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 |
Related structures:
AlphaFold database: A4H7Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.595 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.827 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.416 |
CLV_PCSK_FUR_1 | 681 | 685 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.561 |
DEG_APCC_DBOX_1 | 597 | 605 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 665 | 673 | PF00400 | 0.507 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.483 |
DEG_SCF_FBW7_1 | 206 | 212 | PF00400 | 0.577 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.619 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.615 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.803 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.703 |
DOC_CKS1_1 | 206 | 211 | PF01111 | 0.577 |
DOC_CKS1_1 | 592 | 597 | PF01111 | 0.507 |
DOC_CKS1_1 | 685 | 690 | PF01111 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 720 | 726 | PF00134 | 0.267 |
DOC_MAPK_FxFP_2 | 24 | 27 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 503 | 512 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 579 | 589 | PF00069 | 0.408 |
DOC_MAPK_HePTP_8 | 576 | 588 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 357 | 366 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 451 | 460 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 579 | 588 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 556 | 563 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.539 |
DOC_PP4_FxxP_1 | 24 | 27 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 724 | 727 | PF00568 | 0.495 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 263 | 272 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 598 | 602 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 666 | 670 | PF00244 | 0.507 |
LIG_APCC_ABBA_1 | 586 | 591 | PF00400 | 0.408 |
LIG_BIR_III_2 | 145 | 149 | PF00653 | 0.579 |
LIG_BIR_III_2 | 741 | 745 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.471 |
LIG_Clathr_ClatBox_1 | 526 | 530 | PF01394 | 0.507 |
LIG_EH1_1 | 471 | 479 | PF00400 | 0.507 |
LIG_EVH1_2 | 39 | 43 | PF00568 | 0.488 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.577 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.507 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.532 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.636 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.814 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.408 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.554 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.754 |
LIG_HCF-1_HBM_1 | 785 | 788 | PF13415 | 0.578 |
LIG_LIR_Apic_2 | 352 | 358 | PF02991 | 0.671 |
LIG_LIR_Apic_2 | 578 | 584 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 591 | 595 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 20 | 30 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 697 | 706 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 495 | 499 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.474 |
LIG_MYND_1 | 34 | 38 | PF01753 | 0.478 |
LIG_MYND_1 | 723 | 727 | PF01753 | 0.408 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.408 |
LIG_PCNA_yPIPBox_3 | 463 | 474 | PF02747 | 0.424 |
LIG_Pex14_2 | 22 | 26 | PF04695 | 0.481 |
LIG_Pex14_2 | 701 | 705 | PF04695 | 0.507 |
LIG_PTAP_UEV_1 | 198 | 203 | PF05743 | 0.571 |
LIG_PTB_Apo_2 | 371 | 378 | PF02174 | 0.609 |
LIG_PTB_Phospho_1 | 371 | 377 | PF10480 | 0.614 |
LIG_RPA_C_Fungi | 371 | 383 | PF08784 | 0.576 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.666 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.355 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.408 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.507 |
LIG_SH2_CRK | 650 | 654 | PF00017 | 0.267 |
LIG_SH2_SRC | 788 | 791 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.789 |
LIG_SH2_STAT3 | 377 | 380 | PF00017 | 0.621 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.633 |
LIG_SH3_1 | 269 | 275 | PF00018 | 0.583 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.601 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.772 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.477 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.746 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.600 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.678 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.815 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.729 |
LIG_SUMO_SIM_anti_2 | 457 | 462 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 511 | 516 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 486 | 492 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 604 | 610 | PF11976 | 0.296 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.552 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.524 |
LIG_TRFH_1 | 30 | 34 | PF08558 | 0.476 |
LIG_UBA3_1 | 366 | 371 | PF00899 | 0.605 |
LIG_UBA3_1 | 526 | 533 | PF00899 | 0.507 |
LIG_WRC_WIRS_1 | 493 | 498 | PF05994 | 0.507 |
LIG_WW_1 | 38 | 41 | PF00397 | 0.478 |
MOD_CDK_SPK_2 | 639 | 644 | PF00069 | 0.408 |
MOD_CDK_SPxxK_3 | 382 | 389 | PF00069 | 0.666 |
MOD_CDK_SPxxK_3 | 591 | 598 | PF00069 | 0.507 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.632 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.765 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.718 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.746 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.648 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.717 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.584 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.821 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.769 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.493 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.408 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.408 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.757 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.733 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.816 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.569 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.723 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.561 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.513 |
MOD_CK2_1 | 779 | 785 | PF00069 | 0.809 |
MOD_Cter_Amidation | 681 | 684 | PF01082 | 0.507 |
MOD_GlcNHglycan | 127 | 131 | PF01048 | 0.840 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.758 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.808 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.765 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.783 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.687 |
MOD_GlcNHglycan | 338 | 342 | PF01048 | 0.691 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.518 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.624 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.450 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.357 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.507 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.590 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.558 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.772 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.562 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.578 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.755 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.755 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.804 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.646 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.507 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.811 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.437 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.730 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.719 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.745 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.827 |
MOD_LATS_1 | 150 | 156 | PF00433 | 0.578 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.408 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.507 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.526 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.648 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.599 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.625 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.408 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.807 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.507 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.267 |
MOD_OFUCOSY | 4 | 10 | PF10250 | 0.476 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.599 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.541 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.626 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.408 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.267 |
MOD_PIKK_1 | 548 | 554 | PF00454 | 0.180 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.551 |
MOD_PIKK_1 | 748 | 754 | PF00454 | 0.749 |
MOD_PIKK_1 | 760 | 766 | PF00454 | 0.722 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.828 |
MOD_PKA_1 | 445 | 451 | PF00069 | 0.507 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.784 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.578 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.597 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.507 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.408 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.507 |
MOD_PKB_1 | 167 | 175 | PF00069 | 0.783 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.584 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.507 |
MOD_Plk_1 | 784 | 790 | PF00069 | 0.689 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.588 |
MOD_Plk_2-3 | 665 | 671 | PF00069 | 0.507 |
MOD_Plk_2-3 | 780 | 786 | PF00069 | 0.566 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.530 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.480 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.408 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.507 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.499 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.507 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.610 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.578 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.480 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.563 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.665 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.408 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.408 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.408 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 454 | 457 | PF00179 | 0.408 |
MOD_SUMO_for_1 | 542 | 545 | PF00179 | 0.408 |
MOD_SUMO_for_1 | 625 | 628 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 457 | 462 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_2 | 584 | 590 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 555 | 560 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 650 | 653 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 695 | 698 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.808 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 680 | 683 | PF00400 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTA3 | Leishmania donovani | 76% | 100% |
A4HWB5 | Leishmania infantum | 76% | 100% |
C9ZNW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AQ15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |