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 | 14 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0098588 | bounding membrane of organelle | 4 | 14 |
Related structures:
AlphaFold database: A4H3B8
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 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.365 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 755 | 757 | PF00082 | 0.493 |
CLV_PCSK_PC7_1 | 401 | 407 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 358 | 366 | PF00400 | 0.396 |
DEG_SCF_FBW7_1 | 444 | 451 | PF00400 | 0.501 |
DOC_CKS1_1 | 445 | 450 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 359 | 369 | PF00134 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 359 | 366 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 359 | 366 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 472 | 479 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 496 | 505 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 629 | 637 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.610 |
DOC_MAPK_NFAT4_5 | 69 | 77 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 155 | 161 | PF00149 | 0.354 |
DOC_PP1_RVXF_1 | 470 | 477 | PF00149 | 0.336 |
DOC_PP1_RVXF_1 | 506 | 513 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 652 | 659 | PF00149 | 0.261 |
DOC_PP2B_LxvP_1 | 442 | 445 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.301 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 577 | 583 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 79 | 86 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.374 |
LIG_Actin_WH2_2 | 626 | 641 | PF00022 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 690 | 695 | PF00928 | 0.242 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.339 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.535 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.503 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.353 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.395 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.430 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.413 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.262 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.293 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.599 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.340 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.245 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.285 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.620 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.519 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.355 |
LIG_FHA_2 | 792 | 798 | PF00498 | 0.352 |
LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 531 | 541 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 690 | 700 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 707 | 713 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 720 | 728 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 650 | 656 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 707 | 711 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 820 | 825 | PF02991 | 0.308 |
LIG_MAD2 | 620 | 628 | PF02301 | 0.247 |
LIG_MYND_1 | 336 | 340 | PF01753 | 0.387 |
LIG_Pex14_1 | 691 | 695 | PF04695 | 0.243 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.349 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.581 |
LIG_RPA_C_Fungi | 401 | 413 | PF08784 | 0.340 |
LIG_RPA_C_Fungi | 614 | 626 | PF08784 | 0.294 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.342 |
LIG_SH2_CRK | 822 | 826 | PF00017 | 0.353 |
LIG_SH2_GRB2like | 804 | 807 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 534 | 537 | PF00017 | 0.361 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.399 |
LIG_SH2_SRC | 515 | 518 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 804 | 808 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 727 | 730 | PF00017 | 0.462 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.520 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.531 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.397 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.632 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.504 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.370 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.457 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.515 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.241 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.404 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.412 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.422 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.545 |
LIG_TYR_ITIM | 651 | 656 | PF00017 | 0.297 |
LIG_WW_3 | 275 | 279 | PF00397 | 0.402 |
MOD_CDC14_SPxK_1 | 356 | 359 | PF00782 | 0.400 |
MOD_CDK_SPxK_1 | 353 | 359 | PF00069 | 0.427 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.671 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.477 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.519 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.441 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.527 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.503 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.487 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.679 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.464 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.423 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.412 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.503 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.386 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.482 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.597 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.613 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.372 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.439 |
MOD_GlcNHglycan | 339 | 343 | PF01048 | 0.567 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.595 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.563 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.546 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.559 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.554 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.423 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.404 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.284 |
MOD_GlcNHglycan | 643 | 648 | PF01048 | 0.334 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.435 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.348 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.488 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.473 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.525 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.292 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.478 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.553 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.553 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.501 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.478 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.507 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.248 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.381 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.565 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.387 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.421 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.514 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.380 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.421 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.466 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.466 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.332 |
MOD_N-GLC_1 | 773 | 778 | PF02516 | 0.364 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.505 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.337 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.562 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.562 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.490 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.454 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.394 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.532 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.283 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.502 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.362 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.684 |
MOD_NEK2_2 | 597 | 602 | PF00069 | 0.300 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.412 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.549 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.307 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.411 |
MOD_PK_1 | 406 | 412 | PF00069 | 0.363 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.628 |
MOD_PKA_1 | 755 | 761 | PF00069 | 0.334 |
MOD_PKA_1 | 789 | 795 | PF00069 | 0.330 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.478 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.579 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.577 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.420 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.529 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.349 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.512 |
MOD_PKA_2 | 789 | 795 | PF00069 | 0.356 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.442 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.446 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.394 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.456 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.497 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.423 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.463 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.330 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.507 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.443 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.624 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.585 |
MOD_SUMO_rev_2 | 25 | 32 | PF00179 | 0.475 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 692 | 695 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 723 | 726 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 822 | 825 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 715 | 718 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 789 | 791 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.629 |
TRG_NLS_MonoExtC_3 | 487 | 493 | PF00514 | 0.418 |
TRG_NLS_MonoExtN_4 | 13 | 19 | PF00514 | 0.478 |
TRG_NLS_MonoExtN_4 | 485 | 492 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 823 | 827 | PF00026 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 42% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 59% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 40% | 83% |
A0A3S7WT86 | Leishmania donovani | 41% | 81% |
A0A3S7WWA6 | Leishmania donovani | 42% | 100% |
A0A451EJD9 | Leishmania donovani | 42% | 100% |
A0A451EJF4 | Leishmania donovani | 61% | 100% |
A0A451EJF6 | Leishmania donovani | 62% | 100% |
A0A451EJF8 | Leishmania donovani | 66% | 100% |
A0A451EJF9 | Leishmania donovani | 60% | 96% |
A4H3A9 | Leishmania braziliensis | 62% | 100% |
A4H3B4 | Leishmania braziliensis | 72% | 100% |
A4H3B6 | Leishmania braziliensis | 61% | 100% |
A4H3B7 | Leishmania braziliensis | 45% | 100% |
A4H3B9 | Leishmania braziliensis | 39% | 93% |
A4H4W8 | Leishmania braziliensis | 40% | 100% |
A4HJ20 | Leishmania braziliensis | 59% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 100% |
A4HNK6 | Leishmania braziliensis | 40% | 100% |
A4HRL9 | Leishmania infantum | 59% | 100% |
A4HRM0 | Leishmania infantum | 54% | 100% |
A4HRM1 | Leishmania infantum | 62% | 100% |
A4HRS1 | Leishmania infantum | 60% | 96% |
A4HRS3 | Leishmania infantum | 40% | 83% |
A4HRS5 | Leishmania infantum | 66% | 100% |
A4HZM0 | Leishmania infantum | 42% | 100% |
A4I7C7 | Leishmania infantum | 43% | 100% |
A4IAQ2 | Leishmania infantum | 41% | 100% |
E9AC91 | Leishmania major | 60% | 100% |
E9AC92 | Leishmania major | 60% | 100% |
E9AC94 | Leishmania major | 40% | 70% |
E9AC95 | Leishmania major | 66% | 100% |
E9AC96 | Leishmania major | 60% | 100% |
E9AC98 | Leishmania major | 40% | 83% |
E9AEH8 | Leishmania major | 40% | 100% |
E9AHA6 | Leishmania infantum | 42% | 100% |
E9AIP8 | Leishmania braziliensis | 39% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 84% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
Q4Q5T6 | Leishmania major | 40% | 100% |
Q4QCL8 | Leishmania major | 40% | 100% |
Q4QFJ3 | Leishmania major | 40% | 100% |
Q4QIG9 | Leishmania major | 41% | 100% |
Q7YXU9 | Leishmania major | 40% | 100% |
Q7YXV1 | Leishmania major | 40% | 100% |
Q7YXV2 | Leishmania major | 41% | 100% |