Proteases, aminopeptidase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | yes | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I4T3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0043171 | peptide catabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004177 | aminopeptidase activity | 5 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008233 | peptidase activity | 3 | 13 |
GO:0008237 | metallopeptidase activity | 4 | 13 |
GO:0008238 | exopeptidase activity | 4 | 13 |
GO:0008270 | zinc ion binding | 6 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0046914 | transition metal ion binding | 5 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:0008235 | metalloexopeptidase activity | 5 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
GO:0070006 | metalloaminopeptidase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.451 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.280 |
DOC_CDC14_PxL_1 | 571 | 579 | PF14671 | 0.378 |
DOC_CYCLIN_RxL_1 | 728 | 739 | PF00134 | 0.280 |
DOC_CYCLIN_yCln2_LP_2 | 9 | 15 | PF00134 | 0.419 |
DOC_MAPK_DCC_7 | 248 | 256 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 105 | 115 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 477 | 486 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 480 | 488 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.577 |
DOC_MAPK_RevD_3 | 278 | 292 | PF00069 | 0.443 |
DOC_PP2B_PxIxI_1 | 449 | 455 | PF00149 | 0.411 |
DOC_PP2B_PxIxI_1 | 56 | 62 | PF00149 | 0.378 |
DOC_PP4_FxxP_1 | 624 | 627 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.418 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.378 |
DOC_USP7_UBL2_3 | 615 | 619 | PF12436 | 0.451 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.410 |
LIG_14-3-3_CanoR_1 | 123 | 132 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 470 | 479 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 556 | 560 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 848 | 853 | PF00244 | 0.399 |
LIG_Actin_WH2_2 | 306 | 324 | PF00022 | 0.326 |
LIG_APCC_ABBAyCdc20_2 | 556 | 562 | PF00400 | 0.468 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.632 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 741 | 745 | PF00533 | 0.378 |
LIG_deltaCOP1_diTrp_1 | 317 | 325 | PF00928 | 0.332 |
LIG_deltaCOP1_diTrp_1 | 781 | 790 | PF00928 | 0.404 |
LIG_EH1_1 | 801 | 809 | PF00400 | 0.326 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.354 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.422 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.588 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.381 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.374 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.315 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.306 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.462 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.475 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.287 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.316 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.516 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.353 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.420 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.321 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.300 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.330 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.412 |
LIG_FXI_DFP_1 | 259 | 263 | PF00024 | 0.324 |
LIG_GBD_Chelix_1 | 391 | 399 | PF00786 | 0.326 |
LIG_GBD_Chelix_1 | 807 | 815 | PF00786 | 0.378 |
LIG_IBAR_NPY_1 | 11 | 13 | PF08397 | 0.517 |
LIG_LIR_Apic_2 | 361 | 365 | PF02991 | 0.236 |
LIG_LIR_Apic_2 | 481 | 485 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 184 | 193 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 28 | 39 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 781 | 790 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 822 | 832 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 98 | 107 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 781 | 786 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 822 | 827 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.404 |
LIG_LYPXL_yS_3 | 449 | 452 | PF13949 | 0.381 |
LIG_PALB2_WD40_1 | 302 | 310 | PF16756 | 0.313 |
LIG_PCNA_PIPBox_1 | 104 | 113 | PF02747 | 0.334 |
LIG_PCNA_PIPBox_1 | 598 | 607 | PF02747 | 0.312 |
LIG_PCNA_yPIPBox_3 | 104 | 116 | PF02747 | 0.467 |
LIG_Pex14_1 | 544 | 548 | PF04695 | 0.468 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.345 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.309 |
LIG_Pex14_2 | 604 | 608 | PF04695 | 0.468 |
LIG_Pex14_2 | 786 | 790 | PF04695 | 0.341 |
LIG_Pex14_2 | 824 | 828 | PF04695 | 0.326 |
LIG_PTB_Apo_2 | 535 | 542 | PF02174 | 0.468 |
LIG_Rb_LxCxE_1 | 268 | 289 | PF01857 | 0.341 |
LIG_REV1ctd_RIR_1 | 238 | 247 | PF16727 | 0.377 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.379 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.335 |
LIG_SH2_CRK | 717 | 721 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 536 | 539 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 571 | 575 | PF00017 | 0.420 |
LIG_SH2_PTP2 | 163 | 166 | PF00017 | 0.378 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.516 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.319 |
LIG_SH2_SRC | 536 | 539 | PF00017 | 0.468 |
LIG_SH2_SRC | 571 | 574 | PF00017 | 0.420 |
LIG_SH2_SRC | 649 | 652 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 536 | 540 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 763 | 766 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.386 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.375 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.341 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.326 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.305 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.434 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.408 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.402 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 255 | 261 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 458 | 465 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 484 | 489 | PF11976 | 0.420 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.341 |
LIG_TRAF2_1 | 843 | 846 | PF00917 | 0.334 |
LIG_TRAF2_2 | 144 | 149 | PF00917 | 0.468 |
LIG_UBA3_1 | 379 | 387 | PF00899 | 0.326 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.446 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.387 |
LIG_WRC_WIRS_1 | 601 | 606 | PF05994 | 0.369 |
MOD_CDK_SPxxK_3 | 496 | 503 | PF00069 | 0.545 |
