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: 0 |
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 |
Related structures:
AlphaFold database: E9B447
Term | Name | Level | Count |
---|---|---|---|
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055070 | copper ion homeostasis | 9 | 1 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005507 | copper ion binding | 6 | 5 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 11 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 11 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 11 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 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:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 11 |
GO:0022804 | active transmembrane transporter activity | 3 | 11 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 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:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005375 | copper ion transmembrane transporter activity | 7 | 1 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
GO:0043682 | P-type divalent copper transporter activity | 4 | 1 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 1 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1049 | 1053 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 1151 | 1155 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 482 | 486 | PF00656 | 0.404 |
CLV_NRD_NRD_1 | 1177 | 1179 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 957 | 959 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.413 |
CLV_PCSK_FUR_1 | 241 | 245 | PF00082 | 0.520 |
CLV_PCSK_FUR_1 | 649 | 653 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 1055 | 1057 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 1177 | 1179 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 872 | 874 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 957 | 959 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 1055 | 1057 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 651 | 653 | PF00082 | 0.345 |
CLV_PCSK_PC7_1 | 95 | 101 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 1119 | 1123 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.496 |
CLV_Separin_Metazoa | 891 | 895 | PF03568 | 0.521 |
DEG_APCC_DBOX_1 | 1158 | 1166 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 415 | 423 | PF00400 | 0.627 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.379 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.349 |
DEG_SCF_FBW7_1 | 502 | 508 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 1225 | 1229 | PF00917 | 0.405 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.552 |
DEG_SPOP_SBC_1 | 906 | 910 | PF00917 | 0.494 |
DOC_ANK_TNKS_1 | 698 | 705 | PF00023 | 0.454 |
DOC_CKS1_1 | 502 | 507 | PF01111 | 0.519 |
DOC_CKS1_1 | 842 | 847 | PF01111 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 1200 | 1206 | PF00134 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 369 | 375 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 535 | 541 | PF00134 | 0.326 |
DOC_CYCLIN_yCln2_LP_2 | 57 | 63 | PF00134 | 0.529 |
DOC_MAPK_FxFP_2 | 619 | 622 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 305 | 312 | PF00069 | 0.744 |
DOC_MAPK_gen_1 | 872 | 879 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 99 | 105 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 995 | 1004 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 1067 | 1074 | PF00069 | 0.485 |
DOC_MAPK_RevD_3 | 1163 | 1178 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 1117 | 1123 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 1192 | 1195 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 994 | 997 | PF13499 | 0.349 |
DOC_PP4_FxxP_1 | 619 | 622 | PF00568 | 0.414 |
DOC_USP7_MATH_1 | 1195 | 1199 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 912 | 916 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 930 | 934 | PF00917 | 0.373 |
DOC_WW_Pin1_4 | 1015 | 1020 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 1050 | 1055 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 1127 | 1132 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 841 | 846 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 902 | 907 | PF00397 | 0.468 |
LIG_14-3-3_CanoR_1 | 1013 | 1018 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 625 | 630 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 649 | 659 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 680 | 686 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 780 | 786 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.600 |
LIG_APCC_ABBA_1 | 545 | 550 | PF00400 | 0.451 |
LIG_BIR_III_2 | 807 | 811 | PF00653 | 0.534 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.728 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.534 |
LIG_CaM_IQ_9 | 1165 | 1180 | PF13499 | 0.530 |
LIG_Clathr_ClatBox_1 | 121 | 125 | PF01394 | 0.427 |
LIG_CtBP_PxDLS_1 | 720 | 725 | PF00389 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 817 | 827 | PF00928 | 0.520 |
LIG_EH1_1 | 592 | 600 | PF00400 | 0.513 |
LIG_eIF4E_1 | 593 | 599 | PF01652 | 0.566 |
