Homologous to other eukaryotic P-type Ca2+ ATPases.. For some reason, this group has heavily expanded in Kinetoplastida.. Localization: Endosomal (by homology) / ER (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 13 |
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 | 13 |
Related structures:
AlphaFold database: Q4QED4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005215 | transporter activity | 1 | 7 |
GO:0005388 | P-type calcium transporter activity | 4 | 7 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 7 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 7 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 7 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 7 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 7 |
GO:0015662 | P-type ion transporter activity | 4 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 7 |
GO:0022804 | active transmembrane transporter activity | 3 | 7 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 7 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 7 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.377 |
CLV_NRD_NRD_1 | 1023 | 1025 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 983 | 985 | PF00675 | 0.246 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 983 | 985 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 499 | 501 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.315 |
DEG_APCC_DBOX_1 | 1026 | 1034 | PF00400 | 0.671 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.494 |
DEG_APCC_KENBOX_2 | 293 | 297 | PF00400 | 0.521 |
DOC_ANK_TNKS_1 | 620 | 627 | PF00023 | 0.532 |
DOC_CDC14_PxL_1 | 971 | 979 | PF14671 | 0.260 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.446 |
DOC_CYCLIN_RxL_1 | 778 | 790 | PF00134 | 0.496 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 293 | 302 | PF00134 | 0.487 |
DOC_MAPK_DCC_7 | 689 | 699 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 1024 | 1032 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 498 | 507 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 558 | 566 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 632 | 638 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 857 | 863 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 1024 | 1032 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 617 | 624 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 632 | 640 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 814 | 823 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 98 | 107 | PF00069 | 0.498 |
DOC_MAPK_NFAT4_5 | 1025 | 1033 | PF00069 | 0.575 |
DOC_MAPK_RevD_3 | 842 | 858 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 781 | 788 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.351 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 844 | 847 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 864 | 868 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 961 | 965 | PF00917 | 0.287 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.433 |
DOC_USP7_UBL2_3 | 685 | 689 | PF12436 | 0.536 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 808 | 813 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 834 | 839 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 143 | 148 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 344 | 350 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 5 | 14 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 500 | 509 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 538 | 547 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 559 | 565 | PF00244 | 0.553 |
LIG_14-3-3_CterR_2 | 1047 | 1051 | PF00244 | 0.651 |
LIG_Actin_WH2_2 | 130 | 145 | PF00022 | 0.500 |
LIG_Actin_WH2_2 | 967 | 985 | PF00022 | 0.363 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.359 |
LIG_BIR_III_4 | 433 | 437 | PF00653 | 0.446 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.600 |
LIG_BRCT_BRCA1_1 | 908 | 912 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 919 | 923 | PF00533 | 0.488 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.513 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.467 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.450 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.569 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.521 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.506 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.431 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.457 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.365 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.372 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.494 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.340 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.246 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.288 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.362 |
LIG_FHA_1 | 937 | 943 | PF00498 | 0.267 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.656 |
LIG_FHA_2 | 1016 | 1022 | PF00498 | 0.558 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.474 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.535 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.449 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.444 |
LIG_FHA_2 | 715 | 721 | PF00498 | 0.619 |
LIG_FHA_2 | 835 | 841 | PF00498 | 0.464 |
LIG_FHA_2 | 999 | 1005 | PF00498 | 0.581 |
LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.287 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 761 | 771 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 867 | 877 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 897 | 908 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 761 | 767 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 867 | 872 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 897 | 903 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.598 |
LIG_PCNA_PIPBox_1 | 870 | 879 | PF02747 | 0.286 |
LIG_SH2_CRK | 869 | 873 | PF00017 | 0.305 |
LIG_SH2_PTP2 | 340 | 343 | PF00017 | 0.527 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 532 | 535 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 876 | 879 | PF00017 | 0.318 |
LIG_SH3_1 | 340 | 346 | PF00018 | 0.652 |
LIG_SH3_1 | 990 | 996 | PF00018 | 0.564 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.459 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.680 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.697 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.469 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.355 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.446 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.620 |
LIG_SH3_3 | 809 | 815 | PF00018 | 0.217 |
LIG_SH3_3 | 843 | 849 | PF00018 | 0.446 |
LIG_SH3_3 | 955 | 961 | PF00018 | 0.337 |
LIG_SH3_3 | 990 | 996 | PF00018 | 0.655 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.446 |
LIG_SUMO_SIM_anti_2 | 264 | 270 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 606 | 612 | PF11976 | 0.446 |
LIG_SUMO_SIM_anti_2 | 74 | 79 | PF11976 | 0.304 |
LIG_SUMO_SIM_anti_2 | 755 | 762 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 112 | 118 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 269 | 275 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 277 | 282 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 35 | 40 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 71 | 76 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 720 | 725 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 755 | 762 | PF11976 | 0.497 |
LIG_TRAF2_1 | 1001 | 1004 | PF00917 | 0.650 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.466 |
LIG_TRFH_1 | 462 | 466 | PF08558 | 0.500 |
LIG_UBA3_1 | 232 | 240 | PF00899 | 0.446 |
LIG_UBA3_1 | 392 | 401 | PF00899 | 0.492 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 797 | 802 | PF05994 | 0.302 |
MOD_CDC14_SPxK_1 | 811 | 814 | PF00782 | 0.217 |
MOD_CDK_SPxK_1 | 808 | 814 | PF00069 | 0.217 |
MOD_CDK_SPxxK_3 | 701 | 708 | PF00069 | 0.478 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.646 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.500 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.477 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.508 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.666 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.442 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.791 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.520 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.535 |
MOD_CK1_1 | 964 | 970 | PF00069 | 0.426 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.649 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.457 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.460 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.477 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.500 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.540 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.465 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.544 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.523 |
MOD_CK2_1 | 998 | 1004 | PF00069 | 0.578 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.334 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.236 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.244 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.270 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.220 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.302 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.528 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.268 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.277 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.406 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.438 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.358 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.339 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.289 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.365 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.358 |
MOD_GSK3_1 | 1015 | 1022 | PF00069 | 0.628 |
MOD_GSK3_1 | 1043 | 1050 | PF00069 | 0.706 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.495 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.504 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.509 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.288 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.573 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.457 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.476 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.395 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.602 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.526 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.510 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.304 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.491 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.332 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.430 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.307 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.300 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.269 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.307 |
