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: A4H763
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 | 303 | 307 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.255 |
CLV_PCSK_FUR_1 | 138 | 142 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.255 |
CLV_PCSK_PC1ET2_1 | 630 | 632 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.406 |
CLV_Separin_Metazoa | 49 | 53 | PF03568 | 0.706 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.491 |
DEG_APCC_DBOX_1 | 776 | 784 | PF00400 | 0.455 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.287 |
DOC_ANK_TNKS_1 | 568 | 575 | PF00023 | 0.309 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.567 |
DOC_CKS1_1 | 709 | 714 | PF01111 | 0.249 |
DOC_CKS1_1 | 910 | 915 | PF01111 | 0.455 |
DOC_CYCLIN_RxL_1 | 137 | 145 | PF00134 | 0.507 |
DOC_CYCLIN_RxL_1 | 388 | 396 | PF00134 | 0.211 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.590 |
DOC_MAPK_DCC_7 | 252 | 260 | PF00069 | 0.498 |
DOC_MAPK_DCC_7 | 788 | 796 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 309 | 318 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 788 | 796 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 920 | 930 | PF00069 | 0.566 |
DOC_MAPK_HePTP_8 | 6 | 18 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 252 | 260 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 262 | 269 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 311 | 320 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 788 | 796 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 9 | 18 | PF00069 | 0.601 |
DOC_MAPK_NFAT4_5 | 9 | 17 | PF00069 | 0.595 |
DOC_PP1_RVXF_1 | 628 | 635 | PF00149 | 0.423 |
DOC_PP1_RVXF_1 | 640 | 646 | PF00149 | 0.358 |
DOC_PP1_RVXF_1 | 883 | 890 | PF00149 | 0.231 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.592 |
DOC_PP2B_LxvP_1 | 562 | 565 | PF13499 | 0.255 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.547 |
DOC_SPAK_OSR1_1 | 244 | 248 | PF12202 | 0.553 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.197 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 888 | 892 | PF00917 | 0.211 |
DOC_USP7_UBL2_3 | 605 | 609 | PF12436 | 0.397 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 723 | 728 | PF00397 | 0.224 |
DOC_WW_Pin1_4 | 825 | 830 | PF00397 | 0.197 |
DOC_WW_Pin1_4 | 909 | 914 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.197 |
LIG_14-3-3_CanoR_1 | 445 | 449 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 477 | 482 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 625 | 630 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 650 | 660 | PF00244 | 0.236 |
LIG_14-3-3_CanoR_1 | 671 | 680 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 703 | 713 | PF00244 | 0.205 |
LIG_14-3-3_CanoR_1 | 847 | 854 | PF00244 | 0.212 |
LIG_14-3-3_CanoR_1 | 88 | 98 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 927 | 931 | PF00244 | 0.628 |
LIG_Actin_WH2_2 | 113 | 130 | PF00022 | 0.606 |
LIG_Actin_WH2_2 | 394 | 412 | PF00022 | 0.368 |
LIG_BRCT_BRCA1_1 | 600 | 604 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_1 | 777 | 781 | PF00533 | 0.455 |
LIG_CSL_BTD_1 | 831 | 834 | PF09270 | 0.189 |
LIG_deltaCOP1_diTrp_1 | 300 | 304 | PF00928 | 0.477 |
LIG_deltaCOP1_diTrp_1 | 348 | 355 | PF00928 | 0.508 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.591 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.605 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.608 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.525 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.211 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.204 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.374 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.225 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.291 |
LIG_FHA_1 | 858 | 864 | PF00498 | 0.197 |
LIG_FHA_1 | 919 | 925 | PF00498 | 0.574 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.560 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.557 |
LIG_FHA_2 | 910 | 916 | PF00498 | 0.509 |
LIG_GBD_Chelix_1 | 466 | 474 | PF00786 | 0.211 |
LIG_GBD_Chelix_1 | 98 | 106 | PF00786 | 0.404 |
LIG_IRF3_LxIS_1 | 360 | 367 | PF10401 | 0.570 |
LIG_LIR_Apic_2 | 828 | 834 | PF02991 | 0.189 |
LIG_LIR_Gen_1 | 348 | 357 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 519 | 529 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 739 | 749 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 74 | 83 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 765 | 774 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 92 | 102 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 528 | 534 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 635 | 640 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 739 | 744 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 765 | 769 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 800 | 805 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.613 |
LIG_LRP6_Inhibitor_1 | 769 | 775 | PF00058 | 0.211 |
LIG_LYPXL_yS_3 | 761 | 764 | PF13949 | 0.211 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.528 |
LIG_PCNA_yPIPBox_3 | 309 | 317 | PF02747 | 0.563 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.455 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.526 |
LIG_Pex14_2 | 381 | 385 | PF04695 | 0.455 |
LIG_Pex14_2 | 753 | 757 | PF04695 | 0.211 |
LIG_REV1ctd_RIR_1 | 275 | 283 | PF16727 | 0.489 |
LIG_RPA_C_Fungi | 666 | 678 | PF08784 | 0.258 |
LIG_RPA_C_Fungi | 680 | 692 | PF08784 | 0.334 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.292 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.441 |
LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.536 |
LIG_SH2_SRC | 184 | 187 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 593 | 597 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.211 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.292 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.666 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.570 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.433 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.527 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.388 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.478 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.266 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.292 |
LIG_SH3_3 | 710 | 716 | PF00018 | 0.336 |
LIG_SH3_3 | 867 | 873 | PF00018 | 0.230 |
LIG_SH3_3 | 907 | 913 | PF00018 | 0.292 |
LIG_SUMO_SIM_anti_2 | 453 | 458 | PF11976 | 0.368 |
LIG_SUMO_SIM_anti_2 | 743 | 749 | PF11976 | 0.235 |
LIG_SUMO_SIM_anti_2 | 765 | 771 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 329 | 335 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 678 | 683 | PF11976 | 0.211 |
LIG_SUMO_SIM_par_1 | 818 | 825 | PF11976 | 0.344 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.523 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.618 |
LIG_UBA3_1 | 769 | 775 | PF00899 | 0.211 |
LIG_WRC_WIRS_1 | 222 | 227 | PF05994 | 0.585 |
