Uncharacterized Protein, Uncharacterized
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: 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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4HZ83
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 13 |
GO:0009889 | regulation of biosynthetic process | 4 | 13 |
GO:0010468 | regulation of gene expression | 5 | 13 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 13 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 13 |
GO:0019222 | regulation of metabolic process | 3 | 13 |
GO:0031323 | regulation of cellular metabolic process | 4 | 13 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 13 |
GO:0034248 | regulation of amide metabolic process | 5 | 13 |
GO:0050789 | regulation of biological process | 2 | 13 |
GO:0050794 | regulation of cellular process | 3 | 13 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 13 |
GO:0051246 | regulation of protein metabolic process | 5 | 13 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 13 |
GO:0065007 | biological regulation | 1 | 13 |
GO:0080090 | regulation of primary metabolic process | 4 | 13 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
GO:0004520 | DNA endonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016888 | endodeoxyribonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0017108 | 5'-flap endonuclease activity | 7 | 1 |
GO:0048256 | flap endonuclease activity | 6 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 776 | 780 | PF00656 | 0.761 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 983 | 985 | PF00675 | 0.362 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 983 | 985 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 542 | 544 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 1028 | 1032 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 900 | 904 | PF00082 | 0.313 |
CLV_Separin_Metazoa | 428 | 432 | PF03568 | 0.386 |
CLV_Separin_Metazoa | 817 | 821 | PF03568 | 0.491 |
DEG_APCC_DBOX_1 | 506 | 514 | PF00400 | 0.480 |
DEG_ODPH_VHL_1 | 207 | 218 | PF01847 | 0.461 |
DEG_SCF_FBW7_1 | 481 | 487 | PF00400 | 0.322 |
DEG_SPOP_SBC_1 | 778 | 782 | PF00917 | 0.748 |
DOC_ANK_TNKS_1 | 94 | 101 | PF00023 | 0.608 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.396 |
DOC_CYCLIN_RxL_1 | 217 | 227 | PF00134 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 607 | 613 | PF00134 | 0.562 |
DOC_MAPK_DCC_7 | 290 | 299 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 239 | 248 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 447 | 454 | PF00149 | 0.412 |
DOC_PP1_RVXF_1 | 635 | 641 | PF00149 | 0.562 |
DOC_PP1_RVXF_1 | 788 | 794 | PF00149 | 0.685 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.604 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.326 |
DOC_PP4_MxPP_1 | 155 | 158 | PF00568 | 0.562 |
DOC_PP4_MxPP_1 | 395 | 398 | PF00568 | 0.333 |
DOC_PP4_MxPP_1 | 40 | 43 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.666 |
DOC_USP7_MATH_2 | 316 | 322 | PF00917 | 0.441 |
DOC_WW_Pin1_4 | 1006 | 1011 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 704 | 709 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 924 | 929 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 957 | 962 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 790 | 799 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 814 | 821 | PF00244 | 0.545 |
LIG_Actin_WH2_2 | 210 | 226 | PF00022 | 0.430 |
LIG_Actin_WH2_2 | 653 | 668 | PF00022 | 0.639 |
LIG_Actin_WH2_2 | 675 | 693 | PF00022 | 0.634 |
LIG_Actin_WH2_2 | 968 | 985 | PF00022 | 0.500 |
LIG_APCC_ABBA_1 | 402 | 407 | PF00400 | 0.386 |
LIG_APCC_ABBA_1 | 929 | 934 | PF00400 | 0.504 |
LIG_APCC_ABBAyCdc20_2 | 1028 | 1034 | PF00400 | 0.617 |
LIG_BIR_III_2 | 200 | 204 | PF00653 | 0.581 |
LIG_BIR_III_4 | 629 | 633 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 558 | 562 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_1 | 825 | 829 | PF00533 | 0.577 |
LIG_Clathr_ClatBox_1 | 657 | 661 | PF01394 | 0.557 |
LIG_FHA_1 | 1013 | 1019 | PF00498 | 0.561 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.352 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.261 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.423 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.396 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.416 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.595 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.475 |
LIG_FHA_1 | 832 | 838 | PF00498 | 0.412 |
LIG_FHA_1 | 901 | 907 | PF00498 | 0.535 |
LIG_FHA_1 | 925 | 931 | PF00498 | 0.573 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.431 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.392 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.447 |
LIG_FHA_2 | 828 | 834 | PF00498 | 0.522 |
LIG_FHA_2 | 867 | 873 | PF00498 | 0.522 |
LIG_FHA_2 | 958 | 964 | PF00498 | 0.477 |
LIG_Integrin_RGD_1 | 204 | 206 | PF01839 | 0.779 |
LIG_IRF3_LxIS_1 | 793 | 800 | PF10401 | 0.596 |
