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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0000428 | DNA-directed RNA polymerase complex | 4 | 1 |
GO:0030880 | RNA polymerase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEF3
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 8 |
GO:0006505 | GPI anchor metabolic process | 6 | 8 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 8 |
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006643 | membrane lipid metabolic process | 4 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 8 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 8 |
GO:0006664 | glycolipid metabolic process | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 8 |
GO:0008654 | phospholipid biosynthetic process | 5 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009247 | glycolipid biosynthetic process | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044249 | cellular biosynthetic process | 3 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 8 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 8 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 8 |
GO:0046486 | glycerolipid metabolic process | 4 | 8 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090407 | organophosphate biosynthetic process | 4 | 8 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 8 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
GO:1903509 | liposaccharide metabolic process | 4 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.462 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.812 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 689 | 691 | PF00082 | 0.306 |
CLV_PCSK_PC7_1 | 210 | 216 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.464 |
DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 668 | 676 | PF00400 | 0.383 |
DEG_Kelch_Keap1_1 | 236 | 241 | PF01344 | 0.527 |
DEG_SCF_FBW7_2 | 868 | 874 | PF00400 | 0.752 |
DEG_SIAH_1 | 356 | 364 | PF03145 | 0.528 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.494 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.469 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.495 |
DOC_CKS1_1 | 868 | 873 | PF01111 | 0.748 |
DOC_CYCLIN_RxL_1 | 427 | 437 | PF00134 | 0.375 |
DOC_CYCLIN_RxL_1 | 666 | 673 | PF00134 | 0.383 |
DOC_CYCLIN_yClb1_LxF_4 | 362 | 367 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 747 | 753 | PF00134 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 807 | 813 | PF00134 | 0.679 |
DOC_MAPK_FxFP_2 | 713 | 716 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 328 | 338 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 433 | 442 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 761 | 770 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 373 | 380 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 489 | 498 | PF00069 | 0.288 |
DOC_PP1_RVXF_1 | 362 | 368 | PF00149 | 0.485 |
DOC_PP1_RVXF_1 | 428 | 435 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 747 | 750 | PF13499 | 0.383 |
DOC_PP2B_LxvP_1 | 807 | 810 | PF13499 | 0.603 |
DOC_PP4_FxxP_1 | 713 | 716 | PF00568 | 0.383 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.383 |
DOC_USP7_UBL2_3 | 875 | 879 | PF12436 | 0.752 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 860 | 865 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 867 | 872 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 287 | 296 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 331 | 338 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 433 | 443 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 444 | 452 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 865 | 869 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 418 | 435 | PF00022 | 0.378 |
LIG_Actin_WH2_2 | 551 | 569 | PF00022 | 0.564 |
LIG_BRCT_BRCA1_1 | 603 | 607 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 622 | 626 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.407 |
LIG_deltaCOP1_diTrp_1 | 248 | 255 | PF00928 | 0.527 |
LIG_deltaCOP1_diTrp_1 | 560 | 568 | PF00928 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 620 | 626 | PF00928 | 0.506 |
LIG_DLG_GKlike_1 | 112 | 119 | PF00625 | 0.402 |
LIG_EH1_1 | 695 | 703 | PF00400 | 0.502 |
LIG_eIF4E_1 | 116 | 122 | PF01652 | 0.389 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.557 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.467 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.482 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.417 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.372 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.420 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.353 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.286 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.343 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.610 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.613 |
LIG_FHA_1 | 857 | 863 | PF00498 | 0.572 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.350 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.609 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.542 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.463 |
LIG_FHA_2 | 735 | 741 | PF00498 | 0.323 |
LIG_LIR_Apic_2 | 603 | 609 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 115 | 126 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 396 | 405 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 560 | 570 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 620 | 628 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 705 | 716 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 741 | 751 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 816 | 826 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 96 | 106 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 532 | 537 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 560 | 565 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 705 | 711 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 741 | 747 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.325 |
LIG_LYPXL_SIV_4 | 664 | 672 | PF13949 | 0.383 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.363 |
LIG_PCNA_yPIPBox_3 | 187 | 201 | PF02747 | 0.507 |
LIG_Pex14_1 | 251 | 255 | PF04695 | 0.527 |
LIG_Pex14_1 | 533 | 537 | PF04695 | 0.486 |
LIG_PTB_Apo_2 | 255 | 262 | PF02174 | 0.453 |
LIG_REV1ctd_RIR_1 | 551 | 560 | PF16727 | 0.523 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.434 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.410 |
LIG_SH2_CRK | 684 | 688 | PF00017 | 0.480 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.393 |
LIG_SH2_GRB2like | 79 | 82 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 41 | 44 | PF00017 | 0.375 |
LIG_SH2_PTP2 | 480 | 483 | PF00017 | 0.323 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 694 | 697 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 744 | 747 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 845 | 848 | PF00017 | 0.604 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.518 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.368 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.293 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.481 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.441 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 797 | 803 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 820 | 825 | PF11976 | 0.477 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.461 |
LIG_TRAF2_1 | 291 | 294 | PF00917 | 0.549 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.383 |
LIG_TYR_ITIM | 682 | 687 | PF00017 | 0.523 |
LIG_TYR_ITIM | 742 | 747 | PF00017 | 0.383 |
LIG_TYR_ITIM | 77 | 82 | PF00017 | 0.393 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.523 |
LIG_WRC_WIRS_1 | 724 | 729 | PF05994 | 0.305 |
LIG_WW_3 | 361 | 365 | PF00397 | 0.533 |
MOD_CDC14_SPxK_1 | 872 | 875 | PF00782 | 0.701 |
MOD_CDK_SPK_2 | 860 | 865 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 869 | 875 | PF00069 | 0.691 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.539 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.596 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.479 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.523 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.594 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.323 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.465 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.473 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.489 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.575 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.542 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.434 |
MOD_CK2_1 | 734 | 740 | PF00069 | 0.323 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.461 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.660 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.648 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.677 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.693 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.734 |
MOD_GlcNHglycan | 302 | 306 | PF01048 | 0.795 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.774 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.383 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.281 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.449 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.658 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.424 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.496 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.503 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.528 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.539 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.510 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.294 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.540 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.323 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.364 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.631 |
MOD_GSK3_1 | 809 | 816 | PF00069 | 0.539 |
MOD_GSK3_1 | 856 | 863 | PF00069 | 0.562 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.432 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.700 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.605 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.728 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.564 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.591 |
MOD_N-GLC_2 | 589 | 591 | PF02516 | 0.296 |
MOD_N-GLC_2 | 98 | 100 | PF02516 | 0.678 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.465 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.519 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.521 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.434 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.474 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.237 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.383 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.343 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.323 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.270 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.515 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.430 |
MOD_NEK2_2 | 648 | 653 | PF00069 | 0.323 |
MOD_NEK2_2 | 743 | 748 | PF00069 | 0.425 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.526 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.353 |
MOD_PK_1 | 151 | 157 | PF00069 | 0.473 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.407 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.445 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.489 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.571 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.367 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.351 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.513 |
MOD_PKA_2 | 864 | 870 | PF00069 | 0.646 |
MOD_PKB_1 | 329 | 337 | PF00069 | 0.481 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.510 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.523 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.536 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.397 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.560 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.527 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.516 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.267 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.414 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.425 |
MOD_Plk_1 | 800 | 806 | PF00069 | 0.591 |
MOD_Plk_1 | 822 | 828 | PF00069 | 0.526 |
MOD_Plk_2-3 | 294 | 300 | PF00069 | 0.554 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.405 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.429 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.539 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.577 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.465 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.411 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.375 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.383 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.523 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.606 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.516 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.323 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.239 |
MOD_Plk_4 | 833 | 839 | PF00069 | 0.650 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.494 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.523 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.523 |
MOD_ProDKin_1 | 860 | 866 | PF00069 | 0.693 |
MOD_ProDKin_1 | 867 | 873 | PF00069 | 0.700 |
MOD_SUMO_for_1 | 56 | 59 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_2 | 374 | 380 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_2 | 446 | 452 | PF01217 | 0.352 |
TRG_DiLeu_BaEn_4 | 293 | 299 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 744 | 747 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 687 | 690 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 761 | 764 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 778 | 780 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 839 | 842 | PF00400 | 0.611 |
TRG_ER_diLys_1 | 879 | 882 | PF00400 | 0.697 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C0 | Leptomonas seymouri | 67% | 98% |
A0A0S4IQS6 | Bodo saltans | 25% | 100% |
A4HHK2 | Leishmania braziliensis | 78% | 100% |
E9AE65 | Leishmania major | 95% | 100% |
E9AHJ3 | Leishmania infantum | 99% | 100% |
E9ALM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |