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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HW76
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0106310 | protein serine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.328 |
CLV_C14_Caspase3-7 | 735 | 739 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.657 |
CLV_PCSK_FUR_1 | 539 | 543 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 542 | 548 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 716 | 720 | PF00082 | 0.586 |
DOC_CKS1_1 | 463 | 468 | PF01111 | 0.643 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.548 |
DOC_CKS1_1 | 504 | 509 | PF01111 | 0.538 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 496 | 505 | PF00134 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 473 | 479 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.627 |
DOC_MAPK_gen_1 | 311 | 320 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 61 | 71 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 714 | 721 | PF00069 | 0.604 |
DOC_PP2B_LxvP_1 | 473 | 476 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.326 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 472 | 475 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.570 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 335 | 343 | PF00244 | 0.241 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 625 | 635 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 64 | 71 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 687 | 693 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.590 |
LIG_Actin_WH2_2 | 679 | 695 | PF00022 | 0.631 |
LIG_APCC_ABBA_1 | 262 | 267 | PF00400 | 0.344 |
LIG_APCC_ABBAyCdc20_2 | 125 | 131 | PF00400 | 0.476 |
LIG_APCC_ABBAyCdc20_2 | 306 | 312 | PF00400 | 0.344 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.518 |
LIG_deltaCOP1_diTrp_1 | 417 | 427 | PF00928 | 0.344 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.468 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.204 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.347 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.381 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.607 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.590 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.563 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.412 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.379 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.640 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.590 |
LIG_LIR_Apic_2 | 283 | 287 | PF02991 | 0.302 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 471 | 475 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 506 | 512 | PF02991 | 0.558 |
LIG_LIR_Apic_2 | 629 | 635 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.406 |
LIG_Pex14_1 | 450 | 454 | PF04695 | 0.381 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.511 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.582 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.558 |
LIG_SH2_GRB2like | 252 | 255 | PF00017 | 0.328 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.463 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 681 | 685 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.344 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.573 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.606 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.344 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.467 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.549 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.567 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.564 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.644 |
LIG_SUMO_SIM_anti_2 | 237 | 242 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 441 | 447 | PF11976 | 0.328 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.328 |
LIG_TRFH_1 | 484 | 488 | PF08558 | 0.576 |
LIG_UBA3_1 | 177 | 181 | PF00899 | 0.423 |
LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.328 |
LIG_WRC_WIRS_1 | 469 | 474 | PF05994 | 0.516 |
MOD_CDC14_SPxK_1 | 487 | 490 | PF00782 | 0.571 |
MOD_CDK_SPxK_1 | 484 | 490 | PF00069 | 0.575 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.593 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.564 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.393 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.382 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.369 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.687 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.584 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.642 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.717 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.673 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.740 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.827 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.637 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.631 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.559 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.705 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.797 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.560 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.328 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.359 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.633 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.683 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.616 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.523 |
MOD_Cter_Amidation | 536 | 539 | PF01082 | 0.650 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.690 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.704 |
MOD_GlcNHglycan | 130 | 135 | PF01048 | 0.641 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.488 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.389 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.741 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.397 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.668 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.657 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.692 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.712 |
MOD_GlcNHglycan | 583 | 587 | PF01048 | 0.599 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.696 |
MOD_GlcNHglycan | 653 | 657 | PF01048 | 0.808 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.619 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.631 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.543 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.784 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.606 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.754 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.371 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.554 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.743 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.507 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.582 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.630 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.727 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.588 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.647 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.546 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.612 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.652 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.629 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.668 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.750 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.628 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.705 |
MOD_LATS_1 | 548 | 554 | PF00433 | 0.598 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.569 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.561 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.615 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.540 |
MOD_N-GLC_1 | 712 | 717 | PF02516 | 0.709 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.574 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.522 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.598 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.377 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.333 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.603 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.577 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.730 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.805 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.557 |
MOD_NEK2_2 | 688 | 693 | PF00069 | 0.601 |
MOD_NEK2_2 | 785 | 790 | PF00069 | 0.554 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.590 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.367 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.328 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.570 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.644 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.577 |
MOD_PKA_1 | 541 | 547 | PF00069 | 0.651 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.654 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.446 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.379 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.630 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.572 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.672 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.676 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.568 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.556 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.638 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.611 |
MOD_PKA_2 | 792 | 798 | PF00069 | 0.586 |
MOD_PKB_1 | 580 | 588 | PF00069 | 0.616 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.524 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.344 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.326 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.502 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.581 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.515 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.508 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.553 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.499 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.354 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.333 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.614 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.561 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.579 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.610 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.603 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.790 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.644 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.560 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.699 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.698 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.655 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.673 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.617 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.664 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.607 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.678 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.443 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.544 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.237 |
MOD_SUMO_rev_2 | 653 | 660 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 710 | 715 | PF00179 | 0.601 |
TRG_DiLeu_BaEn_2 | 422 | 428 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.344 |
TRG_NLS_MonoExtN_4 | 604 | 611 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 311 | 316 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 734 | 738 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W1 | Leptomonas seymouri | 44% | 71% |
A0A3S7WT68 | Leishmania donovani | 99% | 73% |
A4H7V0 | Leishmania braziliensis | 76% | 99% |
E9ACA4 | Leishmania major | 25% | 100% |
E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9ALU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QFK4 | Leishmania major | 90% | 98% |