Glycosylation, alpha glucosidase II subunit
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: 5 |
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 | yes | yes: 11, no: 0 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S5H722
Term | Name | Level | Count |
---|---|---|---|
GO:0006491 | N-glycan processing | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009100 | glycoprotein metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:0005975 | carbohydrate metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 12 |
GO:0004558 | alpha-1,4-glucosidase activity | 7 | 7 |
GO:0005488 | binding | 1 | 12 |
GO:0015926 | glucosidase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 12 |
GO:0030246 | carbohydrate binding | 2 | 12 |
GO:0032450 | maltose alpha-glucosidase activity | 8 | 7 |
GO:0090599 | alpha-glucosidase activity | 6 | 8 |
GO:0033919 | glucan 1,3-alpha-glucosidase activity | 8 | 1 |
GO:0090600 | alpha-1,3-glucosidase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.437 |
CLV_PCSK_FUR_1 | 676 | 680 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.336 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.626 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.372 |
DOC_CDC14_PxL_1 | 569 | 577 | PF14671 | 0.321 |
DOC_CKS1_1 | 779 | 784 | PF01111 | 0.567 |
DOC_CYCLIN_RxL_1 | 588 | 596 | PF00134 | 0.307 |
DOC_MAPK_FxFP_2 | 127 | 130 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 316 | 323 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 795 | 801 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.296 |
DOC_PP2B_PxIxI_1 | 613 | 619 | PF00149 | 0.426 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.321 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.292 |
DOC_PP4_FxxP_1 | 516 | 519 | PF00568 | 0.298 |
DOC_PP4_MxPP_1 | 94 | 97 | PF00568 | 0.441 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 741 | 745 | PF00917 | 0.568 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.550 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 599 | 606 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 676 | 686 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 723 | 728 | PF00244 | 0.306 |
LIG_AP2alpha_2 | 687 | 689 | PF02296 | 0.340 |
LIG_BIR_III_4 | 349 | 353 | PF00653 | 0.452 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 549 | 553 | PF00928 | 0.321 |
LIG_deltaCOP1_diTrp_1 | 636 | 643 | PF00928 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 804 | 809 | PF00928 | 0.432 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.404 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.160 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.395 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.355 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.348 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.305 |
LIG_FHA_1 | 741 | 747 | PF00498 | 0.587 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.378 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.390 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.305 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.340 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.238 |
LIG_FHA_2 | 709 | 715 | PF00498 | 0.380 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.509 |
LIG_FHA_2 | 779 | 785 | PF00498 | 0.393 |
LIG_IRF3_LxIS_1 | 497 | 503 | PF10401 | 0.366 |
LIG_KLC1_Yacidic_2 | 704 | 708 | PF13176 | 0.426 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.418 |
LIG_LIR_Apic_2 | 220 | 225 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 78 | 84 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 396 | 405 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 687 | 697 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 744 | 753 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 784 | 793 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 636 | 642 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 687 | 692 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 701 | 705 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 744 | 750 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 784 | 788 | PF02991 | 0.485 |
LIG_MLH1_MIPbox_1 | 378 | 382 | PF16413 | 0.375 |
LIG_Pex14_1 | 366 | 370 | PF04695 | 0.277 |
LIG_Pex14_1 | 377 | 381 | PF04695 | 0.322 |
LIG_Pex14_1 | 639 | 643 | PF04695 | 0.390 |
LIG_Pex14_1 | 805 | 809 | PF04695 | 0.456 |
LIG_PTB_Apo_2 | 501 | 508 | PF02174 | 0.305 |
LIG_PTB_Apo_2 | 731 | 738 | PF02174 | 0.474 |
LIG_PTB_Phospho_1 | 731 | 737 | PF10480 | 0.454 |
LIG_REV1ctd_RIR_1 | 367 | 377 | PF16727 | 0.238 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.298 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.305 |
LIG_SH2_CRK | 747 | 751 | PF00017 | 0.436 |
LIG_SH2_CRK | 759 | 763 | PF00017 | 0.396 |
LIG_SH2_GRB2like | 260 | 263 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 727 | 730 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 747 | 751 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 727 | 731 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 727 | 730 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.502 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.422 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.390 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.305 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.353 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.360 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.288 |
LIG_SH3_3 | 735 | 741 | PF00018 | 0.567 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.580 |
LIG_SH3_3 | 791 | 797 | PF00018 | 0.266 |
LIG_SH3_4 | 50 | 57 | PF00018 | 0.518 |
LIG_SUMO_SIM_anti_2 | 22 | 30 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 12 | 19 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 319 | 325 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.487 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.321 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.305 |
LIG_TYR_ITIM | 757 | 762 | PF00017 | 0.482 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.390 |
LIG_WRC_WIRS_1 | 806 | 811 | PF05994 | 0.497 |
MOD_CDK_SPxK_1 | 225 | 231 | PF00069 | 0.372 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.421 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.565 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.481 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.339 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.283 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.483 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.487 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.426 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.238 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.321 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.411 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.519 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.305 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.468 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.486 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.393 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.300 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.260 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.225 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.361 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.536 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.517 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.352 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.594 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.375 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.563 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.429 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.321 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.333 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.356 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.400 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.462 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.511 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.549 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.433 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.404 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.663 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.457 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.414 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.380 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.420 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.326 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.340 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.305 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.305 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.319 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.294 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.420 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.448 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.342 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.387 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.493 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.392 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.389 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.452 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.340 |
MOD_PK_1 | 795 | 801 | PF00069 | 0.402 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.356 |
MOD_PKA_1 | 795 | 801 | PF00069 | 0.402 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.584 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.375 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.422 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.238 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.364 |
MOD_PKB_1 | 676 | 684 | PF00069 | 0.362 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.453 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.379 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.390 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.368 |
MOD_Plk_2-3 | 265 | 271 | PF00069 | 0.390 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.360 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.321 |
MOD_Plk_2-3 | 709 | 715 | PF00069 | 0.369 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.411 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.464 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.477 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.327 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.390 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.296 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.329 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.356 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.156 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.390 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.304 |
MOD_Plk_4 | 788 | 794 | PF00069 | 0.440 |
MOD_Plk_4 | 795 | 801 | PF00069 | 0.419 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.321 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.532 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.552 |
MOD_SUMO_rev_2 | 299 | 309 | PF00179 | 0.302 |
TRG_DiLeu_BaEn_1 | 556 | 561 | PF01217 | 0.426 |
TRG_DiLeu_BaEn_2 | 519 | 525 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 747 | 750 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 759 | 762 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 675 | 678 | PF00400 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 591 | 596 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5F9 | Leptomonas seymouri | 68% | 99% |
A0A0S4ITP0 | Bodo saltans | 39% | 94% |
A0A0S4JEB6 | Bodo saltans | 47% | 97% |
A0A0S4JFD6 | Bodo saltans | 29% | 85% |
A0A0S4JJL0 | Bodo saltans | 26% | 100% |
A0A1X0P3Y3 | Trypanosomatidae | 30% | 67% |
A0A1X0P7R2 | Trypanosomatidae | 53% | 99% |
A0A3R7MQZ9 | Trypanosoma rangeli | 52% | 99% |
A0A422NT82 | Trypanosoma rangeli | 32% | 77% |
A4H9B4 | Leishmania braziliensis | 82% | 100% |
A4HXN5 | Leishmania infantum | 100% | 100% |
A7LXT0 | Bacteroides ovatus (strain ATCC 8483 / DSM 1896 / JCM 5824 / BCRC 10623 / CCUG 4943 / NCTC 11153) | 27% | 85% |
B9F676 | Oryza sativa subsp. japonica | 43% | 88% |
D0A012 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
D0A8P3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 77% |
D0KQM8 | Saccharolobus solfataricus (strain 98/2) | 32% | 100% |
E9ARE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
F4J6T7 | Arabidopsis thaliana | 31% | 94% |
O00906 | Tetrahymena pyriformis | 26% | 88% |
O04893 | Spinacia oleracea | 32% | 90% |
O04931 | Beta vulgaris | 33% | 89% |
P0CD66 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 32% | 100% |
P10253 | Homo sapiens | 32% | 85% |
P38138 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 85% |
P70699 | Mus musculus | 33% | 85% |
P79403 | Sus scrofa | 44% | 86% |
Q14697 | Homo sapiens | 44% | 86% |
Q43763 | Hordeum vulgare | 32% | 93% |
Q4QE33 | Leishmania major | 93% | 100% |
Q4R4N7 | Macaca fascicularis | 44% | 86% |
Q5AW25 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 100% |
Q5R7A9 | Pongo abelii | 31% | 85% |
Q653V7 | Oryza sativa subsp. japonica | 33% | 92% |
Q6P7A9 | Rattus norvegicus | 33% | 85% |
Q8BHN3 | Mus musculus | 45% | 86% |
Q8BVW0 | Mus musculus | 41% | 90% |
Q8TET4 | Homo sapiens | 41% | 89% |
Q92442 | Mucor javanicus | 28% | 94% |
Q94502 | Dictyostelium discoideum | 43% | 86% |
Q9BE70 | Macaca fascicularis | 43% | 100% |
Q9F234 | Bacillus thermoamyloliquefaciens | 33% | 100% |
Q9FN05 | Arabidopsis thaliana | 41% | 88% |
Q9MYM4 | Bos taurus | 33% | 87% |
Q9P999 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 28% | 100% |
Q9S7Y7 | Arabidopsis thaliana | 30% | 89% |
Q9US55 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 88% |
V5BS12 | Trypanosoma cruzi | 31% | 77% |
V5D5S5 | Trypanosoma cruzi | 53% | 99% |