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: 52 |
NetGPI | no | yes: 0, no: 52 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 53 |
GO:0110165 | cellular anatomical entity | 1 | 53 |
GO:0000139 | Golgi membrane | 5 | 14 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0098588 | bounding membrane of organelle | 4 | 14 |
Related structures:
AlphaFold database: A4H4W8
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 53 |
GO:0006807 | nitrogen compound metabolic process | 2 | 53 |
GO:0008152 | metabolic process | 1 | 53 |
GO:0019538 | protein metabolic process | 3 | 53 |
GO:0036211 | protein modification process | 4 | 53 |
GO:0043170 | macromolecule metabolic process | 3 | 53 |
GO:0043412 | macromolecule modification | 4 | 53 |
GO:0043413 | macromolecule glycosylation | 3 | 53 |
GO:0044238 | primary metabolic process | 2 | 53 |
GO:0070085 | glycosylation | 2 | 53 |
GO:0071704 | organic substance metabolic process | 2 | 53 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 53 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 53 |
GO:0016740 | transferase activity | 2 | 53 |
GO:0016757 | glycosyltransferase activity | 3 | 53 |
GO:0016758 | hexosyltransferase activity | 4 | 53 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.315 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 796 | 800 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 801 | 803 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 730 | 732 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 798 | 800 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 102 | 108 | PF00082 | 0.391 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.438 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.640 |
DEG_SCF_FBW7_1 | 450 | 457 | PF00400 | 0.481 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.338 |
DOC_ANK_TNKS_1 | 380 | 387 | PF00023 | 0.322 |
DOC_CDC14_PxL_1 | 526 | 534 | PF14671 | 0.244 |
DOC_CKS1_1 | 451 | 456 | PF01111 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 448 | 454 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 81 | 87 | PF00134 | 0.595 |
DOC_MAPK_gen_1 | 102 | 111 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 478 | 485 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 534 | 543 | PF00069 | 0.303 |
DOC_MAPK_NFAT4_5 | 478 | 486 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 512 | 519 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 694 | 700 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 448 | 451 | PF13499 | 0.533 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.591 |
DOC_PP2B_PxIxI_1 | 419 | 425 | PF00149 | 0.276 |
DOC_PP4_FxxP_1 | 706 | 709 | PF00568 | 0.270 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.327 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 134 | 142 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 167 | 175 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 478 | 482 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 551 | 558 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 560 | 565 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 630 | 635 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 696 | 700 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 779 | 783 | PF00244 | 0.366 |
LIG_Actin_WH2_2 | 536 | 553 | PF00022 | 0.282 |
LIG_Actin_WH2_2 | 708 | 726 | PF00022 | 0.246 |
LIG_BRCT_BRCA1_1 | 81 | 85 | PF00533 | 0.603 |
LIG_EH_1 | 618 | 622 | PF12763 | 0.356 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.437 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.538 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.484 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.388 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.383 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.642 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.379 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.276 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.346 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.317 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.389 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.408 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.409 |
LIG_LIR_Apic_2 | 500 | 506 | PF02991 | 0.457 |
LIG_LIR_Apic_2 | 557 | 561 | PF02991 | 0.318 |
LIG_LIR_Apic_2 | 704 | 709 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 154 | 159 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 480 | 487 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 537 | 547 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 643 | 651 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.365 |
LIG_NRBOX | 145 | 151 | PF00104 | 0.378 |
LIG_NRBOX | 627 | 633 | PF00104 | 0.349 |
LIG_PCNA_yPIPBox_3 | 143 | 152 | PF02747 | 0.376 |
LIG_Pex14_1 | 591 | 595 | PF04695 | 0.268 |
LIG_SH2_NCK_1 | 374 | 378 | PF00017 | 0.403 |
LIG_SH2_SRC | 651 | 654 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 793 | 797 | PF00017 | 0.374 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 552 | 555 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.331 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.602 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.631 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.342 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.487 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.396 |
LIG_SH3_3 | 706 | 712 | PF00018 | 0.307 |
LIG_SUMO_SIM_anti_2 | 623 | 630 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 643 | 649 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 767 | 772 | PF11976 | 0.294 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.415 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.539 |
LIG_WRC_WIRS_1 | 124 | 129 | PF05994 | 0.410 |
MOD_CDK_SPK_2 | 354 | 359 | PF00069 | 0.478 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.528 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.539 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.592 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.336 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.496 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.561 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.778 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.468 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.443 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.349 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.488 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.638 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.386 |
