Glycosome membrane, GAT1 glycosomal transporterATP-binding cassette D, member 2 ABCD2
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
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: A4I6L1
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 | 11 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0022804 | active transmembrane transporter activity | 3 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140359 | ABC-type transporter activity | 3 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
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 | 732 | 736 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.775 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.598 |
CLV_PCSK_FUR_1 | 813 | 817 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.512 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.256 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.348 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 180 | 192 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 19 | 25 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 141 | 151 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 225 | 233 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 500 | 509 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 595 | 601 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 73 | 80 | PF00069 | 0.519 |
DOC_MAPK_HePTP_8 | 123 | 135 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.193 |
DOC_MAPK_MEF2A_6 | 156 | 163 | PF00069 | 0.219 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 456 | 463 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 531 | 538 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 678 | 686 | PF00069 | 0.559 |
DOC_MAPK_RevD_3 | 680 | 693 | PF00069 | 0.561 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.291 |
DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.575 |
DOC_PP1_RVXF_1 | 647 | 653 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 825 | 832 | PF00149 | 0.770 |
DOC_PP2B_LxvP_1 | 514 | 517 | PF13499 | 0.545 |
DOC_PP4_FxxP_1 | 652 | 655 | PF00568 | 0.466 |
DOC_PP4_MxPP_1 | 51 | 54 | PF00568 | 0.488 |
DOC_SPAK_OSR1_1 | 656 | 660 | PF12202 | 0.479 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 835 | 839 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.494 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.250 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.243 |
LIG_14-3-3_CanoR_1 | 500 | 510 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 629 | 639 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 692 | 696 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 731 | 739 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 750 | 758 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 821 | 829 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.472 |
LIG_Actin_WH2_2 | 44 | 59 | PF00022 | 0.432 |
LIG_Actin_WH2_2 | 546 | 562 | PF00022 | 0.524 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.288 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.523 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.703 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.399 |
LIG_Clathr_ClatBox_1 | 666 | 670 | PF01394 | 0.589 |
LIG_eIF4E_1 | 147 | 153 | PF01652 | 0.434 |
LIG_eIF4E_1 | 158 | 164 | PF01652 | 0.367 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.254 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.416 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.520 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.531 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.524 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.494 |
LIG_FHA_1 | 746 | 752 | PF00498 | 0.642 |
LIG_FHA_1 | 785 | 791 | PF00498 | 0.596 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.470 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.474 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.430 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.578 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.466 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.466 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.694 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.738 |
LIG_GBD_Chelix_1 | 423 | 431 | PF00786 | 0.363 |
LIG_LIR_Apic_2 | 527 | 532 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 570 | 576 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 204 | 212 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 508 | 517 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 616 | 624 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.466 |
LIG_MYND_2 | 765 | 769 | PF01753 | 0.623 |
LIG_NRBOX | 446 | 452 | PF00104 | 0.555 |
LIG_Pex14_1 | 701 | 705 | PF04695 | 0.453 |
LIG_REV1ctd_RIR_1 | 649 | 654 | PF16727 | 0.466 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.411 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.524 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.524 |
LIG_SH2_GRB2like | 698 | 701 | PF00017 | 0.555 |
LIG_SH2_NCK_1 | 113 | 117 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 529 | 532 | PF00017 | 0.524 |
LIG_SH2_SRC | 494 | 497 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 494 | 498 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 676 | 680 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 574 | 577 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.545 |
LIG_SH3_1 | 49 | 55 | PF00018 | 0.438 |
LIG_SH3_1 | 573 | 579 | PF00018 | 0.448 |
LIG_SH3_2 | 52 | 57 | PF14604 | 0.450 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.318 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.537 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.542 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.449 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.412 |
LIG_SH3_3 | 740 | 746 | PF00018 | 0.606 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.726 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.573 |
LIG_SUMO_SIM_par_1 | 511 | 518 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.584 |
LIG_SxIP_EBH_1 | 259 | 268 | PF03271 | 0.318 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.403 |
MOD_CDK_SPK_2 | 777 | 782 | PF00069 | 0.726 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.518 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.390 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.281 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.647 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.566 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.456 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.444 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.543 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.534 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.490 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.430 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.592 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.689 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.479 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.430 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.447 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.696 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.698 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.754 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.656 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.272 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.496 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.593 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.470 |
