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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005886 | plasma membrane | 3 | 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: A4H903
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0005388 | P-type calcium transporter activity | 4 | 4 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 4 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 4 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 4 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 4 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 4 |
GO:0015662 | P-type ion transporter activity | 4 | 4 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 4 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 4 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 4 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 4 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 4 |
GO:0140657 | ATP-dependent activity | 1 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 8 | 14 | PF00089 | 0.274 |
CLV_NRD_NRD_1 | 1045 | 1047 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.159 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 919 | 921 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 1045 | 1047 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.159 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 919 | 921 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.256 |
CLV_PCSK_PC1ET2_1 | 599 | 601 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 770 | 772 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 1070 | 1074 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.245 |
DEG_APCC_DBOX_1 | 1088 | 1096 | PF00400 | 0.629 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.359 |
DEG_APCC_DBOX_1 | 619 | 627 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 919 | 927 | PF00400 | 0.359 |
DEG_APCC_KENBOX_2 | 355 | 359 | PF00400 | 0.518 |
DOC_ANK_TNKS_1 | 682 | 689 | PF00023 | 0.467 |
DOC_CKS1_1 | 517 | 522 | PF01111 | 0.445 |
DOC_CYCLIN_RxL_1 | 842 | 852 | PF00134 | 0.479 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 355 | 364 | PF00134 | 0.483 |
DOC_MAPK_DCC_7 | 751 | 761 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 1074 | 1083 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 1087 | 1094 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 560 | 569 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 620 | 628 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 694 | 700 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 919 | 925 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 1061 | 1073 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 1064 | 1073 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 1074 | 1083 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 1087 | 1094 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 171 | 178 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 679 | 686 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 694 | 702 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 876 | 885 | PF00069 | 0.213 |
DOC_MAPK_NFAT4_5 | 1087 | 1095 | PF00069 | 0.538 |
DOC_MAPK_RevD_3 | 904 | 920 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 843 | 850 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 111 | 114 | PF13499 | 0.333 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.584 |
DOC_PP2B_LxvP_1 | 635 | 638 | PF13499 | 0.364 |
DOC_PP2B_LxvP_1 | 684 | 687 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 906 | 909 | PF13499 | 0.496 |
DOC_SPAK_OSR1_1 | 11 | 15 | PF12202 | 0.443 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 352 | 356 | PF12436 | 0.429 |
DOC_USP7_UBL2_3 | 747 | 751 | PF12436 | 0.429 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 205 | 210 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 41 | 51 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 562 | 571 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 600 | 609 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 621 | 627 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 952 | 960 | PF00244 | 0.221 |
LIG_14-3-3_CterR_2 | 1109 | 1113 | PF00244 | 0.637 |
LIG_Actin_WH2_2 | 1029 | 1047 | PF00022 | 0.360 |
LIG_Actin_WH2_2 | 1056 | 1072 | PF00022 | 0.606 |
LIG_Actin_WH2_2 | 192 | 207 | PF00022 | 0.496 |
LIG_Actin_WH2_2 | 860 | 878 | PF00022 | 0.251 |
LIG_APCC_ABBA_1 | 718 | 723 | PF00400 | 0.399 |
LIG_BIR_III_4 | 495 | 499 | PF00653 | 0.445 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 656 | 660 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 970 | 974 | PF00533 | 0.436 |
LIG_CtBP_PxDLS_1 | 1021 | 1025 | PF00389 | 0.199 |
LIG_FHA_1 | 1000 | 1006 | PF00498 | 0.259 |
LIG_FHA_1 | 1078 | 1084 | PF00498 | 0.698 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.362 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.305 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.641 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.483 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.455 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.422 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.438 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.496 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.478 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.472 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.422 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.452 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.367 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.454 |
