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. | no | 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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HMM8
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 | 3 |
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:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 3 |
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:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0005388 | P-type calcium transporter activity | 4 | 1 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 1 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1051 | 1055 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 704 | 708 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 1100 | 1102 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 797 | 799 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 1102 | 1104 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 1102 | 1104 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 1013 | 1017 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 1096 | 1100 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.265 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.597 |
DOC_ANK_TNKS_1 | 911 | 918 | PF00023 | 0.201 |
DOC_CYCLIN_yCln2_LP_2 | 686 | 692 | PF00134 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 971 | 977 | PF00134 | 0.316 |
DOC_MAPK_DCC_7 | 197 | 205 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 316 | 324 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 387 | 394 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 417 | 423 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 541 | 548 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 798 | 804 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 134 | 143 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 197 | 205 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 387 | 394 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 628 | 635 | PF00069 | 0.605 |
DOC_PP1_RVXF_1 | 1014 | 1021 | PF00149 | 0.627 |
DOC_PP1_RVXF_1 | 593 | 600 | PF00149 | 0.503 |
DOC_PP1_RVXF_1 | 626 | 633 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 861 | 864 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 971 | 974 | PF13499 | 0.388 |
DOC_PP2B_PxIxI_1 | 748 | 754 | PF00149 | 0.489 |
DOC_PP4_FxxP_1 | 1085 | 1088 | PF00568 | 0.771 |
DOC_PP4_FxxP_1 | 609 | 612 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 1078 | 1082 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 759 | 763 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 946 | 950 | PF00917 | 0.532 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.476 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 829 | 834 | PF00397 | 0.301 |
LIG_14-3-3_CanoR_1 | 1067 | 1071 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 791 | 800 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 925 | 933 | PF00244 | 0.279 |
LIG_Actin_WH2_2 | 1054 | 1069 | PF00022 | 0.611 |
LIG_Actin_WH2_2 | 454 | 471 | PF00022 | 0.401 |
LIG_Actin_WH2_2 | 582 | 597 | PF00022 | 0.465 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.593 |
LIG_BRCT_BRCA1_1 | 925 | 929 | PF00533 | 0.317 |
LIG_Clathr_ClatBox_1 | 1026 | 1030 | PF01394 | 0.674 |
LIG_Clathr_ClatBox_1 | 90 | 94 | PF01394 | 0.489 |
LIG_CtBP_PxDLS_1 | 452 | 456 | PF00389 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 153 | 157 | PF00928 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 835 | 842 | PF00928 | 0.336 |
LIG_deltaCOP1_diTrp_1 | 919 | 929 | PF00928 | 0.277 |
LIG_eIF4E_1 | 320 | 326 | PF01652 | 0.489 |
LIG_FAT_LD_1 | 318 | 326 | PF03623 | 0.476 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.316 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.538 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.469 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.475 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.699 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.499 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.544 |
LIG_FHA_1 | 765 | 771 | PF00498 | 0.539 |
LIG_FHA_1 | 855 | 861 | PF00498 | 0.502 |
LIG_FHA_1 | 870 | 876 | PF00498 | 0.416 |
