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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030686 | 90S preribosome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HFF6
Term | Name | Level | Count |
---|---|---|---|
GO:0000447 | endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 745 | 749 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 806 | 810 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 872 | 876 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 990 | 994 | PF00656 | 0.621 |
CLV_MEL_PAP_1 | 278 | 284 | PF00089 | 0.702 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 933 | 935 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 938 | 940 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 953 | 955 | PF00675 | 0.558 |
CLV_PCSK_FUR_1 | 50 | 54 | PF00082 | 0.592 |
CLV_PCSK_FUR_1 | 631 | 635 | PF00082 | 0.512 |
CLV_PCSK_FUR_1 | 930 | 934 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 932 | 934 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 937 | 939 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 983 | 985 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 350 | 352 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 983 | 985 | PF00082 | 0.627 |
CLV_PCSK_PC7_1 | 346 | 352 | PF00082 | 0.660 |
CLV_PCSK_PC7_1 | 933 | 939 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 422 | 426 | PF03568 | 0.761 |
DEG_APCC_DBOX_1 | 826 | 834 | PF00400 | 0.636 |
DEG_SPOP_SBC_1 | 834 | 838 | PF00917 | 0.481 |
DOC_CKS1_1 | 996 | 1001 | PF01111 | 0.533 |
DOC_CYCLIN_RxL_1 | 1 | 11 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 701 | 707 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 223 | 232 | PF00069 | 0.739 |
DOC_MAPK_gen_1 | 274 | 282 | PF00069 | 0.620 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.661 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.728 |
DOC_PP1_RVXF_1 | 2 | 9 | PF00149 | 0.742 |
DOC_PP2B_LxvP_1 | 701 | 704 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 328 | 331 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 1013 | 1017 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 834 | 838 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 871 | 875 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 167 | 171 | PF12436 | 0.682 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.619 |
DOC_USP7_UBL2_3 | 353 | 357 | PF12436 | 0.706 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.436 |
DOC_USP7_UBL2_3 | 477 | 481 | PF12436 | 0.722 |
DOC_USP7_UBL2_3 | 783 | 787 | PF12436 | 0.683 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 995 | 1000 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 123 | 133 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 452 | 461 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 850 | 856 | PF00244 | 0.562 |
LIG_Actin_WH2_2 | 266 | 283 | PF00022 | 0.634 |
LIG_AP2alpha_1 | 795 | 799 | PF02296 | 0.764 |
LIG_BRCT_BRCA1_1 | 502 | 506 | PF00533 | 0.654 |
LIG_EVH1_2 | 891 | 895 | PF00568 | 0.233 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.766 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.593 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.624 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.723 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.742 |
LIG_FHA_1 | 894 | 900 | PF00498 | 0.344 |
LIG_FHA_1 | 959 | 965 | PF00498 | 0.545 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.763 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.628 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.667 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.540 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.578 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.537 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.737 |
LIG_FHA_2 | 841 | 847 | PF00498 | 0.663 |
LIG_FHA_2 | 870 | 876 | PF00498 | 0.420 |
LIG_GBD_Chelix_1 | 977 | 985 | PF00786 | 0.623 |
LIG_LIR_Apic_2 | 607 | 611 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 420 | 427 | PF02991 | 0.765 |
LIG_LIR_Gen_1 | 447 | 454 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 553 | 562 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 859 | 865 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 952 | 958 | PF02991 | 0.525 |
LIG_LYPXL_L_2 | 814 | 823 | PF13949 | 0.648 |
LIG_NRP_CendR_1 | 1052 | 1055 | PF00754 | 0.684 |
LIG_Pex14_1 | 577 | 581 | PF04695 | 0.508 |
LIG_Pex14_2 | 506 | 510 | PF04695 | 0.498 |
LIG_Pex14_2 | 795 | 799 | PF04695 | 0.764 |
LIG_Rb_pABgroove_1 | 712 | 720 | PF01858 | 0.485 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.546 |
LIG_SH2_CRK | 955 | 959 | PF00017 | 0.612 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 919 | 923 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 204 | 207 | PF00017 | 0.610 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 1019 | 1022 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 735 | 738 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 922 | 925 | PF00017 | 0.344 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.750 |
LIG_SH3_3 | 1007 | 1013 | PF00018 | 0.547 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.647 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.736 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.724 |
LIG_SH3_3 | 701 | 707 | PF00018 | 0.444 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.494 |
LIG_SH3_3 | 989 | 995 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 808 | 815 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 893 | 901 | PF11976 | 0.344 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.747 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.567 |
LIG_TRAF2_1 | 331 | 334 | PF00917 | 0.415 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.685 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.604 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.692 |
LIG_TRAF2_1 | 562 | 565 | PF00917 | 0.600 |
LIG_TRAF2_1 | 591 | 594 | PF00917 | 0.673 |
LIG_TRAF2_1 | 768 | 771 | PF00917 | 0.582 |
LIG_TRAF2_1 | 898 | 901 | PF00917 | 0.344 |
LIG_TRAF2_2 | 966 | 971 | PF00917 | 0.703 |
LIG_UBA3_1 | 775 | 783 | PF00899 | 0.436 |
LIG_UBA3_1 | 847 | 856 | PF00899 | 0.569 |
MOD_CK1_1 | 1017 | 1023 | PF00069 | 0.639 |
MOD_CK1_1 | 1025 | 1031 | PF00069 | 0.658 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.586 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.786 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.608 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.626 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.743 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.631 |
MOD_CK1_1 | 803 | 809 | PF00069 | 0.579 |
MOD_CK1_1 | 873 | 879 | PF00069 | 0.233 |
MOD_CK1_1 | 948 | 954 | PF00069 | 0.631 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.671 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.758 |
