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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0071204 | histone pre-mRNA 3'end processing complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QA02
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006398 | mRNA 3'-end processing by stem-loop binding and cleavage | 8 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008334 | histone mRNA metabolic process | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0031124 | mRNA 3'-end processing | 8 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050657 | nucleic acid transport | 6 | 2 |
GO:0050658 | RNA transport | 4 | 2 |
GO:0051028 | mRNA transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051236 | establishment of RNA localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003729 | mRNA binding | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0036002 | pre-mRNA binding | 5 | 2 |
GO:0071207 | histone pre-mRNA stem-loop binding | 6 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.755 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.755 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.680 |
CLV_PCSK_PC7_1 | 671 | 677 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.655 |
CLV_Separin_Metazoa | 262 | 266 | PF03568 | 0.669 |
DEG_COP1_1 | 379 | 387 | PF00400 | 0.707 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.788 |
DEG_SCF_FBW7_1 | 798 | 805 | PF00400 | 0.651 |
DEG_SIAH_1 | 523 | 531 | PF03145 | 0.548 |
DOC_CKS1_1 | 834 | 839 | PF01111 | 0.856 |
DOC_CYCLIN_RxL_1 | 801 | 809 | PF00134 | 0.679 |
DOC_CYCLIN_yCln2_LP_2 | 775 | 781 | PF00134 | 0.563 |
DOC_MAPK_gen_1 | 164 | 175 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 265 | 273 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 411 | 417 | PF00069 | 0.695 |
DOC_MAPK_gen_1 | 790 | 800 | PF00069 | 0.798 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.563 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.562 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.695 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.680 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.646 |
DOC_PP2B_LxvP_1 | 560 | 563 | PF13499 | 0.743 |
DOC_PP2B_LxvP_1 | 645 | 648 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 775 | 778 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.697 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.850 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 712 | 717 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 798 | 803 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 829 | 834 | PF00397 | 0.819 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 355 | 360 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.815 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 685 | 691 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 700 | 707 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 725 | 730 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 738 | 744 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 181 | 198 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.687 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.569 |
LIG_CSL_BTD_1 | 521 | 524 | PF09270 | 0.693 |
LIG_CtBP_PxDLS_1 | 403 | 407 | PF00389 | 0.720 |
LIG_DLG_GKlike_1 | 476 | 484 | PF00625 | 0.571 |
LIG_EVH1_2 | 506 | 510 | PF00568 | 0.662 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.442 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.797 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.632 |
LIG_FHA_1 | 756 | 762 | PF00498 | 0.672 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.731 |
LIG_FHA_1 | 842 | 848 | PF00498 | 0.739 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.566 |
LIG_Integrin_RGD_1 | 114 | 116 | PF01839 | 0.763 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 231 | 239 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 678 | 688 | PF02991 | 0.777 |
LIG_LIR_Gen_1 | 7 | 15 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.760 |
LIG_PDZ_Class_3 | 866 | 871 | PF00595 | 0.661 |
LIG_Pex14_2 | 230 | 234 | PF04695 | 0.566 |
LIG_PTAP_UEV_1 | 384 | 389 | PF05743 | 0.692 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.546 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.482 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.546 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.709 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.661 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.655 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.626 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.707 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.720 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.706 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.664 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.693 |
LIG_SH3_3 | 771 | 777 | PF00018 | 0.629 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.727 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.716 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.719 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.634 |
LIG_WW_2 | 413 | 416 | PF00397 | 0.817 |
MOD_CDC14_SPxK_1 | 409 | 412 | PF00782 | 0.726 |
MOD_CDK_SPK_2 | 106 | 111 | PF00069 | 0.613 |
MOD_CDK_SPK_2 | 406 | 411 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.712 |
MOD_CDK_SPxK_1 | 436 | 442 | PF00069 | 0.694 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.772 |
MOD_CDK_SPxK_1 | 798 | 804 | PF00069 | 0.699 |
MOD_CDK_SPxxK_3 | 404 | 411 | PF00069 | 0.706 |
MOD_CDK_SPxxK_3 | 444 | 451 | PF00069 | 0.687 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.767 |
MOD_CDK_SPxxK_3 | 833 | 840 | PF00069 | 0.852 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.725 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.719 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.560 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.573 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.743 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.629 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.685 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.583 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.646 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.731 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.779 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.760 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.642 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.642 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.411 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.643 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.632 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.728 |
MOD_CK2_1 | 726 | 732 | PF00069 | 0.678 |
MOD_Cter_Amidation | 698 | 701 | PF01082 | 0.591 |
MOD_DYRK1A_RPxSP_1 | 43 | 47 | PF00069 | 0.722 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.754 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.781 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.411 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.655 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.617 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.578 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.769 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.750 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.768 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.774 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.543 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.606 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.727 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.684 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.723 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.663 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.771 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.674 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.623 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.586 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.611 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.741 |
MOD_GlcNHglycan | 837 | 840 | PF01048 | 0.776 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.692 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.513 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.593 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.702 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.677 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.602 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.587 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.805 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.731 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.628 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.767 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.693 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.628 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.680 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.846 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.411 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.804 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.781 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.730 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.808 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.622 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.517 |
MOD_NEK2_2 | 802 | 807 | PF00069 | 0.633 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.370 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.703 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.859 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.784 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.707 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.581 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.389 |
MOD_PKA_1 | 700 | 706 | PF00069 | 0.798 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.389 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.528 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.572 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.760 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.727 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.726 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.697 |
MOD_PKA_2 | 737 | 743 | PF00069 | 0.679 |
MOD_PKA_2 | 841 | 847 | PF00069 | 0.758 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.635 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.564 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.852 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.664 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.712 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.411 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.698 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.632 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.700 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.723 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.669 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.465 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.628 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.794 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.681 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.819 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.758 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.598 |
MOD_ProDKin_1 | 712 | 718 | PF00069 | 0.678 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.682 |
MOD_ProDKin_1 | 798 | 804 | PF00069 | 0.699 |
MOD_ProDKin_1 | 829 | 835 | PF00069 | 0.821 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.792 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.688 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.649 |
TRG_NLS_MonoExtC_3 | 220 | 225 | PF00514 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 95 | 100 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7C9 | Leptomonas seymouri | 40% | 100% |
A0A3Q8IF88 | Leishmania donovani | 88% | 100% |
A4HE27 | Leishmania braziliensis | 63% | 100% |
A4I1D3 | Leishmania infantum | 88% | 100% |
E9AXH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |