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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QIS4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006644 | phospholipid metabolic process | 4 | 9 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 9 |
GO:0006655 | phosphatidylglycerol biosynthetic process | 6 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0008654 | phospholipid biosynthetic process | 5 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 9 |
GO:0032048 | cardiolipin metabolic process | 7 | 9 |
GO:0032049 | cardiolipin biosynthetic process | 7 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0044255 | cellular lipid metabolic process | 3 | 9 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 9 |
GO:0046471 | phosphatidylglycerol metabolic process | 6 | 9 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 9 |
GO:0046486 | glycerolipid metabolic process | 4 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090407 | organophosphate biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0008444 | CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase activity | 6 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017169 | CDP-alcohol phosphatidyltransferase activity | 5 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 648 | 652 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 704 | 708 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.442 |
CLV_PCSK_PC7_1 | 385 | 391 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.382 |
CLV_Separin_Metazoa | 252 | 256 | PF03568 | 0.649 |
DEG_APCC_DBOX_1 | 190 | 198 | PF00400 | 0.578 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.582 |
DEG_APCC_DBOX_1 | 713 | 721 | PF00400 | 0.502 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.742 |
DOC_CYCLIN_RxL_1 | 521 | 534 | PF00134 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.571 |
DOC_MAPK_FxFP_2 | 507 | 510 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 191 | 197 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 299 | 306 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 453 | 460 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 739 | 746 | PF00069 | 0.611 |
DOC_PP1_RVXF_1 | 164 | 170 | PF00149 | 0.580 |
DOC_PP1_RVXF_1 | 615 | 622 | PF00149 | 0.564 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.631 |
DOC_PP4_FxxP_1 | 507 | 510 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.732 |
DOC_USP7_MATH_2 | 670 | 676 | PF00917 | 0.570 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.748 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 531 | 540 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 70 | 76 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 592 | 609 | PF00022 | 0.595 |
LIG_APCC_ABBA_1 | 19 | 24 | PF00400 | 0.587 |
LIG_APCC_ABBAyCdc20_2 | 516 | 522 | PF00400 | 0.521 |
LIG_BIR_III_4 | 78 | 82 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.535 |
LIG_deltaCOP1_diTrp_1 | 500 | 507 | PF00928 | 0.575 |
LIG_EH1_1 | 176 | 184 | PF00400 | 0.529 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.572 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.334 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.550 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.723 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.589 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.746 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.534 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.495 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.569 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.546 |
LIG_FHA_2 | 532 | 538 | PF00498 | 0.567 |
LIG_FHA_2 | 702 | 708 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 505 | 510 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 18 | 25 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 184 | 190 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 288 | 297 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 543 | 553 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.507 |
LIG_NRBOX | 716 | 722 | PF00104 | 0.506 |
LIG_OCRL_FandH_1 | 313 | 325 | PF00620 | 0.536 |
LIG_PALB2_WD40_1 | 346 | 354 | PF16756 | 0.525 |
LIG_PCNA_PIPBox_1 | 98 | 107 | PF02747 | 0.531 |
LIG_PCNA_yPIPBox_3 | 337 | 351 | PF02747 | 0.505 |
LIG_PCNA_yPIPBox_3 | 91 | 105 | PF02747 | 0.641 |
LIG_PDZ_Class_3 | 750 | 755 | PF00595 | 0.622 |
LIG_Pex14_1 | 290 | 294 | PF04695 | 0.588 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.563 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.462 |
LIG_SH2_CRK | 603 | 607 | PF00017 | 0.587 |
LIG_SH2_CRK | 689 | 693 | PF00017 | 0.538 |
LIG_SH2_GRB2like | 284 | 287 | PF00017 | 0.561 |
LIG_SH2_GRB2like | 545 | 548 | PF00017 | 0.505 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.561 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.399 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 455 | 461 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 193 | 199 | PF11976 | 0.605 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.406 |
LIG_TYR_ITIM | 587 | 592 | PF00017 | 0.534 |
LIG_WRC_WIRS_1 | 101 | 106 | PF05994 | 0.521 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.552 |
MOD_CDC14_SPxK_1 | 421 | 424 | PF00782 | 0.657 |
MOD_CDK_SPxK_1 | 383 | 389 | PF00069 | 0.795 |
MOD_CDK_SPxK_1 | 418 | 424 | PF00069 | 0.666 |
MOD_CDK_SPxxK_3 | 383 | 390 | PF00069 | 0.642 |
MOD_CDK_SPxxK_3 | 639 | 646 | PF00069 | 0.683 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.617 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.612 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.743 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.763 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.770 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.749 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.734 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.557 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.736 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.524 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.591 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.715 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.707 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.573 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.633 |
MOD_Cter_Amidation | 629 | 632 | PF01082 | 0.410 |
MOD_DYRK1A_RPxSP_1 | 432 | 436 | PF00069 | 0.729 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.306 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.567 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.577 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.522 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.416 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.497 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.346 |
MOD_GlcNHglycan | 78 | 82 | PF01048 | 0.463 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.528 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.809 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.769 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.804 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.739 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.690 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.709 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.757 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.675 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.516 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.530 |
MOD_LATS_1 | 610 | 616 | PF00433 | 0.522 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.448 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.284 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.545 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.564 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.811 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.540 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.734 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.553 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.453 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.539 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.539 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.505 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.507 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.412 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.664 |
MOD_NEK2_2 | 688 | 693 | PF00069 | 0.511 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.543 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.744 |
MOD_PK_1 | 175 | 181 | PF00069 | 0.462 |
MOD_PK_1 | 612 | 618 | PF00069 | 0.580 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.536 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.542 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.594 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.573 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.690 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.573 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.542 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.543 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.580 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.591 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.755 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.496 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.756 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.492 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.488 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.571 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.571 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.564 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.717 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.781 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.677 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.690 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.759 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.608 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.655 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.501 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.751 |
MOD_SUMO_rev_2 | 127 | 134 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 184 | 194 | PF00179 | 0.603 |
TRG_DiLeu_BaEn_1 | 716 | 721 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_2 | 535 | 541 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_2 | 696 | 702 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 99 | 105 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 689 | 692 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 606 | 608 | PF00400 | 0.586 |
TRG_NES_CRM1_1 | 715 | 729 | PF08389 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILX1 | Leptomonas seymouri | 62% | 100% |
A0A0S4JQL9 | Bodo saltans | 37% | 100% |
A0A3R7KSA0 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5W5 | Leishmania donovani | 92% | 100% |
A4H4W4 | Leishmania braziliensis | 78% | 100% |
A4HT38 | Leishmania infantum | 92% | 100% |
E9AL30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |