Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (by homology)
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: 60 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 53 |
NetGPI | no | yes: 0, no: 53 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
GO:0000139 | Golgi membrane | 5 | 14 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0098588 | bounding membrane of organelle | 4 | 14 |
Related structures:
AlphaFold database: E9AJI6
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 54 |
GO:0006807 | nitrogen compound metabolic process | 2 | 54 |
GO:0008152 | metabolic process | 1 | 54 |
GO:0019538 | protein metabolic process | 3 | 54 |
GO:0036211 | protein modification process | 4 | 54 |
GO:0043170 | macromolecule metabolic process | 3 | 54 |
GO:0043412 | macromolecule modification | 4 | 54 |
GO:0043413 | macromolecule glycosylation | 3 | 54 |
GO:0044238 | primary metabolic process | 2 | 54 |
GO:0070085 | glycosylation | 2 | 54 |
GO:0071704 | organic substance metabolic process | 2 | 54 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 54 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 54 |
GO:0016740 | transferase activity | 2 | 54 |
GO:0016757 | glycosyltransferase activity | 3 | 54 |
GO:0016758 | hexosyltransferase activity | 4 | 54 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.310 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.288 |
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.288 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 796 | 798 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 854 | 856 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 865 | 867 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 881 | 883 | PF00675 | 0.529 |
CLV_PCSK_FUR_1 | 240 | 244 | PF00082 | 0.413 |
CLV_PCSK_FUR_1 | 570 | 574 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 854 | 856 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 865 | 867 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 881 | 883 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 786 | 788 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.386 |
CLV_PCSK_PC7_1 | 267 | 273 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 801 | 805 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 857 | 861 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 865 | 869 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 908 | 912 | PF00082 | 0.473 |
CLV_Separin_Metazoa | 435 | 439 | PF03568 | 0.355 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.312 |
DEG_SCF_FBW7_2 | 112 | 119 | PF00400 | 0.631 |
DOC_ANK_TNKS_1 | 274 | 281 | PF00023 | 0.375 |
DOC_CDC14_PxL_1 | 88 | 96 | PF14671 | 0.631 |
DOC_CYCLIN_RxL_1 | 242 | 254 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 616 | 622 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 301 | 311 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 604 | 611 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 797 | 804 | PF00069 | 0.282 |
DOC_MAPK_gen_1 | 814 | 822 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 881 | 890 | PF00069 | 0.299 |
DOC_MAPK_JIP1_4 | 972 | 978 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 201 | 209 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 248 | 255 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 455 | 462 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 604 | 611 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 817 | 824 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 302 | 309 | PF00149 | 0.346 |
DOC_PP1_RVXF_1 | 680 | 687 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 616 | 619 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 94 | 97 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 960 | 963 | PF13499 | 0.335 |
DOC_PP2B_PxIxI_1 | 457 | 463 | PF00149 | 0.275 |
DOC_PP2B_PxIxI_1 | 972 | 978 | PF00149 | 0.291 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.609 |
DOC_PP4_FxxP_1 | 535 | 538 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.423 |
DOC_USP7_UBL2_3 | 301 | 305 | PF12436 | 0.344 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 919 | 924 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 572 | 577 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 579 | 584 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 787 | 795 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 865 | 874 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 885 | 891 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 302 | 319 | PF00022 | 0.311 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.659 |
LIG_BIR_III_2 | 230 | 234 | PF00653 | 0.591 |
LIG_BIR_III_2 | 970 | 974 | PF00653 | 0.350 |
LIG_BRCT_BRCA1_1 | 481 | 485 | PF00533 | 0.253 |
LIG_Clathr_ClatBox_1 | 742 | 746 | PF01394 | 0.397 |
LIG_CSL_BTD_1 | 960 | 963 | PF09270 | 0.322 |
LIG_deltaCOP1_diTrp_1 | 216 | 221 | PF00928 | 0.558 |
LIG_EVH1_1 | 94 | 98 | PF00568 | 0.646 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.661 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.406 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.477 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.347 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.384 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.490 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.314 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.341 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.665 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.592 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.639 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.339 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.398 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.454 |
LIG_FHA_2 | 839 | 845 | PF00498 | 0.298 |
LIG_FHA_2 | 866 | 872 | PF00498 | 0.310 |
LIG_FHA_2 | 897 | 903 | PF00498 | 0.301 |
LIG_FHA_2 | 920 | 926 | PF00498 | 0.374 |
LIG_LIR_Apic_2 | 534 | 538 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 456 | 465 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 647 | 655 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 688 | 699 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 703 | 712 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 716 | 722 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 833 | 840 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 875 | 884 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 889 | 895 | PF02991 | 0.369 |
LIG_LIR_LC3C_4 | 974 | 978 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 683 | 689 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 703 | 707 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 716 | 721 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 826 | 830 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 833 | 838 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 875 | 880 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 889 | 893 | PF02991 | 0.374 |
LIG_MAD2 | 108 | 116 | PF02301 | 0.630 |
LIG_PDZ_Class_2 | 984 | 989 | PF00595 | 0.283 |
LIG_Pex14_2 | 827 | 831 | PF04695 | 0.280 |
LIG_PTB_Apo_2 | 825 | 832 | PF02174 | 0.293 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.274 |
LIG_SH2_CRK | 550 | 554 | PF00017 | 0.310 |
LIG_SH2_NCK_1 | 487 | 491 | PF00017 | 0.274 |
LIG_SH2_NCK_1 | 704 | 708 | PF00017 | 0.246 |
LIG_SH2_NCK_1 | 835 | 839 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 459 | 462 | PF00017 | 0.265 |
LIG_SH2_SRC | 689 | 692 | PF00017 | 0.353 |
LIG_SH2_SRC | 704 | 707 | PF00017 | 0.255 |
LIG_SH2_SRC | 835 | 838 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 689 | 693 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 704 | 708 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 835 | 839 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 720 | 723 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 905 | 908 | PF00017 | 0.470 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.631 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.429 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.465 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.480 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.414 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.659 |
LIG_SUMO_SIM_anti_2 | 13 | 19 | PF11976 | 0.631 |
LIG_SUMO_SIM_anti_2 | 284 | 289 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 818 | 823 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 974 | 980 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.243 |
LIG_SUMO_SIM_par_1 | 388 | 394 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 818 | 823 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 974 | 980 | PF11976 | 0.302 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.291 |
LIG_TRAF2_1 | 539 | 542 | PF00917 | 0.310 |
LIG_TRAF2_1 | 932 | 935 | PF00917 | 0.353 |
LIG_ULM_U2AF65_1 | 304 | 309 | PF00076 | 0.360 |
LIG_WRC_WIRS_1 | 887 | 892 | PF05994 | 0.273 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.622 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.434 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.429 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.350 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.567 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.419 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.547 |
MOD_CK1_1 | 918 | 924 | PF00069 | 0.466 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.522 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.504 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.592 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.337 |
MOD_CK2_1 | 919 | 925 | PF00069 | 0.532 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.633 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.586 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.466 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.401 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.302 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.560 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.593 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.542 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.404 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.515 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.549 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.571 |
MOD_GlcNHglycan | 917 | 920 | PF01048 | 0.513 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.480 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.577 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.596 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.477 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.654 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.544 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.429 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.549 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.554 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.468 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.447 |
MOD_N-GLC_1 | 945 | 950 | PF02516 | 0.473 |
MOD_N-GLC_2 | 20 | 22 | PF02516 | 0.495 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.558 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.535 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.508 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.372 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.508 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.571 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.319 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.540 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.363 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.325 |
MOD_NEK2_1 | 945 | 950 | PF00069 | 0.406 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.532 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.599 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.560 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.550 |
MOD_PIKK_1 | 762 | 768 | PF00454 | 0.530 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.537 |
MOD_PIKK_1 | 786 | 792 | PF00454 | 0.401 |
MOD_PK_1 | 108 | 114 | PF00069 | 0.557 |
MOD_PKA_1 | 572 | 578 | PF00069 | 0.359 |
MOD_PKA_1 | 786 | 792 | PF00069 | 0.371 |
MOD_PKA_1 | 865 | 871 | PF00069 | 0.357 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.575 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.532 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.512 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.327 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.570 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.407 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.385 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.549 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.379 |
MOD_PKA_2 | 865 | 871 | PF00069 | 0.382 |
MOD_PKA_2 | 915 | 921 | PF00069 | 0.453 |
MOD_PKB_1 | 570 | 578 | PF00069 | 0.358 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.559 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.481 |
MOD_Plk_1 | 730 | 736 | PF00069 | 0.468 |
MOD_Plk_1 | 870 | 876 | PF00069 | 0.393 |
MOD_Plk_1 | 945 | 951 | PF00069 | 0.435 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.313 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.414 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.377 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.489 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.526 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.547 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.275 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.422 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.367 |
MOD_Plk_4 | 889 | 895 | PF00069 | 0.500 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.574 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.465 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.408 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.538 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.384 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.631 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.464 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.356 |
MOD_ProDKin_1 | 919 | 925 | PF00069 | 0.448 |
MOD_SUMO_for_1 | 971 | 974 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 36 | 40 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 965 | 973 | PF00179 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 497 | 502 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 691 | 694 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 835 | 838 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 604 | 606 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 854 | 857 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 865 | 867 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 880 | 882 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 902 | 914 | PF08389 | 0.268 |
TRG_NLS_MonoExtN_4 | 301 | 308 | PF00514 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 30% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 35% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 80% | 100% |
A0A3S7WT86 | Leishmania donovani | 34% | 96% |
A0A3S7WWA6 | Leishmania donovani | 30% | 100% |
A0A451EJD9 | Leishmania donovani | 33% | 100% |
A0A451EJF4 | Leishmania donovani | 33% | 100% |
A0A451EJF6 | Leishmania donovani | 36% | 100% |
A0A451EJF8 | Leishmania donovani | 33% | 100% |
A0A451EJF9 | Leishmania donovani | 36% | 100% |
A4H3A9 | Leishmania braziliensis | 36% | 100% |
A4H3B4 | Leishmania braziliensis | 37% | 100% |
A4H3B6 | Leishmania braziliensis | 37% | 100% |
A4H3B7 | Leishmania braziliensis | 35% | 93% |
A4H3B8 | Leishmania braziliensis | 38% | 100% |
A4H3B9 | Leishmania braziliensis | 62% | 100% |
A4H4W8 | Leishmania braziliensis | 33% | 100% |
A4HJ20 | Leishmania braziliensis | 36% | 100% |
A4HNK6 | Leishmania braziliensis | 32% | 100% |
A4HRL9 | Leishmania infantum | 34% | 100% |
A4HRM0 | Leishmania infantum | 35% | 100% |
A4HRM1 | Leishmania infantum | 36% | 100% |
A4HRS1 | Leishmania infantum | 36% | 100% |
A4HRS3 | Leishmania infantum | 80% | 100% |
A4HRS5 | Leishmania infantum | 33% | 100% |
A4HW87 | Leishmania infantum | 34% | 73% |
A4HZM0 | Leishmania infantum | 30% | 100% |
A4I7C7 | Leishmania infantum | 32% | 100% |
A4IAQ2 | Leishmania infantum | 32% | 100% |
E9AC91 | Leishmania major | 37% | 100% |
E9AC92 | Leishmania major | 36% | 100% |
E9AC94 | Leishmania major | 79% | 100% |
E9AC95 | Leishmania major | 36% | 100% |
E9AC96 | Leishmania major | 36% | 100% |
E9AC98 | Leishmania major | 79% | 100% |
E9AEH8 | Leishmania major | 31% | 100% |
E9AHA6 | Leishmania infantum | 31% | 100% |
E9AIP8 | Leishmania braziliensis | 32% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q5T6 | Leishmania major | 30% | 100% |
Q4QCL8 | Leishmania major | 32% | 100% |
Q4QFJ3 | Leishmania major | 36% | 100% |
Q4QIG9 | Leishmania major | 31% | 100% |
Q7YXU9 | Leishmania major | 31% | 100% |
Q7YXV1 | Leishmania major | 32% | 100% |
Q7YXV2 | Leishmania major | 30% | 100% |