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)
ATPases, P-type ATPase
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. | yes | 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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HXD4
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_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 1066 | 1068 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 940 | 942 | PF00675 | 0.310 |
CLV_PCSK_KEX2_1 | 1066 | 1068 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 940 | 942 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 800 | 802 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 1114 | 1118 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.194 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 791 | 795 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.255 |
CLV_Separin_Metazoa | 706 | 710 | PF03568 | 0.493 |
DEG_APCC_DBOX_1 | 1109 | 1117 | PF00400 | 0.605 |
DEG_APCC_DBOX_1 | 640 | 648 | PF00400 | 0.466 |
DEG_APCC_KENBOX_2 | 376 | 380 | PF00400 | 0.499 |
DEG_SPOP_SBC_1 | 555 | 559 | PF00917 | 0.473 |
DOC_CDC14_PxL_1 | 1054 | 1062 | PF14671 | 0.240 |
DOC_CKS1_1 | 538 | 543 | PF01111 | 0.425 |
DOC_CYCLIN_RxL_1 | 861 | 873 | PF00134 | 0.456 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 376 | 385 | PF00134 | 0.461 |
DOC_MAPK_DCC_7 | 1073 | 1081 | PF00069 | 0.522 |
DOC_MAPK_DCC_7 | 772 | 782 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 1108 | 1115 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 581 | 590 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 641 | 649 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 715 | 721 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 800 | 807 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 940 | 946 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 1073 | 1081 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 1108 | 1115 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 700 | 707 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 715 | 723 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 897 | 906 | PF00069 | 0.194 |
DOC_MAPK_NFAT4_5 | 1108 | 1116 | PF00069 | 0.515 |
DOC_MAPK_RevD_3 | 925 | 941 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 742 | 748 | PF00149 | 0.423 |
DOC_PP1_RVXF_1 | 864 | 871 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 132 | 135 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 705 | 708 | PF13499 | 0.489 |
DOC_PP2B_LxvP_1 | 927 | 930 | PF13499 | 0.477 |
DOC_USP7_MATH_1 | 1044 | 1048 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.248 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 947 | 951 | PF00917 | 0.277 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.603 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.410 |
DOC_USP7_UBL2_3 | 768 | 772 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 784 | 789 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 891 | 896 | PF00397 | 0.277 |
DOC_WW_Pin1_4 | 917 | 922 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 583 | 592 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 621 | 630 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 642 | 648 | PF00244 | 0.528 |
LIG_14-3-3_CterR_2 | 1130 | 1134 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 1050 | 1068 | PF00022 | 0.341 |
LIG_Actin_WH2_2 | 1087 | 1105 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 213 | 228 | PF00022 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.613 |
LIG_BIR_III_4 | 516 | 520 | PF00653 | 0.425 |
LIG_BIR_III_4 | 616 | 620 | PF00653 | 0.500 |
LIG_BRCT_BRCA1_1 | 1002 | 1006 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 541 | 545 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 677 | 681 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 991 | 995 | PF00533 | 0.417 |
LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.245 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.344 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.285 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.625 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.464 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.435 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.408 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.419 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.477 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.462 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.423 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.497 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.433 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.347 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.466 |
LIG_FHA_1 | 871 | 877 | PF00498 | 0.224 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.265 |
LIG_FHA_1 | 965 | 971 | PF00498 | 0.331 |
LIG_FHA_2 | 1082 | 1088 | PF00498 | 0.660 |
LIG_FHA_2 | 1099 | 1105 | PF00498 | 0.541 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.400 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.447 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.500 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.501 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.454 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.547 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.629 |
LIG_FHA_2 | 918 | 924 | PF00498 | 0.441 |
LIG_GBD_Chelix_1 | 311 | 319 | PF00786 | 0.264 |
LIG_GBD_Chelix_1 | 64 | 72 | PF00786 | 0.257 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 486 | 495 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 844 | 854 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 950 | 960 | PF02991 | 0.224 |
LIG_LIR_Gen_1 | 980 | 991 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 844 | 850 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 950 | 955 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 980 | 986 | PF02991 | 0.313 |
LIG_PCNA_PIPBox_1 | 953 | 962 | PF02747 | 0.267 |
LIG_SH2_CRK | 952 | 956 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.497 |
LIG_SH2_SRC | 144 | 147 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 615 | 618 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 959 | 962 | PF00017 | 0.297 |
LIG_SH3_1 | 423 | 429 | PF00018 | 0.607 |
LIG_SH3_3 | 1038 | 1044 | PF00018 | 0.334 |
LIG_SH3_3 | 1074 | 1080 | PF00018 | 0.629 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.419 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.625 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.429 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.425 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.425 |
LIG_SH3_3 | 674 | 680 | PF00018 | 0.614 |
LIG_SH3_3 | 892 | 898 | PF00018 | 0.222 |
LIG_SH3_3 | 926 | 932 | PF00018 | 0.425 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 266 | 271 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 838 | 845 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 118 | 123 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 154 | 159 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 195 | 201 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 216 | 221 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 360 | 365 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 803 | 808 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 838 | 845 | PF11976 | 0.455 |
LIG_TRAF2_1 | 1084 | 1087 | PF00917 | 0.592 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.430 |
LIG_TRFH_1 | 545 | 549 | PF08558 | 0.477 |
LIG_UBA3_1 | 315 | 323 | PF00899 | 0.527 |
LIG_UBA3_1 | 475 | 484 | PF00899 | 0.469 |
LIG_WRC_WIRS_1 | 274 | 279 | PF05994 | 0.434 |
LIG_WRC_WIRS_1 | 880 | 885 | PF05994 | 0.280 |
LIG_WW_2 | 1077 | 1080 | PF00397 | 0.513 |
MOD_CDC14_SPxK_1 | 894 | 897 | PF00782 | 0.194 |
MOD_CDK_SPxK_1 | 891 | 897 | PF00069 | 0.194 |
MOD_CDK_SPxxK_3 | 180 | 187 | PF00069 | 0.621 |
MOD_CDK_SPxxK_3 | 784 | 791 | PF00069 | 0.449 |
MOD_CK1_1 | 1047 | 1053 | PF00069 | 0.411 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.623 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.483 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.639 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.437 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.507 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.454 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.427 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.775 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.492 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.506 |
MOD_CK2_1 | 1081 | 1087 | PF00069 | 0.530 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.434 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.437 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.437 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.494 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.600 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.478 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.490 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.427 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.246 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.311 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.387 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.265 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.216 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.240 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.212 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.337 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.292 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.495 |
MOD_GlcNHglycan | 458 | 462 | PF01048 | 0.353 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.235 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.366 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.410 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.313 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.281 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.326 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.252 |
MOD_GSK3_1 | 1015 | 1022 | PF00069 | 0.425 |
MOD_GSK3_1 | 1044 | 1051 | PF00069 | 0.286 |
MOD_GSK3_1 | 1098 | 1105 | PF00069 | 0.594 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.292 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.259 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.654 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.469 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.464 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.465 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.471 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.458 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.371 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.500 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.540 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.479 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.468 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.286 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.277 |
MOD_N-GLC_1 | 845 | 850 | PF02516 | 0.285 |
MOD_N-GLC_2 | 863 | 865 | PF02516 | 0.226 |
MOD_NEK2_1 | 1000 | 1005 | PF00069 | 0.425 |
MOD_NEK2_1 | 1015 | 1020 | PF00069 | 0.249 |
MOD_NEK2_1 | 1102 | 1107 | PF00069 | 0.496 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.253 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.368 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.268 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.222 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.548 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.418 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.419 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.419 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.667 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.585 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.477 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.430 |
MOD_NEK2_1 | 766 | 771 | PF00069 | 0.526 |
MOD_NEK2_1 | 870 | 875 | PF00069 | 0.273 |
MOD_NEK2_2 | 947 | 952 | PF00069 | 0.322 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.524 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.412 |
MOD_PIKK_1 | 683 | 689 | PF00454 | 0.503 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.469 |
MOD_PK_1 | 54 | 60 | PF00069 | 0.466 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.599 |
MOD_PKA_2 | 1102 | 1108 | PF00069 | 0.494 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.680 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.477 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.464 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.456 |
MOD_PKA_2 | 972 | 978 | PF00069 | 0.275 |
MOD_PKB_1 | 581 | 589 | PF00069 | 0.445 |
MOD_Plk_1 | 1000 | 1006 | PF00069 | 0.425 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.538 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.570 |
MOD_Plk_1 | 845 | 851 | PF00069 | 0.463 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.420 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.426 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.434 |
MOD_Plk_2-3 | 919 | 925 | PF00069 | 0.501 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.420 |
MOD_Plk_4 | 1019 | 1025 | PF00069 | 0.294 |
MOD_Plk_4 | 1033 | 1039 | PF00069 | 0.238 |
MOD_Plk_4 | 1044 | 1050 | PF00069 | 0.274 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.277 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.264 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.435 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.450 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.436 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.406 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.486 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.482 |
MOD_Plk_4 | 947 | 953 | PF00069 | 0.250 |
MOD_Plk_4 | 977 | 983 | PF00069 | 0.249 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.623 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.438 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.604 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.779 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.664 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.440 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.686 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.498 |
MOD_ProDKin_1 | 784 | 790 | PF00069 | 0.452 |
MOD_ProDKin_1 | 891 | 897 | PF00069 | 0.219 |
MOD_ProDKin_1 | 917 | 923 | PF00069 | 0.421 |
MOD_SUMO_for_1 | 288 | 291 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 1121 | 1129 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 430 | 439 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 491 | 498 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 77 | 84 | PF00179 | 0.392 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_1 | 977 | 982 | PF01217 | 0.225 |
TRG_DiLeu_BaEn_2 | 99 | 105 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_4 | 1085 | 1091 | PF01217 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 1055 | 1060 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.685 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 933 | 938 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 952 | 955 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 959 | 962 | PF00928 | 0.280 |
TRG_ER_diArg_1 | 1065 | 1067 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 940 | 942 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 343 | 358 | PF08389 | 0.394 |
TRG_NES_CRM1_1 | 976 | 990 | PF08389 | 0.196 |
TRG_Pf-PMV_PEXEL_1 | 472 | 477 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 998 | 1002 | PF00026 | 0.202 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 29% | 100% |
A0A0N1HWG6 | Leptomonas seymouri | 74% | 100% |
A0A0N1PFH3 | Leptomonas seymouri | 28% | 93% |
A0A0S4J1M1 | Bodo saltans | 30% | 100% |
A0A0S4J5A1 | Bodo saltans | 29% | 100% |
A0A0S4J6U4 | Bodo saltans | 43% | 100% |
A0A0S4JA92 | Bodo saltans | 53% | 100% |
A0A0S4JRV4 | Bodo saltans | 37% | 100% |
A0A0S4KIG5 | Bodo saltans | 28% | 100% |
A0A0S4KNQ6 | Bodo saltans | 38% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 30% | 100% |
A0A1X0NPD9 | Trypanosomatidae | 39% | 100% |
