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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AF31
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 | 3 |
GO:0005388 | P-type calcium transporter activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 3 |
GO:0015662 | P-type ion transporter activity | 4 | 2 |
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 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
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 | 3 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 709 | 713 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 1027 | 1029 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 1105 | 1107 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 796 | 798 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.316 |
CLV_PCSK_KEX2_1 | 1100 | 1102 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 1107 | 1109 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 796 | 798 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 1100 | 1102 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 1107 | 1109 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.262 |
CLV_PCSK_PC7_1 | 1096 | 1102 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 1018 | 1022 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 1028 | 1032 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.331 |
DEG_APCC_DBOX_1 | 1027 | 1035 | PF00400 | 0.582 |
DOC_ANK_TNKS_1 | 40 | 47 | PF00023 | 0.683 |
DOC_CYCLIN_RxL_1 | 546 | 555 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 691 | 697 | PF00134 | 0.657 |
DOC_CYCLIN_yCln2_LP_2 | 976 | 982 | PF00134 | 0.304 |
DOC_MAPK_DCC_7 | 202 | 210 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 1028 | 1034 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 1096 | 1104 | PF00069 | 0.666 |
DOC_MAPK_gen_1 | 321 | 329 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 392 | 399 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 422 | 428 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 546 | 553 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 803 | 809 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.624 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 392 | 399 | PF00069 | 0.619 |
DOC_MAPK_MEF2A_6 | 633 | 640 | PF00069 | 0.646 |
DOC_PP1_RVXF_1 | 1019 | 1026 | PF00149 | 0.564 |
DOC_PP1_RVXF_1 | 598 | 605 | PF00149 | 0.532 |
DOC_PP1_RVXF_1 | 631 | 638 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 866 | 869 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 976 | 979 | PF13499 | 0.346 |
DOC_PP2B_PxIxI_1 | 753 | 759 | PF00149 | 0.485 |
DOC_PP4_FxxP_1 | 1090 | 1093 | PF00568 | 0.785 |
DOC_PP4_FxxP_1 | 614 | 617 | PF00568 | 0.545 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 951 | 955 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.567 |
DOC_USP7_UBL2_3 | 418 | 422 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 722 | 727 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 834 | 839 | PF00397 | 0.291 |
LIG_14-3-3_CanoR_1 | 1072 | 1076 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 796 | 805 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 860 | 868 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 930 | 938 | PF00244 | 0.275 |
LIG_Actin_WH2_2 | 1059 | 1074 | PF00022 | 0.637 |
LIG_Actin_WH2_2 | 587 | 602 | PF00022 | 0.524 |
LIG_BRCT_BRCA1_1 | 152 | 156 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 930 | 934 | PF00533 | 0.291 |
LIG_Clathr_ClatBox_1 | 1031 | 1035 | PF01394 | 0.685 |
LIG_Clathr_ClatBox_1 | 95 | 99 | PF01394 | 0.485 |
LIG_deltaCOP1_diTrp_1 | 158 | 162 | PF00928 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 840 | 847 | PF00928 | 0.322 |
LIG_deltaCOP1_diTrp_1 | 924 | 934 | PF00928 | 0.273 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.485 |
LIG_FAT_LD_1 | 323 | 331 | PF03623 | 0.472 |
LIG_FHA_1 | 1014 | 1020 | PF00498 | 0.501 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.304 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.523 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.466 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.512 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.493 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.690 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.541 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.462 |
LIG_FHA_1 | 860 | 866 | PF00498 | 0.497 |
LIG_FHA_1 | 875 | 881 | PF00498 | 0.422 |
