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: A4IAQ2
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 | 434 | 438 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 740 | 744 | PF00656 | 0.306 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 766 | 768 | PF00082 | 0.574 |
CLV_PCSK_PC7_1 | 775 | 781 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.540 |
CLV_Separin_Metazoa | 268 | 272 | PF03568 | 0.349 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.677 |
DEG_SCF_FBW7_1 | 451 | 458 | PF00400 | 0.483 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.481 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 254 | PF00134 | 0.346 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 630 | 636 | PF00134 | 0.333 |
DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 297 | 306 | PF00069 | 0.396 |
DOC_MAPK_HePTP_8 | 103 | 115 | PF00069 | 0.438 |
DOC_MAPK_JIP1_4 | 297 | 303 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 656 | 665 | PF00069 | 0.298 |
DOC_MAPK_NFAT4_5 | 479 | 487 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 513 | 520 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 542 | 545 | PF13499 | 0.297 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.316 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.412 |
DOC_SPAK_OSR1_1 | 106 | 110 | PF12202 | 0.413 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 808 | 812 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.353 |
DOC_USP7_UBL2_3 | 730 | 734 | PF12436 | 0.335 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 322 | 326 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 426 | 430 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 432 | 436 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 656 | 662 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 675 | 682 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 800 | 805 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.682 |
LIG_Actin_WH2_2 | 661 | 677 | PF00022 | 0.330 |
LIG_Actin_WH2_2 | 751 | 768 | PF00022 | 0.324 |
LIG_APCC_ABBA_1 | 619 | 624 | PF00400 | 0.307 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.393 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.539 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.490 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.356 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.412 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.351 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.404 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.231 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.412 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.330 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.342 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.411 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.483 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.385 |
LIG_FHA_2 | 759 | 765 | PF00498 | 0.336 |
LIG_FHA_2 | 801 | 807 | PF00498 | 0.359 |
LIG_Integrin_RGD_1 | 775 | 777 | PF01839 | 0.570 |
LIG_LIR_Apic_2 | 150 | 155 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.347 |
LIG_LIR_Apic_2 | 503 | 507 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 154 | 160 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 481 | 487 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 538 | 548 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 618 | 627 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 640 | 647 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 696 | 707 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 618 | 622 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 696 | 702 | PF02991 | 0.377 |
LIG_NRBOX | 110 | 116 | PF00104 | 0.308 |
LIG_NRBOX | 625 | 631 | PF00104 | 0.343 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.413 |
LIG_Pex14_2 | 719 | 723 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 207 | 214 | PF02174 | 0.386 |
LIG_PTB_Apo_2 | 636 | 643 | PF02174 | 0.299 |
LIG_PTB_Phospho_1 | 207 | 213 | PF10480 | 0.384 |
LIG_PTB_Phospho_1 | 636 | 642 | PF10480 | 0.272 |
LIG_SH2_CRK | 642 | 646 | PF00017 | 0.300 |
LIG_SH2_CRK | 706 | 710 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 706 | 710 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 793 | 797 | PF00017 | 0.319 |
LIG_SH2_SRC | 793 | 796 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 634 | 638 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 793 | 797 | PF00017 | 0.376 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.383 |
LIG_SH3_1 | 706 | 712 | PF00018 | 0.268 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.512 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.354 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.378 |
LIG_SH3_3 | 706 | 712 | PF00018 | 0.301 |
LIG_SH3_4 | 491 | 498 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 624 | 629 | PF11976 | 0.311 |
LIG_TYR_ITIM | 326 | 331 | PF00017 | 0.444 |
LIG_WRC_WIRS_1 | 616 | 621 | PF05994 | 0.294 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.467 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.440 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.458 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.508 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.306 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.378 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.708 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.325 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.400 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.667 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.477 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.504 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.339 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.639 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.591 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.654 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.714 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.506 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.497 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.533 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.660 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.638 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.510 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.497 |
