Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 19 |
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
Related structures:
AlphaFold database: E9ART6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 19 |
GO:0006811 | monoatomic ion transport | 4 | 19 |
GO:0006812 | monoatomic cation transport | 5 | 19 |
GO:0009987 | cellular process | 1 | 19 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 19 |
GO:0051179 | localization | 1 | 19 |
GO:0051234 | establishment of localization | 2 | 19 |
GO:0055085 | transmembrane transport | 2 | 19 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 19 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 19 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 19 |
GO:0120029 | proton export across plasma membrane | 4 | 19 |
GO:0140115 | export across plasma membrane | 3 | 19 |
GO:0140352 | export from cell | 2 | 19 |
GO:1902600 | proton transmembrane transport | 6 | 19 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006885 | regulation of pH | 8 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 2 |
GO:0030641 | regulation of cellular pH | 7 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051453 | regulation of intracellular pH | 8 | 2 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 20 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0005215 | transporter activity | 1 | 19 |
GO:0005488 | binding | 1 | 20 |
GO:0005524 | ATP binding | 5 | 20 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 19 |
GO:0008553 | P-type proton-exporting transporter activity | 4 | 19 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 19 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 19 |
GO:0015078 | proton transmembrane transporter activity | 5 | 19 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 19 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 19 |
GO:0015662 | P-type ion transporter activity | 4 | 19 |
GO:0016462 | pyrophosphatase activity | 5 | 20 |
GO:0016787 | hydrolase activity | 2 | 20 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 20 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 20 |
GO:0016887 | ATP hydrolysis activity | 7 | 20 |
GO:0017076 | purine nucleotide binding | 4 | 20 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 20 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 19 |
GO:0022804 | active transmembrane transporter activity | 3 | 19 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 19 |
GO:0022857 | transmembrane transporter activity | 2 | 19 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 19 |
GO:0030554 | adenyl nucleotide binding | 5 | 20 |
GO:0032553 | ribonucleotide binding | 3 | 20 |
GO:0032555 | purine ribonucleotide binding | 4 | 20 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 20 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
GO:0036094 | small molecule binding | 2 | 20 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 19 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043168 | anion binding | 3 | 20 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0097367 | carbohydrate derivative binding | 2 | 20 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 19 |
GO:0140657 | ATP-dependent activity | 1 | 19 |
GO:1901265 | nucleoside phosphate binding | 3 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 844 | 848 | PF00656 | 0.382 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.273 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 614 | 616 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.473 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.495 |
DEG_SCF_SKP2-CKS1_1 | 22 | 29 | PF00560 | 0.749 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.479 |
DOC_ANK_TNKS_1 | 224 | 231 | PF00023 | 0.486 |
DOC_CDC14_PxL_1 | 698 | 706 | PF14671 | 0.279 |
DOC_CYCLIN_RxL_1 | 533 | 542 | PF00134 | 0.529 |
DOC_CYCLIN_RxL_1 | 653 | 664 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 58 | PF00134 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.305 |
DOC_MAPK_DCC_7 | 733 | 741 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 512 | 521 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 614 | 622 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 730 | 740 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 445 | 454 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 515 | 523 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 567 | 575 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 614 | 622 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 733 | 741 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 787 | 796 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 863 | 871 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.514 |