LIG_FHA_2 | 1049 | 1055 | PF00498 | 0.734 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.476 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.568 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.473 |
LIG_GBD_Chelix_1 | 288 | 296 | PF00786 | 0.332 |
LIG_IRF3_LxIS_1 | 815 | 822 | PF10401 | 0.506 |
LIG_LIR_Apic_2 | 1082 | 1088 | PF02991 | 0.766 |
LIG_LIR_Apic_2 | 606 | 612 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 1044 | 1053 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 1069 | 1078 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 153 | 162 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 697 | 706 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 707 | 716 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 777 | 788 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 835 | 846 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 1010 | 1015 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 1044 | 1048 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 1069 | 1073 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 319 | 323 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 697 | 701 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 707 | 712 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 77 | 82 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 867 | 873 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 926 | 932 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 969 | 975 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 992 | 998 | PF02991 | 0.276 |
LIG_MYND_3 | 389 | 393 | PF01753 | 0.616 |
LIG_Pex14_1 | 838 | 842 | PF04695 | 0.316 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.301 |
LIG_Pex14_2 | 951 | 955 | PF04695 | 0.468 |
LIG_PTB_Apo_2 | 1014 | 1021 | PF02174 | 0.535 |
LIG_RPA_C_Fungi | 920 | 932 | PF08784 | 0.336 |
LIG_SH2_CRK | 1012 | 1016 | PF00017 | 0.316 |
LIG_SH2_CRK | 639 | 643 | PF00017 | 0.316 |
LIG_SH2_GRB2like | 977 | 980 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.374 |
LIG_SH2_SRC | 434 | 437 | PF00017 | 0.212 |
LIG_SH2_SRC | 639 | 642 | PF00017 | 0.316 |
LIG_SH2_SRC | 977 | 980 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 933 | 936 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 941 | 944 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 977 | 980 | PF00017 | 0.301 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.316 |
LIG_SH3_3 | 940 | 946 | PF00018 | 0.336 |
LIG_Sin3_3 | 332 | 339 | PF02671 | 0.212 |
LIG_SUMO_SIM_anti_2 | 124 | 131 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 811 | 817 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 832 | 838 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 872 | 879 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 1025 | 1033 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 213 | 218 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 555 | 562 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 871 | 879 | PF11976 | 0.212 |
LIG_TRFH_1 | 829 | 833 | PF08558 | 0.301 |
LIG_TYR_ITIM | 931 | 936 | PF00017 | 0.301 |
LIG_UBA3_1 | 1004 | 1013 | PF00899 | 0.330 |
LIG_UBA3_1 | 1018 | 1024 | PF00899 | 0.583 |
LIG_UBA3_1 | 116 | 120 | PF00899 | 0.395 |
LIG_UBA3_1 | 126 | 134 | PF00899 | 0.324 |
LIG_UBA3_1 | 7 | 14 | PF00899 | 0.484 |
LIG_UBA3_1 | 727 | 736 | PF00899 | 0.316 |
LIG_WRC_WIRS_1 | 1045 | 1050 | PF05994 | 0.653 |
LIG_WW_3 | 640 | 644 | PF00397 | 0.301 |
MOD_CDK_SPxxK_3 | 717 | 724 | PF00069 | 0.301 |
MOD_CDK_SPxxK_3 | 745 | 752 | PF00069 | 0.316 |
MOD_CK1_1 | 1069 | 1075 | PF00069 | 0.521 |
MOD_CK1_1 | 1076 | 1082 | PF00069 | 0.537 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.431 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.357 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.327 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.301 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.557 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.316 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.395 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.301 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.333 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.445 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.316 |