LIG_WRC_WIRS_1 | 763 | 768 | PF05994 | 0.292 |
LIG_WRC_WIRS_1 | 816 | 821 | PF05994 | 0.211 |
LIG_WW_3 | 49 | 53 | PF00397 | 0.510 |
MOD_CDK_SPK_2 | 107 | 112 | PF00069 | 0.446 |
MOD_CDK_SPK_2 | 909 | 914 | PF00069 | 0.292 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.477 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.762 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.520 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.474 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.293 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.272 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.343 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.241 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.361 |
MOD_CK1_1 | 723 | 729 | PF00069 | 0.368 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.360 |
MOD_CK1_1 | 845 | 851 | PF00069 | 0.170 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.354 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.518 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.437 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.238 |
MOD_CK2_1 | 909 | 915 | PF00069 | 0.368 |
MOD_CMANNOS | 301 | 304 | PF00535 | 0.316 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.700 |
MOD_GlcNHglycan | 214 | 218 | PF01048 | 0.586 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.588 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.399 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.315 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.361 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.305 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.578 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.477 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.614 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.441 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.505 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.359 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.302 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.335 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.298 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.368 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.267 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.257 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.370 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.368 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.388 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.211 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.258 |
MOD_N-GLC_1 | 798 | 803 | PF02516 | 0.292 |
MOD_N-GLC_1 | 825 | 830 | PF02516 | 0.211 |
MOD_N-GLC_1 | 866 | 871 | PF02516 | 0.209 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.625 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.520 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.388 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.362 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.290 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.350 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.329 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.329 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.259 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.292 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.292 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.282 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.292 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.329 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.259 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.187 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.365 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.172 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.240 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.331 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.211 |
MOD_PIKK_1 | 842 | 848 | PF00454 | 0.211 |
MOD_PK_1 | 31 | 37 | PF00069 | 0.512 |
MOD_PK_1 | 477 | 483 | PF00069 | 0.235 |
MOD_PK_1 | 694 | 700 | PF00069 | 0.211 |
MOD_PKA_1 | 477 | 483 | PF00069 | 0.292 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.587 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.368 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.321 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.205 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.239 |
MOD_PKA_2 | 846 | 852 | PF00069 | 0.271 |
MOD_PKA_2 | 854 | 860 | PF00069 | 0.228 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.439 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.509 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.205 |
MOD_Plk_1 | 798 | 804 | PF00069 | 0.292 |
MOD_Plk_1 | 866 | 872 | PF00069 | 0.211 |
MOD_Plk_2-3 | 174 | 180 | PF00069 | 0.439 |
MOD_Plk_2-3 | 890 | 896 | PF00069 | 0.211 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.496 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.613 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.371 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.163 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.302 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.269 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.308 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.257 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.313 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.394 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.542 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.292 |
MOD_Plk_4 | 815 | 821 | PF00069 | 0.285 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.548 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.499 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.547 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.320 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.379 |
MOD_ProDKin_1 | 723 | 729 | PF00069 | 0.249 |
MOD_ProDKin_1 | 825 | 831 | PF00069 | 0.211 |
MOD_ProDKin_1 | 909 | 915 | PF00069 | 0.292 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 308 | 313 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.205 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 761 | 764 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 611 | 614 | PF00400 | 0.219 |
TRG_ER_diArg_1 | 685 | 687 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 852 | 855 | PF00400 | 0.211 |
TRG_NES_CRM1_1 | 134 | 145 | PF08389 | 0.369 |
TRG_NES_CRM1_1 | 179 | 195 | PF08389 | 0.607 |
TRG_NES_CRM1_1 | 739 | 750 | PF08389 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 140 | 145 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 568 | 573 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDJ1 | Leptomonas seymouri | 50% | 85% |
A0A3S5H6N8 | Leishmania donovani | 71% | 95% |
A1A5B4 | Homo sapiens | 22% | 100% |
A4HVK2 | Leishmania infantum | 71% | 95% |
E9AP98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 94% |
P86044 | Mus musculus | 20% | 100% |
Q4QG80 | Leishmania major | 70% | 100% |