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. | yes | 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: A4H9B4
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 | 317 | 319 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.424 |
CLV_PCSK_FUR_1 | 676 | 680 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.429 |
DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.447 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 |
DOC_CDC14_PxL_1 | 569 | 577 | PF14671 | 0.307 |
DOC_CKS1_1 | 779 | 784 | PF01111 | 0.465 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.318 |
DOC_CYCLIN_RxL_1 | 588 | 596 | PF00134 | 0.294 |
DOC_MAPK_DCC_7 | 666 | 675 | PF00069 | 0.266 |
DOC_MAPK_FxFP_2 | 127 | 130 | PF00069 | 0.402 |
DOC_MAPK_FxFP_2 | 161 | 164 | PF00069 | 0.215 |
DOC_MAPK_gen_1 | 316 | 323 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 795 | 802 | PF00069 | 0.416 |
DOC_MAPK_JIP1_4 | 796 | 802 | PF00069 | 0.274 |
DOC_MAPK_MEF2A_6 | 3 | 10 | PF00069 | 0.653 |
DOC_MAPK_MEF2A_6 | 666 | 675 | PF00069 | 0.266 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.623 |
DOC_PP2B_PxIxI_1 | 613 | 619 | PF00149 | 0.437 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.396 |
DOC_PP4_FxxP_1 | 161 | 164 | PF00568 | 0.215 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.307 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.292 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.215 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.342 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 676 | 686 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 723 | 728 | PF00244 | 0.293 |
LIG_AP2alpha_2 | 687 | 689 | PF02296 | 0.323 |
LIG_BIR_III_4 | 349 | 353 | PF00653 | 0.357 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 358 | 366 | PF00928 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 376 | 382 | PF00928 | 0.245 |
LIG_deltaCOP1_diTrp_1 | 549 | 553 | PF00928 | 0.307 |
LIG_deltaCOP1_diTrp_1 | 636 | 643 | PF00928 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 804 | 809 | PF00928 | 0.423 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.310 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.437 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.171 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.492 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.424 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.571 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.233 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.343 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.335 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.292 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.498 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.540 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.362 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.268 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.335 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.407 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.304 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.326 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.321 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.494 |
LIG_FHA_2 | 779 | 785 | PF00498 | 0.416 |
LIG_IBAR_NPY_1 | 299 | 301 | PF08397 | 0.236 |
LIG_IRF3_LxIS_1 | 497 | 503 | PF10401 | 0.355 |
LIG_KLC1_Yacidic_2 | 704 | 708 | PF13176 | 0.437 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.396 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.215 |
LIG_LIR_Apic_2 | 220 | 225 | PF02991 | 0.307 |
LIG_LIR_Apic_2 | 302 | 306 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 376 | 383 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 396 | 405 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 437 | 444 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 637 | 648 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 687 | 697 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 784 | 793 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 804 | 812 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 636 | 642 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 687 | 692 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 701 | 705 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 784 | 788 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 804 | 809 | PF02991 | 0.208 |
LIG_Pex14_1 | 639 | 643 | PF04695 | 0.386 |
LIG_Pex14_1 | 805 | 809 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 501 | 508 | PF02174 | 0.292 |
LIG_PTB_Apo_2 | 714 | 721 | PF02174 | 0.236 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.292 |
LIG_SH2_CRK | 378 | 382 | PF00017 | 0.266 |
LIG_SH2_CRK | 439 | 443 | PF00017 | 0.335 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.292 |
LIG_SH2_CRK | 759 | 763 | PF00017 | 0.346 |
LIG_SH2_GRB2like | 40 | 43 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 715 | 718 | PF00017 | 0.271 |
LIG_SH2_GRB2like | 727 | 730 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 569 | 573 | PF00017 | 0.321 |
LIG_SH2_SRC | 383 | 386 | PF00017 | 0.215 |
LIG_SH2_SRC | 715 | 718 | PF00017 | 0.215 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 727 | 731 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 727 | 730 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.517 |
LIG_SH3_1 | 595 | 601 | PF00018 | 0.215 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.439 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.386 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.292 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.340 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.313 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.348 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.277 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 12 | 18 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 4 | 10 | PF11976 | 0.552 |
LIG_SUMO_SIM_anti_2 | 91 | 96 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 12 | 18 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 319 | 325 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 798 | 804 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.402 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.307 |
LIG_TRFH_1 | 569 | 573 | PF08558 | 0.259 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.292 |
LIG_TYR_ITIM | 757 | 762 | PF00017 | 0.386 |
LIG_UBA3_1 | 70 | 74 | PF00899 | 0.327 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.386 |
LIG_WRC_WIRS_1 | 806 | 811 | PF05994 | 0.400 |
MOD_CDK_SPxxK_3 | 93 | 100 | PF00069 | 0.296 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.403 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.455 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.215 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.733 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.326 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.460 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.512 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.335 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.437 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.307 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.321 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.253 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.557 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.292 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.366 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.676 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.283 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.361 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.215 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.350 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.545 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.500 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.447 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.307 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.319 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.399 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.461 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.538 |