MOD_Cter_Amidation | 789 | 792 | PF01082 | 0.335 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.316 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.772 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.349 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.689 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.423 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.336 |
MOD_GlcNHglycan | 902 | 905 | PF01048 | 0.391 |
MOD_GlcNHglycan | 913 | 916 | PF01048 | 0.305 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.353 |
MOD_GSK3_1 | 1044 | 1051 | PF00069 | 0.649 |
MOD_GSK3_1 | 1069 | 1076 | PF00069 | 0.532 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.335 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.341 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.406 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.492 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.356 |
MOD_N-GLC_1 | 745 | 750 | PF02516 | 0.301 |
MOD_N-GLC_1 | 778 | 783 | PF02516 | 0.309 |
MOD_NEK2_1 | 1048 | 1053 | PF00069 | 0.659 |
MOD_NEK2_1 | 1066 | 1071 | PF00069 | 0.499 |
MOD_NEK2_1 | 1073 | 1078 | PF00069 | 0.503 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.301 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.316 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.439 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.316 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.316 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.361 |
MOD_NEK2_1 | 966 | 971 | PF00069 | 0.336 |
MOD_NEK2_2 | 824 | 829 | PF00069 | 0.456 |
MOD_NEK2_2 | 946 | 951 | PF00069 | 0.395 |
MOD_PIKK_1 | 1086 | 1092 | PF00454 | 0.693 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.445 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.326 |
MOD_PIKK_1 | 572 | 578 | PF00454 | 0.445 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.356 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.465 |
MOD_PKA_1 | 532 | 538 | PF00069 | 0.301 |
MOD_PKA_1 | 791 | 797 | PF00069 | 0.356 |
MOD_PKA_2 | 1066 | 1072 | PF00069 | 0.516 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.301 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.330 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.395 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.356 |
MOD_PKA_2 | 911 | 917 | PF00069 | 0.307 |
MOD_PKA_2 | 924 | 930 | PF00069 | 0.298 |
MOD_PKA_2 | 946 | 952 | PF00069 | 0.305 |
MOD_PKB_1 | 659 | 667 | PF00069 | 0.259 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.421 |
MOD_Plk_1 | 778 | 784 | PF00069 | 0.309 |
MOD_Plk_2-3 | 1054 | 1060 | PF00069 | 0.435 |
MOD_Plk_2-3 | 854 | 860 | PF00069 | 0.445 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.445 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.489 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.341 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.355 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.395 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.351 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.434 |
MOD_Plk_4 | 876 | 882 | PF00069 | 0.333 |
MOD_Plk_4 | 946 | 952 | PF00069 | 0.301 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.445 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.652 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.301 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.316 |
MOD_ProDKin_1 | 829 | 835 | PF00069 | 0.301 |
MOD_SUMO_rev_2 | 304 | 309 | PF00179 | 0.237 |
MOD_SUMO_rev_2 | 524 | 531 | PF00179 | 0.316 |
MOD_SUMO_rev_2 | 566 | 572 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 720 | 725 | PF00179 | 0.301 |
TRG_DiLeu_BaEn_1 | 567 | 572 | PF01217 | 0.445 |
TRG_DiLeu_BaEn_1 | 811 | 816 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 1012 | 1015 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 1045 | 1048 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 933 | 936 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.236 |