MOD_GlcNHglycan | 738 | 742 | PF01048 | 0.528 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.552 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.476 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.528 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.485 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.485 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.399 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.712 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.457 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.426 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.444 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.376 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.712 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.236 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.679 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.297 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.332 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.659 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.352 |
MOD_LATS_1 | 569 | 575 | PF00433 | 0.201 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.617 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.593 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.545 |
MOD_N-GLC_1 | 693 | 698 | PF02516 | 0.522 |
MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.569 |
MOD_N-GLC_1 | 769 | 774 | PF02516 | 0.515 |
MOD_N-GLC_1 | 800 | 805 | PF02516 | 0.530 |
MOD_N-GLC_2 | 585 | 587 | PF02516 | 0.401 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.453 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.640 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.456 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.387 |
MOD_NEK2_2 | 193 | 198 | PF00069 | 0.550 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.481 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.393 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.662 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.472 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.430 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.215 |
MOD_PIKK_1 | 744 | 750 | PF00454 | 0.353 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.333 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.626 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.599 |
MOD_PK_1 | 234 | 240 | PF00069 | 0.380 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.481 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.684 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.439 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.479 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.465 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.468 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.415 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.423 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.375 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.353 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.665 |
MOD_PKB_1 | 798 | 806 | PF00069 | 0.321 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.417 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.370 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.302 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.362 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.307 |
MOD_Plk_1 | 769 | 775 | PF00069 | 0.326 |
MOD_Plk_1 | 800 | 806 | PF00069 | 0.336 |
MOD_Plk_2-3 | 352 | 358 | PF00069 | 0.413 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.444 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.400 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.409 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.340 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.376 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.327 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.302 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.340 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.295 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.413 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.342 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.353 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.443 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.446 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.493 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.412 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 719 | 722 | PF00179 | 0.267 |
MOD_SUMO_rev_2 | 485 | 493 | PF00179 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.217 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 778 | 780 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 797 | 800 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.681 |
TRG_NLS_MonoExtC_3 | 494 | 500 | PF00514 | 0.335 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 609 | 613 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 77% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 39% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 32% | 82% |
A0A3S7WT86 | Leishmania donovani | 36% | 79% |
A0A3S7WWA6 | Leishmania donovani | 77% | 100% |
A0A451EJD9 | Leishmania donovani | 89% | 100% |
A0A451EJF4 | Leishmania donovani | 37% | 100% |
A0A451EJF6 | Leishmania donovani | 41% | 100% |
A0A451EJF8 | Leishmania donovani | 38% | 100% |
A0A451EJF9 | Leishmania donovani | 39% | 94% |
A4H3A9 | Leishmania braziliensis | 40% | 100% |
A4H3B4 | Leishmania braziliensis | 40% | 100% |
A4H3B6 | Leishmania braziliensis | 38% | 100% |
A4H3B8 | Leishmania braziliensis | 41% | 100% |
A4H3B9 | Leishmania braziliensis | 33% | 100% |
A4H4W8 | Leishmania braziliensis | 55% | 100% |
A4HJ20 | Leishmania braziliensis | 39% | 100% |
A4HNK3 | Leishmania braziliensis | 60% | 99% |
A4HNK6 | Leishmania braziliensis | 55% | 99% |
A4HRL9 | Leishmania infantum | 37% | 100% |
A4HRM0 | Leishmania infantum | 38% | 100% |
A4HRM1 | Leishmania infantum | 41% | 100% |
A4HRS1 | Leishmania infantum | 39% | 94% |
A4HRS3 | Leishmania infantum | 31% | 82% |
A4HRS5 | Leishmania infantum | 38% | 100% |
A4HZM0 | Leishmania infantum | 87% | 100% |
A4I7C7 | Leishmania infantum | 89% | 100% |
E9AC91 | Leishmania major | 40% | 100% |
E9AC92 | Leishmania major | 41% | 100% |
E9AC94 | Leishmania major | 32% | 69% |
E9AC95 | Leishmania major | 37% | 100% |
E9AC96 | Leishmania major | 42% | 100% |
E9AC98 | Leishmania major | 32% | 82% |
E9AEH8 | Leishmania major | 80% | 100% |
E9AHA6 | Leishmania infantum | 90% | 100% |
E9AIP8 | Leishmania braziliensis | 54% | 98% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 82% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4Q5T6 | Leishmania major | 80% | 100% |
Q4QCL8 | Leishmania major | 71% | 100% |
Q4QFJ3 | Leishmania major | 37% | 79% |
Q4QIG9 | Leishmania major | 71% | 100% |
Q7YXU9 | Leishmania major | 70% | 100% |
Q7YXV1 | Leishmania major | 72% | 100% |
Q7YXV2 | Leishmania major | 71% | 100% |