MOD_CK2_1 | 1025 | 1031 | PF00069 | 0.536 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.796 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.666 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.560 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.711 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.753 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.543 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.618 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.732 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.508 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.683 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.397 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.233 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.588 |
MOD_CK2_1 | 840 | 846 | PF00069 | 0.641 |
MOD_CK2_1 | 895 | 901 | PF00069 | 0.344 |
MOD_Cter_Amidation | 478 | 481 | PF01082 | 0.738 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.707 |
MOD_GlcNHglycan | 146 | 150 | PF01048 | 0.665 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.769 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.625 |
MOD_GlcNHglycan | 415 | 419 | PF01048 | 0.503 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.749 |
MOD_GlcNHglycan | 441 | 446 | PF01048 | 0.700 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.610 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.716 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.648 |
MOD_GlcNHglycan | 548 | 552 | PF01048 | 0.740 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.695 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.754 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.685 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.645 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.555 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.763 |
MOD_GlcNHglycan | 804 | 808 | PF01048 | 0.495 |
MOD_GlcNHglycan | 875 | 878 | PF01048 | 0.433 |
MOD_GSK3_1 | 1013 | 1020 | PF00069 | 0.753 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.806 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.746 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.610 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.537 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.722 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.718 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.721 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.777 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.561 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.541 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.721 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.668 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.691 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.233 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.628 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.668 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.580 |
MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.520 |
MOD_N-GLC_1 | 748 | 753 | PF02516 | 0.632 |
MOD_N-GLC_1 | 979 | 984 | PF02516 | 0.593 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.715 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.698 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.713 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.588 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.674 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.335 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.341 |
MOD_NEK2_1 | 833 | 838 | PF00069 | 0.690 |
MOD_NEK2_1 | 851 | 856 | PF00069 | 0.541 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.549 |
MOD_PKA_1 | 785 | 791 | PF00069 | 0.644 |
MOD_PKA_2 | 1034 | 1040 | PF00069 | 0.750 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.673 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.719 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.508 |
MOD_PKA_2 | 949 | 955 | PF00069 | 0.541 |
MOD_PKB_1 | 1003 | 1011 | PF00069 | 0.553 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.579 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.572 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.585 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.536 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.723 |
MOD_Plk_1 | 893 | 899 | PF00069 | 0.344 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.720 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.629 |
MOD_Plk_2-3 | 236 | 242 | PF00069 | 0.706 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.435 |
MOD_Plk_2-3 | 741 | 747 | PF00069 | 0.541 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.686 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.706 |
MOD_Plk_4 | 771 | 777 | PF00069 | 0.578 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.629 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.770 |
MOD_ProDKin_1 | 995 | 1001 | PF00069 | 0.529 |
MOD_SUMO_for_1 | 319 | 322 | PF00179 | 0.631 |
MOD_SUMO_for_1 | 545 | 548 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 104 | 114 | PF00179 | 0.800 |
MOD_SUMO_rev_2 | 177 | 187 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 233 | 239 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 363 | 369 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 402 | 406 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 455 | 461 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 647 | 652 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 706 | 715 | PF00179 | 0.351 |
TRG_DiLeu_BaEn_1 | 457 | 462 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_3 | 770 | 776 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_4 | 457 | 463 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_4 | 647 | 653 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_4 | 684 | 690 | PF01217 | 0.233 |
TRG_DiLeu_BaEn_4 | 860 | 866 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_4 | 900 | 906 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 862 | 865 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 887 | 890 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 955 | 958 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 1051 | 1054 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 631 | 634 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 932 | 934 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 937 | 939 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 953 | 955 | PF00400 | 0.558 |
TRG_NLS_Bipartite_1 | 633 | 654 | PF00514 | 0.444 |
TRG_NLS_MonoCore_2 | 349 | 354 | PF00514 | 0.504 |
TRG_NLS_MonoExtC_3 | 393 | 398 | PF00514 | 0.661 |
TRG_NLS_MonoExtC_3 | 521 | 526 | PF00514 | 0.729 |
TRG_NLS_MonoExtC_3 | 784 | 789 | PF00514 | 0.694 |
TRG_NLS_MonoExtN_4 | 522 | 527 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 783 | 790 | PF00514 | 0.723 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 610 | 614 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 944 | 949 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 983 | 987 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY8 | Leptomonas seymouri | 60% | 100% |
A0A1X0NGP0 | Trypanosomatidae | 38% | 100% |
A0A3R7NCJ6 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X904 | Leishmania donovani | 79% | 100% |
A4IB05 | Leishmania infantum | 79% | 100% |
E9AET3 | Leishmania major | 80% | 100% |
E9B5Y8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5ATL2 | Trypanosoma cruzi | 36% | 100% |