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: E9AP98
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 | 292 | 296 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 756 | 760 | PF00656 | 0.222 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 902 | 904 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 984 | 986 | PF00675 | 0.241 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.492 |
CLV_PCSK_PC7_1 | 12 | 18 | PF00082 | 0.466 |
CLV_PCSK_PC7_1 | 746 | 752 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 750 | 754 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 904 | 908 | PF00082 | 0.396 |
CLV_Separin_Metazoa | 108 | 112 | PF03568 | 0.725 |
DEG_APCC_DBOX_1 | 836 | 844 | PF00400 | 0.454 |
DEG_ODPH_VHL_1 | 483 | 494 | PF01847 | 0.178 |
DEG_SCF_FBW7_1 | 168 | 175 | PF00400 | 0.655 |
DEG_SCF_FBW7_1 | 761 | 767 | PF00400 | 0.178 |
DOC_ANK_TNKS_1 | 628 | 635 | PF00023 | 0.308 |
DOC_CKS1_1 | 761 | 766 | PF01111 | 0.185 |
DOC_CKS1_1 | 973 | 978 | PF01111 | 0.454 |
DOC_CYCLIN_RxL_1 | 744 | 756 | PF00134 | 0.230 |
DOC_CYCLIN_yCln2_LP_2 | 769 | 775 | PF00134 | 0.178 |
DOC_MAPK_DCC_7 | 848 | 856 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 179 | 188 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 848 | 856 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 983 | 993 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 334 | 341 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 848 | 856 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 700 | 706 | PF00149 | 0.356 |
DOC_PP1_RVXF_1 | 944 | 950 | PF00149 | 0.231 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.254 |
DOC_PP2B_LxvP_1 | 769 | 772 | PF13499 | 0.178 |
DOC_PP4_MxPP_1 | 647 | 650 | PF00568 | 0.258 |
DOC_SPAK_OSR1_1 | 948 | 952 | PF12202 | 0.222 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 882 | 886 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.734 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 972 | 977 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 147 | 157 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 316 | 320 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 504 | 508 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 536 | 541 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 582 | 591 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 731 | 740 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 903 | 913 | PF00244 | 0.208 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.598 |
LIG_Actin_WH2_2 | 466 | 484 | PF00022 | 0.366 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.646 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 660 | 664 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_1 | 837 | 841 | PF00533 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 420 | 427 | PF00928 | 0.508 |
LIG_EH1_1 | 641 | 649 | PF00400 | 0.273 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.605 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.487 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.311 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.479 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.371 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.227 |
LIG_FHA_1 | 874 | 880 | PF00498 | 0.291 |
LIG_FHA_1 | 897 | 903 | PF00498 | 0.273 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.231 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.651 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.518 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.628 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.554 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.439 |
LIG_FHA_2 | 761 | 767 | PF00498 | 0.230 |
LIG_FHA_2 | 973 | 979 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 157 | 165 | PF00786 | 0.412 |
LIG_GBD_Chelix_1 | 871 | 879 | PF00786 | 0.185 |
LIG_Integrin_RGD_1 | 76 | 78 | PF01839 | 0.412 |
LIG_IRF3_LxIS_1 | 432 | 439 | PF10401 | 0.567 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 420 | 429 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 433 | 443 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.205 |
LIG_LIR_Gen_1 | 601 | 611 | PF02991 | 0.168 |
LIG_LIR_Gen_1 | 661 | 671 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 799 | 809 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 825 | 834 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 861 | 870 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 588 | 594 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 601 | 606 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 661 | 667 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 699 | 703 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 722 | 728 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 796 | 801 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 825 | 829 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 861 | 865 | PF02991 | 0.506 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.524 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.515 |
LIG_PCNA_yPIPBox_3 | 381 | 389 | PF02747 | 0.550 |
LIG_Pex14_1 | 457 | 461 | PF04695 | 0.454 |
LIG_Pex14_1 | 891 | 895 | PF04695 | 0.239 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.454 |
LIG_Rb_pABgroove_1 | 792 | 800 | PF01858 | 0.273 |
LIG_REV1ctd_RIR_1 | 347 | 355 | PF16727 | 0.475 |
LIG_RPA_C_Fungi | 740 | 752 | PF08784 | 0.332 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.440 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.469 |
LIG_SH2_CRK | 700 | 704 | PF00017 | 0.290 |
LIG_SH2_CRK | 953 | 957 | PF00017 | 0.269 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 134 | 137 | PF00017 | 0.550 |
LIG_SH2_PTP2 | 725 | 728 | PF00017 | 0.269 |
LIG_SH2_PTP2 | 813 | 816 | PF00017 | 0.269 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 798 | 802 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 725 | 728 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 845 | 848 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 895 | 898 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 953 | 956 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 959 | 962 | PF00017 | 0.271 |
LIG_SH3_2 | 110 | 115 | PF14604 | 0.598 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.616 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.695 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.499 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.460 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.383 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.474 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.335 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.290 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.290 |
LIG_SH3_3 | 758 | 764 | PF00018 | 0.270 |
LIG_SH3_3 | 934 | 940 | PF00018 | 0.224 |
LIG_SH3_3 | 970 | 976 | PF00018 | 0.290 |
LIG_Sin3_3 | 489 | 496 | PF02671 | 0.318 |
LIG_SUMO_SIM_anti_2 | 512 | 517 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 825 | 831 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 792 | 799 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 831 | 838 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 878 | 885 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 907 | 916 | PF11976 | 0.185 |
LIG_SxIP_EBH_1 | 731 | 744 | PF03271 | 0.318 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.477 |
LIG_TYR_ITIM | 723 | 728 | PF00017 | 0.184 |
LIG_TYR_ITIM | 951 | 956 | PF00017 | 0.318 |
LIG_UBA3_1 | 663 | 669 | PF00899 | 0.287 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.605 |
LIG_WRC_WIRS_1 | 294 | 299 | PF05994 | 0.564 |
LIG_WRC_WIRS_1 | 360 | 365 | PF05994 | 0.337 |
LIG_WRC_WIRS_1 | 823 | 828 | PF05994 | 0.290 |