LIG_FHA_2 | 1054 | 1060 | PF00498 | 0.738 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.533 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.626 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.567 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.548 |
LIG_GBD_Chelix_1 | 293 | 301 | PF00786 | 0.327 |
LIG_Integrin_isoDGR_2 | 39 | 41 | PF01839 | 0.485 |
LIG_IRF3_LxIS_1 | 820 | 827 | PF10401 | 0.496 |
LIG_LIR_Apic_2 | 1087 | 1093 | PF02991 | 0.781 |
LIG_LIR_Apic_2 | 611 | 617 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 1049 | 1058 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 1074 | 1082 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 521 | 532 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 702 | 711 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 712 | 721 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 782 | 793 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 840 | 851 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 90 | 101 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 1015 | 1020 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 1049 | 1053 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 1074 | 1078 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 702 | 706 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 782 | 788 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 872 | 878 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 931 | 937 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 997 | 1003 | PF02991 | 0.272 |
LIG_MYND_3 | 394 | 398 | PF01753 | 0.615 |
LIG_Pex14_1 | 843 | 847 | PF04695 | 0.304 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.291 |
LIG_Pex14_2 | 956 | 960 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 1019 | 1026 | PF02174 | 0.535 |
LIG_REV1ctd_RIR_1 | 470 | 478 | PF16727 | 0.439 |
LIG_RPA_C_Fungi | 925 | 937 | PF08784 | 0.322 |
LIG_SH2_CRK | 1017 | 1021 | PF00017 | 0.304 |
LIG_SH2_CRK | 644 | 648 | PF00017 | 0.389 |
LIG_SH2_GRB2like | 982 | 985 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.331 |
LIG_SH2_SRC | 644 | 647 | PF00017 | 0.387 |
LIG_SH2_SRC | 982 | 985 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 938 | 941 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 946 | 949 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 982 | 985 | PF00017 | 0.291 |
LIG_SH3_3 | 643 | 649 | PF00018 | 0.394 |
LIG_SH3_3 | 945 | 951 | PF00018 | 0.322 |
LIG_SUMO_SIM_anti_2 | 129 | 136 | PF11976 | 0.359 |
LIG_SUMO_SIM_anti_2 | 143 | 149 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 218 | 223 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 816 | 822 | PF11976 | 0.291 |
LIG_SUMO_SIM_anti_2 | 837 | 843 | PF11976 | 0.304 |
LIG_SUMO_SIM_anti_2 | 877 | 884 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 1030 | 1038 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 129 | 136 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 147 | 153 | PF11976 | 0.215 |
LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 560 | 567 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 575 | 580 | PF11976 | 0.434 |
LIG_TRFH_1 | 834 | 838 | PF08558 | 0.291 |
LIG_TYR_ITIM | 936 | 941 | PF00017 | 0.291 |
LIG_UBA3_1 | 1023 | 1029 | PF00899 | 0.584 |
LIG_UBA3_1 | 732 | 741 | PF00899 | 0.304 |
LIG_WRC_WIRS_1 | 1007 | 1012 | PF05994 | 0.305 |
LIG_WRC_WIRS_1 | 1050 | 1055 | PF05994 | 0.635 |
LIG_WW_3 | 645 | 649 | PF00397 | 0.389 |
MOD_CDK_SPxxK_3 | 722 | 729 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 750 | 757 | PF00069 | 0.304 |
MOD_CK1_1 | 1074 | 1080 | PF00069 | 0.544 |
MOD_CK1_1 | 1081 | 1087 | PF00069 | 0.571 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.428 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.535 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.356 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.314 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.359 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.305 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.391 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.462 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.383 |
MOD_CK1_1 | 994 | 1000 | PF00069 | 0.305 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.395 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.442 |
MOD_CK2_1 | 834 | 840 | PF00069 | 0.304 |
MOD_CK2_1 | 905 | 911 | PF00069 | 0.305 |
