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: 55 |
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: 49 |
NetGPI | no | yes: 0, no: 49 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 15 |
GO:0016020 | membrane | 2 | 50 |
GO:0031090 | organelle membrane | 3 | 15 |
GO:0098588 | bounding membrane of organelle | 4 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 50 |
Related structures:
AlphaFold database: E9AC98
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 50 |
GO:0006807 | nitrogen compound metabolic process | 2 | 50 |
GO:0008152 | metabolic process | 1 | 50 |
GO:0019538 | protein metabolic process | 3 | 50 |
GO:0036211 | protein modification process | 4 | 50 |
GO:0043170 | macromolecule metabolic process | 3 | 50 |
GO:0043412 | macromolecule modification | 4 | 50 |
GO:0043413 | macromolecule glycosylation | 3 | 50 |
GO:0044238 | primary metabolic process | 2 | 50 |
GO:0070085 | glycosylation | 2 | 50 |
GO:0071704 | organic substance metabolic process | 2 | 50 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 50 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 50 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 15 |
GO:0016740 | transferase activity | 2 | 50 |
GO:0016757 | glycosyltransferase activity | 3 | 50 |
GO:0016758 | hexosyltransferase activity | 4 | 50 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.328 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.296 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.395 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 868 | 870 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 884 | 886 | PF00675 | 0.556 |
CLV_PCSK_FUR_1 | 240 | 244 | PF00082 | 0.410 |
CLV_PCSK_FUR_1 | 272 | 276 | PF00082 | 0.588 |
CLV_PCSK_FUR_1 | 574 | 578 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 661 | 663 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 868 | 870 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 884 | 886 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 868 | 872 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 439 | 443 | PF03568 | 0.356 |
DEG_APCC_DBOX_1 | 609 | 617 | PF00400 | 0.324 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 620 | 626 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 963 | 969 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 239 | 247 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 304 | 311 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 817 | 827 | PF00069 | 0.312 |
DOC_MAPK_JIP1_4 | 975 | 981 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 201 | 209 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 248 | 255 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 705 | 714 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 302 | 309 | PF00149 | 0.403 |
DOC_PP1_RVXF_1 | 683 | 690 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 770 | 773 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 963 | 966 | PF13499 | 0.389 |
DOC_PP2B_PxIxI_1 | 461 | 467 | PF00149 | 0.282 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.619 |
DOC_PP4_FxxP_1 | 539 | 542 | PF00568 | 0.363 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.430 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 899 | 904 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 922 | 927 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 199 | 209 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 485 | 489 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 576 | 581 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 585 | 593 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 888 | 894 | PF00244 | 0.339 |
LIG_Actin_WH2_2 | 302 | 319 | PF00022 | 0.361 |
LIG_Actin_WH2_2 | 433 | 449 | PF00022 | 0.377 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.650 |
LIG_BIR_III_2 | 973 | 977 | PF00653 | 0.375 |
LIG_BIR_III_4 | 886 | 890 | PF00653 | 0.346 |
LIG_Clathr_ClatBox_1 | 260 | 264 | PF01394 | 0.222 |
LIG_EVH1_1 | 97 | 101 | PF00568 | 0.637 |
LIG_EVH1_2 | 100 | 104 | PF00568 | 0.625 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.661 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.463 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.508 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.368 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.412 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.493 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.416 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.332 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.242 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.325 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.351 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.671 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.642 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.587 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.497 |
LIG_FHA_2 | 842 | 848 | PF00498 | 0.304 |
LIG_FHA_2 | 869 | 875 | PF00498 | 0.320 |
LIG_FHA_2 | 900 | 906 | PF00498 | 0.322 |
LIG_FHA_2 | 923 | 929 | PF00498 | 0.392 |
LIG_Integrin_RGD_1 | 669 | 671 | PF01839 | 0.595 |
