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: E9B1K4
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 | 723 | 727 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.544 |
CLV_PCSK_FUR_1 | 789 | 793 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.258 |
DOC_CYCLIN_RxL_1 | 180 | 192 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 19 | 25 | PF00134 | 0.479 |
DOC_MAPK_gen_1 | 141 | 151 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 225 | 233 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 491 | 500 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 586 | 592 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.208 |
DOC_MAPK_MEF2A_6 | 156 | 163 | PF00069 | 0.221 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 456 | 463 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 522 | 529 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 669 | 677 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.339 |
DOC_MAPK_RevD_3 | 671 | 684 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.284 |
DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.562 |
DOC_PP1_RVXF_1 | 638 | 644 | PF00149 | 0.507 |
DOC_PP1_RVXF_1 | 801 | 808 | PF00149 | 0.758 |
DOC_PP2B_LxvP_1 | 505 | 508 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 643 | 646 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 807 | 810 | PF00568 | 0.688 |
DOC_PP4_MxPP_1 | 51 | 54 | PF00568 | 0.523 |
DOC_SPAK_OSR1_1 | 647 | 651 | PF12202 | 0.483 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 811 | 815 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 491 | 501 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 620 | 630 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 683 | 687 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 722 | 730 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 797 | 805 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 44 | 59 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 537 | 553 | PF00022 | 0.520 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.402 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.520 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.520 |
LIG_Clathr_ClatBox_1 | 657 | 661 | PF01394 | 0.584 |
LIG_eIF4E_1 | 147 | 153 | PF01652 | 0.431 |
LIG_eIF4E_1 | 158 | 164 | PF01652 | 0.356 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.264 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.528 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.534 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.511 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.541 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.494 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.593 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.498 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.467 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.600 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.458 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.458 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 423 | 431 | PF00786 | 0.357 |
LIG_LIR_Apic_2 | 518 | 523 | PF02991 | 0.520 |
LIG_LIR_Apic_2 | 561 | 567 | PF02991 | 0.440 |
LIG_LIR_Apic_2 | 806 | 810 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 204 | 212 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 607 | 615 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 607 | 613 | PF02991 | 0.508 |
LIG_MYND_1 | 78 | 82 | PF01753 | 0.363 |
LIG_NRBOX | 446 | 452 | PF00104 | 0.559 |
LIG_Pex14_1 | 302 | 306 | PF04695 | 0.383 |
LIG_Pex14_1 | 692 | 696 | PF04695 | 0.459 |
LIG_REV1ctd_RIR_1 | 640 | 645 | PF16727 | 0.458 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.425 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.520 |
LIG_SH2_CRK | 598 | 602 | PF00017 | 0.520 |
LIG_SH2_GRB2like | 689 | 692 | PF00017 | 0.551 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.402 |
LIG_SH2_PTP2 | 520 | 523 | PF00017 | 0.520 |
LIG_SH2_SRC | 485 | 488 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 667 | 671 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 565 | 568 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.564 |
LIG_SH3_1 | 49 | 55 | PF00018 | 0.474 |
LIG_SH3_1 | 564 | 570 | PF00018 | 0.440 |
LIG_SH3_2 | 52 | 57 | PF14604 | 0.477 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.324 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.572 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.537 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.440 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.440 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.611 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.583 |
LIG_SUMO_SIM_par_1 | 502 | 509 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 655 | 661 | PF11976 | 0.578 |
LIG_SxIP_EBH_1 | 259 | 268 | PF03271 | 0.324 |
LIG_TRAF2_1 | 751 | 754 | PF00917 | 0.565 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.154 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.396 |
MOD_CDK_SPxxK_3 | 468 | 475 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.532 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.430 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.313 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.543 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.520 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.478 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.529 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.535 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.518 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.544 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.556 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.483 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.601 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.507 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.410 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.440 |
MOD_CK2_1 | 811 | 817 | PF00069 | 0.711 |
MOD_DYRK1A_RPxSP_1 | 95 | 99 | PF00069 | 0.351 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.676 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.278 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.502 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.638 |