MOD_CDK_SPxxK_3 | 549 | 556 | PF00069 | 0.468 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.523 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.383 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.576 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.349 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.369 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.334 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.490 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.404 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.313 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.420 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.451 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.345 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.378 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.383 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.567 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.319 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.334 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.437 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.341 |
MOD_GlcNHglycan | 639 | 643 | PF01048 | 0.506 |
MOD_GlcNHglycan | 665 | 669 | PF01048 | 0.420 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.317 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.473 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.497 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.375 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.343 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.365 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.432 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.428 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.505 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.445 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.386 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.520 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.444 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.471 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.524 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.336 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.610 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.369 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.344 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.393 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.432 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.312 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.527 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.468 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.410 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.504 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.414 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.397 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.405 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.458 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.555 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.326 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.350 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.529 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.312 |
MOD_PIKK_1 | 758 | 764 | PF00454 | 0.356 |
MOD_PKA_1 | 291 | 297 | PF00069 | 0.402 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.474 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.451 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.420 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.323 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.462 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.341 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.595 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.617 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.485 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.458 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.353 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.288 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.398 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.449 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.513 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.466 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.289 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.537 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.438 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.468 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.339 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.457 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.441 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.541 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.468 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.410 |
MOD_SUMO_for_1 | 157 | 160 | PF00179 | 0.468 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.481 |
TRG_DiLeu_BaEn_2 | 466 | 472 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_2 | 619 | 625 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_4 | 429 | 435 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 644 | 646 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 847 | 850 | PF00400 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 557 | 562 | PF00026 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5R5 | Leptomonas seymouri | 72% | 100% |
A0A0S4IPD6 | Bodo saltans | 41% | 97% |
A0A0S4JBK9 | Bodo saltans | 33% | 100% |
A0A1X0P9F6 | Trypanosomatidae | 51% | 100% |
A0A3S7X2P7 | Leishmania donovani | 99% | 100% |
A0A422NEK9 | Trypanosoma rangeli | 52% | 100% |
A4HHM4 | Leishmania braziliensis | 83% | 100% |
A5HUI5 | Gloydius brevicaudus | 30% | 91% |
A6QPT7 | Bos taurus | 25% | 91% |
C9ZLI0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D0A6I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D3UW23 | Bitis rhinoceros | 30% | 91% |
E9AE86 | Leishmania major | 96% | 100% |
E9AIS1 | Leishmania braziliensis | 28% | 100% |
E9ALJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P15541 | Oryctolagus cuniculus | 26% | 90% |
P15684 | Rattus norvegicus | 25% | 90% |
P16406 | Mus musculus | 31% | 92% |
P40462 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 92% |
P55786 | Homo sapiens | 28% | 94% |
P97629 | Rattus norvegicus | 30% | 85% |
Q0J2B5 | Oryza sativa subsp. japonica | 29% | 99% |
Q0J5V5 | Oryza sativa subsp. japonica | 30% | 99% |
Q11000 | Heliothis virescens | 27% | 86% |
Q11001 | Manduca sexta | 26% | 88% |
Q11011 | Mus musculus | 28% | 94% |
Q4TT88 | Caenorhabditis elegans | 29% | 92% |
Q59KZ1 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 94% |
Q5RFP3 | Pongo abelii | 24% | 90% |
Q6K4E7 | Oryza sativa subsp. japonica | 30% | 99% |
Q6P179 | Homo sapiens | 24% | 90% |
Q6Z6L4 | Oryza sativa subsp. japonica | 30% | 99% |
Q8C129 | Mus musculus | 30% | 85% |
Q8VZH2 | Arabidopsis thaliana | 30% | 99% |
Q9JJ22 | Rattus norvegicus | 24% | 93% |
Q9NZ08 | Homo sapiens | 24% | 92% |
Q9USX1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 98% |
V5BSI2 | Trypanosoma cruzi | 51% | 100% |