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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031510 | SUMO activating enzyme complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QIE7
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0016925 | protein sumoylation | 7 | 8 |
GO:0018193 | peptidyl-amino acid modification | 5 | 8 |
GO:0018205 | peptidyl-lysine modification | 6 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0032446 | protein modification by small protein conjugation | 6 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 8 |
GO:0016874 | ligase activity | 2 | 8 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0019948 | SUMO activating enzyme activity | 3 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.256 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.350 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.481 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.431 |
CLV_PCSK_FUR_1 | 529 | 533 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.350 |
CLV_Separin_Metazoa | 331 | 335 | PF03568 | 0.431 |
CLV_Separin_Metazoa | 689 | 693 | PF03568 | 0.504 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.432 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.282 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.785 |
DEG_SPOP_SBC_1 | 795 | 799 | PF00917 | 0.583 |
DOC_CYCLIN_RxL_1 | 331 | 339 | PF00134 | 0.481 |
DOC_CYCLIN_RxL_1 | 49 | 60 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 529 | 535 | PF00069 | 0.710 |
DOC_MAPK_JIP1_4 | 409 | 415 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 540 | 548 | PF00069 | 0.759 |
DOC_PP1_RVXF_1 | 332 | 338 | PF00149 | 0.481 |
DOC_PP2B_LxvP_1 | 661 | 664 | PF13499 | 0.589 |
DOC_PP2B_LxvP_1 | 691 | 694 | PF13499 | 0.589 |
DOC_PP2B_LxvP_1 | 782 | 785 | PF13499 | 0.769 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.200 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 797 | 802 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 18 | 25 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 321 | 328 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 401 | 410 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 478 | 486 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 583 | 591 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 637 | 641 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 643 | 648 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 705 | 711 | PF00244 | 0.558 |
LIG_Actin_WH2_2 | 462 | 480 | PF00022 | 0.481 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.500 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.500 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.500 |
LIG_BRCT_BRCA1_1 | 739 | 743 | PF00533 | 0.621 |
LIG_Clathr_ClatBox_1 | 64 | 68 | PF01394 | 0.432 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.333 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.294 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.416 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.221 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.705 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.669 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.390 |
LIG_FHA_1 | 786 | 792 | PF00498 | 0.760 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.741 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.497 |
LIG_FHA_2 | 724 | 730 | PF00498 | 0.562 |
LIG_GBD_Chelix_1 | 328 | 336 | PF00786 | 0.432 |
LIG_GBD_Chelix_1 | 469 | 477 | PF00786 | 0.432 |
LIG_LIR_Gen_1 | 228 | 234 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 676 | 687 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 718 | 725 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 676 | 682 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 740 | 746 | PF02991 | 0.592 |
LIG_MAD2 | 518 | 526 | PF02301 | 0.419 |
LIG_NRBOX | 331 | 337 | PF00104 | 0.481 |
LIG_NRBOX | 472 | 478 | PF00104 | 0.432 |
LIG_Pex14_2 | 141 | 145 | PF04695 | 0.334 |
LIG_SH2_NCK_1 | 137 | 141 | PF00017 | 0.384 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 679 | 683 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 708 | 712 | PF00017 | 0.589 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.350 |
LIG_SH2_STAT3 | 195 | 198 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.589 |
LIG_SH3_1 | 531 | 537 | PF00018 | 0.727 |
LIG_SH3_2 | 618 | 623 | PF14604 | 0.556 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.432 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.753 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.591 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.354 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.720 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.483 |
LIG_SUMO_SIM_anti_2 | 472 | 482 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 604 | 609 | PF11976 | 0.649 |
LIG_SUMO_SIM_anti_2 | 831 | 837 | PF11976 | 0.715 |
LIG_SUMO_SIM_par_1 | 342 | 350 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 387 | 394 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 52 | 57 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 638 | 646 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 797 | 805 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 831 | 837 | PF11976 | 0.715 |
LIG_SxIP_EBH_1 | 448 | 461 | PF03271 | 0.481 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.615 |
LIG_TRAF2_1 | 768 | 771 | PF00917 | 0.539 |
LIG_UBA3_1 | 332 | 340 | PF00899 | 0.392 |
LIG_UBA3_1 | 344 | 348 | PF00899 | 0.290 |
MOD_CDK_SPK_2 | 511 | 516 | PF00069 | 0.723 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.801 |
MOD_CDK_SPxxK_3 | 511 | 518 | PF00069 | 0.495 |
MOD_CDK_SPxxK_3 | 533 | 540 | PF00069 | 0.588 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.787 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.438 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.446 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.458 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.356 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.481 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.432 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.706 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.432 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.683 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.767 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.481 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.432 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.787 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.737 |
MOD_CK2_1 | 744 | 750 | PF00069 | 0.567 |
MOD_Cter_Amidation | 117 | 120 | PF01082 | 0.431 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.332 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.411 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.352 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.207 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.418 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.444 |
MOD_GlcNHglycan | 312 | 317 | PF01048 | 0.460 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.434 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.346 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.302 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.432 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.744 |
MOD_GlcNHglycan | 504 | 508 | PF01048 | 0.549 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.810 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.432 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.655 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.654 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.352 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.555 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.774 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.473 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.346 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.447 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.417 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.491 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.406 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.432 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.238 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.337 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.742 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.778 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.350 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.426 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.732 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.444 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.275 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.791 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.157 |
MOD_LATS_1 | 213 | 219 | PF00433 | 0.384 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.373 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.256 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.465 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.497 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.777 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.346 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.429 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.347 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.421 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.355 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.432 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.517 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.492 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.327 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.519 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.803 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.350 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.431 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.474 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.697 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.481 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.599 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.350 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.431 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.429 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.431 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.481 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.717 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.662 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.649 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.397 |
MOD_PKA_2 | 704 | 710 | PF00069 | 0.497 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.432 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.481 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.481 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.350 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.409 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.350 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.392 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.468 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.429 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.406 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.677 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.780 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.484 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.694 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.704 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.699 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.692 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.468 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.687 |
MOD_ProDKin_1 | 797 | 803 | PF00069 | 0.586 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 659 | 662 | PF00179 | 0.332 |
MOD_SUMO_rev_2 | 236 | 246 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 722 | 732 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 831 | 836 | PF01217 | 0.669 |
TRG_DiLeu_BaEn_4 | 342 | 348 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.384 |
TRG_DiLeu_LyEn_5 | 331 | 336 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.350 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.540 |
TRG_LysEnd_GGAAcLL_1 | 832 | 837 | PF00790 | 0.715 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEH2 | Leptomonas seymouri | 50% | 81% |
A0A3R7MNQ1 | Trypanosoma rangeli | 39% | 99% |
A0A3S7WQ47 | Leishmania donovani | 88% | 76% |
A4HTH3 | Leishmania infantum | 89% | 76% |
C9ZPL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AMA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 79% |