LIG_FHA_1 | 850 | 856 | PF00498 | 0.243 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.267 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.419 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.442 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.519 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.469 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.559 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.589 |
LIG_FHA_2 | 897 | 903 | PF00498 | 0.460 |
LIG_GBD_Chelix_1 | 43 | 51 | PF00786 | 0.276 |
LIG_GBD_Chelix_1 | 859 | 867 | PF00786 | 0.223 |
LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 823 | 833 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 844 | 853 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 929 | 939 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 959 | 970 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 984 | 994 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 740 | 745 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 823 | 829 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 844 | 849 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 929 | 934 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 959 | 965 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 984 | 989 | PF02991 | 0.411 |
LIG_MYND_3 | 658 | 662 | PF01753 | 0.359 |
LIG_NRBOX | 862 | 868 | PF00104 | 0.223 |
LIG_PCNA_PIPBox_1 | 932 | 941 | PF02747 | 0.287 |
LIG_PCNA_yPIPBox_3 | 834 | 847 | PF02747 | 0.467 |
LIG_Pex14_1 | 1027 | 1031 | PF04695 | 0.187 |
LIG_SH2_CRK | 931 | 935 | PF00017 | 0.288 |
LIG_SH2_PTP2 | 402 | 405 | PF00017 | 0.514 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 594 | 597 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 938 | 941 | PF00017 | 0.316 |
LIG_SH3_1 | 1052 | 1058 | PF00018 | 0.554 |
LIG_SH3_3 | 1052 | 1058 | PF00018 | 0.649 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.392 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.438 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.620 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.412 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.448 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.445 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.445 |
LIG_SH3_3 | 631 | 637 | PF00018 | 0.414 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.241 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.445 |
LIG_SUMO_SIM_anti_2 | 136 | 141 | PF11976 | 0.278 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 325 | 332 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 668 | 674 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 817 | 824 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 1020 | 1026 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 195 | 200 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 339 | 344 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 782 | 787 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 817 | 824 | PF11976 | 0.472 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.449 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.429 |
LIG_TRFH_1 | 524 | 528 | PF08558 | 0.496 |
LIG_UBA3_1 | 294 | 302 | PF00899 | 0.546 |
LIG_UBA3_1 | 304 | 312 | PF00899 | 0.464 |
LIG_UBA3_1 | 454 | 463 | PF00899 | 0.488 |
LIG_WRC_WIRS_1 | 1028 | 1033 | PF05994 | 0.192 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.454 |
LIG_WRC_WIRS_1 | 859 | 864 | PF05994 | 0.299 |
MOD_CDC14_SPxK_1 | 873 | 876 | PF00782 | 0.213 |
MOD_CDK_SPK_2 | 639 | 644 | PF00069 | 0.359 |
MOD_CDK_SPxK_1 | 870 | 876 | PF00069 | 0.213 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.637 |
MOD_CDK_SPxxK_3 | 763 | 770 | PF00069 | 0.413 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.501 |
MOD_CK1_1 | 1023 | 1029 | PF00069 | 0.357 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.640 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.502 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.456 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.526 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.475 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.703 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.568 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.359 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.454 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.530 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.454 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.457 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.456 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.361 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.498 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.359 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.446 |
MOD_Cter_Amidation | 597 | 600 | PF01082 | 0.265 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.265 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.330 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.284 |
MOD_GlcNHglycan | 212 | 216 | PF01048 | 0.235 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.260 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.231 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.311 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.260 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.510 |
MOD_GlcNHglycan | 437 | 441 | PF01048 | 0.360 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.273 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.177 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.271 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.237 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.246 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.261 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.352 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.413 |