DOC_PP1_RVXF_1 | 656 | 663 | PF00149 | 0.494 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.473 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.615 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 699 | 702 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 903 | 907 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 928 | 932 | PF00917 | 0.817 |
DOC_USP7_UBL2_3 | 147 | 151 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.512 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 926 | 930 | PF12436 | 0.789 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 960 | 965 | PF00397 | 0.766 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 478 | 483 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 658 | 663 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 666 | 672 | PF00244 | 0.314 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.504 |
LIG_APCC_ABBA_1 | 909 | 914 | PF00400 | 0.722 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.756 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.522 |
LIG_CtBP_PxDLS_1 | 561 | 565 | PF00389 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 113 | 122 | PF00928 | 0.252 |
LIG_EH1_1 | 297 | 305 | PF00400 | 0.333 |
LIG_EH1_1 | 448 | 456 | PF00400 | 0.516 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.597 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.523 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.449 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.495 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.467 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.619 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.490 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.681 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.308 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.363 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.508 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.495 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.519 |
LIG_FHA_2 | 857 | 863 | PF00498 | 0.439 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.323 |
LIG_IRF3_LxIS_1 | 792 | 797 | PF10401 | 0.205 |
LIG_LIR_Apic_2 | 498 | 502 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 159 | 170 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 584 | 593 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 693 | 704 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 719 | 727 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 773 | 783 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 790 | 801 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 661 | 665 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 719 | 725 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 773 | 778 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 790 | 796 | PF02991 | 0.171 |
LIG_LIR_Nem_3 | 799 | 804 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 895 | 900 | PF02991 | 0.573 |
LIG_NBox_RRM_1 | 292 | 302 | PF00076 | 0.364 |
LIG_NRBOX | 707 | 713 | PF00104 | 0.315 |
LIG_PALB2_WD40_1 | 770 | 778 | PF16756 | 0.357 |
LIG_PCNA_PIPBox_1 | 493 | 502 | PF02747 | 0.529 |
LIG_PCNA_yPIPBox_3 | 785 | 795 | PF02747 | 0.306 |
LIG_Pex14_1 | 868 | 872 | PF04695 | 0.344 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.306 |
LIG_Pex14_2 | 578 | 582 | PF04695 | 0.504 |
LIG_Pex14_2 | 678 | 682 | PF04695 | 0.314 |
LIG_Pex14_2 | 801 | 805 | PF04695 | 0.314 |
LIG_PTB_Apo_2 | 769 | 776 | PF02174 | 0.394 |
LIG_REV1ctd_RIR_1 | 238 | 247 | PF16727 | 0.486 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.580 |
LIG_SH2_GRB2like | 770 | 773 | PF00017 | 0.370 |
LIG_SH2_SRC | 722 | 725 | PF00017 | 0.564 |
LIG_SH2_SRC | 770 | 773 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.825 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 765 | 769 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 770 | 774 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 765 | 768 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 968 | 971 | PF00017 | 0.675 |
LIG_SH3_2 | 27 | 32 | PF14604 | 0.762 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.769 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.323 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.473 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.479 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.767 |
LIG_SH3_3 | 921 | 927 | PF00018 | 0.694 |
LIG_SH3_4 | 926 | 933 | PF00018 | 0.832 |
LIG_SUMO_SIM_anti_2 | 463 | 470 | PF11976 | 0.557 |
LIG_SUMO_SIM_anti_2 | 753 | 759 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 192 | 199 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 300 | 306 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 307 | 312 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 463 | 470 | PF11976 | 0.523 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.808 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.516 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.598 |
LIG_TRFH_1 | 682 | 686 | PF08558 | 0.418 |
LIG_TYR_ITIM | 720 | 725 | PF00017 | 0.371 |
LIG_UBA3_1 | 791 | 795 | PF00899 | 0.323 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.506 |
LIG_WRC_WIRS_1 | 496 | 501 | PF05994 | 0.314 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.314 |
LIG_WW_3 | 391 | 395 | PF00397 | 0.314 |
LIG_WW_3 | 501 | 505 | PF00397 | 0.305 |
MOD_CDK_SPK_2 | 682 | 687 | PF00069 | 0.482 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.701 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.406 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.622 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.329 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.333 |
MOD_CK1_1 | 806 | 812 | PF00069 | 0.367 |
MOD_CK1_1 | 901 | 907 | PF00069 | 0.578 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.787 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.775 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.323 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.394 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.363 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.357 |
MOD_CK2_1 | 856 | 862 | PF00069 | 0.558 |
MOD_CK2_1 | 954 | 960 | PF00069 | 0.571 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.350 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.425 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.357 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.314 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.434 |
MOD_GlcNHglycan | 902 | 906 | PF01048 | 0.616 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.578 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.598 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.314 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.305 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.310 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.619 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.333 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.373 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.627 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.325 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.314 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.321 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.335 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.314 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.314 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.320 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.333 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.637 |
MOD_N-GLC_1 | 936 | 941 | PF02516 | 0.657 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.472 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.315 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.381 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.288 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.484 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.305 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.375 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.319 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.314 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.343 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.309 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.657 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.480 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.171 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.314 |
MOD_PIKK_1 | 764 | 770 | PF00454 | 0.597 |
MOD_PIKK_1 | 954 | 960 | PF00454 | 0.592 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.646 |
MOD_PK_1 | 478 | 484 | PF00069 | 0.392 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.646 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.448 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.646 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.435 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.666 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.317 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.314 |
MOD_PKB_1 | 594 | 602 | PF00069 | 0.329 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.331 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.305 |
MOD_Plk_1 | 770 | 776 | PF00069 | 0.438 |
MOD_Plk_1 | 936 | 942 | PF00069 | 0.654 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.694 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.380 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.348 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.645 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.401 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.360 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.363 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.314 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.360 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.279 |
MOD_Plk_4 | 741 | 747 | PF00069 | 0.351 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.265 |
