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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HVK2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0006821 | chloride transport | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015698 | inorganic anion transport | 6 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 1 |
GO:1902476 | chloride transmembrane transport | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0005216 | monoatomic ion channel activity | 4 | 1 |
GO:0005253 | monoatomic anion channel activity | 5 | 1 |
GO:0005254 | chloride channel activity | 6 | 1 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 1 |
GO:0015108 | chloride transmembrane transporter activity | 5 | 1 |
GO:0015267 | channel activity | 4 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0022803 | passive transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.564 |
CLV_MEL_PAP_1 | 970 | 976 | PF00089 | 0.298 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 761 | 763 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 967 | 969 | PF00675 | 0.240 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 761 | 763 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 833 | 835 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.245 |
CLV_PCSK_PC7_1 | 12 | 18 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 731 | 737 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 676 | 680 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.571 |
CLV_Separin_Metazoa | 93 | 97 | PF03568 | 0.722 |
DEG_APCC_DBOX_1 | 821 | 829 | PF00400 | 0.452 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.287 |
DOC_ANK_TNKS_1 | 613 | 620 | PF00023 | 0.306 |
DOC_CKS1_1 | 754 | 759 | PF01111 | 0.246 |
DOC_CKS1_1 | 956 | 961 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 729 | 741 | PF00134 | 0.228 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 560 | 566 | PF00134 | 0.439 |
DOC_MAPK_DCC_7 | 833 | 841 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 833 | 841 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 966 | 976 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 833 | 841 | PF00069 | 0.452 |
DOC_MAPK_RevD_3 | 475 | 490 | PF00069 | 0.254 |
DOC_PP1_RVXF_1 | 685 | 691 | PF00149 | 0.355 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.252 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.665 |
DOC_PP4_MxPP_1 | 632 | 635 | PF00568 | 0.256 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 807 | 811 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.289 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.221 |
DOC_WW_Pin1_4 | 955 | 960 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 132 | 142 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 197 | 205 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 489 | 493 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 521 | 530 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 567 | 574 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 670 | 675 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 716 | 725 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 914 | 919 | PF00244 | 0.254 |
LIG_14-3-3_CanoR_1 | 973 | 977 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 170 | 187 | PF00022 | 0.588 |
LIG_Actin_WH2_2 | 451 | 469 | PF00022 | 0.365 |
LIG_APCC_ABBA_1 | 58 | 63 | PF00400 | 0.672 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.620 |
LIG_BRCT_BRCA1_1 | 645 | 649 | PF00533 | 0.289 |
LIG_BRCT_BRCA1_1 | 822 | 826 | PF00533 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 405 | 412 | PF00928 | 0.508 |
LIG_EH1_1 | 626 | 634 | PF00400 | 0.272 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.546 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.601 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.309 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.478 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.371 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.226 |
LIG_FHA_1 | 861 | 867 | PF00498 | 0.288 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.272 |
LIG_FHA_1 | 907 | 913 | PF00498 | 0.242 |
LIG_FHA_1 | 965 | 971 | PF00498 | 0.489 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.638 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.546 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.641 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.550 |
LIG_FHA_2 | 655 | 661 | PF00498 | 0.437 |
LIG_FHA_2 | 746 | 752 | PF00498 | 0.228 |
LIG_FHA_2 | 956 | 962 | PF00498 | 0.506 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.654 |
LIG_GBD_Chelix_1 | 142 | 150 | PF00786 | 0.399 |
LIG_IRF3_LxIS_1 | 417 | 424 | PF10401 | 0.563 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 118 | 127 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 405 | 414 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 646 | 656 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 707 | 718 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 788 | 796 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 810 | 819 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 646 | 652 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 684 | 688 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 810 | 814 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 846 | 850 | PF02991 | 0.504 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.566 |
LIG_NRBOX | 373 | 379 | PF00104 | 0.520 |
LIG_PCNA_yPIPBox_3 | 180 | 193 | PF02747 | 0.576 |
LIG_PCNA_yPIPBox_3 | 366 | 374 | PF02747 | 0.561 |
LIG_Pex14_1 | 442 | 446 | PF04695 | 0.452 |
LIG_Pex14_1 | 876 | 880 | PF04695 | 0.237 |
LIG_Pex14_2 | 354 | 358 | PF04695 | 0.527 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.452 |
LIG_Pex14_2 | 877 | 881 | PF04695 | 0.299 |
LIG_PTB_Apo_2 | 658 | 665 | PF02174 | 0.428 |
LIG_PTB_Phospho_1 | 658 | 664 | PF10480 | 0.454 |
LIG_Rb_pABgroove_1 | 777 | 785 | PF01858 | 0.272 |
LIG_RPA_C_Fungi | 725 | 737 | PF08784 | 0.331 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.448 |
LIG_SH2_CRK | 685 | 689 | PF00017 | 0.289 |
LIG_SH2_CRK | 936 | 940 | PF00017 | 0.268 |
LIG_SH2_NCK_1 | 302 | 306 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 971 | 975 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 119 | 122 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 710 | 713 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 798 | 801 | PF00017 | 0.268 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.522 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 638 | 642 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 783 | 787 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 655 | 658 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 798 | 801 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 830 | 833 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 880 | 883 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 936 | 939 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 942 | 945 | PF00017 | 0.269 |
LIG_SH3_2 | 95 | 100 | PF14604 | 0.594 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.692 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.606 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.518 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.397 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.469 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.333 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.289 |
LIG_SH3_3 | 751 | 757 | PF00018 | 0.391 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.615 |
LIG_SH3_3 | 953 | 959 | PF00018 | 0.289 |
LIG_SH3_4 | 154 | 161 | PF00018 | 0.522 |
LIG_Sin3_3 | 474 | 481 | PF02671 | 0.316 |
LIG_SUMO_SIM_anti_2 | 497 | 502 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 810 | 816 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 777 | 784 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 816 | 823 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 863 | 870 | PF11976 | 0.341 |
LIG_SxIP_EBH_1 | 716 | 729 | PF03271 | 0.316 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.527 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.497 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.647 |
LIG_TRAF2_1 | 772 | 775 | PF00917 | 0.279 |
LIG_TYR_ITIM | 934 | 939 | PF00017 | 0.316 |
LIG_UBA3_1 | 648 | 654 | PF00899 | 0.285 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.566 |
LIG_WRC_WIRS_1 | 279 | 284 | PF05994 | 0.578 |
LIG_WRC_WIRS_1 | 808 | 813 | PF05994 | 0.289 |
MOD_CDK_SPK_2 | 955 | 960 | PF00069 | 0.289 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.456 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.753 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.509 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.596 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.467 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.290 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.340 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.772 |
MOD_CK1_1 | 747 | 753 | PF00069 | 0.357 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.365 |
MOD_CK1_1 | 870 | 876 | PF00069 | 0.362 |
MOD_CK1_1 | 900 | 906 | PF00069 | 0.367 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.547 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.502 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.428 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.268 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.256 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.297 |
MOD_CK2_1 | 955 | 961 | PF00069 | 0.365 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.581 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.670 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.579 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.438 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.392 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.292 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.664 |
MOD_GlcNHglycan | 700 | 704 | PF01048 | 0.401 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.358 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.358 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.589 |
MOD_GlcNHglycan | 892 | 895 | PF01048 | 0.346 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.307 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.575 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.460 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.598 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.597 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.609 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.410 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.359 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.299 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.293 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.306 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.371 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.365 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.313 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.367 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.358 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.346 |
MOD_GSK3_1 | 866 | 873 | PF00069 | 0.331 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.255 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.493 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.557 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.623 |
MOD_N-GLC_1 | 843 | 848 | PF02516 | 0.289 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.596 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.362 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.347 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.326 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.283 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.326 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.256 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.289 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.289 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.289 |
MOD_NEK2_1 | 718 | 723 | PF00069 | 0.326 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.256 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.160 |
MOD_NEK2_1 | 760 | 765 | PF00069 | 0.285 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.268 |
MOD_NEK2_1 | 881 | 886 | PF00069 | 0.284 |
MOD_PKA_1 | 521 | 527 | PF00069 | 0.289 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.524 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.556 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.569 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.365 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.318 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.335 |
MOD_PKA_2 | 738 | 744 | PF00069 | 0.411 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.292 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.418 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.558 |
MOD_Plk_1 | 843 | 849 | PF00069 | 0.289 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.421 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.512 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.572 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.518 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.369 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.160 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.299 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.348 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.278 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.391 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.289 |
MOD_Plk_4 | 860 | 866 | PF00069 | 0.282 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.413 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.538 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.317 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.406 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.376 |
MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.246 |
MOD_ProDKin_1 | 955 | 961 | PF00069 | 0.289 |
MOD_SUMO_rev_2 | 4 | 8 | PF00179 | 0.542 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_3 | 774 | 780 | PF01217 | 0.232 |
TRG_DiLeu_BaEn_4 | 162 | 168 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 345 | 350 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.319 |
TRG_DiLeu_LyEn_5 | 62 | 67 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 798 | 801 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 936 | 939 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 695 | 698 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 730 | 732 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 760 | 762 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 832 | 834 | PF00400 | 0.289 |
TRG_NES_CRM1_1 | 236 | 252 | PF08389 | 0.594 |
TRG_NES_CRM1_1 | 784 | 795 | PF08389 | 0.341 |
TRG_NLS_MonoExtC_3 | 14 | 19 | PF00514 | 0.515 |
TRG_NLS_MonoExtN_4 | 12 | 19 | PF00514 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 613 | 618 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 968 | 972 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDJ1 | Leptomonas seymouri | 50% | 89% |
A0A3S5H6N8 | Leishmania donovani | 99% | 100% |
A2AHL1 | Mus musculus | 23% | 100% |
A4H763 | Leishmania braziliensis | 71% | 99% |
E9AP98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4QG80 | Leishmania major | 92% | 100% |