LIG_FHA_1 | 1016 | 1022 | PF00498 | 0.493 |
LIG_FHA_1 | 1032 | 1038 | PF00498 | 0.454 |
LIG_FHA_1 | 1225 | 1231 | PF00498 | 0.408 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.682 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.725 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.705 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.555 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.708 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.506 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.528 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.323 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.461 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.347 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.480 |
LIG_FHA_1 | 735 | 741 | PF00498 | 0.474 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.534 |
LIG_FHA_1 | 880 | 886 | PF00498 | 0.479 |
LIG_FHA_1 | 893 | 899 | PF00498 | 0.454 |
LIG_FHA_1 | 916 | 922 | PF00498 | 0.349 |
LIG_FHA_1 | 950 | 956 | PF00498 | 0.552 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.535 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.540 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.658 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.721 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.621 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.326 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.505 |
LIG_FHA_2 | 864 | 870 | PF00498 | 0.570 |
LIG_Integrin_isoDGR_2 | 887 | 889 | PF01839 | 0.324 |
LIG_LIR_Apic_2 | 617 | 622 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 358 | 369 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 606 | 616 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 637 | 646 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 817 | 828 | PF02991 | 0.491 |
LIG_LIR_LC3C_4 | 434 | 439 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 637 | 642 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 784 | 788 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 817 | 823 | PF02991 | 0.524 |
LIG_LYPXL_S_1 | 1201 | 1205 | PF13949 | 0.435 |
LIG_LYPXL_SIV_4 | 608 | 616 | PF13949 | 0.374 |
LIG_MAD2 | 693 | 701 | PF02301 | 0.454 |
LIG_MYND_1 | 188 | 192 | PF01753 | 0.761 |
LIG_NRBOX | 1161 | 1167 | PF00104 | 0.502 |
LIG_Pex14_1 | 1185 | 1189 | PF04695 | 0.326 |
LIG_Pex14_2 | 1183 | 1187 | PF04695 | 0.326 |
LIG_Pex14_2 | 238 | 242 | PF04695 | 0.745 |
LIG_Pex14_2 | 576 | 580 | PF04695 | 0.293 |
LIG_Pex14_2 | 581 | 585 | PF04695 | 0.490 |
LIG_Pex14_2 | 788 | 792 | PF04695 | 0.534 |
LIG_Pex14_2 | 823 | 827 | PF04695 | 0.455 |
LIG_REV1ctd_RIR_1 | 1202 | 1209 | PF16727 | 0.541 |
LIG_SH2_CRK | 1189 | 1193 | PF00017 | 0.350 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.380 |
LIG_SH2_SRC | 1098 | 1101 | PF00017 | 0.502 |
LIG_SH2_SRC | 607 | 610 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 1098 | 1102 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.419 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 1064 | 1067 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.198 |
LIG_SH2_STAT5 | 923 | 926 | PF00017 | 0.404 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.783 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.606 |
LIG_SH3_3 | 900 | 906 | PF00018 | 0.349 |
LIG_SH3_4 | 771 | 778 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 1160 | 1167 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 1221 | 1229 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 660 | 668 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 977 | 982 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 1046 | 1053 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 1071 | 1076 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 1190 | 1196 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 261 | 269 | PF11976 | 0.706 |
LIG_SUMO_SIM_par_1 | 596 | 603 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 657 | 663 | PF11976 | 0.607 |
LIG_TRAF2_1 | 867 | 870 | PF00917 | 0.576 |
LIG_UBA3_1 | 1165 | 1173 | PF00899 | 0.522 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.551 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.530 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.350 |
LIG_WW_3 | 995 | 999 | PF00397 | 0.557 |
MOD_CDC14_SPxK_1 | 1053 | 1056 | PF00782 | 0.418 |
MOD_CDC14_SPxK_1 | 303 | 306 | PF00782 | 0.615 |
MOD_CDK_SPK_2 | 1050 | 1055 | PF00069 | 0.418 |
MOD_CDK_SPK_2 | 300 | 305 | PF00069 | 0.615 |
MOD_CDK_SPxK_1 | 1050 | 1056 | PF00069 | 0.418 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.615 |
MOD_CK1_1 | 1172 | 1178 | PF00069 | 0.507 |
MOD_CK1_1 | 1221 | 1227 | PF00069 | 0.315 |
MOD_CK1_1 | 1228 | 1234 | PF00069 | 0.300 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.703 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.636 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.576 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.542 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.473 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.527 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.678 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.378 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.478 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.702 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.349 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.534 |
MOD_CK1_1 | 864 | 870 | PF00069 | 0.509 |
MOD_CK1_1 | 901 | 907 | PF00069 | 0.544 |
MOD_CK1_1 | 915 | 921 | PF00069 | 0.458 |
MOD_CK1_1 | 965 | 971 | PF00069 | 0.534 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.543 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.641 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.612 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.521 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.506 |
MOD_CK2_1 | 863 | 869 | PF00069 | 0.553 |
MOD_CMANNOS | 585 | 588 | PF00535 | 0.426 |
MOD_GlcNHglycan | 1197 | 1200 | PF01048 | 0.350 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.348 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.502 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.394 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.304 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.464 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.363 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.419 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.370 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.393 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.258 |
MOD_GlcNHglycan | 863 | 866 | PF01048 | 0.318 |
MOD_GlcNHglycan | 940 | 943 | PF01048 | 0.327 |
MOD_GlcNHglycan | 949 | 952 | PF01048 | 0.320 |
MOD_GSK3_1 | 1046 | 1053 | PF00069 | 0.562 |
MOD_GSK3_1 | 1221 | 1228 | PF00069 | 0.324 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.691 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.741 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.731 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.725 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.541 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.524 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.606 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.526 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.519 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.469 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.559 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.614 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.660 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.338 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.584 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.362 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.342 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.288 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.544 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.439 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.702 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.452 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.468 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.451 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.623 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.475 |
MOD_LATS_1 | 623 | 629 | PF00433 | 0.302 |
MOD_N-GLC_1 | 1127 | 1132 | PF02516 | 0.284 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.357 |
MOD_N-GLC_1 | 738 | 743 | PF02516 | 0.254 |
MOD_NEK2_1 | 1218 | 1223 | PF00069 | 0.326 |
MOD_NEK2_1 | 1226 | 1231 | PF00069 | 0.326 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.537 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.700 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.681 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.534 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.506 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.541 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.488 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.523 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.553 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.307 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.359 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.380 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.486 |
MOD_NEK2_1 | 790 | 795 | PF00069 | 0.471 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.772 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.449 |
MOD_NEK2_1 | 849 | 854 | PF00069 | 0.450 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.511 |
MOD_NEK2_1 | 879 | 884 | PF00069 | 0.454 |
MOD_NEK2_2 | 373 | 378 | PF00069 | 0.554 |
MOD_NEK2_2 | 614 | 619 | PF00069 | 0.381 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.701 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.527 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.539 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.502 |
MOD_PIKK_1 | 907 | 913 | PF00454 | 0.349 |
MOD_PKA_1 | 651 | 657 | PF00069 | 0.484 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.502 |