TRG_ER_diArg_1 | 1100 | 1103 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 658 | 661 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 681 | 684 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 791 | 793 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 951 | 954 | PF00400 | 0.374 |
TRG_NES_CRM1_1 | 202 | 213 | PF08389 | 0.395 |
TRG_NES_CRM1_1 | 629 | 640 | PF08389 | 0.321 |
TRG_NLS_MonoExtN_4 | 1091 | 1097 | PF00514 | 0.618 |
TRG_NLS_MonoExtN_4 | 733 | 738 | PF00514 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 1024 | 1028 | PF00026 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 661 | 666 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 684 | 688 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 791 | 795 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 30% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 28% | 99% |
A0A0N1PFH3 | Leptomonas seymouri | 81% | 91% |
A0A0S4IM76 | Bodo saltans | 23% | 100% |
A0A0S4J1M1 | Bodo saltans | 29% | 100% |
A0A0S4J5A1 | Bodo saltans | 52% | 100% |
A0A0S4JA92 | Bodo saltans | 29% | 100% |
A0A0S4JRV4 | Bodo saltans | 30% | 100% |
A0A0S4JT33 | Bodo saltans | 22% | 100% |
A0A0S4KIG5 | Bodo saltans | 30% | 100% |
A0A0S4KNQ6 | Bodo saltans | 27% | 99% |
A0A1X0NNY6 | Trypanosomatidae | 30% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 26% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 29% | 97% |
A0A1X0P0Y8 | Trypanosomatidae | 25% | 100% |
A0A1X0P689 | Trypanosomatidae | 69% | 100% |
A0A1X0P724 | Trypanosomatidae | 25% | 100% |
A0A1X0P842 | Trypanosomatidae | 25% | 100% |
A0A381MFJ0 | Leishmania infantum | 25% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 62% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 26% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WPW0 | Leishmania donovani | 26% | 99% |
A0A3S7WUG2 | Leishmania donovani | 29% | 100% |
A0A3S7WV61 | Leishmania donovani | 25% | 100% |
A0A3S7WV68 | Leishmania donovani | 25% | 100% |
A0A3S7X978 | Leishmania donovani | 90% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 31% | 100% |
A0A451EJU6 | Leishmania donovani | 31% | 100% |
A2VDL6 | Bos taurus | 29% | 100% |
A4H3S2 | Leishmania braziliensis | 32% | 100% |
A4H514 | Leishmania braziliensis | 28% | 100% |
A4H903 | Leishmania braziliensis | 30% | 100% |
A4H9Q5 | Leishmania braziliensis | 27% | 100% |
A4HRZ6 | Leishmania infantum | 31% | 100% |
A4HT82 | Leishmania infantum | 26% | 100% |
A4HTF0 | Leishmania infantum | 26% | 100% |
A4HXD4 | Leishmania infantum | 29% | 100% |
A4HY23 | Leishmania infantum | 25% | 100% |
A4IBA6 | Leishmania infantum | 90% | 100% |
A7L9Z8 | Mus musculus | 28% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
D0A564 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D2WKD8 | Sus scrofa | 29% | 100% |
E9AF31 | Leishmania major | 89% | 100% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 99% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 97% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 90% |
G5EBH1 | Caenorhabditis elegans | 24% | 100% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 27% | 78% |
O14983 | Homo sapiens | 30% | 100% |
O22218 | Arabidopsis thaliana | 29% | 100% |
O23087 | Arabidopsis thaliana | 31% | 100% |
O34431 | Bacillus subtilis (strain 168) | 34% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
O46674 | Canis lupus familiaris | 30% | 100% |
O55143 | Mus musculus | 30% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O70228 | Mus musculus | 22% | 100% |
O75110 | Homo sapiens | 21% | 100% |
O75185 | Homo sapiens | 30% | 100% |
O77696 | Sus scrofa | 31% | 100% |
P04074 | Ovis aries | 30% | 100% |
P04191 | Oryctolagus cuniculus | 30% | 100% |
P05023 | Homo sapiens | 30% | 100% |
P05024 | Sus scrofa | 30% | 100% |
P05025 | Tetronarce californica | 29% | 100% |
P06685 | Rattus norvegicus | 29% | 100% |
P06686 | Rattus norvegicus | 29% | 100% |
P06687 | Rattus norvegicus | 30% | 100% |
P09572 | Gallus gallus | 30% | 100% |
P09626 | Rattus norvegicus | 28% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 27% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 27% | 100% |
P11507 | Rattus norvegicus | 30% | 100% |
P11607 | Sus scrofa | 30% | 100% |
P11718 | Leishmania donovani | 26% | 100% |
