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: 15 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9G1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043171 | peptide catabolic process | 4 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004177 | aminopeptidase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008235 | metalloexopeptidase activity | 5 | 2 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0008238 | exopeptidase activity | 4 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0033218 | amide binding | 2 | 2 |
GO:0042277 | peptide binding | 3 | 2 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0070006 | metalloaminopeptidase activity | 6 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 834 | 836 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 834 | 836 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 700 | 702 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 816 | 820 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 834 | 838 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.494 |
CLV_Separin_Metazoa | 563 | 567 | PF03568 | 0.413 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 532 | 536 | PF00917 | 0.347 |
DOC_CYCLIN_RxL_1 | 669 | 680 | PF00134 | 0.490 |
DOC_CYCLIN_RxL_1 | 813 | 824 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 452 | 458 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 568 | 574 | PF00134 | 0.490 |
DOC_MAPK_FxFP_2 | 267 | 270 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 313 | 320 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 384 | 393 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 410 | 417 | PF00069 | 0.490 |
DOC_MAPK_NFAT4_5 | 410 | 418 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 673 | 680 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 829 | 832 | PF13499 | 0.413 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.490 |
DOC_SPAK_OSR1_1 | 493 | 497 | PF12202 | 0.504 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.257 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.278 |
DOC_USP7_MATH_2 | 841 | 847 | PF00917 | 0.490 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 879 | 884 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 557 | 565 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 681 | 688 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 701 | 705 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 847 | 853 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 445 | 463 | PF00022 | 0.490 |
LIG_Actin_WH2_2 | 615 | 632 | PF00022 | 0.388 |
LIG_APCC_ABBA_1 | 260 | 265 | PF00400 | 0.322 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 374 | 378 | PF00533 | 0.381 |
LIG_deltaCOP1_diTrp_1 | 290 | 297 | PF00928 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 340 | 347 | PF00928 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 362 | 369 | PF00928 | 0.376 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.476 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.466 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.351 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.423 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.417 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.423 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.521 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.444 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.425 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.436 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.366 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.438 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.395 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.346 |
LIG_FHA_2 | 736 | 742 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 264 | 270 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 349 | 356 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 580 | 591 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 617 | 625 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 776 | 785 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 617 | 622 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 800 | 805 | PF02991 | 0.409 |
LIG_LYPXL_SIV_4 | 479 | 487 | PF13949 | 0.321 |
LIG_LYPXL_yS_3 | 473 | 476 | PF13949 | 0.367 |
LIG_PALB2_WD40_1 | 324 | 332 | PF16756 | 0.346 |
LIG_PCNA_PIPBox_1 | 428 | 437 | PF02747 | 0.365 |
LIG_PCNA_yPIPBox_3 | 425 | 435 | PF02747 | 0.411 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.413 |
LIG_PTB_Apo_2 | 24 | 31 | PF02174 | 0.374 |
LIG_PTB_Apo_2 | 280 | 287 | PF02174 | 0.490 |
LIG_PTB_Apo_2 | 646 | 653 | PF02174 | 0.413 |
LIG_PTB_Phospho_1 | 646 | 652 | PF10480 | 0.413 |
LIG_SH2_CRK | 583 | 587 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 480 | 484 | PF00017 | 0.341 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.342 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 715 | 719 | PF00017 | 0.379 |
LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 746 | 749 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.160 |
LIG_SH2_STAT5 | 876 | 879 | PF00017 | 0.554 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.476 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.571 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.406 |
LIG_SH3_3 | 702 | 708 | PF00018 | 0.408 |
LIG_SH3_3 | 750 | 756 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 160 | 165 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 484 | 490 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 602 | 608 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 71 | 78 | PF11976 | 0.496 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.413 |
LIG_UBA3_1 | 402 | 410 | PF00899 | 0.346 |
LIG_UBA3_1 | 813 | 819 | PF00899 | 0.457 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 879 | 885 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.439 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.340 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.529 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.365 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.411 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.382 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.490 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.346 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.403 |
MOD_CK2_1 | 683 | 689 | PF00069 | 0.451 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.455 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.490 |
MOD_CK2_1 | 836 | 842 | PF00069 | 0.348 |
MOD_DYRK1A_RPxSP_1 | 238 | 242 | PF00069 | 0.426 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.642 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.490 |
MOD_GlcNHglycan | 306 | 311 | PF01048 | 0.371 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.477 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.351 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.268 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.410 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.388 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.380 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.438 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.420 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.423 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.474 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.373 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.464 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.257 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.456 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.621 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.408 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.365 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.462 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.257 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.436 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.259 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.344 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.338 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.457 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.365 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.335 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.482 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.354 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.409 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.392 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.356 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.429 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.434 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.307 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.457 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.422 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.311 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.346 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.409 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.422 |
MOD_PIKK_1 | 771 | 777 | PF00454 | 0.375 |
MOD_PIKK_1 | 787 | 793 | PF00454 | 0.295 |
MOD_PK_1 | 525 | 531 | PF00069 | 0.555 |
MOD_PK_1 | 808 | 814 | PF00069 | 0.490 |
MOD_PKA_1 | 700 | 706 | PF00069 | 0.413 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.413 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.476 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.346 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.365 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.388 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.413 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.257 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.453 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.396 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.492 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.444 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.365 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.388 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.346 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.357 |
MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.490 |
MOD_Plk_2-3 | 822 | 828 | PF00069 | 0.490 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.400 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.358 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.459 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.457 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.345 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.498 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.417 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.207 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.484 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.381 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.446 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.398 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.380 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.412 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.444 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.347 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.358 |
MOD_ProDKin_1 | 879 | 885 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 884 | 887 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 729 | 734 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 672 | 677 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 678 | 683 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 833 | 835 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 847 | 850 | PF00400 | 0.340 |
TRG_NES_CRM1_1 | 160 | 173 | PF08389 | 0.257 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 695 | 699 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JBK9 | Bodo saltans | 39% | 100% |
A0A1X0NMW3 | Trypanosomatidae | 40% | 100% |
A0A3Q8ICL6 | Leishmania donovani | 93% | 100% |
A0A3R7K1R9 | Trypanosoma rangeli | 40% | 100% |
A0A6J2ATK2 | Acinonyx jubatus | 24% | 89% |
A2RI32 | Lactococcus lactis subsp. cremoris (strain MG1363) | 29% | 100% |
A5HUI5 | Gloydius brevicaudus | 28% | 93% |
A6QPT7 | Bos taurus | 27% | 93% |
D0A6I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D3UW23 | Bitis rhinoceros | 27% | 93% |
E9AHB1 | Leishmania infantum | 93% | 100% |
E9AIS1 | Leishmania braziliensis | 79% | 100% |
E9AY12 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
M3XFH7 | Felis catus | 24% | 89% |
O57579 | Gallus gallus | 25% | 91% |
O93654 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 28% | 100% |
O93655 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 29% | 100% |
O96935 | Plasmodium falciparum (isolate FcB1 / Columbia) | 23% | 82% |
P0C2T8 | Lactococcus lactis subsp. cremoris | 29% | 100% |
P15144 | Homo sapiens | 31% | 92% |
P15145 | Sus scrofa | 27% | 92% |
P15541 | Oryctolagus cuniculus | 27% | 92% |
P15684 | Rattus norvegicus | 27% | 92% |
P16406 | Mus musculus | 27% | 94% |
P32454 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 93% |
P37896 | Lactobacillus delbrueckii subsp. lactis | 28% | 100% |
P37898 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P40462 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 94% |
P50123 | Rattus norvegicus | 28% | 94% |
P55786 | Homo sapiens | 33% | 97% |
P79143 | Canis lupus familiaris | 27% | 91% |
P79171 | Felis catus | 27% | 92% |
P91885 | Manduca sexta | 24% | 94% |
P91887 | Plutella xylostella | 28% | 94% |
P95928 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 31% | 100% |
P97449 | Mus musculus | 26% | 92% |
P97629 | Rattus norvegicus | 28% | 87% |
Q07075 | Homo sapiens | 27% | 93% |
Q0J2B5 | Oryza sativa subsp. japonica | 30% | 100% |
Q0J5V5 | Oryza sativa subsp. japonica | 32% | 100% |
Q10730 | Lactobacillus helveticus | 26% | 100% |
Q10737 | Haemonchus contortus | 29% | 91% |
Q10836 | Rattus norvegicus | 27% | 87% |
Q11000 | Heliothis virescens | 28% | 88% |
Q11001 | Manduca sexta | 25% | 90% |
Q11011 | Mus musculus | 33% | 96% |
Q32LQ0 | Bos taurus | 26% | 93% |
Q48656 | Lactococcus lactis subsp. lactis | 27% | 100% |
Q4TT88 | Caenorhabditis elegans | 31% | 94% |
Q59KZ1 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 96% |
Q5RFP3 | Pongo abelii | 26% | 92% |
Q6K4E7 | Oryza sativa subsp. japonica | 31% | 100% |
Q6P179 | Homo sapiens | 26% | 92% |
Q6Q4G3 | Homo sapiens | 23% | 90% |
Q6Z6L4 | Oryza sativa subsp. japonica | 32% | 100% |
Q8C129 | Mus musculus | 28% | 87% |
Q8K093 | Mus musculus | 27% | 87% |
Q8SQI6 | Encephalitozoon cuniculi (strain GB-M1) | 32% | 100% |
Q8SRG3 | Encephalitozoon cuniculi (strain GB-M1) | 32% | 100% |
Q8VZH2 | Arabidopsis thaliana | 32% | 100% |
Q95334 | Sus scrofa | 27% | 94% |
Q974N6 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 30% | 100% |
Q978U3 | Thermoplasma volcanium (strain ATCC 51530 / DSM 4299 / JCM 9571 / NBRC 15438 / GSS1) | 28% | 100% |
Q97VF1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 29% | 100% |
Q9CIQ1 | Lactococcus lactis subsp. lactis (strain IL1403) | 29% | 100% |
Q9EQH2 | Mus musculus | 31% | 95% |
Q9JJ22 | Rattus norvegicus | 27% | 95% |
Q9NZ08 | Homo sapiens | 27% | 94% |
Q9UIQ6 | Homo sapiens | 30% | 87% |
Q9UKU6 | Homo sapiens | 27% | 87% |
Q9USX1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
V5D7P4 | Trypanosoma cruzi | 40% | 100% |