MOD_GlcNHglycan | 706 | 710 | PF01048 | 0.364 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.399 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.324 |
MOD_GlcNHglycan | 836 | 840 | PF01048 | 0.586 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.457 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.301 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.275 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.448 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.391 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.643 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.685 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.527 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.532 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.690 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.770 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.524 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.781 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.475 |
MOD_LATS_1 | 379 | 385 | PF00433 | 0.518 |
MOD_LATS_1 | 398 | 404 | PF00433 | 0.447 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.273 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.274 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.395 |
MOD_N-GLC_1 | 622 | 627 | PF02516 | 0.266 |
MOD_N-GLC_2 | 542 | 544 | PF02516 | 0.234 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.327 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.251 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.289 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.166 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.289 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.530 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.642 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.538 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.474 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.576 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.564 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.740 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.396 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.416 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.564 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.446 |
MOD_PIKK_1 | 830 | 836 | PF00454 | 0.634 |
MOD_PK_1 | 381 | 387 | PF00069 | 0.466 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.234 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.234 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.337 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.683 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.505 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.480 |
MOD_PKA_2 | 809 | 815 | PF00069 | 0.776 |
MOD_PKA_2 | 820 | 826 | PF00069 | 0.779 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.463 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.399 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.274 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.524 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.532 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.673 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.477 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.490 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.448 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.478 |
MOD_Plk_1 | 734 | 740 | PF00069 | 0.611 |
MOD_Plk_1 | 754 | 760 | PF00069 | 0.709 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.449 |
MOD_Plk_2-3 | 662 | 668 | PF00069 | 0.510 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.379 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.392 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.345 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.279 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.318 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.311 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.516 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.546 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.490 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.493 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.515 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.510 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.559 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.566 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.420 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.676 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.477 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.737 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 760 | 763 | PF00179 | 0.641 |
TRG_DiLeu_BaEn_1 | 662 | 667 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.254 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 548 | 553 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 654 | 657 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 813 | 816 | PF00400 | 0.806 |
TRG_NLS_MonoExtN_4 | 225 | 232 | PF00514 | 0.312 |
TRG_NLS_MonoExtN_4 | 815 | 822 | PF00514 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 551 | 555 | PF00026 | 0.266 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V4 | Leptomonas seymouri | 61% | 98% |
A0A0N1I6W7 | Leptomonas seymouri | 24% | 100% |
A0A0N1I7J3 | Leptomonas seymouri | 28% | 100% |
A0A0S4J3N1 | Bodo saltans | 33% | 90% |
A0A0S4JCM8 | Bodo saltans | 26% | 100% |
A0A0S4JRH8 | Bodo saltans | 21% | 100% |
A0A1X0NJ54 | Trypanosomatidae | 44% | 100% |
A0A1X0P3R6 | Trypanosomatidae | 27% | 100% |
A0A1X0P474 | Trypanosomatidae | 23% | 100% |
A0A3Q8ICD7 | Leishmania donovani | 100% | 100% |
A0A3Q8ICJ2 | Leishmania donovani | 23% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 42% | 100% |
A0A3R7NBD2 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X6Y1 | Leishmania donovani | 28% | 100% |
A0A422NTH3 | Trypanosoma rangeli | 22% | 100% |
A4HFH3 | Leishmania braziliensis | 23% | 100% |
A4HJ32 | Leishmania braziliensis | 77% | 100% |
A4HLP7 | Leishmania braziliensis | 27% | 100% |
A4I2N3 | Leishmania infantum | 24% | 100% |
A4I948 | Leishmania infantum | 28% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D3ZHR2 | Rattus norvegicus | 29% | 100% |
E9AD24 | Leishmania major | 23% | 100% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 97% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
F1RBC8 | Danio rerio | 29% | 100% |
O14678 | Homo sapiens | 25% | 100% |
O89016 | Mus musculus | 25% | 100% |
P16970 | Rattus norvegicus | 30% | 100% |
P28288 | Homo sapiens | 30% | 100% |
P33897 | Homo sapiens | 29% | 100% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 99% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 97% |
P48410 | Mus musculus | 29% | 100% |
P55096 | Mus musculus | 30% | 100% |
P9WQI8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 24% | 100% |
P9WQI9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 24% | 100% |
Q4Q402 | Leishmania major | 28% | 100% |
Q61285 | Mus musculus | 29% | 100% |
Q7JUN3 | Drosophila melanogaster | 28% | 100% |
Q8T8P3 | Dictyostelium discoideum | 30% | 100% |
Q9BHG2 | Leishmania major | 93% | 100% |
Q9QY44 | Rattus norvegicus | 29% | 100% |
Q9UBJ2 | Homo sapiens | 29% | 100% |
V5BPB7 | Trypanosoma cruzi | 28% | 100% |
V5BXE1 | Trypanosoma cruzi | 22% | 100% |