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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030117 | membrane coat | 3 | 12 |
GO:0030120 | vesicle coat | 4 | 12 |
GO:0030127 | COPII vesicle coat | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 6 |
GO:0016020 | membrane | 2 | 6 |
GO:0031090 | organelle membrane | 3 | 6 |
GO:0070971 | endoplasmic reticulum exit site | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4H614
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 11 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0035459 | vesicle cargo loading | 4 | 1 |
GO:0090110 | COPII-coated vesicle cargo loading | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0005096 | GTPase activator activity | 4 | 1 |
GO:0008047 | enzyme activator activity | 3 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030695 | GTPase regulator activity | 4 | 1 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:0140677 | molecular function activator activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 870 | 874 | PF00656 | 0.337 |
CLV_C14_Caspase3-7 | 967 | 971 | PF00656 | 0.318 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 845 | 847 | PF00675 | 0.292 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 732 | 734 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 845 | 847 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 679 | 681 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 732 | 734 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 803 | 805 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 863 | 865 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 977 | 981 | PF00082 | 0.427 |
DEG_APCC_DBOX_1 | 369 | 377 | PF00400 | 0.422 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.575 |
DEG_ODPH_VHL_1 | 430 | 442 | PF01847 | 0.331 |
DEG_SCF_FBW7_2 | 742 | 747 | PF00400 | 0.196 |
DOC_ANK_TNKS_1 | 967 | 974 | PF00023 | 0.422 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.347 |
DOC_CKS1_1 | 741 | 746 | PF01111 | 0.318 |
DOC_CKS1_1 | 758 | 763 | PF01111 | 0.354 |
DOC_CKS1_1 | 892 | 897 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 507 | 515 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 685 | 691 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 1025 | 1031 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 803 | 811 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 845 | 853 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 804 | 813 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 829 | 836 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 846 | 855 | PF00069 | 0.184 |
DOC_MAPK_RevD_3 | 383 | 398 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.337 |
DOC_PP1_RVXF_1 | 731 | 738 | PF00149 | 0.337 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.594 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 478 | 481 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 892 | 895 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 971 | 975 | PF00917 | 0.318 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 794 | 798 | PF12436 | 0.316 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 740 | 745 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 757 | 762 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 853 | 858 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 891 | 896 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 462 | 468 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 684 | 688 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 698 | 704 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 749 | 758 | PF00244 | 0.218 |
LIG_14-3-3_CanoR_1 | 815 | 821 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 845 | 853 | PF00244 | 0.327 |
LIG_Actin_WH2_2 | 342 | 360 | PF00022 | 0.400 |
LIG_Actin_WH2_2 | 389 | 405 | PF00022 | 0.196 |
LIG_APCC_ABBA_1 | 650 | 655 | PF00400 | 0.407 |
LIG_BIR_III_4 | 970 | 974 | PF00653 | 0.316 |
LIG_BRCT_BRCA1_1 | 710 | 714 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 846 | 850 | PF00533 | 0.337 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.493 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.628 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.422 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.400 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.336 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.422 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.390 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.449 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.281 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.331 |
LIG_FHA_1 | 806 | 812 | PF00498 | 0.329 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.162 |
LIG_FHA_2 | 1028 | 1034 | PF00498 | 0.494 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.374 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.449 |
LIG_FHA_2 | 967 | 973 | PF00498 | 0.422 |
LIG_IRF3_LxIS_1 | 850 | 856 | PF10401 | 0.318 |
LIG_LIR_Apic_2 | 739 | 744 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 889 | 895 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 958 | 964 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 554 | 564 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 731 | 742 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 847 | 857 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 923 | 933 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 938 | 946 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 731 | 737 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 835 | 840 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 847 | 853 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 912 | 917 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 923 | 929 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 938 | 942 | PF02991 | 0.299 |
LIG_MAD2 | 510 | 518 | PF02301 | 0.359 |
LIG_MLH1_MIPbox_1 | 846 | 850 | PF16413 | 0.302 |
LIG_MYND_1 | 333 | 337 | PF01753 | 0.374 |
LIG_NRBOX | 805 | 811 | PF00104 | 0.337 |
LIG_PCNA_PIPBox_1 | 282 | 291 | PF02747 | 0.525 |
LIG_PCNA_yPIPBox_3 | 282 | 296 | PF02747 | 0.522 |
LIG_Pex14_1 | 699 | 703 | PF04695 | 0.449 |
LIG_Pex14_1 | 74 | 78 | PF04695 | 0.678 |
LIG_Pex14_2 | 862 | 866 | PF04695 | 0.302 |
LIG_PTAP_UEV_1 | 761 | 766 | PF05743 | 0.611 |
LIG_PTB_Apo_2 | 933 | 940 | PF02174 | 0.359 |
LIG_PTB_Phospho_1 | 933 | 939 | PF10480 | 0.387 |
LIG_Rb_pABgroove_1 | 708 | 716 | PF01858 | 0.449 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.339 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.751 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.482 |
LIG_SH2_GRB2like | 914 | 917 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 939 | 942 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 989 | 992 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 315 | 319 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 549 | 553 | PF00017 | 0.324 |
LIG_SH2_NCK_1 | 769 | 773 | PF00017 | 0.524 |
LIG_SH2_PTP2 | 741 | 744 | PF00017 | 0.196 |
LIG_SH2_STAP1 | 1011 | 1015 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 151 | 154 | PF00017 | 0.581 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 8 | 11 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 1011 | 1014 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 741 | 744 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 849 | 852 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 914 | 917 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 939 | 942 | PF00017 | 0.220 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.753 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.319 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.671 |
LIG_SH3_3 | 752 | 758 | PF00018 | 0.290 |
LIG_SH3_3 | 759 | 765 | PF00018 | 0.440 |
LIG_SH3_3 | 819 | 825 | PF00018 | 0.306 |
LIG_SUMO_SIM_anti_2 | 906 | 912 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 1027 | 1033 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 381 | 387 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 440 | 446 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 562 | 568 | PF11976 | 0.196 |
LIG_SUMO_SIM_par_1 | 594 | 604 | PF11976 | 0.451 |
LIG_TYR_ITIM | 313 | 318 | PF00017 | 0.428 |
LIG_TYR_ITIM | 924 | 929 | PF00017 | 0.449 |
LIG_TYR_ITSM | 5 | 12 | PF00017 | 0.477 |
LIG_UBA3_1 | 1017 | 1026 | PF00899 | 0.462 |
LIG_UBA3_1 | 605 | 612 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 376 | 381 | PF05994 | 0.302 |
LIG_WRC_WIRS_1 | 817 | 822 | PF05994 | 0.337 |
LIG_WRC_WIRS_1 | 837 | 842 | PF05994 | 0.119 |
LIG_WW_1 | 765 | 768 | PF00397 | 0.587 |
MOD_CDK_SPK_2 | 740 | 745 | PF00069 | 0.422 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.521 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.744 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.514 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.493 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.422 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.409 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.601 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.327 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.698 |
MOD_CK1_1 | 818 | 824 | PF00069 | 0.364 |
MOD_CK2_1 | 1027 | 1033 | PF00069 | 0.328 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.526 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.429 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.318 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.406 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.381 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.426 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.337 |
MOD_CK2_1 | 853 | 859 | PF00069 | 0.302 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.711 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.432 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.566 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.733 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.456 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.672 |
MOD_GlcNHglycan | 727 | 730 | PF01048 | 0.363 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.711 |
MOD_GlcNHglycan | 947 | 950 | PF01048 | 0.360 |
MOD_GSK3_1 | 1009 | 1016 | PF00069 | 0.406 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.595 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.712 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.482 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.355 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.409 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.429 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.390 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.236 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.626 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.288 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.682 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.413 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.368 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.455 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.325 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.511 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.293 |
MOD_GSK3_1 | 853 | 860 | PF00069 | 0.302 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.563 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.415 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.510 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.422 |
MOD_N-GLC_1 | 853 | 858 | PF02516 | 0.302 |
MOD_N-GLC_2 | 567 | 569 | PF02516 | 0.422 |
MOD_NEK2_1 | 1020 | 1025 | PF00069 | 0.367 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.305 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.493 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.431 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.354 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.286 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.314 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.318 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.294 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.393 |
MOD_NEK2_1 | 775 | 780 | PF00069 | 0.318 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.318 |
MOD_NEK2_1 | 898 | 903 | PF00069 | 0.411 |
MOD_NEK2_1 | 920 | 925 | PF00069 | 0.318 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.457 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.498 |
MOD_NEK2_2 | 502 | 507 | PF00069 | 0.512 |
MOD_NEK2_2 | 551 | 556 | PF00069 | 0.447 |
MOD_NEK2_2 | 832 | 837 | PF00069 | 0.318 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.664 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.514 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.502 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.414 |
MOD_PK_1 | 751 | 757 | PF00069 | 0.318 |
MOD_PKA_1 | 296 | 302 | PF00069 | 0.569 |
MOD_PKA_1 | 815 | 821 | PF00069 | 0.422 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.500 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.307 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.586 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.449 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.331 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.302 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.356 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.217 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.422 |
MOD_PKA_2 | 844 | 850 | PF00069 | 0.302 |
MOD_PKA_2 | 868 | 874 | PF00069 | 0.359 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.302 |
MOD_PKB_1 | 749 | 757 | PF00069 | 0.302 |
MOD_Plk_1 | 1013 | 1019 | PF00069 | 0.398 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.533 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.429 |
MOD_Plk_1 | 857 | 863 | PF00069 | 0.302 |
MOD_Plk_1 | 898 | 904 | PF00069 | 0.387 |
MOD_Plk_4 | 1013 | 1019 | PF00069 | 0.413 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.449 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.415 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.571 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.387 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.328 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.395 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.302 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.449 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.304 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.318 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.320 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.307 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.231 |
MOD_Plk_4 | 832 | 838 | PF00069 | 0.305 |
MOD_Plk_4 | 920 | 926 | PF00069 | 0.305 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.670 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.687 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.685 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.299 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.521 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.302 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.636 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.437 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.299 |
MOD_ProDKin_1 | 740 | 746 | PF00069 | 0.303 |
MOD_ProDKin_1 | 757 | 763 | PF00069 | 0.399 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.315 |
MOD_ProDKin_1 | 853 | 859 | PF00069 | 0.302 |
MOD_ProDKin_1 | 891 | 897 | PF00069 | 0.435 |
TRG_DiLeu_BaEn_1 | 255 | 260 | PF01217 | 0.527 |
TRG_DiLeu_BaEn_2 | 315 | 321 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 425 | 430 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 559 | 564 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.754 |
TRG_ENDOCYTIC_2 | 817 | 820 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 849 | 852 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.639 |
TRG_ENDOCYTIC_2 | 914 | 917 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 926 | 929 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 939 | 942 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 963 | 966 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 749 | 752 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 814 | 816 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 844 | 846 | PF00400 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.196 |
TRG_Pf-PMV_PEXEL_1 | 539 | 543 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILP6 | Leptomonas seymouri | 69% | 100% |
A0A0N1PDC3 | Leptomonas seymouri | 32% | 100% |
A0A0S4IQK2 | Bodo saltans | 31% | 100% |
A0A0S4JWD1 | Bodo saltans | 45% | 100% |
A0A1X0NM03 | Trypanosomatidae | 31% | 100% |
A0A1X0NRU9 | Trypanosomatidae | 51% | 97% |
A0A221LG88 | Leishmania donovani | 31% | 100% |
A0A3R7KKA5 | Trypanosoma rangeli | 53% | 100% |
A0A3R7L1N0 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WR17 | Leishmania donovani | 88% | 100% |
A1CRW7 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 31% | 100% |
A1D4S4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 31% | 100% |
A2Q8L1 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 31% | 100% |
A2VDL8 | Bos taurus | 31% | 100% |
A3GFA2 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 30% | 100% |
A4HQG3 | Leishmania braziliensis | 32% | 100% |
A4HUE1 | Leishmania infantum | 89% | 100% |
A4IC99 | Leishmania infantum | 31% | 100% |
A4R1J7 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 31% | 100% |
A5DA00 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 30% | 100% |
A5E7S3 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 31% | 100% |
C9ZVF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
D0A3L4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AN41 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AU79 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O74873 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
O94672 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P0CR38 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 32% | 100% |
P0CR39 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 32% | 100% |
P15303 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q01405 | Mus musculus | 31% | 100% |
Q05AS9 | Xenopus tropicalis | 31% | 100% |
Q0CUU1 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 30% | 100% |
Q0US25 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 30% | 100% |
Q15436 | Homo sapiens | 31% | 100% |
Q15437 | Homo sapiens | 32% | 100% |
Q1DY01 | Coccidioides immitis (strain RS) | 31% | 100% |
Q2HB00 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 31% | 100% |
Q2URM9 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 100% |
Q3SZN2 | Bos taurus | 32% | 100% |
Q4PE39 | Ustilago maydis (strain 521 / FGSC 9021) | 32% | 100% |
Q4Q0B5 | Leishmania major | 31% | 100% |
Q4QHI5 | Leishmania major | 87% | 100% |
Q4WK80 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 100% |
Q54T59 | Dictyostelium discoideum | 31% | 100% |
Q5A455 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 100% |
Q5BGR9 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 30% | 100% |
Q5R5G2 | Pongo abelii | 31% | 100% |
Q5R9P3 | Pongo abelii | 31% | 100% |
Q5ZK03 | Gallus gallus | 32% | 100% |
Q6BQT6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 32% | 100% |
Q6C5L5 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
Q6CPH3 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q6FSI6 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
Q6FSK3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 30% | 100% |
Q758M7 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 32% | 100% |
Q7SZE5 | Danio rerio | 32% | 100% |
Q8SQX2 | Encephalitozoon cuniculi (strain GB-M1) | 26% | 100% |
Q9C284 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
Q9D662 | Mus musculus | 32% | 100% |
V5ASV7 | Trypanosoma cruzi | 32% | 100% |
V5DA02 | Trypanosoma cruzi | 54% | 100% |