Overall very similar to animal mitochondrial PGS1 enzymes, with one key difference: instead a a transit signal, the Kinetoplastid variant has membrane anchor.
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:0005739 | mitochondrion | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4H4W4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 11 |
GO:0006655 | phosphatidylglycerol biosynthetic process | 6 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0008654 | phospholipid biosynthetic process | 5 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0032048 | cardiolipin metabolic process | 7 | 11 |
GO:0032049 | cardiolipin biosynthetic process | 7 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 11 |
GO:0046471 | phosphatidylglycerol metabolic process | 6 | 11 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 11 |
GO:0046486 | glycerolipid metabolic process | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008444 | CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase activity | 6 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017169 | CDP-alcohol phosphatidyltransferase activity | 5 | 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: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:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.605 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.502 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.571 |
DEG_APCC_DBOX_1 | 587 | 595 | PF00400 | 0.608 |
DEG_APCC_DBOX_1 | 714 | 722 | PF00400 | 0.516 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.702 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.769 |
DEG_SPOP_SBC_1 | 414 | 418 | PF00917 | 0.607 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.778 |
DOC_CYCLIN_RxL_1 | 525 | 538 | PF00134 | 0.588 |
DOC_MAPK_FxFP_2 | 511 | 514 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 197 | 203 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 303 | 310 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 457 | 464 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 740 | 747 | PF00069 | 0.602 |
DOC_PP1_RVXF_1 | 170 | 176 | PF00149 | 0.598 |
DOC_PP1_RVXF_1 | 619 | 626 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.608 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 364 | 368 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 457 | 464 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 535 | 544 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 635 | 645 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 727 | 734 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 596 | 613 | PF00022 | 0.627 |
LIG_APCC_ABBA_1 | 19 | 24 | PF00400 | 0.625 |
LIG_APCC_ABBAyCdc20_2 | 520 | 526 | PF00400 | 0.517 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.705 |
LIG_deltaCOP1_diTrp_1 | 504 | 511 | PF00928 | 0.602 |
LIG_EH1_1 | 182 | 190 | PF00400 | 0.561 |
LIG_eIF4E_1 | 507 | 513 | PF01652 | 0.415 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.572 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.345 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.574 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.738 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.633 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.606 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.758 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.515 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.701 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.502 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.544 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.499 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.528 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.567 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.516 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.599 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.584 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.702 |
LIG_LIR_Apic_2 | 509 | 514 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 132 | 143 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 190 | 196 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 439 | 447 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 506 | 516 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 546 | 557 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.526 |
LIG_NRBOX | 717 | 723 | PF00104 | 0.533 |
LIG_OCRL_FandH_1 | 317 | 329 | PF00620 | 0.562 |
LIG_PALB2_WD40_1 | 350 | 358 | PF16756 | 0.524 |
LIG_PCNA_PIPBox_1 | 104 | 113 | PF02747 | 0.529 |
LIG_PCNA_yPIPBox_3 | 341 | 355 | PF02747 | 0.545 |
LIG_PCNA_yPIPBox_3 | 97 | 111 | PF02747 | 0.622 |
LIG_PDZ_Class_3 | 751 | 756 | PF00595 | 0.616 |
LIG_Pex14_1 | 294 | 298 | PF04695 | 0.603 |
LIG_SH2_CRK | 288 | 292 | PF00017 | 0.587 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.615 |
LIG_SH2_CRK | 690 | 694 | PF00017 | 0.558 |
LIG_SH2_GRB2like | 288 | 291 | PF00017 | 0.586 |
LIG_SH2_GRB2like | 549 | 552 | PF00017 | 0.515 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 553 | 557 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.397 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.443 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.649 |
LIG_SUMO_SIM_anti_2 | 184 | 190 | PF11976 | 0.556 |
LIG_SUMO_SIM_anti_2 | 459 | 465 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 199 | 205 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 459 | 465 | PF11976 | 0.454 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.451 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.555 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.378 |
LIG_TYR_ITIM | 591 | 596 | PF00017 | 0.536 |
LIG_UBA3_1 | 206 | 212 | PF00899 | 0.581 |
LIG_UBA3_1 | 297 | 305 | PF00899 | 0.522 |
LIG_UBA3_1 | 718 | 724 | PF00899 | 0.523 |
LIG_WRC_WIRS_1 | 107 | 112 | PF05994 | 0.535 |
LIG_WRC_WIRS_1 | 508 | 513 | PF05994 | 0.550 |
LIG_WRC_WIRS_1 | 553 | 558 | PF05994 | 0.513 |
MOD_CDK_SPxK_1 | 387 | 393 | PF00069 | 0.796 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.580 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.624 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.657 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.761 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.761 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.799 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.756 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.772 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.790 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.572 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.675 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.546 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.588 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.460 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.588 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.603 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.505 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.735 |
MOD_Cter_Amidation | 633 | 636 | PF01082 | 0.447 |
MOD_DYRK1A_RPxSP_1 | 436 | 440 | PF00069 | 0.754 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.308 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.533 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.600 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.547 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.433 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.591 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.520 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.320 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.362 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.570 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.530 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.345 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.454 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.565 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.754 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.796 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.711 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.718 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.724 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.703 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.773 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.499 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.629 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.554 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.677 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.547 |
MOD_LATS_1 | 614 | 620 | PF00433 | 0.558 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.425 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.282 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.524 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.347 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.583 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.766 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.532 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.698 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.558 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.444 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.539 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.565 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.519 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.520 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.512 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.640 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.691 |
MOD_NEK2_2 | 689 | 694 | PF00069 | 0.525 |
MOD_PIKK_1 | 728 | 734 | PF00454 | 0.619 |
MOD_PK_1 | 616 | 622 | PF00069 | 0.578 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.562 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.553 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.692 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.624 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.580 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.639 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.530 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.597 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.586 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.581 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.569 |
MOD_Plk_1 | 616 | 622 | PF00069 | 0.393 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.614 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.611 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.450 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.454 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.614 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.760 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.482 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.438 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.790 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.444 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.506 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.598 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.598 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.789 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.738 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.730 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.686 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.621 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.500 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.731 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 190 | 200 | PF00179 | 0.622 |
TRG_DiLeu_BaEn_1 | 346 | 351 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 717 | 722 | PF01217 | 0.544 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_2 | 539 | 545 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_2 | 697 | 703 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_4 | 540 | 546 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 690 | 693 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.561 |
TRG_ER_FFAT_2 | 34 | 43 | PF00635 | 0.506 |
TRG_NES_CRM1_1 | 460 | 471 | PF08389 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILX1 | Leptomonas seymouri | 61% | 100% |
A0A0S4JQL9 | Bodo saltans | 35% | 100% |
A0A3R7KSA0 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H5W5 | Leishmania donovani | 79% | 100% |
A4HT38 | Leishmania infantum | 78% | 100% |
C9ZUU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AL30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QIS4 | Leishmania major | 78% | 99% |
V5ATE0 | Trypanosoma cruzi | 48% | 100% |