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 |
Related structures:
AlphaFold database: E9AL26
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.787 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 703 | 705 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 792 | 796 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 702 | 704 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 794 | 796 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 817 | 819 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 490 | 492 | PF00082 | 0.761 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.827 |
CLV_PCSK_PC1ET2_1 | 817 | 819 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.828 |
CLV_PCSK_SKI1_1 | 818 | 822 | PF00082 | 0.548 |
DEG_SCF_FBW7_1 | 370 | 375 | PF00400 | 0.843 |
DEG_SPOP_SBC_1 | 339 | 343 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 348 | 352 | PF00917 | 0.721 |
DOC_ANK_TNKS_1 | 666 | 673 | PF00023 | 0.535 |
DOC_CKS1_1 | 463 | 468 | PF01111 | 0.552 |
DOC_CKS1_1 | 697 | 702 | PF01111 | 0.816 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 509 | 515 | PF00134 | 0.550 |
DOC_MAPK_DCC_7 | 287 | 296 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 817 | 828 | PF00069 | 0.742 |
DOC_MAPK_MEF2A_6 | 287 | 296 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 424 | 431 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 464 | 473 | PF00069 | 0.746 |
DOC_MAPK_MEF2A_6 | 821 | 830 | PF00069 | 0.688 |
DOC_MAPK_RevD_3 | 427 | 443 | PF00069 | 0.536 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.739 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 686 | 689 | PF00568 | 0.737 |
DOC_PP4_MxPP_1 | 698 | 701 | PF00568 | 0.682 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.743 |
DOC_USP7_UBL2_3 | 486 | 490 | PF12436 | 0.781 |
DOC_USP7_UBL2_3 | 553 | 557 | PF12436 | 0.737 |
DOC_USP7_UBL2_3 | 595 | 599 | PF12436 | 0.754 |
DOC_USP7_UBL2_3 | 817 | 821 | PF12436 | 0.503 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.838 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 696 | 701 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 709 | 714 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 729 | 734 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 836 | 841 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 196 | 202 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 242 | 249 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 287 | 291 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 394 | 400 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 491 | 501 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 507 | 512 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 526 | 534 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 536 | 544 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 703 | 713 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 736 | 741 | PF00244 | 0.810 |
LIG_14-3-3_CanoR_1 | 754 | 759 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 775 | 779 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.420 |
LIG_BRCT_BRCA1_1 | 758 | 762 | PF00533 | 0.739 |
LIG_deltaCOP1_diTrp_1 | 181 | 189 | PF00928 | 0.411 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.471 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.266 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.459 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.733 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.746 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.806 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.411 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.761 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.623 |
LIG_Integrin_isoDGR_2 | 763 | 765 | PF01839 | 0.729 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 684 | 689 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 4 | 12 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 69 | 76 | PF02991 | 0.448 |
LIG_LIR_LC3C_4 | 28 | 32 | PF02991 | 0.477 |
LIG_LIR_LC3C_4 | 428 | 432 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 4 | 9 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.374 |
LIG_MAD2 | 553 | 561 | PF02301 | 0.815 |
LIG_PALB2_WD40_1 | 100 | 108 | PF16756 | 0.411 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.411 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.406 |
LIG_SH2_STAT3 | 635 | 638 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 740 | 743 | PF00017 | 0.746 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.407 |
LIG_SH3_1 | 300 | 306 | PF00018 | 0.738 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.511 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.724 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.775 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.693 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.756 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.717 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.791 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.589 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.744 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.684 |
LIG_SH3_3 | 708 | 714 | PF00018 | 0.755 |
LIG_SH3_4 | 599 | 606 | PF00018 | 0.798 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 428 | 433 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 233 | 238 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 354 | 363 | PF11976 | 0.754 |
LIG_SUMO_SIM_par_1 | 428 | 433 | PF11976 | 0.547 |
LIG_TRAF2_1 | 777 | 780 | PF00917 | 0.642 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.411 |
LIG_WW_3 | 284 | 288 | PF00397 | 0.733 |
LIG_WW_3 | 324 | 328 | PF00397 | 0.740 |
LIG_WW_3 | 577 | 581 | PF00397 | 0.820 |
LIG_WW_3 | 699 | 703 | PF00397 | 0.812 |
MOD_CDC14_SPxK_1 | 585 | 588 | PF00782 | 0.733 |
MOD_CDK_SPxK_1 | 321 | 327 | PF00069 | 0.740 |
MOD_CDK_SPxK_1 | 582 | 588 | PF00069 | 0.736 |
MOD_CDK_SPxK_1 | 696 | 702 | PF00069 | 0.824 |
MOD_CDK_SPxxK_3 | 321 | 328 | PF00069 | 0.741 |
MOD_CDK_SPxxK_3 | 678 | 685 | PF00069 | 0.686 |
