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 | 10 |
GO:0030684 | preribosome | 3 | 10 |
GO:0032040 | small-subunit processome | 4 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
GO:0030689 | Noc complex | 3 | 1 |
GO:0030692 | Noc4p-Nop14p complex | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4H3F7
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 9 |
GO:0042254 | ribosome biogenesis | 5 | 9 |
GO:0044085 | cellular component biogenesis | 3 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 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:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 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:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.695 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 471 | 475 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.233 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 899 | 903 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 841 | 843 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 887 | 889 | PF00675 | 0.631 |
CLV_PCSK_FUR_1 | 231 | 235 | PF00082 | 0.450 |
CLV_PCSK_FUR_1 | 855 | 859 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 819 | 821 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 827 | 829 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 841 | 843 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 846 | 848 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 819 | 821 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 827 | 829 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 846 | 848 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 857 | 859 | PF00082 | 0.304 |
CLV_PCSK_PC7_1 | 823 | 829 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 842 | 848 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 816 | 820 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.627 |
DEG_APCC_DBOX_1 | 887 | 895 | PF00400 | 0.527 |
DEG_COP1_1 | 397 | 405 | PF00400 | 0.632 |
DEG_SCF_FBW7_1 | 676 | 682 | PF00400 | 0.233 |
DEG_SPOP_SBC_1 | 894 | 898 | PF00917 | 0.788 |
DOC_ANK_TNKS_1 | 61 | 68 | PF00023 | 0.725 |
DOC_CKS1_1 | 582 | 587 | PF01111 | 0.369 |
DOC_CKS1_1 | 676 | 681 | PF01111 | 0.233 |
DOC_CKS1_1 | 754 | 759 | PF01111 | 0.233 |
DOC_CYCLIN_RxL_1 | 257 | 270 | PF00134 | 0.557 |
DOC_MAPK_DCC_7 | 399 | 407 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 399 | 407 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 559 | 566 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 722 | 729 | PF00069 | 0.233 |
DOC_PP2B_LxvP_1 | 640 | 643 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 657 | 660 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 743 | 746 | PF13499 | 0.477 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 747 | 751 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.787 |
DOC_USP7_MATH_2 | 84 | 90 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 880 | 884 | PF12436 | 0.583 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.814 |
LIG_14-3-3_CanoR_1 | 124 | 132 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 352 | 361 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 559 | 563 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 831 | 839 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 607 | 622 | PF00022 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.511 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.810 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.630 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_1 | 569 | 573 | PF00533 | 0.369 |
LIG_Clathr_ClatBox_1 | 540 | 544 | PF01394 | 0.352 |
LIG_CSL_BTD_1 | 754 | 757 | PF09270 | 0.485 |
LIG_EH_1 | 92 | 96 | PF12763 | 0.749 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.740 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.505 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.540 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.588 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.389 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.446 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.389 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.691 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.511 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.653 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.722 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.562 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.546 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.532 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.416 |
LIG_GBD_Chelix_1 | 611 | 619 | PF00786 | 0.444 |
LIG_HP1_1 | 643 | 647 | PF01393 | 0.444 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 492 | 503 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 584 | 594 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 607 | 616 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 856 | 866 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 856 | 862 | PF02991 | 0.401 |
LIG_MYND_3 | 659 | 663 | PF01753 | 0.485 |
LIG_NRBOX | 515 | 521 | PF00104 | 0.444 |
LIG_NRBOX | 610 | 616 | PF00104 | 0.344 |
LIG_NRBOX | 737 | 743 | PF00104 | 0.444 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.519 |
LIG_SH2_CRK | 859 | 863 | PF00017 | 0.485 |
LIG_SH2_GRB2like | 859 | 862 | PF00017 | 0.485 |
LIG_SH2_SRC | 565 | 568 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.385 |
LIG_SH3_1 | 722 | 728 | PF00018 | 0.444 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.713 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.357 |
LIG_SH3_3 | 722 | 728 | PF00018 | 0.444 |
LIG_SH3_3 | 751 | 757 | PF00018 | 0.483 |
LIG_SH3_5 | 574 | 578 | PF00018 | 0.344 |
LIG_Sin3_3 | 538 | 545 | PF02671 | 0.352 |
LIG_SUMO_SIM_par_1 | 530 | 535 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 539 | 544 | PF11976 | 0.317 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.657 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.525 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.605 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.642 |
LIG_TRAF2_1 | 903 | 906 | PF00917 | 0.543 |
LIG_UBA3_1 | 562 | 571 | PF00899 | 0.444 |
LIG_UBA3_1 | 615 | 620 | PF00899 | 0.444 |
LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.520 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.630 |
LIG_WRC_WIRS_1 | 788 | 793 | PF05994 | 0.401 |
MOD_CDC14_SPxK_1 | 702 | 705 | PF00782 | 0.485 |
MOD_CDK_SPxK_1 | 699 | 705 | PF00069 | 0.485 |
MOD_CDK_SPxxK_3 | 243 | 250 | PF00069 | 0.545 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.636 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.607 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.737 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.653 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.690 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.715 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.632 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.424 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.425 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.508 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.648 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.666 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.650 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.634 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.573 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.564 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.758 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.385 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.730 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.661 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.716 |
MOD_GlcNHglycan | 161 | 166 | PF01048 | 0.610 |
MOD_GlcNHglycan | 172 | 178 | PF01048 | 0.593 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.389 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.609 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.609 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.598 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.550 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.742 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.489 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.387 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.414 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.414 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.376 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.758 |
MOD_GlcNHglycan | 891 | 894 | PF01048 | 0.710 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.702 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.619 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.739 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.664 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.519 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.614 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.417 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.750 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.665 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.568 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.597 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.357 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.420 |
MOD_GSK3_1 | 831 | 838 | PF00069 | 0.485 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.778 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.691 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.781 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.450 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.645 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.787 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.587 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.471 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.530 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.644 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.540 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.474 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.355 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.345 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.349 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.397 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.452 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.553 |
MOD_NEK2_2 | 787 | 792 | PF00069 | 0.401 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.645 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.621 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.604 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.686 |
MOD_PIKK_1 | 861 | 867 | PF00454 | 0.474 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.662 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.520 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.648 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.710 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.535 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.669 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.608 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.635 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.416 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.354 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.629 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.627 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.427 |
MOD_Plk_1 | 835 | 841 | PF00069 | 0.485 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.595 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.747 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.625 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.253 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.408 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.485 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.233 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.783 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.547 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.369 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.296 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.485 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.419 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.449 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.369 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.815 |
MOD_SUMO_for_1 | 811 | 814 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 821 | 829 | PF00179 | 0.369 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 666 | 671 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_4 | 384 | 390 | PF01217 | 0.501 |
TRG_DiLeu_BaEn_4 | 715 | 721 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 657 | 662 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 702 | 707 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 709 | 714 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 798 | 803 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 825 | 830 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 791 | 794 | PF00400 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 712 | 716 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 794 | 798 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 820 | 824 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 831 | 836 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1III2 | Leptomonas seymouri | 56% | 100% |
A0A1X0NK23 | Trypanosomatidae | 35% | 92% |
A0A3S5H513 | Leishmania donovani | 79% | 100% |
A4HRR1 | Leishmania infantum | 80% | 100% |
C9ZJ50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 95% |
E9ACE0 | Leishmania major | 78% | 100% |
E9AJM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 97% |
V5AQ76 | Trypanosoma cruzi | 40% | 100% |