MOD_Cter_Amidation | 672 | 675 | PF01082 | 0.371 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.490 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.497 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.617 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.543 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.448 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.381 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.516 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.586 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.540 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.649 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.392 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.464 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.444 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.365 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.478 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.507 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.455 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.519 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.397 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.495 |
MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.330 |
MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.425 |
MOD_N-GLC_2 | 42 | 44 | PF02516 | 0.494 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.561 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.492 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.485 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.364 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.414 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.433 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.681 |
MOD_NEK2_2 | 285 | 290 | PF00069 | 0.449 |
MOD_NEK2_2 | 636 | 641 | PF00069 | 0.327 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.508 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.565 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.486 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.553 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.457 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.389 |
MOD_PKA_1 | 144 | 150 | PF00069 | 0.439 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.513 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.514 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.513 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.570 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.473 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.516 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.553 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.444 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.322 |
MOD_PKA_2 | 695 | 701 | PF00069 | 0.295 |
MOD_PKA_2 | 778 | 784 | PF00069 | 0.365 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.503 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.515 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.453 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.512 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.526 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.337 |
MOD_Plk_2-3 | 65 | 71 | PF00069 | 0.510 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.335 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.465 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.560 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.549 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.421 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.402 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.429 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.378 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.335 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.508 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.426 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.368 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.392 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.522 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.601 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.473 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.552 |
MOD_SUMO_rev_2 | 176 | 184 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 229 | 235 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 722 | 732 | PF00179 | 0.345 |
TRG_DiLeu_BaEn_1 | 643 | 648 | PF01217 | 0.286 |
TRG_DiLeu_BaEn_1 | 728 | 733 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 54 | 59 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 627 | 632 | PF01217 | 0.313 |
TRG_DiLeu_LyEn_5 | 728 | 733 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.499 |
TRG_NLS_MonoExtC_3 | 797 | 802 | PF00514 | 0.308 |
TRG_NLS_MonoExtN_4 | 796 | 802 | PF00514 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 630 | 634 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 730 | 734 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 64% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 37% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 33% | 82% |
A0A3S7WT86 | Leishmania donovani | 36% | 79% |
A0A3S7WWA6 | Leishmania donovani | 64% | 100% |
A0A451EJD9 | Leishmania donovani | 57% | 100% |
A0A451EJF4 | Leishmania donovani | 38% | 100% |
A0A451EJF6 | Leishmania donovani | 39% | 100% |
A0A451EJF8 | Leishmania donovani | 36% | 100% |
A0A451EJF9 | Leishmania donovani | 40% | 94% |
A4H3A9 | Leishmania braziliensis | 40% | 100% |
A4H3B4 | Leishmania braziliensis | 38% | 100% |
A4H3B6 | Leishmania braziliensis | 39% | 100% |
A4H3B8 | Leishmania braziliensis | 40% | 100% |
A4H3B9 | Leishmania braziliensis | 33% | 100% |
A4HJ20 | Leishmania braziliensis | 37% | 100% |
A4HNK3 | Leishmania braziliensis | 95% | 100% |
A4HNK6 | Leishmania braziliensis | 93% | 100% |
A4HRL9 | Leishmania infantum | 38% | 100% |
A4HRM0 | Leishmania infantum | 36% | 100% |
A4HRM1 | Leishmania infantum | 40% | 100% |
A4HRS1 | Leishmania infantum | 40% | 94% |
A4HRS3 | Leishmania infantum | 33% | 82% |
A4HRS5 | Leishmania infantum | 36% | 100% |
A4HZM0 | Leishmania infantum | 57% | 100% |
A4I7C7 | Leishmania infantum | 58% | 100% |
A4IAQ2 | Leishmania infantum | 55% | 100% |
E9AC91 | Leishmania major | 37% | 100% |
E9AC92 | Leishmania major | 39% | 100% |
E9AC94 | Leishmania major | 33% | 100% |
E9AC95 | Leishmania major | 35% | 100% |
E9AC96 | Leishmania major | 40% | 100% |
E9AC98 | Leishmania major | 33% | 100% |
E9AEH8 | Leishmania major | 58% | 100% |
E9AHA6 | Leishmania infantum | 57% | 100% |
E9AIP8 | Leishmania braziliensis | 90% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 82% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4Q5T6 | Leishmania major | 58% | 100% |
Q4QCL8 | Leishmania major | 62% | 100% |
Q4QFJ3 | Leishmania major | 36% | 79% |
Q4QIG9 | Leishmania major | 62% | 100% |
Q7YXU9 | Leishmania major | 63% | 100% |
Q7YXV1 | Leishmania major | 63% | 100% |
Q7YXV2 | Leishmania major | 62% | 100% |