MOD_Plk_4 | 770 | 776 | PF00069 | 0.407 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.171 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.305 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.449 |
MOD_Plk_4 | 836 | 842 | PF00069 | 0.343 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.722 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.431 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.323 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.451 |
MOD_ProDKin_1 | 960 | 966 | PF00069 | 0.756 |
MOD_SUMO_rev_2 | 371 | 379 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 501 | 510 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 514 | 524 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 78 | 85 | PF00179 | 0.379 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_4 | 371 | 377 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 860 | 865 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 689 | 692 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 793 | 796 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 872 | 875 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 593 | 596 | PF00400 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 537 | 542 | PF00026 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y1 | Leptomonas seymouri | 26% | 96% |
A0A0N1PFH3 | Leptomonas seymouri | 26% | 80% |
A0A0S4INU6 | Bodo saltans | 23% | 80% |
A0A0S4IVK7 | Bodo saltans | 70% | 100% |
A0A0S4J1M1 | Bodo saltans | 26% | 89% |
A0A0S4J6U4 | Bodo saltans | 23% | 89% |
A0A0S4JA92 | Bodo saltans | 26% | 96% |
A0A0S4JRV4 | Bodo saltans | 27% | 96% |
A0A0S4JT33 | Bodo saltans | 40% | 100% |
A0A1X0NL00 | Trypanosomatidae | 69% | 100% |
A0A1X0NNY6 | Trypanosomatidae | 28% | 97% |
A0A1X0NPD9 | Trypanosomatidae | 25% | 88% |
A0A1X0P689 | Trypanosomatidae | 27% | 93% |
A0A1X0P720 | Trypanosomatidae | 84% | 100% |
A0A1X0P724 | Trypanosomatidae | 72% | 100% |
A0A1X0P7A1 | Trypanosomatidae | 82% | 100% |
A0A1X0P842 | Trypanosomatidae | 65% | 97% |
A0A381MFJ0 | Leishmania infantum | 96% | 100% |
A0A3R7KM63 | Trypanosoma rangeli | 25% | 94% |
A0A3R7MRX8 | Trypanosoma rangeli | 26% | 94% |
A0A3S5H5E7 | Leishmania donovani | 25% | 100% |
A0A3S5H5Y9 | Leishmania donovani | 24% | 88% |
A0A3S5IRL5 | Trypanosoma rangeli | 80% | 100% |
A0A3S7WPW0 | Leishmania donovani | 25% | 87% |
A0A3S7WV61 | Leishmania donovani | 96% | 100% |
A0A3S7WV68 | Leishmania donovani | 95% | 100% |
A0A3S7X978 | Leishmania donovani | 26% | 88% |
A0A422NP08 | Trypanosoma rangeli | 67% | 100% |
A0R3Y2 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 26% | 100% |
A2VDL6 | Bos taurus | 26% | 95% |
A4H514 | Leishmania braziliensis | 25% | 87% |
A4H9Q5 | Leishmania braziliensis | 91% | 100% |
A4HMM8 | Leishmania braziliensis | 24% | 88% |
A4HSA9 | Leishmania infantum | 28% | 100% |
A4HT82 | Leishmania infantum | 24% | 100% |
A4HTF0 | Leishmania infantum | 24% | 100% |
A4HY23 | Leishmania infantum | 95% | 100% |
A4IBA6 | Leishmania infantum | 26% | 88% |
A7L9Z8 | Mus musculus | 27% | 100% |
C9ZUN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 90% |
C9ZZN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
D0A564 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 79% | 100% |
D0ZTB2 | Salmonella typhimurium (strain 14028s / SGSC 2262) | 30% | 100% |
D2WKD8 | Sus scrofa | 26% | 95% |
E9AF31 | Leishmania major | 26% | 88% |
E9AL76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AL78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B686 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 80% |
O22218 | Arabidopsis thaliana | 25% | 95% |
O34431 | Bacillus subtilis (strain 168) | 26% | 100% |
O43108 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
O64806 | Arabidopsis thaliana | 26% | 96% |
O75185 | Homo sapiens | 26% | 100% |
O81108 | Arabidopsis thaliana | 26% | 96% |
O97198 | Leishmania major | 26% | 100% |
P04074 | Ovis aries | 27% | 95% |
P05023 | Homo sapiens | 26% | 95% |
P05024 | Sus scrofa | 26% | 95% |
P05025 | Tetronarce californica | 25% | 95% |
P05030 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P06685 | Rattus norvegicus | 27% | 95% |
P06686 | Rattus norvegicus | 26% | 95% |
P07038 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 34% | 100% |
P09572 | Gallus gallus | 26% | 95% |
P09626 | Rattus norvegicus | 26% | 94% |
P09627 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P0A505 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 25% | 100% |
P0ABB8 | Escherichia coli (strain K12) | 30% | 100% |
P0ABB9 | Escherichia coli O157:H7 | 30% | 100% |
P11718 | Leishmania donovani | 96% | 100% |
P12522 | Leishmania donovani | 95% | 100% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P13607 | Drosophila melanogaster | 25% | 94% |
P17326 | Artemia franciscana | 25% | 98% |
P18907 | Equus caballus | 26% | 95% |
P19156 | Sus scrofa | 26% | 94% |