P13585 | Gallus gallus | 30% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P13607 | Drosophila melanogaster | 27% | 100% |
P13637 | Homo sapiens | 30% | 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) | 37% | 100% |
P22700 | Drosophila melanogaster | 31% | 100% |
P24797 | Gallus gallus | 29% | 100% |
P24798 | Gallus gallus | 29% | 100% |
P25489 | Catostomus commersonii | 28% | 100% |
P27112 | Oryctolagus cuniculus | 28% | 100% |
P28774 | Artemia franciscana | 29% | 100% |
P30714 | Rhinella marina | 29% | 100% |
P35315 | Trypanosoma brucei brucei | 31% | 100% |
P35316 | Artemia franciscana | 29% | 100% |
P35317 | Hydra vulgaris | 29% | 100% |
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) | 29% | 100% |
P50993 | Homo sapiens | 29% | 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% |
P54679 | Dictyostelium discoideum | 26% | 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 | 32% | 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) | 35% | 100% |
Q03669 | Gallus gallus | 29% | 100% |
Q08435 | Nicotiana plumbaginifolia | 26% | 100% |
Q08436 | Nicotiana plumbaginifolia | 25% | 100% |
Q08DA1 | Bos taurus | 30% | 100% |
Q0VCY0 | Bos taurus | 30% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q13733 | Homo sapiens | 29% | 100% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 30% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 28% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 28% | 100% |
Q37145 | Arabidopsis thaliana | 30% | 100% |
Q3TYU2 | Mus musculus | 23% | 91% |
Q42556 | Arabidopsis thaliana | 25% | 100% |
Q42883 | Solanum lycopersicum | 31% | 100% |
Q4QDN7 | Leishmania major | 25% | 100% |
Q4QDN8 | Leishmania major | 25% | 100% |
Q4QED4 | Leishmania major | 29% | 100% |
Q4QIM6 | Leishmania major | 28% | 100% |
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 | 28% | 100% |
Q5RDR3 | Pongo abelii | 29% | 100% |
Q64392 | Cavia porcellus | 29% | 100% |
Q64436 | Mus musculus | 29% | 100% |
Q64518 | Mus musculus | 32% | 100% |
Q64541 | Rattus norvegicus | 28% | 100% |
Q64542 | Rattus norvegicus | 27% | 92% |
Q64566 | Rattus norvegicus | 29% | 100% |
Q64578 | Rattus norvegicus | 30% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 28% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 30% | 100% |
Q6PIC6 | Mus musculus | 30% | 100% |
Q6PIE5 | Mus musculus | 29% | 100% |
Q6RWA9 | Taenia solium | 29% | 100% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 34% | 100% |
Q7PPA5 | Anopheles gambiae | 30% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 26% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 29% | 100% |
Q80XR2 | Mus musculus | 29% | 100% |
Q8R429 | Mus musculus | 30% | 100% |
Q8R4C1 | Rattus norvegicus | 29% | 100% |
Q8VDN2 | Mus musculus | 29% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 30% | 100% |
Q92030 | Anguilla anguilla | 28% | 100% |
Q92036 | Rhinella marina | 28% | 100% |
Q92105 | Pelophylax lessonae | 30% | 100% |
Q92123 | Xenopus laevis | 29% | 100% |
Q92126 | Xenopus laevis | 27% | 100% |
Q93084 | Homo sapiens | 31% | 100% |
Q95Z93 | Leishmania major | 31% | 100% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CTG6 | Mus musculus | 21% | 94% |
Q9H7F0 | Homo sapiens | 22% | 90% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 85% |
Q9LF79 | Arabidopsis thaliana | 30% | 100% |
Q9LIK7 | Arabidopsis thaliana | 27% | 100% |
Q9LU41 | Arabidopsis thaliana | 27% | 100% |
Q9LV11 | Arabidopsis thaliana | 25% | 100% |
Q9LY77 | Arabidopsis thaliana | 26% | 100% |
Q9M2L4 | Arabidopsis thaliana | 28% | 100% |
Q9N0Z6 | Oryctolagus cuniculus | 29% | 100% |
Q9R0K7 | Mus musculus | 30% | 92% |
Q9SGG3 | Arabidopsis thaliana | 21% | 90% |
Q9SJB3 | Arabidopsis thaliana | 23% | 100% |
Q9SY55 | Arabidopsis thaliana | 30% | 100% |
Q9SZR1 | Arabidopsis thaliana | 29% | 100% |
Q9TV52 | Oryctolagus cuniculus | 28% | 100% |
Q9WV27 | Mus musculus | 28% | 100% |
Q9XES1 | Arabidopsis thaliana | 32% | 100% |
Q9YGL9 | Gallus gallus | 31% | 100% |
Q9YH26 | Oreochromis mossambicus | 29% | 100% |
Q9Z1W8 | Mus musculus | 28% | 100% |
V5B873 | Trypanosoma cruzi | 24% | 100% |
V5BHZ2 | Trypanosoma cruzi | 67% | 100% |
V5BLM1 | Trypanosoma cruzi | 31% | 100% |