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.472 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.522 |
MOD_PKA_2 | 919 | 925 | PF00069 | 0.445 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.477 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.494 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.459 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.380 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.316 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.407 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.455 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.375 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.466 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.323 |
MOD_Plk_1 | 912 | 918 | PF00069 | 0.455 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.513 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.560 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.499 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.546 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.480 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.476 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.341 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.484 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.533 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.480 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.466 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.323 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.486 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.308 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.455 |
MOD_Plk_4 | 937 | 943 | PF00069 | 0.373 |
MOD_Plk_4 | 979 | 985 | PF00069 | 0.327 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.455 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.262 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.457 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.524 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.516 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.541 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.266 |
MOD_ProDKin_1 | 951 | 957 | PF00069 | 0.371 |
MOD_ProDKin_1 | 985 | 991 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 584 | 587 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 20 | 27 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 237 | 247 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 976 | 983 | PF00179 | 0.237 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_1 | 912 | 917 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 838 | 841 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 844 | 847 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 943 | 946 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 639 | 641 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 822 | 824 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 570 | 574 | PF00026 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 75% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 30% | 92% |
A0A0N1I8I8 | Leptomonas seymouri | 28% | 84% |
A0A0N1PFH3 | Leptomonas seymouri | 31% | 84% |
A0A0S4INU6 | Bodo saltans | 21% | 84% |
A0A0S4J1M1 | Bodo saltans | 28% | 94% |
A0A0S4J5A1 | Bodo saltans | 32% | 96% |
A0A0S4J6U4 | Bodo saltans | 27% | 94% |
A0A0S4JA92 | Bodo saltans | 28% | 100% |
A0A0S4JRV4 | Bodo saltans | 31% | 100% |
A0A0S4KIG5 | Bodo saltans | 63% | 100% |
A0A0S4KNQ6 | Bodo saltans | 29% | 92% |
A0A1X0NNY6 | Trypanosomatidae | 68% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 27% | 93% |
A0A1X0NPJ3 | Trypanosomatidae | 20% | 83% |
A0A1X0NTI6 | Trypanosomatidae | 28% | 90% |
A0A1X0P0Y8 | Trypanosomatidae | 26% | 93% |
A0A1X0P689 | Trypanosomatidae | 31% | 98% |
A0A3R7KM63 | Trypanosoma rangeli | 27% | 99% |
A0A3R7MRX8 | Trypanosoma rangeli | 31% | 99% |
A0A3S5H5Y9 | Leishmania donovani | 27% | 93% |
A0A3S5H614 | Leishmania donovani | 21% | 82% |
A0A3S5ISK9 | Trypanosoma rangeli | 27% | 96% |
A0A3S7WPW0 | Leishmania donovani | 27% | 92% |
A0A3S7WUG2 | Leishmania donovani | 30% | 100% |
A0A3S7X978 | Leishmania donovani | 31% | 92% |
A0A422NTS7 | Trypanosoma rangeli | 65% | 100% |