MOD_GlcNHglycan | 697 | 701 | PF01048 | 0.368 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.464 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.464 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.295 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.390 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.382 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.527 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.553 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.544 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.759 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.523 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.498 |
MOD_LATS_1 | 379 | 385 | PF00433 | 0.524 |
MOD_LATS_1 | 398 | 404 | PF00433 | 0.465 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.279 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.261 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.416 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.283 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.597 |
MOD_N-GLC_2 | 533 | 535 | PF02516 | 0.240 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.334 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.243 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.282 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.199 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.320 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.291 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.527 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.565 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.458 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.465 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.574 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.624 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.402 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.422 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.563 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.462 |
MOD_PK_1 | 381 | 387 | PF00069 | 0.483 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.240 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.240 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.336 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.493 |
MOD_PKA_2 | 785 | 791 | PF00069 | 0.787 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.788 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.493 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.390 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.261 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.520 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.529 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.681 |
MOD_Plk_1 | 588 | 594 | PF00069 | 0.469 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.520 |
MOD_Plk_1 | 652 | 658 | PF00069 | 0.458 |
MOD_Plk_1 | 725 | 731 | PF00069 | 0.578 |
MOD_Plk_2-3 | 626 | 632 | PF00069 | 0.441 |
MOD_Plk_2-3 | 653 | 659 | PF00069 | 0.504 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.429 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.409 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.377 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.272 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.324 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.377 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.511 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.551 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.507 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.520 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.507 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.504 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.550 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.567 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.459 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.742 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.489 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.578 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.564 |
MOD_SUMO_for_1 | 751 | 754 | PF00179 | 0.634 |
MOD_SUMO_rev_2 | 458 | 465 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 761 | 766 | PF00179 | 0.578 |
TRG_DiLeu_BaEn_1 | 653 | 658 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.273 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 539 | 544 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 645 | 648 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 789 | 792 | PF00400 | 0.782 |
TRG_NLS_MonoExtN_4 | 225 | 232 | PF00514 | 0.307 |
TRG_NLS_MonoExtN_4 | 791 | 798 | PF00514 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 542 | 546 | PF00026 | 0.283 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V4 | Leptomonas seymouri | 65% | 95% |
A0A0N1I6W7 | Leptomonas seymouri | 22% | 100% |
A0A0N1I7J3 | Leptomonas seymouri | 28% | 100% |
A0A0S4JCM8 | Bodo saltans | 27% | 100% |
A0A0S4JRH8 | Bodo saltans | 21% | 100% |
A0A1X0NJ54 | Trypanosomatidae | 44% | 100% |
A0A1X0P3R6 | Trypanosomatidae | 28% | 100% |
A0A1X0P474 | Trypanosomatidae | 22% | 100% |
A0A3Q8ICD7 | Leishmania donovani | 90% | 97% |
A0A3Q8ICJ2 | Leishmania donovani | 23% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 43% | 100% |
A0A3R7NBD2 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X6Y1 | Leishmania donovani | 28% | 100% |
A0A422NTH3 | Trypanosoma rangeli | 21% | 100% |
A4HFH3 | Leishmania braziliensis | 23% | 100% |
A4HJ32 | Leishmania braziliensis | 76% | 100% |
A4HLP7 | Leishmania braziliensis | 27% | 100% |
A4I2N3 | Leishmania infantum | 22% | 100% |
A4I6L1 | Leishmania infantum | 90% | 97% |
A4I948 | Leishmania infantum | 28% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D3ZHR2 | Rattus norvegicus | 28% | 100% |
E9AD24 | Leishmania major | 23% | 100% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
F1RBC8 | Danio rerio | 28% | 100% |
O14678 | Homo sapiens | 26% | 100% |
O89016 | Mus musculus | 25% | 100% |
P16970 | Rattus norvegicus | 30% | 100% |
P28288 | Homo sapiens | 31% | 100% |
P33897 | Homo sapiens | 30% | 100% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 96% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 94% |
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 | 29% | 100% |
Q9BHG2 | Leishmania major | 89% | 100% |
Q9QY44 | Rattus norvegicus | 29% | 100% |
Q9UBJ2 | Homo sapiens | 29% | 100% |
V5BPB7 | Trypanosoma cruzi | 28% | 100% |
V5BXE1 | Trypanosoma cruzi | 21% | 100% |