Palmitoyltransferase. Leishmaniids have +2 extra TM segments at the N-terminus while all other Kinetoplastids typically only have the 4 core ones.. Localization: ER (by homology)
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HZD7
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.740 |
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.762 |
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.805 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 480 | 482 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.504 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.709 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.530 |
DEG_APCC_DBOX_1 | 511 | 519 | PF00400 | 0.604 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.726 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.500 |
DOC_CYCLIN_RxL_1 | 459 | 470 | PF00134 | 0.398 |
DOC_CYCLIN_RxL_1 | 497 | 506 | PF00134 | 0.694 |
DOC_CYCLIN_yCln2_LP_2 | 424 | 430 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 13 | 20 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.713 |
DOC_MAPK_gen_1 | 551 | 559 | PF00069 | 0.652 |
DOC_MAPK_HePTP_8 | 549 | 561 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 13 | 22 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.668 |
DOC_MAPK_MEF2A_6 | 552 | 561 | PF00069 | 0.685 |
DOC_MAPK_RevD_3 | 237 | 252 | PF00069 | 0.738 |
DOC_PP1_RVXF_1 | 36 | 43 | PF00149 | 0.595 |
DOC_PP1_RVXF_1 | 498 | 505 | PF00149 | 0.692 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.763 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.438 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.810 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.552 |
DOC_USP7_UBL2_3 | 517 | 521 | PF12436 | 0.656 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.869 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 264 | 273 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 528 | 535 | PF00244 | 0.652 |
LIG_AP2alpha_1 | 504 | 508 | PF02296 | 0.675 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.749 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.744 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.530 |
LIG_CaM_NSCaTE_8 | 377 | 384 | PF13499 | 0.473 |
LIG_Clathr_ClatBox_1 | 296 | 300 | PF01394 | 0.737 |
LIG_deltaCOP1_diTrp_1 | 540 | 546 | PF00928 | 0.683 |
LIG_DLG_GKlike_1 | 251 | 258 | PF00625 | 0.661 |
LIG_EH1_1 | 443 | 451 | PF00400 | 0.443 |
LIG_eIF4E_1 | 459 | 465 | PF01652 | 0.534 |
LIG_eIF4E_1 | 579 | 585 | PF01652 | 0.723 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.718 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.816 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.666 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.796 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.604 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.473 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.406 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.348 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.558 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.315 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.723 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.824 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.717 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.595 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.639 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.660 |
LIG_HP1_1 | 74 | 78 | PF01393 | 0.321 |
LIG_IBAR_NPY_1 | 494 | 496 | PF08397 | 0.565 |
LIG_Integrin_RGD_1 | 226 | 228 | PF01839 | 0.601 |
LIG_LIR_Apic_2 | 109 | 115 | PF02991 | 0.788 |
LIG_LIR_Apic_2 | 491 | 495 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 455 | 465 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 581 | 590 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 72 | 83 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.835 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 581 | 585 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.300 |
LIG_LYPXL_SIV_4 | 427 | 435 | PF13949 | 0.438 |
LIG_NRBOX | 292 | 298 | PF00104 | 0.622 |
LIG_NRBOX | 77 | 83 | PF00104 | 0.473 |
LIG_Pex14_1 | 562 | 566 | PF04695 | 0.681 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.707 |
LIG_Pex14_2 | 504 | 508 | PF04695 | 0.675 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.753 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.534 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.591 |
LIG_SH2_GRB2like | 125 | 128 | PF00017 | 0.679 |
LIG_SH2_GRB2like | 459 | 462 | PF00017 | 0.534 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.473 |
LIG_SH2_SRC | 125 | 128 | PF00017 | 0.788 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.746 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.705 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.329 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.831 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.733 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.709 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.764 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.438 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.759 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.736 |
LIG_TYR_ITIM | 387 | 392 | PF00017 | 0.353 |
LIG_TYR_ITIM | 73 | 78 | PF00017 | 0.534 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.638 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.534 |
LIG_WRC_WIRS_1 | 566 | 571 | PF05994 | 0.658 |
LIG_WRC_WIRS_1 | 579 | 584 | PF05994 | 0.487 |
LIG_WRC_WIRS_1 | 84 | 89 | PF05994 | 0.534 |
LIG_WW_1 | 107 | 110 | PF00397 | 0.675 |
LIG_WW_2 | 209 | 212 | PF00397 | 0.808 |
LIG_WW_3 | 309 | 313 | PF00397 | 0.640 |
MOD_CDC14_SPxK_1 | 171 | 174 | PF00782 | 0.820 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.534 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.627 |
MOD_CDK_SPK_2 | 168 | 173 | PF00069 | 0.630 |
MOD_CDK_SPK_2 | 189 | 194 | PF00069 | 0.708 |
MOD_CDK_SPxK_1 | 168 | 174 | PF00069 | 0.815 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.534 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.854 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.743 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.492 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.443 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.620 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.534 |
MOD_CMANNOS | 374 | 377 | PF00535 | 0.534 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.652 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.554 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.793 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.657 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.752 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.753 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.710 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.781 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.597 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.635 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.534 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.473 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.400 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.460 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.607 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.561 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.541 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.769 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.587 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.401 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.459 |
MOD_N-GLC_2 | 344 | 346 | PF02516 | 0.460 |
MOD_N-GLC_2 | 358 | 360 | PF02516 | 0.375 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.821 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.521 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.592 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.375 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.456 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.316 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.473 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.357 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.553 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.600 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.473 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.796 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.763 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.598 |
MOD_PKA_1 | 528 | 534 | PF00069 | 0.688 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.720 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.508 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.443 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.627 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.651 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.673 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.854 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.534 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.511 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.503 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.532 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.374 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.441 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.464 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.219 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.788 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.758 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.857 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.534 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.620 |
MOD_SUMO_for_1 | 520 | 523 | PF00179 | 0.554 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.443 |
TRG_DiLeu_LyEn_5 | 589 | 594 | PF01217 | 0.723 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.534 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.566 |
TRG_NES_CRM1_1 | 154 | 166 | PF08389 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 402 | 407 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 551 | 555 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IAF5 | Leishmania donovani | 100% | 84% |
A4HC51 | Leishmania braziliensis | 69% | 100% |
E9AVC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QC55 | Leishmania major | 92% | 100% |
Q4QC56 | Leishmania major | 92% | 100% |