A0A451EJU6 | Leishmania donovani | 86% | 100% |
A2VDL6 | Bos taurus | 32% | 100% |
A4H514 | Leishmania braziliensis | 28% | 91% |
A4H903 | Leishmania braziliensis | 27% | 92% |
A4HLF4 | Leishmania braziliensis | 26% | 86% |
A4HMM8 | Leishmania braziliensis | 32% | 93% |
A4HRZ6 | Leishmania infantum | 86% | 100% |
A4HT82 | Leishmania infantum | 29% | 100% |
A4HTD0 | Leishmania infantum | 22% | 82% |
A4HTF0 | Leishmania infantum | 27% | 100% |
A4HXD4 | Leishmania infantum | 30% | 100% |
A4IBA6 | Leishmania infantum | 31% | 92% |
A7L9Z8 | Mus musculus | 33% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 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) | 26% | 93% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 25% | 100% |
D2WKD8 | Sus scrofa | 32% | 100% |
D3K0R6 | Bos taurus | 27% | 85% |
E9AF31 | Leishmania major | 31% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 93% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 92% |
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) | 28% | 72% |
O14022 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 94% |
O14072 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 85% |
O14983 | Homo sapiens | 49% | 100% |
O22218 | Arabidopsis thaliana | 29% | 100% |
O23087 | Arabidopsis thaliana | 44% | 97% |
O34431 | Bacillus subtilis (strain 168) | 34% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 35% | 100% |
O46674 | Canis lupus familiaris | 49% | 100% |
O55143 | Mus musculus | 49% | 98% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
O64806 | Arabidopsis thaliana | 27% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 78% |
O75185 | Homo sapiens | 32% | 100% |
O77696 | Sus scrofa | 49% | 100% |
O81108 | Arabidopsis thaliana | 29% | 100% |
P04074 | Ovis aries | 32% | 100% |
P04191 | Oryctolagus cuniculus | 49% | 100% |
P05023 | Homo sapiens | 32% | 100% |
P05024 | Sus scrofa | 31% | 100% |
P05025 | Tetronarce californica | 32% | 100% |
P06685 | Rattus norvegicus | 31% | 100% |
P06686 | Rattus norvegicus | 32% | 100% |
P06687 | Rattus norvegicus | 32% | 100% |
P09572 | Gallus gallus | 32% | 100% |
P09626 | Rattus norvegicus | 32% | 99% |
P09627 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P11505 | Rattus norvegicus | 30% | 84% |
P11506 | Rattus norvegicus | 30% | 82% |
P11507 | Rattus norvegicus | 48% | 98% |
P11607 | Sus scrofa | 49% | 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 | 32% | 100% |
P16615 | Homo sapiens | 49% | 98% |
P17326 | Artemia franciscana | 31% | 100% |
P18596 | Rattus norvegicus | 49% | 100% |
P18907 | Equus caballus | 32% | 100% |
P19156 | Sus scrofa | 32% | 99% |
P19456 | Arabidopsis thaliana | 26% | 100% |
P20020 | Homo sapiens | 30% | 84% |
P20431 | Arabidopsis thaliana | 26% | 100% |
P20647 | Oryctolagus cuniculus | 49% | 98% |
P20648 | Homo sapiens | 32% | 99% |
P20649 | Arabidopsis thaliana | 25% | 100% |
P22180 | Solanum lycopersicum | 25% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 99% |
P22700 | Drosophila melanogaster | 48% | 100% |
P23220 | Sus scrofa | 30% | 84% |
P23634 | Homo sapiens | 29% | 83% |
P24797 | Gallus gallus | 33% | 100% |
P24798 | Gallus gallus | 32% | 100% |
P25489 | Catostomus commersonii | 32% | 100% |
P27112 | Oryctolagus cuniculus | 32% | 99% |
P28774 | Artemia franciscana | 31% | 100% |
P30714 | Rhinella marina | 31% | 100% |
P35315 | Trypanosoma brucei brucei | 65% | 100% |
P35316 | Artemia franciscana | 48% | 100% |
P35317 | Hydra vulgaris | 30% | 99% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 35% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 34% | 100% |
P39986 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 84% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 31% | 100% |
P50993 | Homo sapiens | 32% | 100% |
P50996 | Canis lupus familiaris | 32% | 99% |
P50997 | Canis lupus familiaris | 31% | 100% |
P54209 | Dunaliella bioculata | 47% | 99% |
P54210 | Dunaliella acidophila | 26% | 93% |
P54678 | Dictyostelium discoideum | 29% | 92% |
P54707 | Homo sapiens | 30% | 99% |
P54708 | Rattus norvegicus | 32% | 99% |
P57709 | Bos taurus | 33% | 100% |
P58165 | Oreochromis mossambicus | 30% | 92% |
