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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QHU9
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 2 |
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006631 | fatty acid metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019752 | carboxylic acid metabolic process | 5 | 2 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 2 |
GO:0043436 | oxoacid metabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000062 | fatty-acyl-CoA binding | 4 | 8 |
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008289 | lipid binding | 2 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0033218 | amide binding | 2 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0120227 | acyl-CoA binding | 3 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:1901567 | fatty acid derivative binding | 3 | 8 |
GO:1901681 | sulfur compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 734 | 738 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 976 | 980 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 879 | 881 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 994 | 996 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 997 | 999 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 879 | 881 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 981 | 983 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 981 | 983 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 879 | 883 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 943 | 947 | PF00082 | 0.262 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.620 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.601 |
DEG_APCC_DBOX_1 | 871 | 879 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 747 | 751 | PF00917 | 0.664 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.715 |
DOC_CYCLIN_RxL_1 | 305 | 313 | PF00134 | 0.647 |
DOC_CYCLIN_RxL_1 | 653 | 663 | PF00134 | 0.638 |
DOC_CYCLIN_yCln2_LP_2 | 112 | 118 | PF00134 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 92 | 98 | PF00134 | 0.638 |
DOC_MAPK_gen_1 | 533 | 541 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 700 | 711 | PF00069 | 0.709 |
DOC_MAPK_MEF2A_6 | 502 | 510 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 595 | 604 | PF00069 | 0.287 |
DOC_MAPK_MEF2A_6 | 83 | 91 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 929 | 938 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.308 |
DOC_PP1_RVXF_1 | 500 | 506 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 933 | 939 | PF00149 | 0.514 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.233 |
DOC_PP4_FxxP_1 | 591 | 594 | PF00568 | 0.478 |
DOC_PP4_MxPP_1 | 824 | 827 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 742 | 746 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 807 | 811 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 897 | 901 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 908 | 912 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 822 | 827 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 217 | 225 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 321 | 331 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 410 | 415 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 525 | 531 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 535 | 539 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 649 | 657 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 806 | 812 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 859 | 865 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 982 | 992 | PF00244 | 0.580 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.746 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 597 | 601 | PF00533 | 0.357 |
LIG_CaM_IQ_9 | 59 | 75 | PF13499 | 0.539 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.459 |
LIG_deltaCOP1_diTrp_1 | 784 | 792 | PF00928 | 0.689 |
LIG_EVH1_1 | 486 | 490 | PF00568 | 0.478 |
LIG_EVH1_2 | 487 | 491 | PF00568 | 0.478 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.736 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.720 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.723 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.559 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.641 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.677 |
LIG_FHA_2 | 650 | 656 | PF00498 | 0.666 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.695 |
LIG_FHA_2 | 868 | 874 | PF00498 | 0.688 |
LIG_FHA_2 | 944 | 950 | PF00498 | 0.462 |
LIG_HCF-1_HBM_1 | 79 | 82 | PF13415 | 0.586 |
LIG_LIR_Gen_1 | 14 | 22 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 455 | 465 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 577 | 583 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 598 | 609 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 967 | 977 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 598 | 604 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 655 | 660 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 686 | 692 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 710 | 716 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 967 | 972 | PF02991 | 0.462 |
LIG_MYND_2 | 373 | 377 | PF01753 | 0.626 |
LIG_Pex14_2 | 401 | 405 | PF04695 | 0.607 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.392 |
LIG_Pex14_2 | 505 | 509 | PF04695 | 0.380 |
LIG_Pex14_2 | 597 | 601 | PF04695 | 0.357 |
LIG_Pex14_2 | 657 | 661 | PF04695 | 0.604 |
LIG_Pex14_2 | 938 | 942 | PF04695 | 0.514 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 714 | 718 | PF00017 | 0.627 |
LIG_SH2_STAT3 | 984 | 987 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 984 | 987 | PF00017 | 0.462 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.718 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.705 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.652 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.675 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.484 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.580 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 390 | 395 | PF11976 | 0.628 |
LIG_SUMO_SIM_anti_2 | 707 | 713 | PF11976 | 0.642 |
LIG_SUMO_SIM_anti_2 | 88 | 94 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.632 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 93 | 102 | PF11976 | 0.648 |
LIG_TRAF2_1 | 723 | 726 | PF00917 | 0.665 |
LIG_TRAF2_1 | 802 | 805 | PF00917 | 0.723 |
LIG_TYR_ITIM | 711 | 716 | PF00017 | 0.636 |
LIG_UBA3_1 | 563 | 568 | PF00899 | 0.444 |
LIG_UBA3_1 | 620 | 627 | PF00899 | 0.647 |
LIG_UBA3_1 | 990 | 999 | PF00899 | 0.611 |
MOD_CDC14_SPxK_1 | 640 | 643 | PF00782 | 0.664 |
MOD_CDK_SPK_2 | 590 | 595 | PF00069 | 0.442 |
MOD_CDK_SPxK_1 | 229 | 235 | PF00069 | 0.821 |
MOD_CDK_SPxK_1 | 637 | 643 | PF00069 | 0.674 |
MOD_CDK_SPxK_1 | 783 | 789 | PF00069 | 0.678 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.646 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.665 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.689 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.505 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.570 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.572 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.643 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.728 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.739 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.616 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.635 |