P19456 | Arabidopsis thaliana | 37% | 100% |
P19657 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P20431 | Arabidopsis thaliana | 36% | 100% |
P20648 | Homo sapiens | 28% | 94% |
P20649 | Arabidopsis thaliana | 37% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 100% |
P22180 | Solanum lycopersicum | 36% | 100% |
P24545 | Zygosaccharomyces rouxii | 35% | 100% |
P24797 | Gallus gallus | 26% | 96% |
P24798 | Gallus gallus | 24% | 96% |
P25489 | Catostomus commersonii | 26% | 95% |
P27112 | Oryctolagus cuniculus | 26% | 94% |
P28774 | Artemia franciscana | 24% | 97% |
P28876 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 96% |
P28877 | Candida albicans | 33% | 100% |
P30714 | Rhinella marina | 26% | 95% |
P35317 | Hydra vulgaris | 26% | 94% |
P36640 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 30% | 100% |
P37278 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 30% | 100% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 28% | 100% |
P49380 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 35% | 100% |
P50993 | Homo sapiens | 26% | 95% |
P50996 | Canis lupus familiaris | 27% | 94% |
P50997 | Canis lupus familiaris | 27% | 95% |
P54210 | Dunaliella acidophila | 36% | 88% |
P54211 | Dunaliella bioculata | 37% | 86% |
P54678 | Dictyostelium discoideum | 26% | 87% |
P54679 | Dictyostelium discoideum | 34% | 92% |
P54707 | Homo sapiens | 25% | 94% |
P54708 | Rattus norvegicus | 26% | 94% |
P57709 | Bos taurus | 26% | 100% |
P58312 | Oreochromis mossambicus | 25% | 96% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 28% | 100% |
P78036 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 27% | 100% |
P83970 | Triticum aestivum | 35% | 100% |
P98194 | Homo sapiens | 26% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 28% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 28% | 100% |
P9WPT0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 25% | 100% |
P9WPT1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 25% | 100% |
Q03194 | Nicotiana plumbaginifolia | 36% | 100% |
Q07421 | Ajellomyces capsulatus | 34% | 100% |
Q08435 | Nicotiana plumbaginifolia | 37% | 100% |
Q08436 | Nicotiana plumbaginifolia | 36% | 100% |
Q08DA1 | Bos taurus | 27% | 95% |
Q13733 | Homo sapiens | 24% | 95% |
Q21286 | Caenorhabditis elegans | 23% | 81% |
Q2QMX9 | Oryza sativa subsp. japonica | 27% | 95% |
Q2QY12 | Oryza sativa subsp. japonica | 24% | 94% |
Q2RAS0 | Oryza sativa subsp. japonica | 25% | 96% |
Q37145 | Arabidopsis thaliana | 26% | 95% |
Q42556 | Arabidopsis thaliana | 36% | 100% |
Q43128 | Arabidopsis thaliana | 36% | 100% |
Q4QDN7 | Leishmania major | 95% | 100% |
Q4QDN8 | Leishmania major | 95% | 100% |
Q4QIM6 | Leishmania major | 23% | 100% |
Q4QIM8 | Leishmania major | 24% | 100% |
Q4VNC0 | Homo sapiens | 22% | 80% |
Q4VNC1 | Homo sapiens | 21% | 81% |
Q58623 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 37% | 100% |
Q5R5K5 | Pongo abelii | 26% | 100% |
Q5RCD8 | Pongo abelii | 26% | 95% |
Q5RDR3 | Pongo abelii | 26% | 95% |
Q5XF90 | Mus musculus | 22% | 82% |
Q5ZKB7 | Gallus gallus | 21% | 81% |
Q64392 | Cavia porcellus | 24% | 94% |
Q64436 | Mus musculus | 26% | 94% |
Q64541 | Rattus norvegicus | 24% | 95% |
Q65X71 | Oryza sativa subsp. japonica | 26% | 95% |
Q6ATV4 | Oryza sativa subsp. japonica | 26% | 94% |
Q6PIE5 | Mus musculus | 26% | 95% |
Q6RWA9 | Taenia solium | 24% | 96% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 30% | 100% |
Q7X8B5 | Oryza sativa subsp. japonica | 25% | 90% |
Q7XEK4 | Oryza sativa subsp. japonica | 24% | 94% |
Q7XPY2 | Oryza sativa subsp. japonica | 35% | 100% |
Q8RUN1 | Oryza sativa subsp. japonica | 24% | 93% |
Q8VDN2 | Mus musculus | 26% | 95% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 28% | 100% |
Q8YPE9 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 23% | 100% |
Q92030 | Anguilla anguilla | 26% | 95% |
Q92123 | Xenopus laevis | 26% | 95% |
Q92126 | Xenopus laevis | 26% | 94% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 27% | 100% |
Q9HDW7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 75% |
Q9LF79 | Arabidopsis thaliana | 24% | 91% |
Q9LU41 | Arabidopsis thaliana | 24% | 90% |
Q9LV11 | Arabidopsis thaliana | 37% | 100% |
Q9LY32 | Arabidopsis thaliana | 36% | 100% |
Q9LY77 | Arabidopsis thaliana | 25% | 94% |
Q9M2A0 | Arabidopsis thaliana | 35% | 100% |
Q9M2L4 | Arabidopsis thaliana | 26% | 95% |
Q9N0Z6 | Oryctolagus cuniculus | 26% | 95% |
Q9R0K7 | Mus musculus | 25% | 81% |
Q9SH76 | Arabidopsis thaliana | 35% | 100% |
Q9SJB3 | Arabidopsis thaliana | 36% | 100% |
Q9SU58 | Arabidopsis thaliana | 36% | 100% |
Q9SZR1 | Arabidopsis thaliana | 25% | 91% |
Q9TV52 | Oryctolagus cuniculus | 25% | 89% |
Q9WV27 | Mus musculus | 24% | 94% |
Q9YH26 | Oreochromis mossambicus | 25% | 95% |
Q9Z1W8 | Mus musculus | 26% | 94% |
V5BDL7 | Trypanosoma cruzi | 68% | 100% |
V5BHZ2 | Trypanosoma cruzi | 27% | 94% |