MOD_PKA_2 | 1158 | 1164 | PF00069 | 0.518 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.771 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.768 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.484 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.534 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.502 |
MOD_PKB_1 | 1011 | 1019 | PF00069 | 0.349 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.740 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.724 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.557 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.692 |
MOD_Plk_1 | 752 | 758 | PF00069 | 0.492 |
MOD_Plk_1 | 816 | 822 | PF00069 | 0.508 |
MOD_Plk_1 | 974 | 980 | PF00069 | 0.526 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.730 |
MOD_Plk_2-3 | 59 | 65 | PF00069 | 0.521 |
MOD_Plk_2-3 | 708 | 714 | PF00069 | 0.468 |
MOD_Plk_2-3 | 949 | 955 | PF00069 | 0.502 |
MOD_Plk_4 | 1032 | 1038 | PF00069 | 0.496 |
MOD_Plk_4 | 1158 | 1164 | PF00069 | 0.519 |
MOD_Plk_4 | 1221 | 1227 | PF00069 | 0.380 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.526 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.728 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.528 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.340 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.354 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.446 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.307 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.182 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.305 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.505 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.480 |
MOD_Plk_4 | 752 | 758 | PF00069 | 0.448 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.524 |
MOD_Plk_4 | 828 | 834 | PF00069 | 0.486 |
MOD_Plk_4 | 898 | 904 | PF00069 | 0.485 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.543 |
MOD_Plk_4 | 962 | 968 | PF00069 | 0.555 |
MOD_ProDKin_1 | 1015 | 1021 | PF00069 | 0.496 |
MOD_ProDKin_1 | 1050 | 1056 | PF00069 | 0.418 |
MOD_ProDKin_1 | 1127 | 1133 | PF00069 | 0.484 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.782 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.645 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.537 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.612 |
MOD_ProDKin_1 | 841 | 847 | PF00069 | 0.468 |
MOD_ProDKin_1 | 902 | 908 | PF00069 | 0.468 |
MOD_SUMO_for_1 | 1054 | 1057 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 151 | 159 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 339 | 348 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 404 | 408 | PF00179 | 0.622 |
TRG_DiLeu_BaEn_1 | 1020 | 1025 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_1 | 267 | 272 | PF01217 | 0.756 |
TRG_DiLeu_BaEn_1 | 660 | 665 | PF01217 | 0.588 |
TRG_DiLeu_BaEn_4 | 267 | 273 | PF01217 | 0.745 |
TRG_DiLeu_BaLyEn_6 | 552 | 557 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 998 | 1003 | PF01217 | 0.421 |
TRG_DiLeu_LyEn_5 | 267 | 272 | PF01217 | 0.747 |
TRG_ENDOCYTIC_2 | 1180 | 1183 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 1189 | 1192 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 1202 | 1205 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 1176 | 1178 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 871 | 873 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 957 | 960 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 133 | 147 | PF08389 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 1111 | 1115 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 520 | 524 | PF00026 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 693 | 698 | PF00026 | 0.254 |
TRG_Pf-PMV_PEXEL_1 | 943 | 947 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFW0 | Leptomonas seymouri | 59% | 100% |
A0A0S4J742 | Bodo saltans | 40% | 100% |
A0A1X0P531 | Trypanosomatidae | 49% | 100% |
A0A3Q8IGY9 | Leishmania donovani | 91% | 100% |
A0A422NN19 | Trypanosoma rangeli | 50% | 100% |
A3AWA4 | Oryza sativa subsp. japonica | 34% | 100% |
A4HLS1 | Leishmania braziliensis | 80% | 100% |
A4I980 | Leishmania infantum | 91% | 100% |
B9DFX7 | Arabidopsis thaliana | 28% | 100% |
D0A5R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
O59666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P35670 | Homo sapiens | 30% | 85% |
P38995 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P49015 | Cricetulus griseus | 32% | 84% |
P70705 | Rattus norvegicus | 31% | 84% |
Q04656 | Homo sapiens | 33% | 83% |
Q4Q3X8 | Leishmania major | 90% | 100% |
Q59385 | Escherichia coli (strain K12) | 33% | 100% |
Q64430 | Mus musculus | 33% | 84% |
Q64446 | Mus musculus | 33% | 85% |
Q64535 | Rattus norvegicus | 33% | 86% |
Q6H7M3 | Oryza sativa subsp. japonica | 35% | 100% |
Q8XD24 | Escherichia coli O157:H7 | 33% | 100% |
Q8Z8S4 | Salmonella typhi | 34% | 100% |
Q8ZR95 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 33% | 100% |
Q9KPZ7 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 100% |
Q9S7J8 | Arabidopsis thaliana | 35% | 100% |
Q9SH30 | Arabidopsis thaliana | 33% | 100% |
Q9XT50 | Ovis aries | 34% | 83% |