LIG_LIR_Apic_2 | 496 | 501 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 52 | 58 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 448 | 458 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 476 | 486 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 487 | 495 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 601 | 612 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 720 | 730 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 794 | 801 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 921 | 931 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 987 | 998 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 729 | 735 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 794 | 799 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 874 | 880 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 969 | 975 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 987 | 993 | PF02991 | 0.444 |
LIG_NRBOX | 938 | 944 | PF00104 | 0.562 |
LIG_PCNA_PIPBox_1 | 210 | 219 | PF02747 | 0.436 |
LIG_PCNA_PIPBox_1 | 584 | 593 | PF02747 | 0.418 |
LIG_PCNA_yPIPBox_3 | 204 | 217 | PF02747 | 0.492 |
LIG_PCNA_yPIPBox_3 | 973 | 986 | PF02747 | 0.562 |
LIG_Pex14_1 | 640 | 644 | PF04695 | 0.490 |
LIG_Pex14_1 | 877 | 881 | PF04695 | 0.491 |
LIG_Pex14_2 | 571 | 575 | PF04695 | 0.352 |
LIG_Pex14_2 | 732 | 736 | PF04695 | 0.516 |
LIG_Pex14_2 | 911 | 915 | PF04695 | 0.538 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.327 |
LIG_SH2_NCK_1 | 524 | 528 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 946 | 949 | PF00017 | 0.491 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 881 | 885 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 881 | 884 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 1044 | 1047 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 735 | 738 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 796 | 799 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 946 | 949 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 994 | 997 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 999 | 1002 | PF00017 | 0.514 |
LIG_SH3_3 | 1004 | 1010 | PF00018 | 0.626 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.556 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.522 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.569 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.629 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.506 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.597 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.309 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.513 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.484 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.596 |
LIG_SH3_3 | 697 | 703 | PF00018 | 0.700 |
LIG_SH3_3 | 858 | 864 | PF00018 | 0.494 |
LIG_SH3_3 | 925 | 931 | PF00018 | 0.577 |
LIG_SH3_3 | 946 | 952 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 655 | 662 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 244 | 249 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 655 | 662 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 685 | 693 | PF11976 | 0.571 |
LIG_TRAF2_1 | 869 | 872 | PF00917 | 0.567 |
LIG_TRAF2_1 | 960 | 963 | PF00917 | 0.491 |
LIG_TYR_ITIM | 522 | 527 | PF00017 | 0.326 |
LIG_TYR_ITIM | 944 | 949 | PF00017 | 0.491 |
LIG_TYR_ITSM | 792 | 799 | PF00017 | 0.605 |
LIG_UBA3_1 | 15 | 23 | PF00899 | 0.611 |
LIG_UBA3_1 | 278 | 284 | PF00899 | 0.419 |
LIG_UBA3_1 | 618 | 627 | PF00899 | 0.562 |
LIG_WRC_WIRS_1 | 228 | 233 | PF05994 | 0.388 |
LIG_WRC_WIRS_1 | 727 | 732 | PF05994 | 0.531 |
LIG_WW_1 | 951 | 954 | PF00397 | 0.562 |
MOD_CDK_SPK_2 | 704 | 709 | PF00069 | 0.676 |
MOD_CDK_SPxxK_3 | 957 | 964 | PF00069 | 0.562 |
MOD_CK1_1 | 1005 | 1011 | PF00069 | 0.594 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.436 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.385 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.339 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.390 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.578 |
MOD_CK1_1 | 913 | 919 | PF00069 | 0.503 |
MOD_CK2_1 | 1005 | 1011 | PF00069 | 0.622 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.442 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.366 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.421 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.354 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.353 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.522 |
MOD_CK2_1 | 957 | 963 | PF00069 | 0.483 |
MOD_CMANNOS | 640 | 643 | PF00535 | 0.309 |
MOD_Cter_Amidation | 716 | 719 | PF01082 | 0.352 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.785 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.633 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.775 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.553 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.515 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.580 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.753 |
MOD_GlcNHglycan | 912 | 915 | PF01048 | 0.339 |
MOD_GSK3_1 | 1002 | 1009 | PF00069 | 0.576 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.408 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.555 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.363 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.377 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.315 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.617 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.373 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.300 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.348 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.394 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.516 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.583 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.639 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.612 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.518 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.488 |