MOD_CK2_1 | 704 | 710 | PF00069 | 0.627 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.702 |
MOD_CK2_1 | 810 | 816 | PF00069 | 0.759 |
MOD_CK2_1 | 867 | 873 | PF00069 | 0.684 |
MOD_CMANNOS | 966 | 969 | PF00535 | 0.262 |
MOD_Cter_Amidation | 522 | 525 | PF01082 | 0.695 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.470 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.507 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.565 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.471 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.702 |
MOD_GlcNHglycan | 45 | 49 | PF01048 | 0.453 |
MOD_GlcNHglycan | 464 | 468 | PF01048 | 0.779 |
MOD_GlcNHglycan | 517 | 522 | PF01048 | 0.702 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.640 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.384 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.431 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.500 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.633 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.519 |
MOD_GlcNHglycan | 812 | 815 | PF01048 | 0.531 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.532 |
MOD_GlcNHglycan | 917 | 920 | PF01048 | 0.258 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.634 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.739 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.713 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.629 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.539 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.611 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.523 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.442 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.343 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.383 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.636 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.776 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.659 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.754 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.772 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.668 |
MOD_N-GLC_1 | 850 | 855 | PF02516 | 0.489 |
MOD_N-GLC_2 | 275 | 277 | PF02516 | 0.414 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.691 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.658 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.435 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.653 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.471 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.570 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.487 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.492 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.413 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.546 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.359 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.720 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.726 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.799 |
MOD_NEK2_1 | 923 | 928 | PF00069 | 0.512 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.501 |
MOD_NEK2_1 | 994 | 999 | PF00069 | 0.611 |
MOD_PIKK_1 | 796 | 802 | PF00454 | 0.743 |
MOD_PIKK_1 | 983 | 989 | PF00454 | 0.415 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.658 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.660 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.715 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.761 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.453 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.649 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.736 |
MOD_PKA_2 | 858 | 864 | PF00069 | 0.658 |
MOD_PKA_2 | 928 | 934 | PF00069 | 0.431 |
MOD_PKB_1 | 217 | 225 | PF00069 | 0.694 |
MOD_PKB_1 | 524 | 532 | PF00069 | 0.488 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.663 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.466 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.548 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.360 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.606 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.635 |
MOD_Plk_2-3 | 844 | 850 | PF00069 | 0.670 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.698 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.679 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.694 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.579 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.700 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.469 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.453 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.451 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.307 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.648 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.603 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.563 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.669 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.714 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.695 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.739 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.751 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.704 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.520 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.440 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.455 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.695 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.642 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.692 |
MOD_ProDKin_1 | 822 | 828 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 930 | 936 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 976 | 983 | PF00179 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.630 |
TRG_DiLeu_BaLyEn_6 | 371 | 376 | PF01217 | 0.655 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 939 | 942 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 988 | 991 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 700 | 702 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 705 | 708 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 878 | 880 | PF00400 | 0.693 |
TRG_NLS_Bipartite_1 | 981 | 999 | PF00514 | 0.572 |
TRG_NLS_MonoExtC_3 | 994 | 999 | PF00514 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 542 | 546 | PF00026 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 658 | 663 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7G9 | Leptomonas seymouri | 53% | 100% |
A0A3S7WQP7 | Leishmania donovani | 94% | 100% |
A4H5Q6 | Leishmania braziliensis | 72% | 82% |
A4HTZ6 | Leishmania infantum | 94% | 100% |
D0A9G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AMS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |