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:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042555 | MCM complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AKD9
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0032392 | DNA geometric change | 7 | 7 |
GO:0032508 | DNA duplex unwinding | 8 | 7 |
GO:0051276 | chromosome organization | 5 | 7 |
GO:0071103 | DNA conformation change | 6 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.259 |
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 930 | 932 | PF00675 | 0.665 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 930 | 932 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 931 | 935 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 943 | 951 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 617 | 621 | PF00917 | 0.553 |
DOC_ANK_TNKS_1 | 180 | 187 | PF00023 | 0.575 |
DOC_ANK_TNKS_1 | 3 | 10 | PF00023 | 0.669 |
DOC_ANK_TNKS_1 | 472 | 479 | PF00023 | 0.690 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.664 |
DOC_CYCLIN_RxL_1 | 784 | 794 | PF00134 | 0.375 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 775 | 784 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 429 | 438 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 563 | 570 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 583 | 590 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 775 | 784 | PF00069 | 0.355 |
DOC_MAPK_NFAT4_5 | 563 | 571 | PF00069 | 0.553 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.632 |
DOC_PP1_RVXF_1 | 785 | 792 | PF00149 | 0.368 |
DOC_PP2B_LxvP_1 | 363 | 366 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 780 | 783 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 686 | 689 | PF00568 | 0.467 |
DOC_SPAK_OSR1_1 | 724 | 728 | PF12202 | 0.443 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 830 | 834 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 920 | 924 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 861 | 866 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 547 | 553 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 611 | 615 | PF00244 | 0.394 |
LIG_CtBP_PxDLS_1 | 558 | 563 | PF00389 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 29 | 36 | PF00928 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 56 | 62 | PF00928 | 0.427 |
LIG_EH1_1 | 958 | 966 | PF00400 | 0.257 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.511 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.553 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.473 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.557 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.478 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.473 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.556 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.391 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.467 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.550 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.710 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.390 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.467 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.467 |
LIG_FHA_2 | 886 | 892 | PF00498 | 0.467 |
LIG_Integrin_RGD_1 | 120 | 122 | PF01839 | 0.527 |
LIG_Integrin_RGD_1 | 473 | 475 | PF01839 | 0.695 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 723 | 731 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 723 | 728 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 905 | 909 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.553 |
LIG_MYND_1 | 798 | 802 | PF01753 | 0.260 |
LIG_PALB2_WD40_1 | 540 | 548 | PF16756 | 0.467 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.422 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.408 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 894 | 898 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 812 | 815 | PF00017 | 0.407 |
LIG_SH2_STAT3 | 894 | 897 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 812 | 815 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 997 | 1000 | PF00017 | 0.375 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.725 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.688 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.449 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 587 | 593 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.724 |
LIG_SUMO_SIM_par_1 | 963 | 970 | PF11976 | 0.500 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.461 |
LIG_UBA3_1 | 556 | 563 | PF00899 | 0.467 |
LIG_WRC_WIRS_1 | 903 | 908 | PF05994 | 0.444 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.467 |
MOD_CDK_SPK_2 | 861 | 866 | PF00069 | 0.467 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.659 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.467 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.716 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.786 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.556 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.545 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.629 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.520 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.467 |
MOD_CK1_1 | 843 | 849 | PF00069 | 0.519 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.476 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.467 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.519 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.648 |
MOD_Cter_Amidation | 928 | 931 | PF01082 | 0.724 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.339 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.353 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.652 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.611 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.535 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.474 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.642 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.732 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.618 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.460 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.386 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.267 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.683 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.590 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.565 |
MOD_GlcNHglycan | 922 | 925 | PF01048 | 0.586 |
MOD_GlcNHglycan | 974 | 977 | PF01048 | 0.423 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.525 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.467 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.700 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.629 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.272 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.646 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.602 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.416 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.469 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.485 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.540 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.627 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.584 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.617 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.608 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.467 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.598 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.267 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.690 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.464 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.681 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.579 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.477 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.467 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.467 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.516 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.467 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.374 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.668 |
MOD_NEK2_1 | 859 | 864 | PF00069 | 0.311 |
MOD_NEK2_1 | 898 | 903 | PF00069 | 0.467 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.548 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.511 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.662 |
MOD_OFUCOSY | 616 | 623 | PF10250 | 0.267 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.444 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.746 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.506 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.648 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.467 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.375 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.556 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.587 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.462 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.479 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.570 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.689 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.467 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.467 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.418 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.546 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.467 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.467 |
MOD_Plk_1 | 859 | 865 | PF00069 | 0.431 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.693 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.399 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.467 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.693 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.563 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.467 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.467 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.379 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.467 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.659 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.467 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.509 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.604 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.606 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.640 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.467 |
MOD_ProDKin_1 | 861 | 867 | PF00069 | 0.460 |
MOD_SUMO_for_1 | 879 | 882 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 659 | 668 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 664 | 669 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 985 | 990 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 930 | 932 | PF00400 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 981 | 985 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM6 | Leptomonas seymouri | 64% | 99% |
A0A3S5H5H2 | Leishmania donovani | 89% | 100% |
A4H477 | Leishmania braziliensis | 79% | 99% |
A4HSF2 | Leishmania infantum | 89% | 100% |
F4KAB8 | Arabidopsis thaliana | 26% | 100% |
Q4QJG9 | Leishmania major | 88% | 99% |