MOD_GSK3_1 | 866 | 873 | PF00069 | 0.567 |
MOD_LATS_1 | 515 | 521 | PF00433 | 0.409 |
MOD_LATS_1 | 716 | 722 | PF00433 | 0.538 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.562 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.837 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.496 |
MOD_N-GLC_1 | 784 | 789 | PF02516 | 0.502 |
MOD_N-GLC_1 | 895 | 900 | PF02516 | 0.362 |
MOD_N-GLC_2 | 378 | 380 | PF02516 | 0.569 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.589 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.573 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.409 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.341 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.421 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.359 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.369 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.418 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.578 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.787 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.481 |
MOD_NEK2_1 | 895 | 900 | PF00069 | 0.552 |
MOD_NEK2_1 | 910 | 915 | PF00069 | 0.341 |
MOD_NEK2_1 | 967 | 972 | PF00069 | 0.548 |
MOD_NEK2_1 | 986 | 991 | PF00069 | 0.363 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.459 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.463 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.419 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.352 |
MOD_PIKK_1 | 617 | 623 | PF00454 | 0.507 |
MOD_PIKK_1 | 977 | 983 | PF00454 | 0.562 |
MOD_PK_1 | 1002 | 1008 | PF00069 | 0.608 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.436 |
MOD_PKA_1 | 718 | 724 | PF00069 | 0.512 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.428 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.411 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.542 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.431 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.590 |
MOD_Plk_1 | 895 | 901 | PF00069 | 0.562 |
MOD_Plk_1 | 916 | 922 | PF00069 | 0.568 |
MOD_Plk_1 | 986 | 992 | PF00069 | 0.562 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.670 |
MOD_Plk_2-3 | 866 | 872 | PF00069 | 0.424 |
MOD_Plk_4 | 1002 | 1008 | PF00069 | 0.539 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.611 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.418 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.266 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.393 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.421 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.394 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.291 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.561 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.610 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.592 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.503 |
MOD_ProDKin_1 | 1006 | 1012 | PF00069 | 0.628 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.452 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.365 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.362 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.612 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.654 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.543 |
MOD_ProDKin_1 | 704 | 710 | PF00069 | 0.649 |
MOD_ProDKin_1 | 924 | 930 | PF00069 | 0.545 |
MOD_ProDKin_1 | 957 | 963 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 406 | 411 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 862 | 869 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 963 | 972 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 603 | 608 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_1 | 963 | 968 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 218 | 223 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 653 | 658 | PF01217 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 925 | 930 | PF01217 | 0.577 |
TRG_DiLeu_LyEn_5 | 963 | 968 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 1044 | 1047 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 796 | 799 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 964 | 967 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 982 | 984 | PF00400 | 0.581 |
TRG_NES_CRM1_1 | 406 | 420 | PF08389 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 361 | 366 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 900 | 904 | PF00026 | 0.276 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9J9 | Leptomonas seymouri | 75% | 77% |
A0A1X0NZ14 | Trypanosomatidae | 47% | 86% |
A0A1X0P1K6 | Trypanosomatidae | 23% | 100% |
A0A3S7WWH1 | Leishmania donovani | 100% | 76% |
A0A422N7G4 | Trypanosoma rangeli | 43% | 100% |
A4HBS9 | Leishmania braziliensis | 92% | 100% |
D0A1F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 86% |
E9AV50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q38C92 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 46% | 86% |
Q4QCD1 | Leishmania major | 97% | 100% |
V5AYD9 | Trypanosoma cruzi | 43% | 86% |
V5BX20 | Trypanosoma cruzi | 22% | 100% |