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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0046860 | glycosome membrane | 7 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HJ32
Term | Name | Level | Count |
---|---|---|---|
GO:0000038 | very long-chain fatty acid metabolic process | 5 | 1 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0006635 | fatty acid beta-oxidation | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009062 | fatty acid catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015849 | organic acid transport | 5 | 1 |
GO:0015908 | fatty acid transport | 6 | 1 |
GO:0015909 | long-chain fatty acid transport | 7 | 1 |
GO:0015910 | long-chain fatty acid import into peroxisome | 5 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016054 | organic acid catabolic process | 4 | 1 |
GO:0019395 | fatty acid oxidation | 5 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0030258 | lipid modification | 4 | 1 |
GO:0032365 | intracellular lipid transport | 4 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0034440 | lipid oxidation | 5 | 1 |
GO:0042760 | very long-chain fatty acid catabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046395 | carboxylic acid catabolic process | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1902001 | fatty acid transmembrane transport | 5 | 1 |
GO:1903825 | organic acid transmembrane transport | 3 | 1 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005215 | transporter activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0022804 | active transmembrane transporter activity | 3 | 10 |
GO:0022857 | transmembrane transporter activity | 2 | 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:0042626 | ATPase-coupled transmembrane transporter activity | 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:0140359 | ABC-type transporter activity | 3 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0005319 | lipid transporter activity | 2 | 1 |
GO:0005324 | long-chain fatty acid transporter activity | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 733 | 737 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 810 | 812 | PF00675 | 0.558 |
CLV_PCSK_FUR_1 | 808 | 812 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 808 | 810 | PF00082 | 0.557 |
CLV_PCSK_PC7_1 | 805 | 811 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.242 |
DEG_SCF_FBW7_1 | 825 | 832 | PF00400 | 0.588 |
DEG_SCF_FBW7_2 | 779 | 785 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.180 |
DOC_AGCK_PIF_1 | 291 | 296 | PF00069 | 0.307 |
DOC_CKS1_1 | 779 | 784 | PF01111 | 0.600 |
DOC_CKS1_1 | 826 | 831 | PF01111 | 0.631 |
DOC_MAPK_gen_1 | 142 | 152 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 596 | 602 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.237 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.195 |
DOC_MAPK_MEF2A_6 | 157 | 164 | PF00069 | 0.204 |
DOC_MAPK_MEF2A_6 | 532 | 539 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 679 | 687 | PF00069 | 0.543 |
DOC_MAPK_RevD_3 | 681 | 694 | PF00069 | 0.547 |
DOC_PP1_RVXF_1 | 229 | 235 | PF00149 | 0.266 |
DOC_PP1_RVXF_1 | 628 | 634 | PF00149 | 0.386 |
DOC_PP1_RVXF_1 | 648 | 654 | PF00149 | 0.492 |
DOC_PP1_RVXF_1 | 820 | 827 | PF00149 | 0.734 |
DOC_PP2B_LxvP_1 | 515 | 518 | PF13499 | 0.521 |
DOC_PP4_FxxP_1 | 653 | 656 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 826 | 829 | PF00568 | 0.679 |
DOC_PP4_MxPP_1 | 51 | 54 | PF00568 | 0.514 |
DOC_SPAK_OSR1_1 | 657 | 661 | PF12202 | 0.467 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.536 |
DOC_USP7_MATH_2 | 782 | 788 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 712 | 717 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 800 | 805 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 825 | 830 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 157 | 163 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.236 |
LIG_14-3-3_CanoR_1 | 693 | 697 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 732 | 740 | PF00244 | 0.622 |
LIG_Actin_WH2_2 | 547 | 563 | PF00022 | 0.507 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 547 | 551 | PF00533 | 0.507 |
LIG_Clathr_ClatBox_1 | 667 | 671 | PF01394 | 0.573 |
LIG_EH1_1 | 181 | 189 | PF00400 | 0.366 |
LIG_eIF4E_1 | 159 | 165 | PF01652 | 0.334 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.216 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.260 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.513 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.519 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.438 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.492 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.474 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.366 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.598 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.403 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.442 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.475 |
LIG_FHA_2 | 779 | 785 | PF00498 | 0.671 |
LIG_FHA_2 | 826 | 832 | PF00498 | 0.691 |
LIG_GBD_Chelix_1 | 424 | 432 | PF00786 | 0.344 |
LIG_LIR_Apic_2 | 528 | 533 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 571 | 577 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 146 | 156 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 295 | 305 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.180 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 617 | 625 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.180 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 606 | 611 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.521 |
LIG_NRBOX | 447 | 453 | PF00104 | 0.513 |
LIG_Pex14_1 | 287 | 291 | PF04695 | 0.265 |
LIG_Pex14_1 | 702 | 706 | PF04695 | 0.446 |
LIG_REV1ctd_RIR_1 | 650 | 655 | PF16727 | 0.442 |
LIG_RPA_C_Fungi | 152 | 164 | PF08784 | 0.256 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.378 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.378 |
LIG_SH2_GRB2like | 699 | 702 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 159 | 162 | PF00017 | 0.337 |
LIG_SH2_PTP2 | 530 | 533 | PF00017 | 0.378 |
LIG_SH2_SRC | 719 | 722 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 114 | 118 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 677 | 681 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 114 | 117 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 575 | 578 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.440 |
LIG_SH3_1 | 574 | 580 | PF00018 | 0.261 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.337 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.540 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.440 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.297 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.297 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.500 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.640 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.772 |
LIG_SUMO_SIM_par_1 | 163 | 168 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 512 | 519 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 635 | 642 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 665 | 671 | PF11976 | 0.468 |
LIG_SxIP_EBH_1 | 260 | 269 | PF03271 | 0.337 |
LIG_TRAF2_1 | 782 | 785 | PF00917 | 0.504 |
LIG_UBA3_1 | 351 | 357 | PF00899 | 0.256 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.378 |
MOD_CDK_SPK_2 | 778 | 783 | PF00069 | 0.639 |
