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: A4I1D3
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 | 0.764 |
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 | 0.553 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.827 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.713 |
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 | 0.553 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.393 |
CLV_PCSK_PC7_1 | 688 | 694 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 795 | 799 | PF00082 | 0.736 |
CLV_Separin_Metazoa | 262 | 266 | PF03568 | 0.641 |
DEG_COP1_1 | 379 | 387 | PF00400 | 0.694 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.755 |
DOC_CKS1_1 | 825 | 830 | PF01111 | 0.797 |
DOC_CYCLIN_RxL_1 | 473 | 484 | PF00134 | 0.682 |
DOC_CYCLIN_RxL_1 | 792 | 800 | PF00134 | 0.674 |
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 | 0.641 |
DOC_MAPK_gen_1 | 411 | 417 | PF00069 | 0.793 |
DOC_MAPK_gen_1 | 781 | 791 | PF00069 | 0.694 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.641 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.593 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.691 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.642 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.742 |
DOC_PP2B_LxvP_1 | 552 | 555 | PF13499 | 0.705 |
DOC_PP2B_LxvP_1 | 636 | 639 | PF13499 | 0.669 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.653 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.720 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 703 | 708 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.769 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 355 | 360 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 451 | 458 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 676 | 682 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 692 | 698 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 716 | 721 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 729 | 735 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 767 | 773 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.566 |
LIG_Actin_WH2_2 | 181 | 198 | PF00022 | 0.593 |
LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.657 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.620 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.582 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.614 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.620 |
LIG_CSL_BTD_1 | 521 | 524 | PF09270 | 0.665 |
LIG_CtBP_PxDLS_1 | 403 | 407 | PF00389 | 0.707 |
LIG_EVH1_2 | 205 | 209 | PF00568 | 0.467 |
LIG_EVH1_2 | 506 | 510 | PF00568 | 0.733 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.581 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.749 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.573 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.723 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.724 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.687 |
LIG_FHA_1 | 833 | 839 | PF00498 | 0.701 |
LIG_Integrin_RGD_1 | 114 | 116 | PF01839 | 0.722 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 231 | 239 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 669 | 679 | PF02991 | 0.729 |
LIG_LIR_Gen_1 | 7 | 15 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.694 |
LIG_Pex14_2 | 230 | 234 | PF04695 | 0.678 |
LIG_PTAP_UEV_1 | 384 | 389 | PF05743 | 0.684 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.670 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.593 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.693 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.766 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.662 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.579 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.775 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.732 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.762 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.627 |
LIG_SH3_3 | 745 | 751 | PF00018 | 0.616 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.697 |
LIG_SH3_3 | 839 | 845 | PF00018 | 0.724 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.705 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.656 |
LIG_WW_2 | 413 | 416 | PF00397 | 0.788 |
MOD_CDC14_SPxK_1 | 409 | 412 | PF00782 | 0.788 |
MOD_CDK_SPK_2 | 406 | 411 | PF00069 | 0.779 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.782 |
MOD_CDK_SPxK_1 | 436 | 442 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.728 |
MOD_CDK_SPxK_1 | 789 | 795 | PF00069 | 0.749 |
MOD_CDK_SPxxK_3 | 404 | 411 | PF00069 | 0.778 |
MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.630 |
MOD_CDK_SPxxK_3 | 444 | 451 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.730 |
MOD_CDK_SPxxK_3 | 566 | 573 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 789 | 796 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 824 | 831 | PF00069 | 0.796 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.659 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.558 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.674 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.593 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.726 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.646 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.724 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.568 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.604 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.630 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.593 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.695 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.705 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.671 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.620 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.730 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.362 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.671 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.694 |
MOD_Cter_Amidation | 162 | 165 | PF01082 | 0.295 |
MOD_DYRK1A_RPxSP_1 | 43 | 47 | PF00069 | 0.700 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.777 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.677 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.470 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.700 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.696 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.656 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.792 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.703 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.691 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.561 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.507 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.605 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.732 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.732 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.758 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.528 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.738 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.643 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.600 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.628 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.733 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.619 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.586 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.470 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.603 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.582 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.729 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.669 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.719 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.657 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.613 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.531 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.664 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.767 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.486 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.331 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.764 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.735 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.494 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.753 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.546 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.668 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.406 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.759 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.745 |
MOD_PIKK_1 | 656 | 662 | PF00454 | 0.784 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.754 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.557 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.406 |
MOD_PKA_1 | 692 | 698 | PF00069 | 0.685 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.406 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.644 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.587 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.657 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.713 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.778 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.739 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.623 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.717 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.603 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.794 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.635 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.668 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.622 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.470 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.766 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.690 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.773 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.611 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.661 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.562 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.502 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.588 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.755 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.527 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.645 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.623 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.723 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.563 |
MOD_ProDKin_1 | 703 | 709 | PF00069 | 0.695 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.559 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.749 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.769 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.742 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.672 |
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 | 0.825 |
TRG_NLS_MonoExtC_3 | 220 | 225 | PF00514 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 750 | 755 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF88 | Leishmania donovani | 99% | 100% |
A4HE27 | Leishmania braziliensis | 62% | 97% |
E9AXH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QA02 | Leishmania major | 88% | 100% |