A0A1X0NTI6 | Trypanosomatidae | 59% | 100% |
A0A1X0P0Y8 | Trypanosomatidae | 38% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 40% | 100% |
A0A3R7MRX8 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 39% | 100% |
A0A3S5ISK9 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WPW0 | Leishmania donovani | 39% | 100% |
A0A3S7WUG2 | Leishmania donovani | 100% | 100% |
A0A422NTS7 | Trypanosoma rangeli | 29% | 100% |
A0A451EJU6 | Leishmania donovani | 29% | 100% |
A4H3S2 | Leishmania braziliensis | 30% | 100% |
A4H514 | Leishmania braziliensis | 39% | 100% |
A4H903 | Leishmania braziliensis | 87% | 100% |
A4HMM8 | Leishmania braziliensis | 29% | 100% |
A4HRZ6 | Leishmania infantum | 29% | 100% |
A4HT82 | Leishmania infantum | 38% | 97% |
A4HTF0 | Leishmania infantum | 40% | 96% |
C9ZPL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A4V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D3K0R6 | Bos taurus | 35% | 94% |
E9AJY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AR29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
G5E829 | Mus musculus | 39% | 93% |
J9VQQ3 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 36% | 80% |
O14983 | Homo sapiens | 30% | 100% |
O22218 | Arabidopsis thaliana | 36% | 100% |
O23087 | Arabidopsis thaliana | 30% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 100% |
O46674 | Canis lupus familiaris | 29% | 100% |
O55143 | Mus musculus | 29% | 100% |
O64806 | Arabidopsis thaliana | 38% | 100% |
O75185 | Homo sapiens | 28% | 100% |
O77696 | Sus scrofa | 31% | 100% |
O81108 | Arabidopsis thaliana | 37% | 100% |
P04191 | Oryctolagus cuniculus | 30% | 100% |
P11505 | Rattus norvegicus | 39% | 93% |
P11506 | Rattus norvegicus | 40% | 91% |
P11507 | Rattus norvegicus | 29% | 100% |
P11607 | Sus scrofa | 28% | 100% |
P13585 | Gallus gallus | 30% | 100% |
P13587 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P16615 | Homo sapiens | 30% | 100% |
P18596 | Rattus norvegicus | 30% | 100% |
P20020 | Homo sapiens | 39% | 93% |
P20647 | Oryctolagus cuniculus | 29% | 100% |
P22700 | Drosophila melanogaster | 29% | 100% |
P23220 | Sus scrofa | 39% | 93% |
P23634 | Homo sapiens | 35% | 91% |
P25489 | Catostomus commersonii | 28% | 100% |
P28774 | Artemia franciscana | 29% | 100% |
P35315 | Trypanosoma brucei brucei | 29% | 100% |
P35316 | Artemia franciscana | 29% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 29% | 100% |
P38929 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 97% |
P54209 | Dunaliella bioculata | 28% | 100% |
P54678 | Dictyostelium discoideum | 40% | 100% |
P54708 | Rattus norvegicus | 28% | 100% |
P57709 | Bos taurus | 28% | 100% |
P58165 | Oreochromis mossambicus | 38% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P70083 | Makaira nigricans | 30% | 100% |
P98194 | Homo sapiens | 27% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q00779 | Felis catus | 29% | 100% |
Q00804 | Oryctolagus cuniculus | 34% | 93% |
Q01814 | Homo sapiens | 40% | 91% |
Q01896 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q03669 | Gallus gallus | 30% | 100% |
Q0VCY0 | Bos taurus | 30% | 100% |
Q12691 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q12697 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 77% |
Q13733 | Homo sapiens | 27% | 100% |
Q16720 | Homo sapiens | 36% | 93% |
Q292Q0 | Drosophila pseudoobscura pseudoobscura | 29% | 100% |
Q2QMX9 | Oryza sativa subsp. japonica | 37% | 100% |
Q2QY12 | Oryza sativa subsp. japonica | 36% | 100% |
Q2RAS0 | Oryza sativa subsp. japonica | 37% | 100% |
Q37145 | Arabidopsis thaliana | 38% | 100% |
Q4Q490 | Leishmania major | 35% | 95% |
Q4QED4 | Leishmania major | 96% | 100% |
Q4QIM6 | Leishmania major | 39% | 100% |
Q4QIM8 | Leishmania major | 39% | 100% |
Q4VNC0 | Homo sapiens | 22% | 93% |
Q5R5K5 | Pongo abelii | 28% | 100% |
Q5XF89 | Mus musculus | 20% | 93% |
Q64392 | Cavia porcellus | 27% | 100% |
Q64518 | Mus musculus | 30% | 100% |
Q64541 | Rattus norvegicus | 27% | 100% |
Q64542 | Rattus norvegicus | 35% | 94% |
Q64566 | Rattus norvegicus | 27% | 100% |
Q64568 | Rattus norvegicus | 35% | 90% |
Q64578 | Rattus norvegicus | 30% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 36% | 100% |
Q6ATV4 | Oryza sativa subsp. japonica | 38% | 100% |
Q6Q477 | Mus musculus | 33% | 94% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 28% | 100% |
Q7PPA5 | Anopheles gambiae | 29% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 37% | 100% |
Q7XEK4 | Oryza sativa subsp. japonica | 36% | 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) | 28% | 100% |
Q92105 | Pelophylax lessonae | 30% | 100% |
Q93084 | Homo sapiens | 30% | 100% |
Q95Z93 | Leishmania major | 30% | 100% |
Q98SH2 | Gallus gallus | 36% | 94% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 88% |
Q9LF79 | Arabidopsis thaliana | 35% | 100% |
Q9LIK7 | Arabidopsis thaliana | 35% | 100% |
Q9LU41 | Arabidopsis thaliana | 36% | 100% |
Q9LY77 | Arabidopsis thaliana | 36% | 100% |
Q9M2L4 | Arabidopsis thaliana | 36% | 100% |
Q9NQ11 | Homo sapiens | 23% | 96% |
Q9R0K7 | Mus musculus | 37% | 95% |
Q9SY55 | Arabidopsis thaliana | 28% | 100% |
Q9SZR1 | Arabidopsis thaliana | 37% | 100% |
Q9TV52 | Oryctolagus cuniculus | 27% | 100% |
Q9WV27 | Mus musculus | 27% | 100% |
Q9YGL9 | Gallus gallus | 30% | 100% |
Q9Z1W8 | Mus musculus | 27% | 100% |
V5B873 | Trypanosoma cruzi | 40% | 100% |
V5BLM1 | Trypanosoma cruzi | 28% | 100% |