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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 7 |
GO:0005929 | cilium | 4 | 8 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0099080 | supramolecular complex | 2 | 7 |
GO:0099081 | supramolecular polymer | 3 | 7 |
GO:0099512 | supramolecular fiber | 4 | 7 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H6X0
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0018095 | protein polyglutamylation | 7 | 8 |
GO:0018193 | peptidyl-amino acid modification | 5 | 8 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 8 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 8 |
GO:0016881 | acid-amino acid ligase activity | 4 | 8 |
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 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.775 |
CLV_PCSK_FUR_1 | 101 | 105 | PF00082 | 0.567 |
CLV_PCSK_FUR_1 | 328 | 332 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.326 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
DEG_SCF_FBW7_1 | 83 | 89 | PF00400 | 0.688 |
DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.606 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.688 |
DOC_MAPK_gen_1 | 196 | 204 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 619 | 627 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 619 | 627 | PF00069 | 0.553 |
DOC_MAPK_NFAT4_5 | 620 | 628 | PF00069 | 0.553 |
DOC_MAPK_RevD_3 | 184 | 197 | PF00069 | 0.606 |
DOC_PP1_RVXF_1 | 707 | 714 | PF00149 | 0.542 |
DOC_PP1_RVXF_1 | 777 | 783 | PF00149 | 0.518 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.825 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 755 | 759 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.677 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 250 | 259 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 415 | 419 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 451 | 457 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 56 | 66 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.672 |
LIG_Actin_WH2_2 | 704 | 722 | PF00022 | 0.534 |
LIG_APCC_ABBA_1 | 475 | 480 | PF00400 | 0.513 |
LIG_BIR_III_4 | 174 | 178 | PF00653 | 0.643 |
LIG_BIR_III_4 | 433 | 437 | PF00653 | 0.468 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 575 | 579 | PF00533 | 0.642 |
LIG_deltaCOP1_diTrp_1 | 354 | 359 | PF00928 | 0.475 |
LIG_eIF4E_1 | 609 | 615 | PF01652 | 0.513 |
LIG_eIF4E_1 | 736 | 742 | PF01652 | 0.513 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.665 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.486 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.501 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.513 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.602 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.644 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.616 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.425 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.799 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.537 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.513 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.513 |
LIG_FHA_2 | 761 | 767 | PF00498 | 0.513 |
LIG_Integrin_isoDGR_2 | 223 | 225 | PF01839 | 0.596 |
LIG_LIR_Apic_2 | 468 | 472 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 354 | 362 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 641 | 652 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 687 | 695 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 641 | 647 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 687 | 691 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 732 | 736 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 810 | 815 | PF02991 | 0.569 |
LIG_MAD2 | 779 | 787 | PF02301 | 0.513 |
LIG_PCNA_PIPBox_1 | 659 | 668 | PF02747 | 0.513 |
LIG_PDZ_Class_2 | 812 | 817 | PF00595 | 0.455 |
LIG_Pex14_2 | 478 | 482 | PF04695 | 0.511 |
LIG_Pex14_2 | 688 | 692 | PF04695 | 0.461 |
LIG_PTB_Apo_2 | 707 | 714 | PF02174 | 0.513 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.513 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.513 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.480 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.553 |
LIG_SH2_CRK | 716 | 720 | PF00017 | 0.513 |
LIG_SH2_CRK | 738 | 742 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 626 | 629 | PF00017 | 0.526 |
LIG_SH2_SRC | 604 | 607 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 738 | 742 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.511 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.810 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.643 |
LIG_SH3_3 | 778 | 784 | PF00018 | 0.523 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.663 |
LIG_SUMO_SIM_anti_2 | 199 | 205 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 452 | 458 | PF11976 | 0.482 |
LIG_TYR_ITAM | 395 | 416 | PF00017 | 0.513 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.513 |
LIG_TYR_ITIM | 714 | 719 | PF00017 | 0.513 |
LIG_WRC_WIRS_1 | 456 | 461 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 525 | 530 | PF05994 | 0.563 |
LIG_WW_1 | 783 | 786 | PF00397 | 0.511 |
LIG_WW_2 | 90 | 93 | PF00397 | 0.608 |
MOD_CDK_SPK_2 | 573 | 578 | PF00069 | 0.550 |
MOD_CDK_SPxxK_3 | 529 | 536 | PF00069 | 0.533 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.708 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.578 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.767 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.691 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.660 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.482 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.716 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.722 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.608 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.492 |
MOD_CK1_1 | 758 | 764 | PF00069 | 0.534 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.690 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.689 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.653 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.662 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.596 |
MOD_Cter_Amidation | 617 | 620 | PF01082 | 0.353 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.647 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.653 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.671 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.688 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.730 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.834 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.776 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.692 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.661 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.326 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.336 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.765 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.717 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.600 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.566 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.824 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.786 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.611 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.715 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.562 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.763 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.641 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.636 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.716 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.653 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.626 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.468 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.534 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.678 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.513 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.563 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.682 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.697 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.340 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.682 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.523 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.493 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.732 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.632 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.646 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.768 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.320 |
MOD_N-GLC_1 | 753 | 758 | PF02516 | 0.312 |
MOD_N-GLC_1 | 774 | 779 | PF02516 | 0.232 |
MOD_N-GLC_2 | 567 | 569 | PF02516 | 0.628 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.711 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.513 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.573 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.684 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.437 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.513 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.513 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.513 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.513 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.591 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.470 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.471 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.611 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.513 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.513 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.623 |
MOD_PKA_1 | 103 | 109 | PF00069 | 0.671 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.664 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.511 |
MOD_PKA_1 | 519 | 525 | PF00069 | 0.496 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.642 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.671 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.664 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.762 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.478 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.513 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.513 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.833 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.647 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.595 |
MOD_Plk_1 | 774 | 780 | PF00069 | 0.432 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.632 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.638 |
MOD_Plk_2-3 | 729 | 735 | PF00069 | 0.511 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.560 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.577 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.478 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.389 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.639 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.650 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.679 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.632 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.528 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.702 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.602 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.513 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.686 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.593 |
MOD_SUMO_for_1 | 126 | 129 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 344 | 350 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 517 | 522 | PF00179 | 0.468 |
TRG_AP2beta_CARGO_1 | 641 | 651 | PF09066 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 764 | 769 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 810 | 815 | PF01217 | 0.291 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 798 | 801 | PF00400 | 0.488 |
TRG_NES_CRM1_1 | 660 | 675 | PF08389 | 0.513 |
TRG_NLS_MonoCore_2 | 55 | 60 | PF00514 | 0.625 |
TRG_NLS_MonoCore_2 | 99 | 104 | PF00514 | 0.610 |
TRG_NLS_MonoExtC_3 | 99 | 104 | PF00514 | 0.635 |
TRG_NLS_MonoExtN_4 | 100 | 107 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 56 | 61 | PF00514 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 161 | 166 | PF00026 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 767 | 771 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDX5 | Leptomonas seymouri | 61% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 24% | 100% |
A4H8G3 | Leishmania braziliensis | 72% | 95% |
A4HWT7 | Leishmania infantum | 100% | 100% |
A4HYN9 | Leishmania infantum | 24% | 100% |
E9AID0 | Leishmania braziliensis | 24% | 100% |
E9AQJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QCW7 | Leishmania major | 23% | 100% |
Q4QEY2 | Leishmania major | 89% | 99% |