Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (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: 60 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 53 |
NetGPI | no | yes: 0, no: 53 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
GO:0000139 | Golgi membrane | 5 | 13 |
GO:0031090 | organelle membrane | 3 | 13 |
GO:0098588 | bounding membrane of organelle | 4 | 13 |
Related structures:
AlphaFold database: A4H3A9
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 54 |
GO:0006807 | nitrogen compound metabolic process | 2 | 54 |
GO:0008152 | metabolic process | 1 | 54 |
GO:0019538 | protein metabolic process | 3 | 54 |
GO:0036211 | protein modification process | 4 | 54 |
GO:0043170 | macromolecule metabolic process | 3 | 54 |
GO:0043412 | macromolecule modification | 4 | 54 |
GO:0043413 | macromolecule glycosylation | 3 | 54 |
GO:0044238 | primary metabolic process | 2 | 54 |
GO:0070085 | glycosylation | 2 | 54 |
GO:0071704 | organic substance metabolic process | 2 | 54 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 54 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 54 |
GO:0016740 | transferase activity | 2 | 54 |
GO:0016757 | glycosyltransferase activity | 3 | 54 |
GO:0016758 | hexosyltransferase activity | 4 | 54 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.389 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 676 | 678 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.571 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.634 |
CLV_PCSK_PC7_1 | 562 | 568 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.528 |
DEG_SCF_FBW7_1 | 354 | 361 | PF00400 | 0.514 |
DOC_CKS1_1 | 355 | 360 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 24 | 36 | PF00134 | 0.359 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.559 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 382 | 389 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 521 | 530 | PF00069 | 0.321 |
DOC_MAPK_RevD_3 | 10 | 25 | PF00069 | 0.204 |
DOC_PP1_RVXF_1 | 380 | 387 | PF00149 | 0.378 |
DOC_PP1_RVXF_1 | 416 | 423 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 574 | 580 | PF00149 | 0.266 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.403 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 315 | 325 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 44 | 53 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 475 | 479 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 543 | 549 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 562 | 566 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 653 | 657 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 86 | 93 | PF00244 | 0.367 |
LIG_Actin_WH2_2 | 152 | 168 | PF00022 | 0.473 |
LIG_Actin_WH2_2 | 552 | 568 | PF00022 | 0.294 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.403 |
LIG_BIR_III_2 | 664 | 668 | PF00653 | 0.291 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.407 |
LIG_Clathr_ClatBox_1 | 506 | 510 | PF01394 | 0.217 |
LIG_CtBP_PxDLS_1 | 246 | 250 | PF00389 | 0.381 |
LIG_eIF4E_1 | 501 | 507 | PF01652 | 0.224 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.598 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.370 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.433 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.365 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.457 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.431 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.262 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.536 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.374 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.322 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.292 |
LIG_FHA_2 | 702 | 708 | PF00498 | 0.319 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 708 | 714 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 542 | 550 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 597 | 605 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 623 | 629 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.304 |
LIG_NRBOX | 508 | 514 | PF00104 | 0.238 |
LIG_NRBOX | 555 | 561 | PF00104 | 0.279 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.295 |
LIG_Pex14_1 | 699 | 703 | PF04695 | 0.281 |
LIG_REV1ctd_RIR_1 | 617 | 626 | PF16727 | 0.290 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.290 |
LIG_SH2_CRK | 711 | 715 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 285 | 289 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 681 | 685 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 711 | 715 | PF00017 | 0.293 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.311 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.344 |
LIG_SH2_SRC | 425 | 428 | PF00017 | 0.394 |
LIG_SH2_SRC | 615 | 618 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 625 | 629 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.445 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.466 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.338 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.402 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.534 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.317 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.367 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.339 |
LIG_SH3_5 | 610 | 614 | PF00018 | 0.228 |
LIG_SUMO_SIM_anti_2 | 15 | 20 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.238 |
LIG_SUMO_SIM_par_1 | 245 | 253 | PF11976 | 0.389 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.348 |
LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.543 |
LIG_WW_3 | 184 | 188 | PF00397 | 0.444 |
MOD_CDC14_SPxK_1 | 26 | 29 | PF00782 | 0.428 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.433 |
MOD_CDK_SPxxK_3 | 23 | 30 | PF00069 | 0.434 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.406 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.602 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.481 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.488 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.679 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.496 |
MOD_Cter_Amidation | 22 | 25 | PF01082 | 0.439 |
MOD_Cter_Amidation | 632 | 635 | PF01082 | 0.374 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.601 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.610 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.469 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.487 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.564 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.489 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.416 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.531 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.597 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.610 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.265 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.451 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.498 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.478 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.554 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.666 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.453 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.687 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.533 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.558 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.587 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.393 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.403 |
MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.534 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.443 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.494 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.439 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.325 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.348 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.562 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.496 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.462 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.406 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.532 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.305 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.696 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.551 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.458 |
MOD_PKA_1 | 393 | 399 | PF00069 | 0.641 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.577 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.637 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.597 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.436 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.335 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.386 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.439 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.428 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.455 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.420 |
MOD_Plk_2-3 | 248 | 254 | PF00069 | 0.547 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.312 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.497 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.468 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.521 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.394 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.445 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.496 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.602 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.611 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.405 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.350 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 508 | 513 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 42% | 88% |
A0A3S5H4Y6 | Leishmania donovani | 62% | 89% |
A0A3S5H4Y9 | Leishmania donovani | 38% | 72% |
A0A3S7WT86 | Leishmania donovani | 40% | 70% |
A0A3S7WWA6 | Leishmania donovani | 42% | 88% |
A0A451EJD9 | Leishmania donovani | 40% | 88% |
A0A451EJF4 | Leishmania donovani | 65% | 88% |
A0A451EJF6 | Leishmania donovani | 55% | 100% |
A0A451EJF8 | Leishmania donovani | 56% | 93% |
A0A451EJF9 | Leishmania donovani | 53% | 83% |
A4H3B4 | Leishmania braziliensis | 79% | 88% |
A4H3B5 | Leishmania braziliensis | 94% | 100% |
A4H3B6 | Leishmania braziliensis | 86% | 99% |
A4H3B7 | Leishmania braziliensis | 51% | 67% |
A4H3B8 | Leishmania braziliensis | 62% | 86% |
A4H3B9 | Leishmania braziliensis | 40% | 80% |
A4H4W8 | Leishmania braziliensis | 40% | 88% |
A4HJ20 | Leishmania braziliensis | 86% | 88% |
A4HNK3 | Leishmania braziliensis | 42% | 100% |
A4HNK6 | Leishmania braziliensis | 40% | 90% |
A4HRL9 | Leishmania infantum | 65% | 88% |
A4HRM0 | Leishmania infantum | 64% | 97% |
A4HRM1 | Leishmania infantum | 55% | 100% |
A4HRS1 | Leishmania infantum | 53% | 83% |
A4HRS3 | Leishmania infantum | 39% | 72% |
A4HRS5 | Leishmania infantum | 56% | 93% |
A4HZM0 | Leishmania infantum | 40% | 88% |
A4I7C7 | Leishmania infantum | 41% | 88% |
A4IAQ2 | Leishmania infantum | 40% | 88% |
E9AC91 | Leishmania major | 64% | 100% |
E9AC92 | Leishmania major | 63% | 100% |
E9AC95 | Leishmania major | 54% | 100% |
E9AC96 | Leishmania major | 55% | 100% |
E9AC98 | Leishmania major | 38% | 72% |
E9AEH8 | Leishmania major | 41% | 100% |
E9AHA6 | Leishmania infantum | 39% | 88% |
E9AIP8 | Leishmania braziliensis | 40% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 88% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 90% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 93% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 72% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 97% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 88% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 88% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 88% |
Q4Q5T6 | Leishmania major | 41% | 100% |
Q4QCL8 | Leishmania major | 42% | 100% |
Q4QFJ3 | Leishmania major | 40% | 70% |
Q4QIG9 | Leishmania major | 42% | 100% |
Q7YXU9 | Leishmania major | 42% | 100% |
Q7YXV1 | Leishmania major | 42% | 100% |
Q7YXV2 | Leishmania major | 41% | 100% |