MOD_CDK_SPxxK_3 | 696 | 703 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 729 | 736 | PF00069 | 0.741 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.356 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.366 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.183 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.411 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.652 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.639 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.838 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.829 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.692 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.854 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.752 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.725 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.824 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.821 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.680 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.471 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.733 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.733 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.563 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.554 |
MOD_CK2_1 | 774 | 780 | PF00069 | 0.665 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.383 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.411 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.329 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.701 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.784 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.672 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.525 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.551 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.689 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.741 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.710 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.511 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.670 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.411 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.411 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.511 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.703 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.707 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.786 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.794 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.697 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.847 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.750 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.742 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.744 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.725 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.722 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.485 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.411 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.403 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.560 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.694 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.423 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.210 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.560 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.386 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.371 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.369 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.704 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.710 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.411 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.700 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.423 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.511 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.749 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.403 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.753 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.549 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.411 |
MOD_PK_1 | 507 | 513 | PF00069 | 0.835 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.411 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.767 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.662 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.732 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.765 |
MOD_PKB_1 | 327 | 335 | PF00069 | 0.633 |
MOD_PKB_1 | 505 | 513 | PF00069 | 0.835 |
MOD_PKB_1 | 702 | 710 | PF00069 | 0.741 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.411 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.347 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.419 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.406 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.413 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.566 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.393 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.354 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.411 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.511 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.590 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.737 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.802 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.753 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.782 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.840 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.807 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.780 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.751 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.642 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.698 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.736 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.709 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.783 |
MOD_ProDKin_1 | 696 | 702 | PF00069 | 0.780 |
MOD_ProDKin_1 | 709 | 715 | PF00069 | 0.694 |
MOD_ProDKin_1 | 729 | 735 | PF00069 | 0.702 |
MOD_ProDKin_1 | 836 | 842 | PF00069 | 0.565 |
MOD_SUMO_for_1 | 441 | 444 | PF00179 | 0.681 |
MOD_SUMO_rev_2 | 133 | 139 | PF00179 | 0.354 |
MOD_SUMO_rev_2 | 362 | 366 | PF00179 | 0.762 |
MOD_SUMO_rev_2 | 642 | 647 | PF00179 | 0.651 |
TRG_DiLeu_BaEn_2 | 519 | 525 | PF01217 | 0.828 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.842 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.832 |
TRG_ER_diArg_1 | 701 | 704 | PF00400 | 0.818 |
TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.598 |
TRG_NLS_MonoExtC_3 | 813 | 818 | PF00514 | 0.584 |
TRG_NLS_MonoExtN_4 | 325 | 331 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 489 | 494 | PF00514 | 0.734 |
TRG_Pf-PMV_PEXEL_1 | 526 | 531 | PF00026 | 0.750 |
TRG_Pf-PMV_PEXEL_1 | 704 | 708 | PF00026 | 0.826 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD87 | Leptomonas seymouri | 48% | 100% |
A0A3S7WPQ0 | Leishmania donovani | 86% | 100% |
A4H4W0 | Leishmania braziliensis | 66% | 96% |
A4HT34 | Leishmania infantum | 86% | 100% |
Q4QIS8 | Leishmania major | 86% | 100% |