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: E9ASB8
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_NRD_NRD_1 | 107 | 109 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.440 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.669 |
DEG_ODPH_VHL_1 | 11 | 24 | PF01847 | 0.639 |
DEG_SCF_FBW7_1 | 451 | 458 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.411 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.337 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 254 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 632 | 638 | PF00134 | 0.427 |
DOC_MAPK_DCC_7 | 14 | 24 | PF00069 | 0.668 |
DOC_MAPK_gen_1 | 107 | 114 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 232 | 238 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 297 | 306 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 47 | 54 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 495 | 502 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 82 | 88 | PF00069 | 0.650 |
DOC_MAPK_JIP1_4 | 297 | 303 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 107 | 116 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 535 | 544 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 627 | 634 | PF00069 | 0.305 |
DOC_MAPK_NFAT4_5 | 479 | 487 | PF00069 | 0.338 |
DOC_MAPK_NFAT4_5 | 627 | 635 | PF00069 | 0.293 |
DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.379 |
DOC_PP1_RVXF_1 | 513 | 520 | PF00149 | 0.439 |
DOC_PP1_RVXF_1 | 587 | 593 | PF00149 | 0.311 |
DOC_PP1_RVXF_1 | 596 | 602 | PF00149 | 0.305 |
DOC_PP1_RVXF_1 | 769 | 776 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.519 |
DOC_PP2B_LxvP_1 | 542 | 545 | PF13499 | 0.311 |
DOC_PP2B_LxvP_1 | 632 | 635 | PF13499 | 0.402 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.401 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.332 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.293 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.358 |
DOC_USP7_UBL2_3 | 722 | 726 | PF12436 | 0.319 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 322 | 326 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 426 | 430 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 501 | 505 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 562 | 570 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 677 | 684 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 691 | 700 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 771 | 776 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 801 | 807 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 93 | 100 | PF00244 | 0.703 |
LIG_Actin_WH2_2 | 537 | 554 | PF00022 | 0.276 |
LIG_Actin_WH2_2 | 663 | 679 | PF00022 | 0.327 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.347 |
LIG_DLG_GKlike_1 | 180 | 187 | PF00625 | 0.335 |
LIG_EH_1 | 618 | 622 | PF12763 | 0.370 |
LIG_EH1_1 | 642 | 650 | PF00400 | 0.241 |
LIG_EVH1_2 | 84 | 88 | PF00568 | 0.632 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.457 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.711 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.495 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.483 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.350 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.435 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.338 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.377 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.682 |
LIG_FHA_1 | 780 | 786 | PF00498 | 0.328 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.336 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.420 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.410 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.466 |
LIG_FHA_2 | 803 | 809 | PF00498 | 0.344 |
LIG_Integrin_RGD_1 | 777 | 779 | PF01839 | 0.565 |
LIG_LIR_Apic_2 | 150 | 155 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 503 | 507 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 154 | 160 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 481 | 487 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 538 | 548 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 642 | 651 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 698 | 708 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.377 |
LIG_NRBOX | 627 | 633 | PF00104 | 0.341 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.409 |
LIG_Pex14_2 | 721 | 725 | PF04695 | 0.265 |
LIG_RPA_C_Fungi | 175 | 187 | PF08784 | 0.400 |
LIG_SH2_CRK | 570 | 574 | PF00017 | 0.355 |
LIG_SH2_CRK | 708 | 712 | PF00017 | 0.307 |
LIG_SH2_CRK | 795 | 799 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 708 | 712 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 795 | 799 | PF00017 | 0.362 |
LIG_SH2_PTP2 | 644 | 647 | PF00017 | 0.266 |
LIG_SH2_SRC | 795 | 798 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 636 | 640 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 720 | 723 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 784 | 787 | PF00017 | 0.435 |
LIG_SH3_1 | 708 | 714 | PF00018 | 0.301 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.597 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.459 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.452 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.390 |
LIG_SH3_3 | 708 | 714 | PF00018 | 0.348 |
LIG_SH3_4 | 491 | 498 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 115 | 121 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 627 | 633 | PF11976 | 0.385 |
LIG_TYR_ITIM | 326 | 331 | PF00017 | 0.541 |
LIG_TYR_ITIM | 568 | 573 | PF00017 | 0.318 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.514 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.512 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.447 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.489 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.422 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.282 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.633 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.380 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.222 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.551 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.502 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.489 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.581 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.601 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.365 |
MOD_CK2_1 | 739 | 745 | PF00069 | 0.400 |
MOD_CK2_1 | 802 | 808 | PF00069 | 0.355 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.478 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.589 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.617 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.641 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.468 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.624 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.545 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.533 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.627 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.348 |
MOD_GlcNHglycan | 812 | 815 | PF01048 | 0.403 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.596 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.482 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.571 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.459 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.640 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.480 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.529 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.643 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.588 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.531 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.476 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.490 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.634 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.355 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.342 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.581 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.464 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.425 |
MOD_LATS_1 | 91 | 97 | PF00433 | 0.523 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.451 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.394 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.380 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.406 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.432 |
MOD_N-GLC_1 | 802 | 807 | PF02516 | 0.409 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.361 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.545 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.573 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.454 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.416 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.346 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.280 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.591 |
MOD_NEK2_2 | 193 | 198 | PF00069 | 0.625 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.514 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.456 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.571 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.539 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.556 |
MOD_PIKK_1 | 746 | 752 | PF00454 | 0.409 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.397 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.597 |
MOD_PKA_1 | 64 | 70 | PF00069 | 0.565 |
MOD_PKA_1 | 771 | 777 | PF00069 | 0.309 |
MOD_PKA_1 | 801 | 807 | PF00069 | 0.332 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.635 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.502 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.489 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.402 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.545 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.574 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.495 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.519 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.443 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.442 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.569 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.404 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.602 |
MOD_PKB_1 | 769 | 777 | PF00069 | 0.318 |
MOD_PKB_1 | 800 | 808 | PF00069 | 0.362 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.474 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.476 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.575 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.420 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.505 |
MOD_Plk_2-3 | 352 | 358 | PF00069 | 0.492 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.318 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.497 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.484 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.491 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.408 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.466 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.377 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.344 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.520 |
MOD_Plk_4 | 771 | 777 | PF00069 | 0.396 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.453 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.528 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.371 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.457 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.524 |
MOD_SUMO_for_1 | 721 | 724 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 485 | 493 | PF00179 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 624 | 629 | PF01217 | 0.348 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.384 |
TRG_NLS_MonoCore_2 | 558 | 563 | PF00514 | 0.325 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 74% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 38% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 34% | 82% |
A0A3S7WT86 | Leishmania donovani | 36% | 79% |
A0A3S7WWA6 | Leishmania donovani | 74% | 100% |
A0A451EJD9 | Leishmania donovani | 80% | 100% |
A0A451EJF4 | Leishmania donovani | 40% | 100% |
A0A451EJF6 | Leishmania donovani | 40% | 100% |
A0A451EJF8 | Leishmania donovani | 36% | 100% |
A0A451EJF9 | Leishmania donovani | 41% | 94% |
A4H3A9 | Leishmania braziliensis | 40% | 100% |
A4H3B4 | Leishmania braziliensis | 40% | 100% |
A4H3B6 | Leishmania braziliensis | 39% | 98% |
A4H3B8 | Leishmania braziliensis | 42% | 100% |
A4H3B9 | Leishmania braziliensis | 36% | 100% |
A4H4W8 | Leishmania braziliensis | 59% | 100% |
A4HJ20 | Leishmania braziliensis | 38% | 100% |
A4HNK3 | Leishmania braziliensis | 66% | 100% |
A4HNK6 | Leishmania braziliensis | 59% | 100% |
A4HRL9 | Leishmania infantum | 40% | 100% |
A4HRM0 | Leishmania infantum | 38% | 100% |
A4HRM1 | Leishmania infantum | 40% | 100% |
A4HRS1 | Leishmania infantum | 41% | 94% |
A4HRS3 | Leishmania infantum | 31% | 82% |
A4HRS5 | Leishmania infantum | 36% | 100% |
A4HZM0 | Leishmania infantum | 81% | 100% |
A4I7C7 | Leishmania infantum | 81% | 100% |
A4IAQ2 | Leishmania infantum | 78% | 100% |
E9AC91 | Leishmania major | 41% | 100% |
E9AC92 | Leishmania major | 41% | 100% |
E9AC94 | Leishmania major | 32% | 100% |
E9AC95 | Leishmania major | 36% | 100% |
E9AC96 | Leishmania major | 41% | 100% |
E9AC98 | Leishmania major | 32% | 100% |
E9AEH8 | Leishmania major | 78% | 100% |
E9AHA6 | Leishmania infantum | 80% | 100% |
E9AIP8 | Leishmania braziliensis | 59% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q5T6 | Leishmania major | 80% | 100% |
Q4QCL8 | Leishmania major | 71% | 100% |
Q4QFJ3 | Leishmania major | 36% | 79% |
Q4QIG9 | Leishmania major | 72% | 100% |
Q7YXU9 | Leishmania major | 71% | 100% |
Q7YXV1 | Leishmania major | 73% | 100% |
Q7YXV2 | Leishmania major | 72% | 100% |