MOD_Cter_Amidation | 794 | 797 | PF01082 | 0.324 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.592 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.304 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.334 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.803 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.300 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.322 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.378 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.594 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.558 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.293 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.331 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.323 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.811 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.482 |
MOD_GSK3_1 | 925 | 932 | PF00069 | 0.496 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.287 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.346 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.779 |
MOD_N-GLC_1 | 750 | 755 | PF02516 | 0.291 |
MOD_NEK2_1 | 1053 | 1058 | PF00069 | 0.615 |
MOD_NEK2_1 | 1071 | 1076 | PF00069 | 0.524 |
MOD_NEK2_1 | 1078 | 1083 | PF00069 | 0.538 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.524 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.291 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.304 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.431 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.304 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.304 |
MOD_NEK2_1 | 942 | 947 | PF00069 | 0.346 |
MOD_NEK2_1 | 991 | 996 | PF00069 | 0.305 |
MOD_NEK2_2 | 829 | 834 | PF00069 | 0.406 |
MOD_NEK2_2 | 951 | 956 | PF00069 | 0.382 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.438 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.533 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.313 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.550 |
MOD_PIKK_1 | 796 | 802 | PF00454 | 0.354 |
MOD_PIKK_1 | 869 | 875 | PF00454 | 0.305 |
MOD_PKA_1 | 537 | 543 | PF00069 | 0.291 |
MOD_PKA_1 | 796 | 802 | PF00069 | 0.344 |
MOD_PKA_2 | 1071 | 1077 | PF00069 | 0.537 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.291 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.291 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.497 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.344 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.305 |
MOD_PKA_2 | 929 | 935 | PF00069 | 0.288 |
MOD_PKA_2 | 951 | 957 | PF00069 | 0.295 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.414 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.439 |
MOD_Plk_2-3 | 707 | 713 | PF00069 | 0.462 |
MOD_Plk_2-3 | 859 | 865 | PF00069 | 0.438 |
MOD_Plk_4 | 1006 | 1012 | PF00069 | 0.232 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.418 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.327 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.428 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.462 |
MOD_Plk_4 | 784 | 790 | PF00069 | 0.291 |
MOD_Plk_4 | 829 | 835 | PF00069 | 0.414 |
MOD_Plk_4 | 881 | 887 | PF00069 | 0.320 |
MOD_Plk_4 | 951 | 957 | PF00069 | 0.291 |
MOD_Plk_4 | 991 | 997 | PF00069 | 0.521 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.438 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.624 |
MOD_ProDKin_1 | 722 | 728 | PF00069 | 0.388 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.304 |
MOD_ProDKin_1 | 834 | 840 | PF00069 | 0.291 |
MOD_SUMO_for_1 | 547 | 550 | PF00179 | 0.305 |
MOD_SUMO_rev_2 | 529 | 536 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 540 | 547 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 571 | 577 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 725 | 730 | PF00179 | 0.386 |
TRG_DiLeu_BaEn_1 | 572 | 577 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_1 | 816 | 821 | PF01217 | 0.291 |
TRG_ENDOCYTIC_2 | 1017 | 1020 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 1050 | 1053 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 938 | 941 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 1105 | 1108 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 686 | 689 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 796 | 798 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 956 | 959 | PF00400 | 0.331 |
TRG_NES_CRM1_1 | 207 | 218 | PF08389 | 0.382 |
TRG_NES_CRM1_1 | 634 | 645 | PF08389 | 0.354 |
TRG_NLS_MonoExtN_4 | 1096 | 1103 | PF00514 | 0.642 |