MOD_CDK_SPK_2 | 800 | 805 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.685 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.636 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.316 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.180 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.304 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.419 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.690 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.702 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.321 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.329 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.351 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.378 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.301 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.606 |
MOD_CK2_1 | 825 | 831 | PF00069 | 0.640 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.755 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.295 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.278 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.532 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.737 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.590 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.500 |
MOD_GlcNHglycan | 784 | 789 | PF01048 | 0.612 |
MOD_GlcNHglycan | 817 | 820 | PF01048 | 0.490 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.482 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.277 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.398 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.380 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.425 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.638 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.411 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.714 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.400 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.689 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.683 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.655 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.666 |
MOD_LATS_1 | 380 | 386 | PF00433 | 0.337 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.259 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.180 |
MOD_N-GLC_1 | 623 | 628 | PF02516 | 0.321 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.518 |
MOD_N-GLC_2 | 543 | 545 | PF02516 | 0.261 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.311 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.259 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.319 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.183 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.476 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.408 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.313 |
MOD_NEK2_1 | 726 | 731 | PF00069 | 0.451 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.633 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.337 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.442 |
MOD_NEK2_2 | 480 | 485 | PF00069 | 0.449 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.562 |
MOD_PK_1 | 163 | 169 | PF00069 | 0.256 |
MOD_PK_1 | 382 | 388 | PF00069 | 0.321 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.269 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.394 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.180 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.332 |
MOD_PKA_2 | 804 | 810 | PF00069 | 0.696 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.502 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.214 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.378 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.378 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.311 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.286 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.319 |
MOD_Plk_1 | 735 | 741 | PF00069 | 0.458 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.349 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.393 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.256 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.333 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.337 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.453 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.364 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.367 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.378 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.364 |
MOD_Plk_4 | 735 | 741 | PF00069 | 0.418 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.784 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.704 |
MOD_ProDKin_1 | 712 | 718 | PF00069 | 0.331 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.697 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.639 |
MOD_ProDKin_1 | 800 | 806 | PF00069 | 0.666 |
MOD_ProDKin_1 | 825 | 831 | PF00069 | 0.558 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.786 |
MOD_SUMO_rev_2 | 483 | 492 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 663 | 668 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 549 | 554 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 655 | 658 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 808 | 811 | PF00400 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 552 | 556 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V4 | Leptomonas seymouri | 63% | 97% |
A0A0N1I6W7 | Leptomonas seymouri | 22% | 100% |
A0A0N1I7J3 | Leptomonas seymouri | 26% | 100% |
A0A0S4JCM8 | Bodo saltans | 27% | 100% |
A0A0S4JRH8 | Bodo saltans | 21% | 100% |
A0A1X0NJ54 | Trypanosomatidae | 42% | 100% |
A0A1X0P3R6 | Trypanosomatidae | 27% | 100% |
A0A1X0P474 | Trypanosomatidae | 20% | 100% |
A0A1X0P748 | Trypanosomatidae | 21% | 66% |
A0A3Q8ICD7 | Leishmania donovani | 77% | 99% |
A0A3Q8ICJ2 | Leishmania donovani | 22% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 42% | 100% |
A0A3R7NBD2 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X6Y1 | Leishmania donovani | 26% | 100% |
A0A422NTH3 | Trypanosoma rangeli | 21% | 100% |
A4HFH3 | Leishmania braziliensis | 23% | 100% |
A4HLP7 | Leishmania braziliensis | 26% | 100% |
A4I2N3 | Leishmania infantum | 22% | 100% |
A4I6L1 | Leishmania infantum | 77% | 99% |
A4I948 | Leishmania infantum | 26% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D3ZHR2 | Rattus norvegicus | 28% | 100% |
E9AD24 | Leishmania major | 22% | 100% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
F1RBC8 | Danio rerio | 27% | 100% |
O14678 | Homo sapiens | 25% | 100% |
O89016 | Mus musculus | 25% | 100% |
P16970 | Rattus norvegicus | 31% | 100% |
P28288 | Homo sapiens | 30% | 100% |
P33897 | Homo sapiens | 28% | 100% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 98% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 96% |
P45221 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 100% |
P48410 | Mus musculus | 28% | 100% |
P55096 | Mus musculus | 31% | 100% |
Q4Q402 | Leishmania major | 26% | 100% |
Q61285 | Mus musculus | 28% | 100% |
Q6NLC1 | Arabidopsis thaliana | 23% | 100% |
Q7JUN3 | Drosophila melanogaster | 27% | 100% |
Q8T8P3 | Dictyostelium discoideum | 29% | 100% |
Q9BHG2 | Leishmania major | 78% | 100% |
Q9QY44 | Rattus norvegicus | 28% | 100% |
Q9UBJ2 | Homo sapiens | 27% | 100% |
V5BPB7 | Trypanosoma cruzi | 27% | 100% |
V5BXE1 | Trypanosoma cruzi | 21% | 100% |