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: 47 |
NetGPI | no | yes: 0, no: 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 48 |
GO:0110165 | cellular anatomical entity | 1 | 48 |
GO:0000139 | Golgi membrane | 5 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
Related structures:
AlphaFold database: A0A451EJF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 48 |
GO:0006807 | nitrogen compound metabolic process | 2 | 48 |
GO:0008152 | metabolic process | 1 | 48 |
GO:0019538 | protein metabolic process | 3 | 48 |
GO:0036211 | protein modification process | 4 | 48 |
GO:0043170 | macromolecule metabolic process | 3 | 48 |
GO:0043412 | macromolecule modification | 4 | 48 |
GO:0043413 | macromolecule glycosylation | 3 | 48 |
GO:0044238 | primary metabolic process | 2 | 48 |
GO:0070085 | glycosylation | 2 | 48 |
GO:0071704 | organic substance metabolic process | 2 | 48 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 48 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 48 |
GO:0016740 | transferase activity | 2 | 48 |
GO:0016757 | glycosyltransferase activity | 3 | 48 |
GO:0016758 | hexosyltransferase activity | 4 | 48 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.363 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.377 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 129 | 135 | PF00082 | 0.377 |
CLV_PCSK_PC7_1 | 231 | 237 | PF00082 | 0.412 |
CLV_PCSK_PC7_1 | 378 | 384 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 531 | 539 | PF00400 | 0.320 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.439 |
DEG_SCF_FBW7_1 | 274 | 281 | PF00400 | 0.593 |
DEG_SCF_FBW7_2 | 243 | 250 | PF00400 | 0.355 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.390 |
DOC_CKS1_1 | 107 | 112 | PF01111 | 0.409 |
DOC_CKS1_1 | 275 | 280 | PF01111 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.394 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.621 |
DOC_MAPK_gen_1 | 434 | 441 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 451 | 458 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 502 | 511 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 302 | 309 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 434 | 441 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 59 | 67 | PF00069 | 0.397 |
DOC_PP1_RVXF_1 | 300 | 307 | PF00149 | 0.406 |
DOC_PP1_RVXF_1 | 336 | 343 | PF00149 | 0.519 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.620 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.340 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.401 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.372 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.385 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 179 | 187 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 31 | 38 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.373 |
LIG_14-3-3_CterR_2 | 651 | 654 | PF00244 | 0.323 |
LIG_Actin_WH2_2 | 73 | 89 | PF00022 | 0.429 |
LIG_BRCT_BRCA1_1 | 641 | 645 | PF00533 | 0.294 |
LIG_EVH1_1 | 386 | 390 | PF00568 | 0.380 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.400 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.548 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.434 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.527 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.351 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.603 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.522 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.569 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.413 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.392 |
LIG_Integrin_RGD_1 | 573 | 575 | PF01839 | 0.395 |
LIG_LIR_Apic_2 | 277 | 283 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 109 | 118 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 138 | 143 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 361 | 371 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 522 | 530 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 522 | 527 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 644 | 650 | PF02991 | 0.325 |
LIG_NRP_CendR_1 | 651 | 654 | PF00754 | 0.372 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.311 |
LIG_PTB_Apo_2 | 630 | 637 | PF02174 | 0.284 |
LIG_PTB_Phospho_1 | 630 | 636 | PF10480 | 0.278 |
LIG_RPA_C_Fungi | 446 | 458 | PF08784 | 0.301 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.423 |
LIG_SH2_GRB2like | 477 | 480 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 364 | 367 | PF00017 | 0.330 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.418 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 634 | 638 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 558 | 561 | PF00017 | 0.261 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.473 |
LIG_SH3_1 | 385 | 391 | PF00018 | 0.379 |
LIG_SH3_2 | 387 | 392 | PF14604 | 0.382 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.574 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.610 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.371 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.478 |
LIG_SH3_CIN85_PxpxPR_1 | 387 | 392 | PF14604 | 0.385 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.388 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.433 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.569 |
LIG_TYR_ITSM | 107 | 114 | PF00017 | 0.393 |
LIG_WW_3 | 389 | 393 | PF00397 | 0.410 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.384 |
MOD_CDK_SPK_2 | 406 | 411 | PF00069 | 0.517 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.413 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.514 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.712 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.405 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.538 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.351 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.522 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.589 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.603 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.418 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.519 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.386 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.285 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.637 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.567 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.407 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.539 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.515 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.553 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.654 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.277 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.571 |
MOD_GlcNHglycan | 563 | 567 | PF01048 | 0.340 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.405 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.721 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.567 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.482 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.552 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.487 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.402 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.539 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.389 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.347 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.540 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.574 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.409 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.310 |
MOD_N-GLC_1 | 632 | 637 | PF02516 | 0.325 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.411 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.513 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.409 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.555 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.549 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.523 |
MOD_PKA_1 | 254 | 260 | PF00069 | 0.402 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.644 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.586 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.423 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.552 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.571 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.585 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.372 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.378 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.404 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.407 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.309 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.291 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.330 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.339 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.414 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.299 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.540 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.393 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.365 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.456 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.444 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.625 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.541 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.531 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.505 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 39% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 75% | 100% |
A0A3S7WWA6 | Leishmania donovani | 39% | 100% |
A0A451EJD9 | Leishmania donovani | 41% | 100% |
A0A451EJF4 | Leishmania donovani | 75% | 100% |
A0A451EJF8 | Leishmania donovani | 61% | 85% |
A0A451EJF9 | Leishmania donovani | 96% | 76% |
A4H3A9 | Leishmania braziliensis | 55% | 100% |
A4H3B4 | Leishmania braziliensis | 60% | 100% |
A4H3B5 | Leishmania braziliensis | 51% | 99% |
A4H3B6 | Leishmania braziliensis | 55% | 100% |
A4H3B8 | Leishmania braziliensis | 62% | 100% |
A4H3B9 | Leishmania braziliensis | 39% | 100% |
A4H4W8 | Leishmania braziliensis | 39% | 100% |
A4HJ20 | Leishmania braziliensis | 55% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 96% |
A4HNK6 | Leishmania braziliensis | 40% | 100% |
A4HRL9 | Leishmania infantum | 75% | 100% |
A4HRM0 | Leishmania infantum | 63% | 100% |
A4HRM1 | Leishmania infantum | 99% | 100% |
A4HRS1 | Leishmania infantum | 95% | 100% |
A4HRS5 | Leishmania infantum | 61% | 100% |
A4HZM0 | Leishmania infantum | 40% | 100% |
A4I7C7 | Leishmania infantum | 41% | 100% |
A4IAQ2 | Leishmania infantum | 41% | 100% |
E9AC91 | Leishmania major | 69% | 100% |
E9AC92 | Leishmania major | 67% | 100% |
E9AC95 | Leishmania major | 60% | 100% |
E9AC96 | Leishmania major | 90% | 100% |
E9AEH8 | Leishmania major | 41% | 100% |
E9AHA6 | Leishmania infantum | 40% | 100% |
E9AIP8 | Leishmania braziliensis | 41% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 66% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q4Q5T6 | Leishmania major | 41% | 100% |
Q4QCL8 | Leishmania major | 41% | 100% |
Q4QIG9 | Leishmania major | 41% | 100% |
Q7YXU9 | Leishmania major | 39% | 100% |
Q7YXV1 | Leishmania major | 40% | 100% |
Q7YXV2 | Leishmania major | 40% | 100% |