Fatty acid metabolism, Choline/Carnitine o-acyltransferase-like
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:0005739 | mitochondrion | 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:0110165 | cellular anatomical entity | 1 | 5 |
GO:0016020 | membrane | 2 | 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HYI3
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006575 | cellular modified amino acid metabolic process | 3 | 1 |
GO:0006577 | amino-acid betaine metabolic process | 4 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009437 | carnitine metabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016746 | acyltransferase activity | 3 | 10 |
GO:0004095 | carnitine O-palmitoyltransferase activity | 7 | 1 |
GO:0008374 | O-acyltransferase activity | 5 | 1 |
GO:0016406 | carnitine O-acyltransferase activity | 6 | 1 |
GO:0016409 | palmitoyltransferase activity | 5 | 1 |
GO:0016416 | O-palmitoyltransferase activity | 6 | 1 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.187 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.276 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.185 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 427 | 429 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.234 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 715 | 717 | PF00082 | 0.271 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 778 | 786 | PF00400 | 0.434 |
DEG_SCF_FBW7_2 | 289 | 295 | PF00400 | 0.348 |
DOC_CKS1_1 | 107 | 112 | PF01111 | 0.335 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.408 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.404 |
DOC_CKS1_1 | 753 | 758 | PF01111 | 0.434 |
DOC_CYCLIN_RxL_1 | 467 | 477 | PF00134 | 0.402 |
DOC_CYCLIN_RxL_1 | 592 | 600 | PF00134 | 0.471 |
DOC_CYCLIN_RxL_1 | 776 | 783 | PF00134 | 0.434 |
DOC_CYCLIN_yClb1_LxF_4 | 594 | 599 | PF00134 | 0.471 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 779 | 785 | PF00134 | 0.434 |
DOC_MAPK_DCC_7 | 59 | 69 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 355 | 365 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 368 | 376 | PF00069 | 0.353 |
DOC_MAPK_HePTP_8 | 523 | 535 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 297 | 304 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 526 | 535 | PF00069 | 0.451 |
DOC_PP1_RVXF_1 | 25 | 31 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 593 | 600 | PF00149 | 0.390 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.253 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 321 | 324 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 583 | 586 | PF00568 | 0.492 |
DOC_SPAK_OSR1_1 | 598 | 602 | PF12202 | 0.430 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 834 | 838 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.264 |
DOC_USP7_UBL2_3 | 577 | 581 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 766 | 770 | PF12436 | 0.434 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 752 | 757 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 803 | 808 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 229 | 237 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 499 | 503 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 610 | 618 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 630 | 638 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 687 | 696 | PF00244 | 0.436 |
LIG_ActinCP_TwfCPI_2 | 177 | 186 | PF01115 | 0.497 |
LIG_APCC_ABBA_1 | 531 | 536 | PF00400 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.558 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 812 | 816 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_2 | 692 | 698 | PF00533 | 0.434 |
LIG_CaM_NSCaTE_8 | 129 | 136 | PF13499 | 0.339 |
LIG_Clathr_ClatBox_1 | 398 | 402 | PF01394 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 260 | 267 | PF00928 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 536 | 545 | PF00928 | 0.471 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.471 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.405 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.459 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.515 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.387 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.428 |
LIG_FHA_1 | 843 | 849 | PF00498 | 0.486 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.311 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.471 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.526 |
LIG_FHA_2 | 753 | 759 | PF00498 | 0.432 |
LIG_LIR_Apic_2 | 112 | 117 | PF02991 | 0.353 |
LIG_LIR_Apic_2 | 118 | 122 | PF02991 | 0.292 |
LIG_LIR_Apic_2 | 278 | 284 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 359 | 366 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 518 | 525 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 536 | 546 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 647 | 657 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 667 | 678 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 820 | 829 | PF02991 | 0.492 |
LIG_LIR_LC3C_4 | 520 | 525 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 543 | 548 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 820 | 826 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.302 |
LIG_LRP6_Inhibitor_1 | 317 | 325 | PF00058 | 0.312 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.445 |
LIG_NRBOX | 393 | 399 | PF00104 | 0.434 |
LIG_PCNA_PIPBox_1 | 201 | 210 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 201 | 212 | PF02747 | 0.471 |
LIG_Pex14_1 | 100 | 104 | PF04695 | 0.349 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.471 |
LIG_Pex14_2 | 545 | 549 | PF04695 | 0.471 |
LIG_REV1ctd_RIR_1 | 174 | 179 | PF16727 | 0.533 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.430 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 670 | 674 | PF00017 | 0.440 |
LIG_SH2_PTP2 | 823 | 826 | PF00017 | 0.471 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 659 | 662 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 823 | 826 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.349 |
LIG_SH3_2 | 591 | 596 | PF14604 | 0.451 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.566 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.516 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.391 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.387 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.377 |
LIG_SH3_3 | 801 | 807 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 348 | 353 | PF11976 | 0.471 |
LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 397 | 404 | PF11976 | 0.471 |
LIG_SxIP_EBH_1 | 337 | 347 | PF03271 | 0.404 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.471 |
LIG_TRAF2_1 | 711 | 714 | PF00917 | 0.537 |
LIG_TRAF2_1 | 729 | 732 | PF00917 | 0.400 |
LIG_TRAF2_1 | 751 | 754 | PF00917 | 0.402 |
LIG_TYR_ITIM | 668 | 673 | PF00017 | 0.434 |
LIG_TYR_ITIM | 821 | 826 | PF00017 | 0.404 |
LIG_UBA3_1 | 301 | 309 | PF00899 | 0.409 |
LIG_ULM_U2AF65_1 | 765 | 770 | PF00076 | 0.434 |
LIG_WRC_WIRS_1 | 475 | 480 | PF05994 | 0.471 |
LIG_WRC_WIRS_1 | 542 | 547 | PF05994 | 0.471 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.350 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.347 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.461 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.433 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.507 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.461 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.451 |
MOD_CK1_1 | 752 | 758 | PF00069 | 0.431 |
MOD_CK1_1 | 836 | 842 | PF00069 | 0.393 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.424 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.433 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.484 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.443 |
MOD_Cter_Amidation | 424 | 427 | PF01082 | 0.271 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.271 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.262 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.295 |
MOD_GlcNHglycan | 556 | 560 | PF01048 | 0.295 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.252 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.331 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.211 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.213 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.218 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.324 |
MOD_GlcNHglycan | 860 | 864 | PF01048 | 0.382 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.474 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.437 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.433 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.338 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.473 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.456 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.412 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.416 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.471 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.482 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.475 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.440 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.393 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.290 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.423 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.213 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.235 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.294 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.428 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.438 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.525 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.394 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.434 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.443 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.301 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.482 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.467 |
MOD_NEK2_1 | 764 | 769 | PF00069 | 0.406 |
MOD_NEK2_1 | 822 | 827 | PF00069 | 0.391 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.553 |
MOD_NEK2_2 | 207 | 212 | PF00069 | 0.456 |
MOD_NEK2_2 | 789 | 794 | PF00069 | 0.402 |
MOD_OFUCOSY | 75 | 80 | PF10250 | 0.339 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.652 |
MOD_PIKK_1 | 619 | 625 | PF00454 | 0.464 |
MOD_PIKK_1 | 749 | 755 | PF00454 | 0.524 |
MOD_PKA_1 | 426 | 432 | PF00069 | 0.471 |
