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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S7WQP7
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000062 | fatty-acyl-CoA binding | 4 | 9 |
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0008289 | lipid binding | 2 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0033218 | amide binding | 2 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0120227 | acyl-CoA binding | 3 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:1901567 | fatty acid derivative binding | 3 | 9 |
GO:1901681 | sulfur compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 686 | 690 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 736 | 740 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 975 | 979 | PF00656 | 0.520 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 878 | 880 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 993 | 995 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 996 | 998 | PF00675 | 0.423 |
CLV_PCSK_FUR_1 | 525 | 529 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 702 | 704 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 878 | 880 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 980 | 982 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 980 | 982 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 942 | 946 | PF00082 | 0.253 |
DEG_APCC_DBOX_1 | 308 | 316 | PF00400 | 0.596 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.584 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.701 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.714 |
DOC_CYCLIN_RxL_1 | 306 | 314 | PF00134 | 0.658 |
DOC_CYCLIN_RxL_1 | 655 | 665 | PF00134 | 0.680 |
DOC_CYCLIN_yCln2_LP_2 | 112 | 118 | PF00134 | 0.469 |
DOC_CYCLIN_yCln2_LP_2 | 92 | 98 | PF00134 | 0.626 |
DOC_MAPK_gen_1 | 525 | 532 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 702 | 713 | PF00069 | 0.709 |
DOC_MAPK_MEF2A_6 | 503 | 511 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 597 | 606 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 83 | 91 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 928 | 937 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 422 | 429 | PF00149 | 0.299 |
DOC_PP1_RVXF_1 | 501 | 507 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 932 | 938 | PF00149 | 0.520 |
DOC_PP4_FxxP_1 | 593 | 596 | PF00568 | 0.479 |
DOC_PP4_MxPP_1 | 823 | 826 | PF00568 | 0.692 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 744 | 748 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 753 | 757 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 806 | 810 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 896 | 900 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 907 | 911 | PF00917 | 0.655 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 749 | 754 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 821 | 826 | PF00397 | 0.767 |
LIG_14-3-3_CanoR_1 | 217 | 226 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 411 | 416 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 537 | 541 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 651 | 659 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 805 | 811 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 858 | 864 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 981 | 991 | PF00244 | 0.562 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.745 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.281 |
LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 599 | 603 | PF00533 | 0.383 |
LIG_CaM_IQ_9 | 59 | 75 | PF13499 | 0.534 |
LIG_CtBP_PxDLS_1 | 445 | 449 | PF00389 | 0.483 |
LIG_deltaCOP1_diTrp_1 | 783 | 791 | PF00928 | 0.684 |
LIG_EVH1_1 | 487 | 491 | PF00568 | 0.467 |
LIG_EVH1_2 | 488 | 492 | PF00568 | 0.463 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.737 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.746 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.720 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.524 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.660 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.634 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.675 |
LIG_FHA_2 | 684 | 690 | PF00498 | 0.719 |
LIG_FHA_2 | 729 | 735 | PF00498 | 0.635 |
LIG_FHA_2 | 757 | 763 | PF00498 | 0.691 |
LIG_FHA_2 | 867 | 873 | PF00498 | 0.699 |
LIG_FHA_2 | 943 | 949 | PF00498 | 0.453 |
LIG_HCF-1_HBM_1 | 79 | 82 | PF13415 | 0.572 |
LIG_LIR_Gen_1 | 14 | 22 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 425 | 436 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 579 | 585 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 966 | 976 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 657 | 662 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 688 | 694 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 966 | 971 | PF02991 | 0.453 |
LIG_MYND_2 | 374 | 378 | PF01753 | 0.659 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.610 |
LIG_Pex14_2 | 506 | 510 | PF04695 | 0.399 |
LIG_Pex14_2 | 599 | 603 | PF04695 | 0.383 |
LIG_Pex14_2 | 659 | 663 | PF04695 | 0.611 |
LIG_Pex14_2 | 937 | 941 | PF04695 | 0.505 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 716 | 720 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 983 | 986 | PF00017 | 0.453 |
LIG_SH3_1 | 228 | 234 | PF00018 | 0.692 |
LIG_SH3_2 | 231 | 236 | PF14604 | 0.696 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.744 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.833 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.660 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.702 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.501 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.690 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.661 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.627 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 391 | 396 | PF11976 | 0.666 |
LIG_SUMO_SIM_anti_2 | 709 | 715 | PF11976 | 0.672 |
LIG_SUMO_SIM_anti_2 | 88 | 94 | PF11976 | 0.618 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.687 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.593 |
LIG_TRAF2_1 | 516 | 519 | PF00917 | 0.444 |
LIG_TRAF2_1 | 725 | 728 | PF00917 | 0.687 |
LIG_TRAF2_1 | 801 | 804 | PF00917 | 0.719 |
LIG_TRAF2_1 | 869 | 872 | PF00917 | 0.626 |
LIG_TYR_ITIM | 713 | 718 | PF00017 | 0.668 |
LIG_UBA3_1 | 565 | 570 | PF00899 | 0.415 |
LIG_UBA3_1 | 622 | 629 | PF00899 | 0.660 |
LIG_UBA3_1 | 989 | 998 | PF00899 | 0.624 |
MOD_CDC14_SPxK_1 | 642 | 645 | PF00782 | 0.684 |
MOD_CDK_SPK_2 | 592 | 597 | PF00069 | 0.428 |
MOD_CDK_SPxK_1 | 230 | 236 | PF00069 | 0.817 |
MOD_CDK_SPxK_1 | 639 | 645 | PF00069 | 0.690 |
MOD_CDK_SPxK_1 | 782 | 788 | PF00069 | 0.673 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.602 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.684 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.687 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.643 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.554 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.544 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.458 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.677 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.683 |
MOD_CK1_1 | 792 | 798 | PF00069 | 0.727 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.606 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.639 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.618 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.703 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.702 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.748 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.702 |
MOD_CK2_1 | 906 | 912 | PF00069 | 0.581 |
MOD_CMANNOS | 965 | 968 | PF00535 | 0.253 |
MOD_Cter_Amidation | 523 | 526 | PF01082 | 0.712 |
MOD_DYRK1A_RPxSP_1 | 230 | 234 | PF00069 | 0.725 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.489 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.479 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.347 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.537 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.586 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.601 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.472 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.737 |
MOD_GlcNHglycan | 45 | 49 | PF01048 | 0.449 |
MOD_GlcNHglycan | 465 | 469 | PF01048 | 0.783 |
MOD_GlcNHglycan | 518 | 523 | PF01048 | 0.673 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.622 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.346 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.369 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.489 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.607 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.473 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.638 |
MOD_GlcNHglycan | 898 | 901 | PF01048 | 0.561 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.248 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.632 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.727 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.793 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.716 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.252 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.537 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.616 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.492 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.437 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.320 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.383 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.640 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.766 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.803 |
MOD_GSK3_1 | 821 | 828 | PF00069 | 0.783 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.690 |
MOD_N-GLC_1 | 849 | 854 | PF02516 | 0.489 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.603 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.775 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.692 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.636 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.584 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.560 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.588 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.432 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.473 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.444 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.506 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.333 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.740 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.674 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.811 |
MOD_NEK2_1 | 922 | 927 | PF00069 | 0.494 |
MOD_NEK2_1 | 993 | 998 | PF00069 | 0.641 |
MOD_PIKK_1 | 795 | 801 | PF00454 | 0.761 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.647 |
MOD_PK_1 | 528 | 534 | PF00069 | 0.425 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.628 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.717 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.716 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.464 |
MOD_PKA_2 | 650 | 656 | PF00069 | 0.668 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.719 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.658 |
MOD_PKB_1 | 217 | 225 | PF00069 | 0.729 |
MOD_PKB_1 | 526 | 534 | PF00069 | 0.500 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.644 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.582 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.538 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.409 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.609 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.640 |
MOD_Plk_2-3 | 728 | 734 | PF00069 | 0.632 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.658 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.631 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.643 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.721 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.667 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.725 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.493 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.414 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.271 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.672 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.546 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.689 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.731 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.679 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.751 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.787 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.689 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.562 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.434 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.466 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.661 |
MOD_ProDKin_1 | 749 | 755 | PF00069 | 0.739 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.726 |
MOD_ProDKin_1 | 821 | 827 | PF00069 | 0.769 |
MOD_SUMO_rev_2 | 929 | 935 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 975 | 982 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 985 | 990 | PF00179 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.707 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 938 | 941 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 987 | 990 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.767 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 702 | 704 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 707 | 710 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 877 | 879 | PF00400 | 0.711 |
TRG_NES_CRM1_1 | 391 | 403 | PF08389 | 0.544 |
TRG_NLS_Bipartite_1 | 980 | 998 | PF00514 | 0.585 |
TRG_NLS_MonoExtC_3 | 226 | 231 | PF00514 | 0.643 |
TRG_NLS_MonoExtC_3 | 993 | 998 | PF00514 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 309 | 313 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 660 | 665 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7G9 | Leptomonas seymouri | 54% | 100% |
A0A422N766 | Trypanosoma rangeli | 28% | 100% |
A4H5Q6 | Leishmania braziliensis | 73% | 100% |
A4HTZ6 | Leishmania infantum | 99% | 100% |
D0A9G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AMS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QHU9 | Leishmania major | 94% | 100% |