MOD_GSK3_1 | 1023 | 1030 | PF00069 | 0.305 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.278 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.488 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.418 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.482 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.481 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.759 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.519 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.648 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.478 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.440 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.449 |
MOD_GSK3_1 | 784 | 791 | PF00069 | 0.446 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.488 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.306 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.311 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.296 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.173 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.272 |
MOD_N-GLC_1 | 824 | 829 | PF02516 | 0.305 |
MOD_N-GLC_1 | 841 | 846 | PF02516 | 0.195 |
MOD_N-GLC_1 | 987 | 992 | PF02516 | 0.159 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.388 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.287 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.242 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.567 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.437 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.438 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.438 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.594 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.496 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.474 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.465 |
MOD_NEK2_1 | 849 | 854 | PF00069 | 0.292 |
MOD_NEK2_1 | 979 | 984 | PF00069 | 0.445 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.273 |
MOD_NEK2_2 | 555 | 560 | PF00069 | 0.359 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.538 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.431 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.435 |
MOD_PIKK_1 | 737 | 743 | PF00454 | 0.359 |
MOD_PKA_1 | 406 | 412 | PF00069 | 0.619 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.633 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.496 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.577 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.476 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.359 |
MOD_PKA_2 | 951 | 957 | PF00069 | 0.295 |
MOD_PKB_1 | 560 | 568 | PF00069 | 0.464 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.507 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.502 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.421 |
MOD_Plk_1 | 824 | 830 | PF00069 | 0.484 |
MOD_Plk_1 | 979 | 985 | PF00069 | 0.445 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.454 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.445 |
MOD_Plk_2-3 | 898 | 904 | PF00069 | 0.520 |
MOD_Plk_4 | 1012 | 1018 | PF00069 | 0.258 |
MOD_Plk_4 | 1023 | 1029 | PF00069 | 0.294 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.283 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.454 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.469 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.455 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.608 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.469 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.440 |
MOD_Plk_4 | 825 | 831 | PF00069 | 0.503 |
MOD_Plk_4 | 858 | 864 | PF00069 | 0.376 |
MOD_Plk_4 | 926 | 932 | PF00069 | 0.269 |
MOD_Plk_4 | 956 | 962 | PF00069 | 0.268 |
MOD_Plk_4 | 981 | 987 | PF00069 | 0.386 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.613 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.640 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.458 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.778 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.399 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.460 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.579 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.413 |
MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.238 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.440 |
MOD_SUMO_for_1 | 1063 | 1066 | PF00179 | 0.484 |
MOD_SUMO_for_1 | 267 | 270 | PF00179 | 0.496 |
MOD_SUMO_for_1 | 729 | 732 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 1100 | 1108 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_1 | 956 | 961 | PF01217 | 0.245 |
TRG_DiLeu_BaEn_2 | 78 | 84 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_4 | 79 | 85 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 425 | 430 | PF01217 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 449 | 454 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 912 | 917 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 931 | 934 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 938 | 941 | PF00928 | 0.299 |
TRG_ER_diArg_1 | 1044 | 1046 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 607 | 610 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 919 | 921 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 322 | 337 | PF08389 | 0.413 |
TRG_NES_CRM1_1 | 955 | 969 | PF08389 | 0.215 |
TRG_NLS_MonoExtN_4 | 405 | 410 | PF00514 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 20 | 25 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.183 |
TRG_Pf-PMV_PEXEL_1 | 451 | 456 | PF00026 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.214 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 27% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 74% | 100% |
A0A0N1PFH3 | Leptomonas seymouri | 29% | 92% |
A0A0S4J1M1 | Bodo saltans | 29% | 100% |
A0A0S4J5A1 | Bodo saltans | 29% | 100% |
A0A0S4J6U4 | Bodo saltans | 42% | 100% |
A0A0S4JA92 | Bodo saltans | 52% | 100% |
A0A0S4JRV4 | Bodo saltans | 37% | 100% |
A0A0S4KIG5 | Bodo saltans | 28% | 100% |
A0A0S4KNQ6 | Bodo saltans | 37% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 28% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 39% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 58% | 98% |
A0A1X0P0Y8 | Trypanosomatidae | 38% | 100% |
A0A1X0P689 | Trypanosomatidae | 28% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 39% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 39% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WPW0 | Leishmania donovani | 38% | 99% |
A0A3S7WUG2 | Leishmania donovani | 87% | 98% |
A0A3S7X6H3 | Leishmania donovani | 35% | 93% |
A0A3S7X978 | Leishmania donovani | 29% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 29% | 100% |
A0A451EJU6 | Leishmania donovani | 28% | 100% |
A4H3S2 | Leishmania braziliensis | 27% | 94% |
A4H514 | Leishmania braziliensis | 39% | 100% |
A4HMM8 | Leishmania braziliensis | 30% | 100% |
A4HRZ6 | Leishmania infantum | 29% | 100% |
A4HT82 | Leishmania infantum | 39% | 100% |
A4HTF0 | Leishmania infantum | 41% | 100% |
A4HXD4 | Leishmania infantum | 87% | 98% |
A4I8W5 | Leishmania infantum | 35% | 93% |
A4IBA6 | Leishmania infantum | 29% | 100% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D3K0R6 | Bos taurus | 35% | 92% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 91% |
G5E829 | Mus musculus | 35% | 91% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 37% | 79% |
O14983 | Homo sapiens | 32% | 100% |
O22218 | Arabidopsis thaliana | 36% | 100% |
O23087 | Arabidopsis thaliana | 30% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 100% |
O43861 | Homo sapiens | 24% | 97% |
O46674 | Canis lupus familiaris | 31% | 100% |
O55143 | Mus musculus | 31% | 100% |
O64806 | Arabidopsis thaliana | 37% | 100% |
O74431 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 85% |
O77696 | Sus scrofa | 31% | 100% |
O81108 | Arabidopsis thaliana | 37% | 100% |
P04191 | Oryctolagus cuniculus | 31% | 100% |
P11505 | Rattus norvegicus | 35% | 91% |
P11506 | Rattus norvegicus | 40% | 90% |
P11507 | Rattus norvegicus | 31% | 100% |
P11607 | Sus scrofa | 31% | 100% |
P13585 | Gallus gallus | 31% | 100% |
P16615 | Homo sapiens | 31% | 100% |
P18596 | Rattus norvegicus | 30% | 100% |
P20020 | Homo sapiens | 35% | 91% |
P20647 | Oryctolagus cuniculus | 31% | 100% |
P22700 | Drosophila melanogaster | 29% | 100% |
P23220 | Sus scrofa | 35% | 91% |
P23634 | Homo sapiens | 36% | 90% |
P35315 | Trypanosoma brucei brucei | 27% | 100% |
P35316 | Artemia franciscana | 29% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 29% | 100% |
P54209 | Dunaliella bioculata | 29% | 100% |
P54678 | Dictyostelium discoideum | 39% | 100% |
P54708 | Rattus norvegicus | 28% | 100% |
P57709 | Bos taurus | 28% | 100% |
P58165 | Oreochromis mossambicus | 39% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70083 | Makaira nigricans | 30% | 100% |
P98194 | Homo sapiens | 28% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q00779 | Felis catus | 31% | 100% |
Q00804 | Oryctolagus cuniculus | 35% | 91% |
Q01814 | Homo sapiens | 40% | 90% |
Q03669 | Gallus gallus | 31% | 100% |
Q0VCY0 | Bos taurus | 31% | 100% |
Q12697 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 20% | 76% |
Q13733 | Homo sapiens | 28% | 100% |
Q16720 | Homo sapiens | 36% | 91% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 29% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 37% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 36% | 100% |
Q37145 | Arabidopsis thaliana | 37% | 100% |
Q3TYU2 | Mus musculus | 21% | 92% |
Q42883 | Solanum lycopersicum | 29% | 100% |
Q4QED4 | Leishmania major | 88% | 100% |
Q4QIM6 | Leishmania major | 39% | 100% |
Q4QIM8 | Leishmania major | 39% | 100% |
Q4VNC0 | Homo sapiens | 23% | 91% |
Q5R5K5 | Pongo abelii | 28% | 100% |
Q5XF89 | Mus musculus | 21% | 91% |
Q64392 | Cavia porcellus | 27% | 100% |
Q64518 | Mus musculus | 30% | 100% |
Q64541 | Rattus norvegicus | 28% | 100% |
Q64542 | Rattus norvegicus | 35% | 93% |
Q64566 | Rattus norvegicus | 28% | 100% |
Q64568 | Rattus norvegicus | 34% | 88% |
Q64578 | Rattus norvegicus | 32% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 35% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6DFW5 | Mus musculus | 23% | 95% |
Q6Q477 | Mus musculus | 35% | 92% |
Q7PPA5 | Anopheles gambiae | 29% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 35% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 36% | 100% |
Q80XR2 | Mus musculus | 28% | 100% |
Q8R429 | Mus musculus | 31% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 36% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 29% | 100% |
Q92105 | Pelophylax lessonae | 32% | 100% |
Q93084 | Homo sapiens | 30% | 100% |
Q95JN5 | Macaca fascicularis | 20% | 91% |
Q95Z93 | Leishmania major | 29% | 100% |
Q98SH2 | Gallus gallus | 35% | 92% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9CTG6 | Mus musculus | 23% | 95% |
Q9H7F0 | Homo sapiens | 20% | 91% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 86% |
Q9LF79 | Arabidopsis thaliana | 35% | 100% |
Q9LU41 | Arabidopsis thaliana | 36% | 100% |
Q9LY77 | Arabidopsis thaliana | 36% | 100% |
Q9M2L4 | Arabidopsis thaliana | 37% | 100% |
Q9NQ11 | Homo sapiens | 22% | 94% |
Q9R0K7 | Mus musculus | 37% | 93% |
Q9SY55 | Arabidopsis thaliana | 28% | 100% |
Q9SZR1 | Arabidopsis thaliana | 37% | 100% |
Q9TV52 | Oryctolagus cuniculus | 27% | 100% |
Q9WV27 | Mus musculus | 28% | 100% |
Q9YGL9 | Gallus gallus | 30% | 100% |
Q9Z1W8 | Mus musculus | 28% | 100% |
V5B873 | Trypanosoma cruzi | 40% | 100% |
V5BHZ2 | Trypanosoma cruzi | 30% | 100% |
V5BLM1 | Trypanosoma cruzi | 29% | 100% |
V5BNZ8 | Trypanosoma cruzi | 22% | 89% |