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 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9B4U5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0030258 | lipid modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0046839 | phospholipid dephosphorylation | 5 | 7 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046164 | alcohol catabolic process | 4 | 1 |
GO:0046174 | polyol catabolic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 1 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0004439 | phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | 8 | 1 |
GO:0034593 | phosphatidylinositol bisphosphate phosphatase activity | 7 | 1 |
GO:0034595 | phosphatidylinositol phosphate 5-phosphatase activity | 7 | 1 |
GO:0052866 | phosphatidylinositol phosphate phosphatase activity | 6 | 1 |
GO:0106019 | phosphatidylinositol-4,5-bisphosphate phosphatase activity | 8 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.355 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.668 |
CLV_PCSK_FUR_1 | 529 | 533 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.722 |
CLV_PCSK_PC7_1 | 112 | 118 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.641 |
CLV_Separin_Metazoa | 174 | 178 | PF03568 | 0.249 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 616 | 620 | PF00917 | 0.567 |
DOC_CYCLIN_RxL_1 | 77 | 88 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 137 | 143 | PF00134 | 0.396 |
DOC_CYCLIN_yCln2_LP_2 | 610 | 616 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 301 | 308 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 733 | 743 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 77 | 86 | PF00069 | 0.519 |
DOC_MAPK_HePTP_8 | 341 | 353 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 21 | 29 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 77 | 86 | PF00069 | 0.479 |
DOC_MIT_MIM_1 | 461 | 469 | PF04212 | 0.349 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.356 |
DOC_PP1_RVXF_1 | 537 | 543 | PF00149 | 0.294 |
DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.412 |
DOC_PP2B_LxvP_1 | 703 | 706 | PF13499 | 0.529 |
DOC_PP4_FxxP_1 | 388 | 391 | PF00568 | 0.387 |
DOC_PP4_FxxP_1 | 569 | 572 | PF00568 | 0.571 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.553 |
DOC_SPAK_OSR1_1 | 738 | 742 | PF12202 | 0.355 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.262 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.400 |
DOC_USP7_UBL2_3 | 369 | 373 | PF12436 | 0.429 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 224 | 232 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 728 | 735 | PF00244 | 0.312 |
LIG_AP2alpha_1 | 253 | 257 | PF02296 | 0.321 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 565 | 569 | PF00533 | 0.567 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 243 | 253 | PF00928 | 0.370 |
LIG_deltaCOP1_diTrp_1 | 507 | 512 | PF00928 | 0.367 |
LIG_deltaCOP1_diTrp_1 | 533 | 542 | PF00928 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 677 | 685 | PF00928 | 0.360 |
LIG_eIF4E_1 | 354 | 360 | PF01652 | 0.312 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.386 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.332 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.362 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.205 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.490 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.406 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.356 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.528 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.417 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.580 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.426 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.503 |
LIG_FHA_2 | 620 | 626 | PF00498 | 0.569 |
LIG_HCF-1_HBM_1 | 452 | 455 | PF13415 | 0.351 |
LIG_LIR_Apic_2 | 385 | 391 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 566 | 572 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 656 | 662 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 677 | 683 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 243 | 254 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 424 | 432 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 482 | 487 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 507 | 516 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 589 | 598 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 482 | 486 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 507 | 512 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 707 | 712 | PF02991 | 0.454 |
LIG_PCNA_yPIPBox_3 | 116 | 129 | PF02747 | 0.326 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.471 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.321 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.518 |
LIG_Pex14_2 | 505 | 509 | PF04695 | 0.367 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.319 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 483 | 486 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 158 | 162 | PF00017 | 0.349 |
LIG_SH2_NCK_1 | 721 | 725 | PF00017 | 0.334 |
LIG_SH2_SRC | 158 | 161 | PF00017 | 0.361 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.284 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 23 | 28 | PF11976 | 0.205 |
LIG_SUMO_SIM_anti_2 | 701 | 707 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 32 | 38 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 701 | 707 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 742 | 747 | PF11976 | 0.378 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.287 |
LIG_TRAF2_1 | 594 | 597 | PF00917 | 0.535 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.317 |
LIG_UBA3_1 | 313 | 320 | PF00899 | 0.333 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.362 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.513 |
LIG_WW_1 | 155 | 158 | PF00397 | 0.421 |
LIG_WW_1 | 513 | 516 | PF00397 | 0.302 |
MOD_CDK_SPxxK_3 | 468 | 475 | PF00069 | 0.421 |
MOD_CDK_SPxxK_3 | 49 | 56 | PF00069 | 0.522 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.409 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.547 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.481 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.519 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.458 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.462 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.500 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.283 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.409 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.529 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.562 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.498 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.526 |
MOD_Cter_Amidation | 354 | 357 | PF01082 | 0.507 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.768 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.523 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.648 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.697 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.510 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.556 |
MOD_GlcNHglycan | 564 | 568 | PF01048 | 0.705 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.788 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.768 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.730 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.726 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.670 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.719 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.593 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.513 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.496 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.350 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.374 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.503 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.391 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.360 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.460 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.504 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.491 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.377 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.450 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.441 |
MOD_N-GLC_2 | 144 | 146 | PF02516 | 0.574 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.508 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.383 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.322 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.420 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.334 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.195 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.280 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.497 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.400 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.538 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.456 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.489 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.488 |
MOD_NEK2_2 | 723 | 728 | PF00069 | 0.412 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.402 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.487 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.535 |
MOD_PKA_1 | 223 | 229 | PF00069 | 0.470 |
MOD_PKA_1 | 373 | 379 | PF00069 | 0.383 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.446 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.282 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.503 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.336 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.302 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.416 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.443 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.390 |
MOD_PKA_2 | 727 | 733 | PF00069 | 0.315 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.567 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.515 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.487 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.548 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.342 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.409 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.246 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.416 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.260 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.401 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.538 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.477 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.423 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.487 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.607 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.426 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 174 | 184 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 245 | 254 | PF00179 | 0.386 |
MOD_SUMO_rev_2 | 294 | 303 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 594 | 603 | PF00179 | 0.544 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.330 |
TRG_DiLeu_BaEn_1 | 491 | 496 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 469 | 474 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 529 | 532 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 735 | 738 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.485 |
TRG_ER_FFAT_2 | 435 | 447 | PF00635 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 543 | 548 | PF00026 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 631 | 636 | PF00026 | 0.779 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDQ6 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IFD8 | Leishmania donovani | 90% | 100% |
A0A422NU02 | Trypanosoma rangeli | 36% | 99% |
A4I9T4 | Leishmania infantum | 90% | 100% |
Q4Q381 | Leishmania major | 89% | 100% |