MOD_N-GLC_1 | 762 | 767 | PF02516 | 0.301 |
MOD_N-GLC_2 | 780 | 782 | PF02516 | 0.249 |
MOD_NEK2_1 | 1019 | 1024 | PF00069 | 0.571 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.578 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.433 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.452 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.459 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.639 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.290 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.500 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.419 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.466 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.563 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.290 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.304 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.244 |
MOD_NEK2_1 | 917 | 922 | PF00069 | 0.548 |
MOD_NEK2_1 | 932 | 937 | PF00069 | 0.370 |
MOD_NEK2_2 | 864 | 869 | PF00069 | 0.349 |
MOD_PIKK_1 | 1045 | 1051 | PF00454 | 0.573 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.559 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.558 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.626 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.500 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.575 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.487 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.462 |
MOD_PKA_2 | 889 | 895 | PF00069 | 0.305 |
MOD_PKB_1 | 498 | 506 | PF00069 | 0.470 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.441 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.570 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.593 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.613 |
MOD_Plk_1 | 762 | 768 | PF00069 | 0.488 |
MOD_Plk_1 | 917 | 923 | PF00069 | 0.446 |
MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.457 |
MOD_Plk_2-3 | 17 | 23 | PF00069 | 0.437 |
MOD_Plk_2-3 | 836 | 842 | PF00069 | 0.538 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.459 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.470 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.469 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.434 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.427 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.288 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.532 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.307 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.489 |
MOD_Plk_4 | 864 | 870 | PF00069 | 0.293 |
MOD_Plk_4 | 894 | 900 | PF00069 | 0.271 |
MOD_Plk_4 | 936 | 942 | PF00069 | 0.257 |
MOD_Plk_4 | 950 | 956 | PF00069 | 0.230 |
MOD_Plk_4 | 961 | 967 | PF00069 | 0.293 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.457 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.672 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.459 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.737 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.536 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.480 |
MOD_ProDKin_1 | 808 | 814 | PF00069 | 0.259 |
MOD_ProDKin_1 | 834 | 840 | PF00069 | 0.444 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.649 |
MOD_SUMO_for_1 | 205 | 208 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 347 | 357 | PF00179 | 0.775 |
MOD_SUMO_rev_2 | 408 | 415 | PF00179 | 0.415 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_1 | 894 | 899 | PF01217 | 0.246 |
TRG_DiLeu_BaEn_2 | 16 | 22 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 1002 | 1008 | PF01217 | 0.630 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.670 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 850 | 855 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 972 | 977 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 869 | 872 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 876 | 879 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 857 | 859 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 982 | 984 | PF00400 | 0.509 |
TRG_NES_CRM1_1 | 260 | 275 | PF08389 | 0.417 |
TRG_NES_CRM1_1 | 893 | 907 | PF08389 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 30% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 75% | 94% |
A0A0N1PFH3 | Leptomonas seymouri | 29% | 87% |
A0A0S4J1M1 | Bodo saltans | 30% | 96% |
A0A0S4J6U4 | Bodo saltans | 44% | 97% |
A0A0S4JA92 | Bodo saltans | 54% | 100% |
A0A0S4JRV4 | Bodo saltans | 37% | 100% |
A0A0S4KIG5 | Bodo saltans | 29% | 100% |
A0A0S4KNQ6 | Bodo saltans | 38% | 94% |
A0A1X0NNY6 | Trypanosomatidae | 31% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 39% | 95% |
A0A1X0NPJ3 | Trypanosomatidae | 23% | 85% |
A0A1X0NTI6 | Trypanosomatidae | 61% | 93% |
A0A1X0P0Y8 | Trypanosomatidae | 38% | 96% |
A0A1X0P689 | Trypanosomatidae | 28% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 40% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 40% | 95% |
A0A3S5ISK9 | Trypanosoma rangeli | 37% | 99% |
A0A3S7WPW0 | Leishmania donovani | 40% | 94% |
A0A3S7WUG2 | Leishmania donovani | 96% | 93% |
A0A3S7X6H3 | Leishmania donovani | 35% | 88% |