MOD_CDK_SPK_2 | 972 | 977 | PF00069 | 0.290 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.570 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.426 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.735 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.538 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.611 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.466 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.554 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.291 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.342 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.185 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.363 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.366 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.790 |
MOD_CK1_1 | 885 | 891 | PF00069 | 0.364 |
MOD_CK1_1 | 915 | 921 | PF00069 | 0.369 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.564 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.458 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.432 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.185 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.269 |
MOD_CK2_1 | 972 | 978 | PF00069 | 0.366 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.640 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.561 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.438 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.391 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.637 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.229 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.548 |
MOD_GlcNHglycan | 715 | 719 | PF01048 | 0.412 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.360 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.360 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.683 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.347 |
MOD_GlcNHglycan | 916 | 920 | PF01048 | 0.293 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.578 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.526 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.416 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.588 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.583 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.626 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.353 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.358 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.397 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.301 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.294 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.584 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.312 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.372 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.366 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.595 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.315 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.366 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.331 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.377 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.332 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.256 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.398 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.538 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.532 |
MOD_N-GLC_1 | 858 | 863 | PF02516 | 0.290 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.643 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.561 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.461 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.360 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.504 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.349 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.327 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.285 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.327 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.258 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.290 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.290 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.327 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.258 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.161 |
MOD_NEK2_1 | 775 | 780 | PF00069 | 0.287 |
MOD_NEK2_1 | 881 | 886 | PF00069 | 0.269 |
MOD_NEK2_1 | 896 | 901 | PF00069 | 0.286 |
MOD_NEK2_2 | 898 | 903 | PF00069 | 0.185 |
MOD_PK_1 | 536 | 542 | PF00069 | 0.233 |
MOD_PKA_1 | 536 | 542 | PF00069 | 0.290 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.585 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.581 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.366 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.319 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.327 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.423 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.388 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.540 |
MOD_Plk_1 | 858 | 864 | PF00069 | 0.290 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.579 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.380 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.555 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.610 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.529 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.369 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.161 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.301 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.349 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.256 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.218 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.279 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.504 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.393 |
MOD_Plk_4 | 764 | 770 | PF00069 | 0.185 |
MOD_Plk_4 | 822 | 828 | PF00069 | 0.290 |
MOD_Plk_4 | 861 | 867 | PF00069 | 0.311 |
MOD_Plk_4 | 875 | 881 | PF00069 | 0.283 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.623 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.540 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.496 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.322 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.409 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.247 |
MOD_ProDKin_1 | 972 | 978 | PF00069 | 0.290 |
MOD_SUMO_rev_2 | 4 | 8 | PF00179 | 0.580 |
TRG_DiLeu_BaEn_1 | 790 | 795 | PF01217 | 0.184 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.308 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 700 | 703 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 725 | 728 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 801 | 804 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 813 | 816 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 953 | 956 | PF00928 | 0.269 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 627 | 629 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 684 | 687 | PF00400 | 0.202 |
TRG_ER_diArg_1 | 745 | 747 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 749 | 751 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 847 | 849 | PF00400 | 0.290 |
TRG_NES_CRM1_1 | 251 | 267 | PF08389 | 0.545 |
TRG_NES_CRM1_1 | 799 | 810 | PF08389 | 0.342 |
TRG_NLS_MonoExtC_3 | 14 | 19 | PF00514 | 0.548 |
TRG_NLS_MonoExtN_4 | 12 | 19 | PF00514 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 343 | 347 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 387 | 391 | PF00026 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 628 | 633 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 687 | 691 | PF00026 | 0.197 |
TRG_Pf-PMV_PEXEL_1 | 890 | 894 | PF00026 | 0.185 |
TRG_Pf-PMV_PEXEL_1 | 985 | 989 | PF00026 | 0.383 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDJ1 | Leptomonas seymouri | 50% | 91% |
A0A3S5H6N8 | Leishmania donovani | 82% | 100% |
A1A5B4 | Homo sapiens | 22% | 100% |
A4H763 | Leishmania braziliensis | 69% | 100% |
A4HVK2 | Leishmania infantum | 83% | 100% |
Q4KMQ2 | Homo sapiens | 22% | 100% |
Q4QG80 | Leishmania major | 82% | 97% |