GPI anchor biosynthesis, mannosyltransferase-II
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031501 | mannosyltransferase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HXW9
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 7 |
GO:0006505 | GPI anchor metabolic process | 6 | 7 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 7 |
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006643 | membrane lipid metabolic process | 4 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 7 |
GO:0006664 | glycolipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 7 |
GO:0008654 | phospholipid biosynthetic process | 5 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009247 | glycolipid biosynthetic process | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 7 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 7 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:1903509 | liposaccharide metabolic process | 4 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000009 | alpha-1,6-mannosyltransferase activity | 6 | 7 |
GO:0000030 | mannosyltransferase activity | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004376 | glycolipid mannosyltransferase activity | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016757 | glycosyltransferase activity | 3 | 7 |
GO:0016758 | hexosyltransferase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.690 |
DEG_APCC_DBOX_1 | 493 | 501 | PF00400 | 0.653 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.412 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.694 |
DEG_SCF_FBW7_1 | 392 | 399 | PF00400 | 0.605 |
DEG_SCF_FBW7_2 | 209 | 215 | PF00400 | 0.792 |
DOC_AGCK_PIF_1 | 565 | 570 | PF00069 | 0.354 |
DOC_CDC14_PxL_1 | 136 | 144 | PF14671 | 0.412 |
DOC_CKS1_1 | 209 | 214 | PF01111 | 0.756 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 360 | PF00134 | 0.680 |
DOC_CYCLIN_yCln2_LP_2 | 439 | 445 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 578 | 584 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 183 | 190 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 2 | 11 | PF00069 | 0.691 |
DOC_MAPK_gen_1 | 557 | 564 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 613 | 622 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 2 | 11 | PF00069 | 0.625 |
DOC_MAPK_RevD_3 | 514 | 530 | PF00069 | 0.397 |
DOC_PP1_RVXF_1 | 31 | 38 | PF00149 | 0.422 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.746 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 578 | 581 | PF13499 | 0.412 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.330 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.262 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.385 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 231 | 241 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 26 | 35 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 330 | 335 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 409 | 419 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 654 | 660 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 680 | 684 | PF00244 | 0.530 |
LIG_APCC_ABBA_1 | 298 | 303 | PF00400 | 0.429 |
LIG_APCC_ABBA_1 | 39 | 44 | PF00400 | 0.605 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.346 |
LIG_CaM_NSCaTE_8 | 560 | 567 | PF13499 | 0.420 |
LIG_eIF4E_1 | 559 | 565 | PF01652 | 0.354 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.346 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.756 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.555 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.357 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.420 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.573 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.637 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.456 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.630 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.514 |
LIG_GBD_Chelix_1 | 67 | 75 | PF00786 | 0.514 |
LIG_LIR_Apic_2 | 189 | 193 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 5 | 16 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 615 | 625 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 682 | 692 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 563 | 568 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 615 | 620 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.417 |
LIG_LYPXL_S_1 | 551 | 555 | PF13949 | 0.546 |
LIG_LYPXL_yS_3 | 552 | 555 | PF13949 | 0.346 |
LIG_MYND_1 | 491 | 495 | PF01753 | 0.667 |
LIG_NRBOX | 635 | 641 | PF00104 | 0.385 |
LIG_NRBOX | 661 | 667 | PF00104 | 0.412 |
LIG_PCNA_PIPBox_1 | 328 | 337 | PF02747 | 0.683 |
LIG_Pex14_1 | 406 | 410 | PF04695 | 0.562 |
LIG_RPA_C_Fungi | 273 | 285 | PF08784 | 0.514 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.343 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.619 |
LIG_SH2_PTP2 | 166 | 169 | PF00017 | 0.514 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.617 |
LIG_SH2_SRC | 42 | 45 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 453 | 456 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.402 |
LIG_SH3_1 | 206 | 212 | PF00018 | 0.697 |
LIG_SH3_1 | 356 | 362 | PF00018 | 0.707 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.410 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.697 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.514 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.707 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.422 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.544 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 679 | 685 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 507 | 512 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 580 | 586 | PF11976 | 0.514 |
LIG_SxIP_EBH_1 | 381 | 390 | PF03271 | 0.648 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.522 |
LIG_TRFH_1 | 37 | 41 | PF08558 | 0.422 |
LIG_ULM_U2AF65_1 | 613 | 618 | PF00076 | 0.422 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.412 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.687 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.422 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.514 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.425 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.397 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.791 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.614 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.546 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.412 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.534 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.577 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.518 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.667 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.665 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.447 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.425 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.402 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.486 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.514 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.534 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.607 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.585 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.493 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.390 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.568 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.371 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.421 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.385 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.541 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.293 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.446 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.424 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.492 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.295 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.322 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.466 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.412 |
MOD_NEK2_2 | 560 | 565 | PF00069 | 0.424 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.518 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.514 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.514 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.514 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.411 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.472 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.588 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.409 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.412 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.412 |
MOD_PKB_1 | 24 | 32 | PF00069 | 0.293 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.573 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.438 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.256 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.424 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.502 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.412 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.599 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.614 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.412 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.385 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.514 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.408 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.470 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.769 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.412 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.604 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.597 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.293 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 404 | 407 | PF00179 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 66 | 71 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 276 | 279 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL0 | Leptomonas seymouri | 52% | 100% |
A0A3S7WV16 | Leishmania donovani | 99% | 100% |
A4H9K3 | Leishmania braziliensis | 75% | 100% |
E9ARN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QDU6 | Leishmania major | 91% | 100% |