MOD_PKA_1 | 498 | 504 | PF00069 | 0.471 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.517 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.507 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.597 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.387 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.429 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.492 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.451 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.387 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.524 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.493 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.479 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.414 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.404 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.471 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.434 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.478 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.322 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.288 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.600 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.419 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.471 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.411 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.402 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.536 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.477 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.379 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.331 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.330 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.347 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.372 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.387 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.403 |
MOD_ProDKin_1 | 752 | 758 | PF00069 | 0.433 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.390 |
MOD_ProDKin_1 | 803 | 809 | PF00069 | 0.392 |
MOD_SUMO_rev_2 | 491 | 500 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 707 | 717 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_1 | 714 | 719 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_2 | 469 | 475 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_4 | 556 | 562 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.467 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 823 | 826 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 596 | 599 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.387 |
TRG_NES_CRM1_1 | 389 | 403 | PF08389 | 0.471 |
TRG_NLS_Bipartite_1 | 577 | 599 | PF00514 | 0.479 |
TRG_NLS_MonoExtN_4 | 594 | 599 | PF00514 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.263 |
TRG_Pf-PMV_PEXEL_1 | 212 | 217 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 571 | 575 | PF00026 | 0.204 |
TRG_Pf-PMV_PEXEL_1 | 716 | 721 | PF00026 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 779 | 783 | PF00026 | 0.230 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E3 | Leptomonas seymouri | 23% | 100% |
A0A0N1I7U1 | Leptomonas seymouri | 74% | 100% |
A0A0N1IK11 | Leptomonas seymouri | 23% | 100% |
A0A0S4JAG1 | Bodo saltans | 25% | 100% |
A0A0S4JRL8 | Bodo saltans | 35% | 100% |
A0A0S4KE24 | Bodo saltans | 30% | 100% |
A0A1X0NT49 | Trypanosomatidae | 24% | 100% |
A0A1X0NT60 | Trypanosomatidae | 25% | 100% |
A0A1X0NZS6 | Trypanosomatidae | 24% | 100% |
A0A1X0P523 | Trypanosomatidae | 26% | 100% |
A0A1X0P5Y2 | Trypanosomatidae | 39% | 100% |
A0A3R7L2D0 | Trypanosoma rangeli | 25% | 100% |
A0A3S5IQT1 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WVN3 | Leishmania donovani | 100% | 100% |
A0A422NAV0 | Trypanosoma rangeli | 23% | 100% |
A0A422NSK2 | Trypanosoma rangeli | 24% | 100% |
A4HAA3 | Leishmania braziliensis | 89% | 100% |
B2ZGJ1 | Danio rerio | 26% | 100% |
C9ZL75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZRI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A627 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9ASA7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
F1LN46 | Rattus norvegicus | 32% | 100% |
O19094 | Bos taurus | 24% | 100% |
P07668 | Drosophila melanogaster | 23% | 100% |
P11466 | Rattus norvegicus | 24% | 100% |
P13222 | Sus scrofa | 27% | 100% |
P18886 | Rattus norvegicus | 26% | 100% |
P23786 | Homo sapiens | 26% | 100% |
P28329 | Homo sapiens | 27% | 100% |
P32198 | Rattus norvegicus | 31% | 100% |
P32738 | Rattus norvegicus | 26% | 100% |
P32756 | Caenorhabditis elegans | 23% | 100% |
P32796 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P43155 | Homo sapiens | 25% | 100% |
P47934 | Mus musculus | 25% | 100% |
P50416 | Homo sapiens | 32% | 100% |
P52825 | Mus musculus | 27% | 100% |
P52826 | Columba livia | 26% | 100% |
P80235 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P97742 | Mus musculus | 32% | 100% |
Q00614 | Candida tropicalis | 24% | 100% |
Q03059 | Mus musculus | 26% | 100% |
Q2KJB7 | Bos taurus | 26% | 100% |
Q4QD55 | Leishmania major | 97% | 100% |
Q58DK1 | Bos taurus | 29% | 100% |
Q5U3U3 | Danio rerio | 26% | 100% |
Q60HG9 | Macaca fascicularis | 26% | 100% |
Q63704 | Rattus norvegicus | 30% | 100% |
Q68Y62 | Equus caballus | 32% | 100% |
Q6P4X5 | Xenopus tropicalis | 25% | 100% |
Q704S8 | Rattus norvegicus | 25% | 100% |
Q7ZXE1 | Xenopus laevis | 26% | 100% |
Q8BGD5 | Mus musculus | 33% | 100% |
Q8HY46 | Sus scrofa | 29% | 100% |
Q8TCG5 | Homo sapiens | 34% | 100% |
Q90YJ9 | Gallus gallus | 27% | 100% |
Q924X2 | Mus musculus | 30% | 100% |
Q92523 | Homo sapiens | 31% | 100% |
Q9DC50 | Mus musculus | 24% | 100% |
Q9UKG9 | Homo sapiens | 25% | 100% |
V5BH74 | Trypanosoma cruzi | 24% | 100% |
V5BQH8 | Trypanosoma cruzi | 25% | 100% |
V5D4R1 | Trypanosoma cruzi | 41% | 100% |
V5DBT5 | Trypanosoma cruzi | 25% | 100% |