TRG_NLS_MonoExtN_4 | 738 | 743 | PF00514 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 1029 | 1033 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 592 | 597 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 666 | 671 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 689 | 693 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 796 | 800 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 30% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 27% | 99% |
A0A0N1PFH3 | Leptomonas seymouri | 83% | 91% |
A0A0S4J1M1 | Bodo saltans | 29% | 100% |
A0A0S4J5A1 | Bodo saltans | 50% | 100% |
A0A0S4JA92 | Bodo saltans | 27% | 100% |
A0A0S4JRV4 | Bodo saltans | 30% | 100% |
A0A0S4JT33 | Bodo saltans | 22% | 100% |
A0A0S4KIG5 | Bodo saltans | 31% | 100% |
A0A0S4KNQ6 | Bodo saltans | 27% | 99% |
A0A1X0NNY6 | Trypanosomatidae | 30% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 27% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 28% | 98% |
A0A1X0P0Y8 | Trypanosomatidae | 25% | 100% |
A0A1X0P689 | Trypanosomatidae | 69% | 100% |
A0A1X0P720 | Trypanosomatidae | 25% | 100% |
A0A1X0P724 | Trypanosomatidae | 24% | 100% |
A0A1X0P7A1 | Trypanosomatidae | 24% | 100% |
A0A381MFJ0 | Leishmania infantum | 27% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 62% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 26% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WPW0 | Leishmania donovani | 25% | 99% |
A0A3S7WV61 | Leishmania donovani | 27% | 100% |
A0A3S7WV68 | Leishmania donovani | 27% | 100% |
A0A3S7X978 | Leishmania donovani | 97% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 30% | 100% |
A0A451EJU6 | Leishmania donovani | 30% | 100% |
A2VDL6 | Bos taurus | 29% | 100% |
A4H3S2 | Leishmania braziliensis | 31% | 100% |
A4H514 | Leishmania braziliensis | 26% | 98% |
A4H9Q5 | Leishmania braziliensis | 27% | 100% |
A4HMM8 | Leishmania braziliensis | 89% | 100% |
A4HRZ6 | Leishmania infantum | 31% | 100% |
A4HT82 | Leishmania infantum | 27% | 100% |
A4HTF0 | Leishmania infantum | 26% | 100% |
A4HY23 | Leishmania infantum | 27% | 100% |
A4IBA6 | Leishmania infantum | 97% | 100% |
A7L9Z8 | Mus musculus | 27% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A564 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D2WKD8 | Sus scrofa | 30% | 100% |
D3K0R6 | Bos taurus | 28% | 92% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 99% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 98% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 91% |
F1Q4S1 | Danio rerio | 23% | 99% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 26% | 78% |
O14983 | Homo sapiens | 30% | 100% |
O22218 | Arabidopsis thaliana | 28% | 100% |
O23087 | Arabidopsis thaliana | 32% | 100% |
O34431 | Bacillus subtilis (strain 168) | 34% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 29% | 100% |
O46674 | Canis lupus familiaris | 30% | 100% |
O55143 | Mus musculus | 29% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O70228 | Mus musculus | 22% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 84% |
O75110 | Homo sapiens | 22% | 100% |
O77696 | Sus scrofa | 31% | 100% |
O81108 | Arabidopsis thaliana | 29% | 100% |
P04074 | Ovis aries | 30% | 100% |
P04191 | Oryctolagus cuniculus | 30% | 100% |
P05023 | Homo sapiens | 30% | 100% |
P05024 | Sus scrofa | 30% | 100% |
P05025 | Tetronarce californica | 30% | 100% |
P06685 | Rattus norvegicus | 30% | 100% |
P06686 | Rattus norvegicus | 29% | 100% |
P06687 | Rattus norvegicus | 31% | 100% |
P09572 | Gallus gallus | 30% | 100% |
P09626 | Rattus norvegicus | 29% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 26% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 26% | 100% |
P11507 | Rattus norvegicus | 29% | 100% |
P11607 | Sus scrofa | 30% | 100% |
P13585 | Gallus gallus | 31% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P13607 | Drosophila melanogaster | 28% | 100% |
P13637 | Homo sapiens | 31% | 100% |
P16615 | Homo sapiens | 30% | 100% |
P17326 | Artemia franciscana | 28% | 100% |
P18596 | Rattus norvegicus | 31% | 100% |
P18907 | Equus caballus | 31% | 100% |
P19156 | Sus scrofa | 29% | 100% |
P20647 | Oryctolagus cuniculus | 30% | 100% |
P20648 | Homo sapiens | 29% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P22700 | Drosophila melanogaster | 31% | 100% |
P23634 | Homo sapiens | 28% | 89% |
P24797 | Gallus gallus | 30% | 100% |
P24798 | Gallus gallus | 31% | 100% |
P25489 | Catostomus commersonii | 29% | 100% |
P27112 | Oryctolagus cuniculus | 29% | 100% |
P28774 | Artemia franciscana | 29% | 100% |
P30714 | Rhinella marina | 30% | 100% |
P35315 | Trypanosoma brucei brucei | 30% | 100% |
P35316 | Artemia franciscana | 28% | 100% |
P35317 | Hydra vulgaris | 30% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 34% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 35% | 100% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 30% | 100% |
P49380 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 100% |
P50993 | Homo sapiens | 30% | 100% |
P50996 | Canis lupus familiaris | 29% | 100% |
P50997 | Canis lupus familiaris | 30% | 100% |
P54209 | Dunaliella bioculata | 31% | 100% |
P54210 | Dunaliella acidophila | 25% | 100% |
P54211 | Dunaliella bioculata | 24% | 98% |
P54678 | Dictyostelium discoideum | 29% | 99% |
P54679 | Dictyostelium discoideum | 25% | 100% |
P54707 | Homo sapiens | 28% | 100% |
P54708 | Rattus norvegicus | 28% | 100% |
P57709 | Bos taurus | 30% | 100% |
P58312 | Oreochromis mossambicus | 29% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 31% | 100% |
P70083 | Makaira nigricans | 30% | 100% |
P70704 | Mus musculus | 22% | 95% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 30% | 100% |
P92939 | Arabidopsis thaliana | 31% | 100% |
P98194 | Homo sapiens | 30% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 31% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 31% | 100% |
Q00779 | Felis catus | 30% | 100% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q03669 | Gallus gallus | 29% | 100% |
Q08436 | Nicotiana plumbaginifolia | 24% | 100% |
Q08DA1 | Bos taurus | 30% | 100% |
Q0VCY0 | Bos taurus | 30% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 30% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 28% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 28% | 100% |
Q3TYU2 | Mus musculus | 23% | 91% |
Q42883 | Solanum lycopersicum | 32% | 100% |
Q4QDN7 | Leishmania major | 26% | 100% |
Q4QDN8 | Leishmania major | 26% | 100% |
Q4QIM6 | Leishmania major | 27% | 99% |
Q4QIM8 | Leishmania major | 27% | 100% |
Q58623 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 30% | 100% |
Q5R5K5 | Pongo abelii | 30% | 100% |
Q5RCD8 | Pongo abelii | 30% | 100% |
Q5RDR3 | Pongo abelii | 31% | 100% |
Q64392 | Cavia porcellus | 29% | 100% |
Q64518 | Mus musculus | 32% | 100% |
Q64541 | Rattus norvegicus | 28% | 100% |
Q64542 | Rattus norvegicus | 27% | 92% |
Q64566 | Rattus norvegicus | 30% | 100% |
Q64578 | Rattus norvegicus | 29% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 27% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 30% | 100% |
Q6PIC6 | Mus musculus | 31% | 100% |
Q6PIE5 | Mus musculus | 29% | 100% |
Q6RWA9 | Taenia solium | 29% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 33% | 100% |
Q7PPA5 | Anopheles gambiae | 30% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 27% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 28% | 100% |
Q80XR2 | Mus musculus | 30% | 100% |
Q8R429 | Mus musculus | 30% | 100% |
Q8R4C1 | Rattus norvegicus | 29% | 100% |
Q8VDN2 | Mus musculus | 30% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 30% | 100% |
Q92030 | Anguilla anguilla | 29% | 100% |
Q92036 | Rhinella marina | 29% | 100% |
Q92105 | Pelophylax lessonae | 30% | 100% |
Q92123 | Xenopus laevis | 30% | 100% |
Q92126 | Xenopus laevis | 28% | 100% |
Q93084 | Homo sapiens | 31% | 100% |
Q95Z93 | Leishmania major | 31% | 100% |
Q98SH2 | Gallus gallus | 28% | 92% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CTG6 | Mus musculus | 21% | 95% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 86% |
Q9LF79 | Arabidopsis thaliana | 30% | 100% |
Q9LIK7 | Arabidopsis thaliana | 27% | 100% |
Q9LU41 | Arabidopsis thaliana | 29% | 100% |
Q9LV11 | Arabidopsis thaliana | 24% | 100% |
Q9LY77 | Arabidopsis thaliana | 27% | 100% |
Q9M2A0 | Arabidopsis thaliana | 24% | 100% |
Q9M2L4 | Arabidopsis thaliana | 28% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 30% | 100% |
Q9R0K7 | Mus musculus | 29% | 93% |
Q9SY55 | Arabidopsis thaliana | 31% | 100% |
Q9SZR1 | Arabidopsis thaliana | 29% | 100% |
Q9TV52 | Oryctolagus cuniculus | 29% | 100% |
Q9WV27 | Mus musculus | 28% | 100% |
Q9XES1 | Arabidopsis thaliana | 32% | 100% |
Q9YGL9 | Gallus gallus | 31% | 100% |
Q9YH26 | Oreochromis mossambicus | 29% | 100% |
Q9Z1W8 | Mus musculus | 29% | 100% |
V5B873 | Trypanosoma cruzi | 24% | 100% |
V5BHZ2 | Trypanosoma cruzi | 68% | 100% |
V5BLM1 | Trypanosoma cruzi | 31% | 100% |