MOD_LATS_1 | 327 | 333 | PF00433 | 0.297 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.538 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.428 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.442 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.255 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.658 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.444 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.433 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.215 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.429 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.325 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.215 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.312 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.292 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.292 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.276 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.283 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.405 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.328 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.357 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.335 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.485 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.357 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.326 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.215 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.297 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.340 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.306 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.284 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.398 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.215 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.347 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.479 |
MOD_PKB_1 | 676 | 684 | PF00069 | 0.345 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.472 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.481 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.271 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.386 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.344 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.357 |
MOD_Plk_2-3 | 265 | 271 | PF00069 | 0.386 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.307 |
MOD_Plk_2-3 | 709 | 715 | PF00069 | 0.359 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.430 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.452 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.323 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.300 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.386 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.452 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.284 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.315 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.344 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.188 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.386 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.307 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.226 |
MOD_Plk_4 | 741 | 747 | PF00069 | 0.472 |
MOD_Plk_4 | 788 | 794 | PF00069 | 0.427 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.464 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.307 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.489 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.470 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.314 |
MOD_SUMO_for_1 | 49 | 52 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 556 | 561 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_2 | 519 | 525 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_2 | 715 | 721 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 66 | 71 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.213 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 759 | 762 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 675 | 678 | PF00400 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 591 | 596 | PF00026 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5F9 | Leptomonas seymouri | 68% | 99% |
A0A0S4ITP0 | Bodo saltans | 38% | 94% |
A0A0S4JEB6 | Bodo saltans | 45% | 97% |
A0A0S4JFD6 | Bodo saltans | 28% | 85% |
A0A0S4JJL0 | Bodo saltans | 27% | 100% |
A0A1X0P3Y3 | Trypanosomatidae | 30% | 67% |
A0A1X0P7R2 | Trypanosomatidae | 53% | 99% |
A0A3R7MQZ9 | Trypanosoma rangeli | 51% | 99% |
A0A3S5H722 | Leishmania donovani | 82% | 100% |
A0A422NT82 | Trypanosoma rangeli | 32% | 77% |
A4HXN5 | Leishmania infantum | 82% | 100% |
A7LXT0 | Bacteroides ovatus (strain ATCC 8483 / DSM 1896 / JCM 5824 / BCRC 10623 / CCUG 4943 / NCTC 11153) | 26% | 85% |
B3PEE6 | Cellvibrio japonicus (strain Ueda107) | 26% | 100% |
B9F676 | Oryza sativa subsp. japonica | 42% | 88% |
D0A012 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D0A8P3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 77% |
D0KQM8 | Saccharolobus solfataricus (strain 98/2) | 31% | 100% |
E9ARE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
O00906 | Tetrahymena pyriformis | 24% | 88% |
O04893 | Spinacia oleracea | 32% | 90% |
O04931 | Beta vulgaris | 31% | 89% |
P0CD66 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 31% | 100% |
P10253 | Homo sapiens | 31% | 85% |
P31434 | Escherichia coli (strain K12) | 26% | 100% |
P38138 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 85% |
P70699 | Mus musculus | 33% | 85% |
P79403 | Sus scrofa | 43% | 86% |
P96793 | Lactiplantibacillus pentosus | 25% | 100% |
Q14697 | Homo sapiens | 43% | 86% |
Q43763 | Hordeum vulgare | 30% | 93% |
Q4QE33 | Leishmania major | 82% | 100% |
Q4R4N7 | Macaca fascicularis | 43% | 86% |
Q5AW25 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 24% | 100% |
Q5R7A9 | Pongo abelii | 30% | 85% |
Q653V7 | Oryza sativa subsp. japonica | 32% | 92% |
Q6P7A9 | Rattus norvegicus | 32% | 85% |
Q8BHN3 | Mus musculus | 44% | 86% |
Q8BVW0 | Mus musculus | 40% | 90% |
Q8TET4 | Homo sapiens | 40% | 89% |
Q92442 | Mucor javanicus | 26% | 94% |
Q94502 | Dictyostelium discoideum | 39% | 86% |
Q9BE70 | Macaca fascicularis | 41% | 100% |
Q9F234 | Bacillus thermoamyloliquefaciens | 36% | 100% |
Q9FN05 | Arabidopsis thaliana | 39% | 88% |
Q9MYM4 | Bos taurus | 31% | 87% |
Q9P999 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 29% | 100% |
Q9S7Y7 | Arabidopsis thaliana | 31% | 89% |
Q9US55 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 88% |
V5BS12 | Trypanosoma cruzi | 31% | 77% |
V5D5S5 | Trypanosoma cruzi | 52% | 99% |