P58312 | Oreochromis mossambicus | 31% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 34% | 100% |
P70083 | Makaira nigricans | 49% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 29% | 100% |
P90747 | Caenorhabditis elegans | 23% | 87% |
P92939 | Arabidopsis thaliana | 45% | 97% |
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 | 28% | 84% |
Q01814 | Homo sapiens | 29% | 82% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q03194 | Nicotiana plumbaginifolia | 26% | 100% |
Q03669 | Gallus gallus | 48% | 98% |
Q08DA1 | Bos taurus | 32% | 100% |
Q0VCY0 | Bos taurus | 50% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q13733 | Homo sapiens | 32% | 100% |
Q16720 | Homo sapiens | 28% | 84% |
Q21286 | Caenorhabditis elegans | 22% | 85% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 48% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 27% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 27% | 99% |
Q2RAS0 | Oryza sativa subsp. japonica | 27% | 100% |
Q37145 | Arabidopsis thaliana | 30% | 100% |
Q3TYU2 | Mus musculus | 21% | 84% |
Q42556 | Arabidopsis thaliana | 24% | 100% |
Q42883 | Solanum lycopersicum | 44% | 98% |
Q4QED4 | Leishmania major | 30% | 100% |
Q4QII2 | Leishmania major | 21% | 82% |
Q4QIM6 | Leishmania major | 26% | 100% |
Q4QIM8 | Leishmania major | 28% | 100% |
Q4VNC0 | Homo sapiens | 22% | 84% |
Q5R5K5 | Pongo abelii | 33% | 100% |
Q5RCD8 | Pongo abelii | 32% | 100% |
Q5RDR3 | Pongo abelii | 32% | 100% |
Q5ZKB7 | Gallus gallus | 22% | 85% |
Q64392 | Cavia porcellus | 31% | 99% |
Q64436 | Mus musculus | 32% | 99% |
Q64518 | Mus musculus | 49% | 100% |
Q64541 | Rattus norvegicus | 30% | 100% |
Q64542 | Rattus norvegicus | 27% | 85% |
Q64566 | Rattus norvegicus | 33% | 100% |
Q64568 | Rattus norvegicus | 27% | 81% |
Q64578 | Rattus norvegicus | 50% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 27% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 28% | 99% |
Q6PIC6 | Mus musculus | 32% | 100% |
Q6PIE5 | Mus musculus | 32% | 100% |
Q6Q477 | Mus musculus | 31% | 85% |
Q6RWA9 | Taenia solium | 32% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 34% | 100% |
Q7PPA5 | Anopheles gambiae | 48% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 27% | 94% |
Q7XEK4 | Oryza sativa subsp. japonica | 31% | 99% |
Q80XR2 | Mus musculus | 33% | 100% |
Q8R429 | Mus musculus | 50% | 100% |
Q8R4C1 | Rattus norvegicus | 33% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 29% | 98% |
Q8VDN2 | Mus musculus | 31% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 35% | 100% |
Q92030 | Anguilla anguilla | 32% | 100% |
Q92036 | Rhinella marina | 29% | 98% |
Q92105 | Pelophylax lessonae | 49% | 100% |
Q92123 | Xenopus laevis | 32% | 100% |
Q92126 | Xenopus laevis | 31% | 99% |
Q93084 | Homo sapiens | 48% | 100% |
Q95JN5 | Macaca fascicularis | 21% | 84% |
Q95Z93 | Leishmania major | 86% | 100% |
Q98SH2 | Gallus gallus | 28% | 85% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 34% | 100% |
Q9CTG6 | Mus musculus | 21% | 88% |
Q9H7F0 | Homo sapiens | 21% | 84% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 79% |
Q9LF79 | Arabidopsis thaliana | 29% | 95% |
Q9LIK7 | Arabidopsis thaliana | 30% | 100% |
Q9LU41 | Arabidopsis thaliana | 28% | 94% |
Q9LV11 | Arabidopsis thaliana | 25% | 100% |
Q9LY32 | Arabidopsis thaliana | 26% | 100% |
Q9LY77 | Arabidopsis thaliana | 30% | 99% |
Q9M2A0 | Arabidopsis thaliana | 25% | 100% |
Q9M2L4 | Arabidopsis thaliana | 29% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 32% | 100% |
Q9NQ11 | Homo sapiens | 21% | 87% |
Q9R0K7 | Mus musculus | 27% | 86% |
Q9SH76 | Arabidopsis thaliana | 24% | 100% |
Q9SJB3 | Arabidopsis thaliana | 25% | 100% |
Q9SU58 | Arabidopsis thaliana | 25% | 100% |
Q9SY55 | Arabidopsis thaliana | 47% | 100% |
Q9SZR1 | Arabidopsis thaliana | 29% | 96% |
Q9TV52 | Oryctolagus cuniculus | 30% | 94% |
Q9WV27 | Mus musculus | 30% | 99% |
Q9XES1 | Arabidopsis thaliana | 45% | 97% |
Q9YGL9 | Gallus gallus | 48% | 100% |
Q9YH26 | Oreochromis mossambicus | 31% | 100% |
Q9Z1W8 | Mus musculus | 32% | 99% |
V5B873 | Trypanosoma cruzi | 28% | 93% |
V5BHZ2 | Trypanosoma cruzi | 31% | 99% |
V5BLM1 | Trypanosoma cruzi | 66% | 100% |
V5BPC6 | Trypanosoma cruzi | 26% | 97% |