A0A3S7X978 | Leishmania donovani | 28% | 95% |
A0A451EJU6 | Leishmania donovani | 30% | 100% |
A4H3S2 | Leishmania braziliensis | 30% | 100% |
A4H514 | Leishmania braziliensis | 40% | 93% |
A4H903 | Leishmania braziliensis | 88% | 94% |
A4HLF4 | Leishmania braziliensis | 35% | 88% |
A4HMM8 | Leishmania braziliensis | 29% | 95% |
A4HRZ6 | Leishmania infantum | 30% | 100% |
A4HT82 | Leishmania infantum | 39% | 100% |
A4HTF0 | Leishmania infantum | 41% | 100% |
A4HXD4 | Leishmania infantum | 96% | 93% |
A4I8W5 | Leishmania infantum | 35% | 88% |
A4IBA6 | Leishmania infantum | 28% | 95% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 98% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 96% |
D3K0R6 | Bos taurus | 35% | 87% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 95% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 94% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 93% |
E9B3T4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 88% |
G5E829 | Mus musculus | 39% | 86% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 37% | 74% |
O14983 | Homo sapiens | 31% | 100% |
O22218 | Arabidopsis thaliana | 37% | 100% |
O23087 | Arabidopsis thaliana | 30% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
O46674 | Canis lupus familiaris | 29% | 100% |
O55143 | Mus musculus | 29% | 100% |
O64806 | Arabidopsis thaliana | 38% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 80% |
O75185 | Homo sapiens | 28% | 100% |
O77696 | Sus scrofa | 30% | 100% |
O81108 | Arabidopsis thaliana | 38% | 100% |
P04191 | Oryctolagus cuniculus | 30% | 100% |
P11505 | Rattus norvegicus | 39% | 86% |
P11506 | Rattus norvegicus | 40% | 85% |
P11507 | Rattus norvegicus | 29% | 100% |
P11607 | Sus scrofa | 29% | 100% |
P13585 | Gallus gallus | 31% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 96% |
P16615 | Homo sapiens | 29% | 100% |
P18596 | Rattus norvegicus | 30% | 100% |
P20647 | Oryctolagus cuniculus | 29% | 100% |
P22189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
P22700 | Drosophila melanogaster | 29% | 100% |
P23634 | Homo sapiens | 35% | 85% |
P25489 | Catostomus commersonii | 28% | 100% |
P28774 | Artemia franciscana | 27% | 100% |
P35316 | Artemia franciscana | 29% | 100% |
P35317 | Hydra vulgaris | 28% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 29% | 100% |
P38929 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 90% |
P54209 | Dunaliella bioculata | 30% | 100% |
P54678 | Dictyostelium discoideum | 40% | 94% |
P54707 | Homo sapiens | 28% | 100% |
P54708 | Rattus norvegicus | 28% | 100% |
P57709 | Bos taurus | 27% | 100% |
P58165 | Oreochromis mossambicus | 38% | 95% |
P70083 | Makaira nigricans | 30% | 100% |
P98194 | Homo sapiens | 27% | 100% |
Q00779 | Felis catus | 29% | 100% |
Q00804 | Oryctolagus cuniculus | 34% | 86% |
Q01814 | Homo sapiens | 40% | 85% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 96% |
Q03669 | Gallus gallus | 28% | 100% |
Q0VCY0 | Bos taurus | 30% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 96% |
Q12697 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 20% | 71% |
Q13733 | Homo sapiens | 28% | 100% |
Q16720 | Homo sapiens | 37% | 86% |
Q21286 | Caenorhabditis elegans | 20% | 87% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 29% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 38% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 37% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 37% | 100% |
Q37145 | Arabidopsis thaliana | 38% | 100% |
Q3TYU2 | Mus musculus | 21% | 86% |
Q4Q490 | Leishmania major | 36% | 88% |
Q4QIM6 | Leishmania major | 40% | 100% |
Q4QIM8 | Leishmania major | 40% | 100% |
Q4VNC0 | Homo sapiens | 22% | 86% |
Q5R5K5 | Pongo abelii | 27% | 100% |
Q5XF89 | Mus musculus | 20% | 86% |
Q64392 | Cavia porcellus | 27% | 100% |
Q64518 | Mus musculus | 30% | 100% |
Q64541 | Rattus norvegicus | 27% | 100% |
Q64542 | Rattus norvegicus | 36% | 87% |
Q64566 | Rattus norvegicus | 27% | 100% |
Q64568 | Rattus norvegicus | 37% | 84% |
Q64578 | Rattus norvegicus | 30% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 37% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6DFW5 | Mus musculus | 23% | 89% |
Q6Q477 | Mus musculus | 34% | 87% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 29% | 100% |
Q7PPA5 | Anopheles gambiae | 29% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 36% | 97% |
Q7XEK4 | Oryza sativa subsp. japonica | 37% | 100% |
Q80XR2 | Mus musculus | 27% | 100% |
Q8R429 | Mus musculus | 30% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 35% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 29% | 100% |
Q92105 | Pelophylax lessonae | 30% | 100% |
Q93084 | Homo sapiens | 29% | 100% |
Q95Z93 | Leishmania major | 31% | 100% |
Q98SH2 | Gallus gallus | 37% | 87% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 27% | 100% |
Q9CTG6 | Mus musculus | 22% | 90% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 81% |
Q9LF79 | Arabidopsis thaliana | 35% | 98% |
Q9LU41 | Arabidopsis thaliana | 36% | 97% |
Q9M2L4 | Arabidopsis thaliana | 37% | 100% |
Q9R0K7 | Mus musculus | 38% | 88% |
Q9SY55 | Arabidopsis thaliana | 29% | 100% |
Q9SZR1 | Arabidopsis thaliana | 37% | 98% |
Q9TV52 | Oryctolagus cuniculus | 27% | 96% |
Q9WV27 | Mus musculus | 27% | 100% |
Q9YGL9 | Gallus gallus | 29% | 100% |
Q9Z1W8 | Mus musculus | 28% | 100% |
V5B873 | Trypanosoma cruzi | 40% | 95% |
V5BLM1 | Trypanosoma cruzi | 29% | 100% |
V5BPC6 | Trypanosoma cruzi | 39% | 99% |