LIG_LIR_Apic_2 | 538 | 542 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 264 | 273 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 461 | 469 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 651 | 659 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 691 | 702 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 708 | 718 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 719 | 725 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 836 | 843 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 878 | 887 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 892 | 898 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 686 | 692 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 708 | 714 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 719 | 724 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 829 | 833 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 836 | 841 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 878 | 883 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 892 | 896 | PF02991 | 0.388 |
LIG_NRBOX | 395 | 401 | PF00104 | 0.379 |
LIG_PDZ_Class_2 | 987 | 992 | PF00595 | 0.302 |
LIG_Pex14_1 | 219 | 223 | PF04695 | 0.578 |
LIG_Pex14_2 | 830 | 834 | PF04695 | 0.306 |
LIG_PTB_Apo_2 | 326 | 333 | PF02174 | 0.395 |
LIG_PTB_Apo_2 | 828 | 835 | PF02174 | 0.327 |
LIG_PTB_Phospho_1 | 326 | 332 | PF10480 | 0.391 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.338 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.275 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 491 | 495 | PF00017 | 0.275 |
LIG_SH2_NCK_1 | 707 | 711 | PF00017 | 0.252 |
LIG_SH2_NCK_1 | 838 | 842 | PF00017 | 0.298 |
LIG_SH2_PTP2 | 463 | 466 | PF00017 | 0.271 |
LIG_SH2_PTP2 | 711 | 714 | PF00017 | 0.314 |
LIG_SH2_SRC | 332 | 335 | PF00017 | 0.361 |
LIG_SH2_SRC | 692 | 695 | PF00017 | 0.362 |
LIG_SH2_SRC | 707 | 710 | PF00017 | 0.259 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 407 | 411 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 692 | 696 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 707 | 711 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 838 | 842 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 908 | 911 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 913 | 916 | PF00017 | 0.424 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.653 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.636 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.420 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.426 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.494 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.398 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.319 |
LIG_SH3_3 | 770 | 776 | PF00018 | 0.403 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.663 |
LIG_SUMO_SIM_anti_2 | 13 | 19 | PF11976 | 0.632 |
LIG_SUMO_SIM_anti_2 | 284 | 289 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 821 | 826 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 823 | 829 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 977 | 983 | PF11976 | 0.313 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.632 |
LIG_TRAF2_1 | 512 | 515 | PF00917 | 0.295 |
LIG_TRAF2_1 | 543 | 546 | PF00917 | 0.344 |
LIG_TYR_ITIM | 489 | 494 | PF00017 | 0.543 |
LIG_ULM_U2AF65_1 | 304 | 309 | PF00076 | 0.457 |
LIG_WRC_WIRS_1 | 568 | 573 | PF05994 | 0.379 |
MOD_CDK_SPK_2 | 605 | 610 | PF00069 | 0.435 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.603 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.467 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.484 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.345 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.567 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.433 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.377 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.537 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.421 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.592 |
MOD_CK1_1 | 921 | 927 | PF00069 | 0.474 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.566 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.656 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.427 |
MOD_CK2_1 | 922 | 928 | PF00069 | 0.546 |
MOD_Cter_Amidation | 726 | 729 | PF01082 | 0.423 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.547 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.505 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.533 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.309 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.547 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.450 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.581 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.550 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.397 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.580 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.567 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.538 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.516 |
MOD_GlcNHglycan | 967 | 970 | PF01048 | 0.514 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.588 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.498 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.620 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.522 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.539 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.416 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.556 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.305 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.545 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.574 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.495 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.514 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.495 |
MOD_N-GLC_1 | 948 | 953 | PF02516 | 0.480 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.585 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.566 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.369 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.582 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.550 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.322 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.444 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.336 |
MOD_NEK2_1 | 849 | 854 | PF00069 | 0.327 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.652 |
MOD_NEK2_2 | 754 | 759 | PF00069 | 0.524 |
MOD_NEK2_2 | 823 | 828 | PF00069 | 0.333 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.493 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.572 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.549 |
MOD_PIKK_1 | 765 | 771 | PF00454 | 0.523 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.564 |
MOD_PK_1 | 39 | 45 | PF00069 | 0.503 |
MOD_PK_1 | 447 | 453 | PF00069 | 0.367 |
MOD_PKA_1 | 576 | 582 | PF00069 | 0.364 |
MOD_PKA_1 | 661 | 667 | PF00069 | 0.698 |
MOD_PKA_1 | 868 | 874 | PF00069 | 0.370 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.575 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.530 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.475 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.316 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.571 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.456 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.392 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.411 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.640 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.582 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.577 |
MOD_PKA_2 | 868 | 874 | PF00069 | 0.397 |
MOD_PKA_2 | 918 | 924 | PF00069 | 0.465 |
MOD_PKB_1 | 574 | 582 | PF00069 | 0.367 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.462 |
MOD_Plk_1 | 873 | 879 | PF00069 | 0.409 |
MOD_Plk_1 | 948 | 954 | PF00069 | 0.444 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.576 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.513 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.320 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.506 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.409 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.493 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.544 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.537 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.368 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.585 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.417 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.634 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.403 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.471 |
MOD_ProDKin_1 | 899 | 905 | PF00069 | 0.388 |
MOD_ProDKin_1 | 922 | 928 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 665 | 668 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 968 | 976 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_2 | 844 | 850 | PF01217 | 0.327 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 501 | 506 | PF01217 | 0.294 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 838 | 841 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 728 | 731 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 857 | 860 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 868 | 870 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 883 | 885 | PF00400 | 0.415 |
TRG_NLS_MonoExtN_4 | 239 | 246 | PF00514 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 633 | 637 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 33% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 35% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 91% | 100% |
A0A3S7WT86 | Leishmania donovani | 36% | 100% |
A0A3S7WWA6 | Leishmania donovani | 33% | 100% |
A0A451EJD9 | Leishmania donovani | 32% | 100% |
A0A451EJF4 | Leishmania donovani | 35% | 100% |
A0A451EJF8 | Leishmania donovani | 35% | 100% |
A0A451EJF9 | Leishmania donovani | 38% | 100% |
A4H3A9 | Leishmania braziliensis | 38% | 100% |
A4H3B4 | Leishmania braziliensis | 39% | 100% |
A4H3B6 | Leishmania braziliensis | 38% | 100% |
A4H3B8 | Leishmania braziliensis | 40% | 100% |
A4H3B9 | Leishmania braziliensis | 64% | 100% |
A4H4W8 | Leishmania braziliensis | 33% | 100% |
A4HJ20 | Leishmania braziliensis | 38% | 100% |
A4HNK6 | Leishmania braziliensis | 33% | 100% |
A4HRL9 | Leishmania infantum | 34% | 100% |
A4HRM0 | Leishmania infantum | 35% | 100% |
A4HRS1 | Leishmania infantum | 38% | 100% |
A4HRS3 | Leishmania infantum | 91% | 100% |
A4HRS5 | Leishmania infantum | 35% | 100% |
A4HZM0 | Leishmania infantum | 32% | 100% |
A4I7C7 | Leishmania infantum | 33% | 100% |
A4IAQ2 | Leishmania infantum | 32% | 100% |
E9AC91 | Leishmania major | 38% | 100% |
E9AC92 | Leishmania major | 38% | 100% |
E9AC94 | Leishmania major | 100% | 100% |
E9AC95 | Leishmania major | 34% | 93% |
E9AC96 | Leishmania major | 38% | 100% |
E9AEH8 | Leishmania major | 33% | 100% |
E9AHA6 | Leishmania infantum | 32% | 100% |
E9AIP8 | Leishmania braziliensis | 31% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q4Q5T6 | Leishmania major | 32% | 100% |
Q4QCL8 | Leishmania major | 32% | 100% |
Q4QFJ3 | Leishmania major | 37% | 96% |
Q4QIG9 | Leishmania major | 32% | 100% |
Q7YXU9 | Leishmania major | 33% | 100% |
Q7YXV1 | Leishmania major | 33% | 100% |
Q7YXV2 | Leishmania major | 32% | 100% |