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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071204 | histone pre-mRNA 3'end processing complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AXH0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006398 | mRNA 3'-end processing by stem-loop binding and cleavage | 8 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008334 | histone mRNA metabolic process | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 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:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003729 | mRNA binding | 5 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0036002 | pre-mRNA binding | 5 | 1 |
GO:0071207 | histone pre-mRNA stem-loop binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.727 |
CLV_PCSK_FUR_1 | 76 | 80 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.727 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 816 | 820 | PF00082 | 0.744 |
CLV_Separin_Metazoa | 262 | 266 | PF03568 | 0.664 |
DEG_APCC_DBOX_1 | 411 | 419 | PF00400 | 0.536 |
DEG_COP1_1 | 376 | 387 | PF00400 | 0.667 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.566 |
DEG_SCF_FBW7_1 | 541 | 548 | PF00400 | 0.520 |
DOC_CKS1_1 | 656 | 661 | PF01111 | 0.498 |
DOC_CKS1_1 | 846 | 851 | PF01111 | 0.788 |
DOC_CYCLIN_RxL_1 | 486 | 497 | PF00134 | 0.694 |
DOC_CYCLIN_RxL_1 | 813 | 821 | PF00134 | 0.677 |
DOC_MAPK_gen_1 | 164 | 175 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 265 | 273 | PF00069 | 0.679 |
DOC_MAPK_gen_1 | 411 | 417 | PF00069 | 0.773 |
DOC_MAPK_gen_1 | 802 | 812 | PF00069 | 0.705 |
DOC_MAPK_gen_1 | 852 | 859 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.679 |
DOC_MAPK_MEF2A_6 | 852 | 859 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.593 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 517 | 520 | PF13499 | 0.745 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.728 |
DOC_PP2B_LxvP_1 | 657 | 660 | PF13499 | 0.669 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.534 |
DOC_PP4_FxxP_1 | 523 | 526 | PF00568 | 0.674 |
DOC_PP4_MxPP_1 | 621 | 624 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 724 | 729 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 845 | 850 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 355 | 360 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 489 | 494 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 508 | 517 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 750 | 757 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 181 | 198 | PF00022 | 0.593 |
LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.683 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.619 |
LIG_BRCT_BRCA1_1 | 624 | 628 | PF00533 | 0.595 |
LIG_BRCT_BRCA1_1 | 790 | 794 | PF00533 | 0.637 |
LIG_CSL_BTD_1 | 534 | 537 | PF09270 | 0.673 |
LIG_CtBP_PxDLS_1 | 403 | 407 | PF00389 | 0.707 |
LIG_EVH1_2 | 519 | 523 | PF00568 | 0.727 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.535 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.754 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.590 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.730 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.615 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.686 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.688 |
LIG_Integrin_RGD_1 | 114 | 116 | PF01839 | 0.743 |
LIG_LIR_Apic_2 | 129 | 134 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 424 | 429 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 231 | 239 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 690 | 700 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.657 |
LIG_Pex14_2 | 230 | 234 | PF04695 | 0.667 |
LIG_PTAP_UEV_1 | 384 | 389 | PF05743 | 0.681 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 757 | 761 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.661 |
LIG_SH3_2 | 429 | 434 | PF14604 | 0.548 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.593 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.693 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.561 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.749 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.517 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.769 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.733 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.546 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.529 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.769 |
LIG_SH3_3 | 860 | 866 | PF00018 | 0.699 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.701 |
LIG_SUMO_SIM_par_1 | 489 | 494 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 855 | 861 | PF11976 | 0.528 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.678 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.518 |
LIG_WW_2 | 413 | 416 | PF00397 | 0.764 |
MOD_CDC14_SPxK_1 | 154 | 157 | PF00782 | 0.521 |
MOD_CDC14_SPxK_1 | 409 | 412 | PF00782 | 0.771 |
MOD_CDK_SPK_2 | 406 | 411 | PF00069 | 0.766 |
MOD_CDK_SPK_2 | 444 | 449 | PF00069 | 0.526 |
MOD_CDK_SPxK_1 | 151 | 157 | PF00069 | 0.522 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.768 |
MOD_CDK_SPxK_1 | 436 | 442 | PF00069 | 0.690 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.741 |
MOD_CDK_SPxK_1 | 810 | 816 | PF00069 | 0.747 |
MOD_CDK_SPxxK_3 | 404 | 411 | PF00069 | 0.770 |
MOD_CDK_SPxxK_3 | 457 | 464 | PF00069 | 0.592 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.736 |
MOD_CDK_SPxxK_3 | 810 | 817 | PF00069 | 0.604 |
MOD_CDK_SPxxK_3 | 845 | 852 | PF00069 | 0.787 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.643 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.532 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.646 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.575 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.519 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.705 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.626 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.602 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.725 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.582 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.692 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.708 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.645 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.704 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.362 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.670 |
MOD_CK2_1 | 738 | 744 | PF00069 | 0.707 |
MOD_DYRK1A_RPxSP_1 | 43 | 47 | PF00069 | 0.698 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.786 |
MOD_GlcNHglycan | 17 | 22 | PF01048 | 0.553 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.470 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.728 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.672 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.613 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.785 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.622 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.713 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.573 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.519 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.734 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.769 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.529 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.729 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.643 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.608 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.591 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.662 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.633 |
MOD_GlcNHglycan | 849 | 852 | PF01048 | 0.723 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.591 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.470 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.619 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.727 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.670 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.702 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.623 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.594 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.607 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.643 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.628 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.600 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.553 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.671 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.682 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.609 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.562 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.763 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.534 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.486 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.764 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.540 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.743 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.567 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.534 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.768 |
MOD_NEK2_1 | 818 | 823 | PF00069 | 0.548 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.656 |
MOD_NEK2_2 | 503 | 508 | PF00069 | 0.523 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.406 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.531 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.518 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.776 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.788 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.558 |
MOD_PIKK_1 | 803 | 809 | PF00454 | 0.769 |
MOD_PIKK_1 | 841 | 847 | PF00454 | 0.612 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.406 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.406 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.620 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.584 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.566 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.718 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.776 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.622 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.549 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.565 |
MOD_PKA_2 | 853 | 859 | PF00069 | 0.708 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.807 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.607 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.470 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.760 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.689 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.767 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.566 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.560 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.515 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.596 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.633 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.501 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.774 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.649 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.524 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.583 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.730 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.628 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.576 |
MOD_ProDKin_1 | 724 | 730 | PF00069 | 0.700 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.572 |
MOD_ProDKin_1 | 810 | 816 | PF00069 | 0.747 |
MOD_ProDKin_1 | 845 | 851 | PF00069 | 0.750 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 413 | 418 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.776 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.674 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.803 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.655 |
TRG_NLS_MonoExtC_3 | 220 | 225 | PF00514 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF88 | Leishmania donovani | 84% | 100% |
A4HE27 | Leishmania braziliensis | 62% | 97% |
A4I1D3 | Leishmania infantum | 84% | 100% |
Q4QA02 | Leishmania major | 83% | 100% |