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: A0A451EJF9
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 | 672 | 676 | PF00656 | 0.316 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 591 | 593 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 338 | 344 | PF00082 | 0.521 |
CLV_PCSK_PC7_1 | 440 | 446 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 587 | 593 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.533 |
CLV_Separin_Metazoa | 213 | 217 | PF03568 | 0.345 |
DEG_APCC_DBOX_1 | 397 | 405 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 740 | 748 | PF00400 | 0.282 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.635 |
DEG_SCF_FBW7_1 | 483 | 490 | PF00400 | 0.479 |
DEG_SCF_FBW7_2 | 452 | 459 | PF00400 | 0.315 |
DEG_SPOP_SBC_1 | 670 | 674 | PF00917 | 0.335 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.340 |
DOC_CKS1_1 | 484 | 489 | PF01111 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 124 | 135 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 157 | 164 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 643 | 650 | PF00069 | 0.290 |
DOC_MAPK_gen_1 | 660 | 667 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 711 | 720 | PF00069 | 0.277 |
DOC_MAPK_JIP1_4 | 125 | 131 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 124 | 131 | PF00069 | 0.718 |
DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 511 | 518 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 535 | 544 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 643 | 650 | PF00069 | 0.268 |
DOC_PP1_RVXF_1 | 509 | 516 | PF00149 | 0.336 |
DOC_PP1_RVXF_1 | 545 | 552 | PF00149 | 0.434 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 667 | 670 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 595 | 598 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.663 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 216 | 223 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 463 | 468 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 690 | 694 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 713 | 719 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.664 |
LIG_14-3-3_CterR_2 | 860 | 863 | PF00244 | 0.295 |
LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.373 |
LIG_APCC_ABBA_1 | 146 | 151 | PF00400 | 0.398 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.615 |
LIG_BRCT_BRCA1_1 | 850 | 854 | PF00533 | 0.265 |
LIG_eIF4E_1 | 209 | 215 | PF01652 | 0.362 |
LIG_EVH1_1 | 595 | 599 | PF00568 | 0.327 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.324 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.437 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.530 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.497 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.341 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.651 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.377 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.418 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.305 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.338 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.416 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.499 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.337 |
LIG_FHA_2 | 832 | 838 | PF00498 | 0.321 |
LIG_Integrin_RGD_1 | 782 | 784 | PF01839 | 0.537 |
LIG_LIR_Apic_2 | 486 | 492 | PF02991 | 0.367 |
LIG_LIR_Apic_2 | 533 | 539 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 27 | 38 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 318 | 327 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 347 | 352 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 553 | 564 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 570 | 580 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 731 | 739 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 746 | 754 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 731 | 736 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 761 | 767 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 853 | 859 | PF02991 | 0.298 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.276 |
LIG_NRP_CendR_1 | 860 | 863 | PF00754 | 0.516 |
LIG_PTB_Apo_2 | 839 | 846 | PF02174 | 0.256 |
LIG_PTB_Phospho_1 | 839 | 845 | PF10480 | 0.253 |
LIG_RPA_C_Fungi | 655 | 667 | PF08784 | 0.299 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.387 |
LIG_SH2_GRB2like | 686 | 689 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 22 | 25 | PF00017 | 0.496 |
LIG_SH2_PTP2 | 573 | 576 | PF00017 | 0.362 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.399 |
LIG_SH2_SRC | 554 | 557 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 554 | 558 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 843 | 847 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 767 | 770 | PF00017 | 0.256 |
LIG_SH2_STAT3 | 843 | 846 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 768 | 771 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 830 | 833 | PF00017 | 0.457 |
LIG_SH3_1 | 594 | 600 | PF00018 | 0.384 |
LIG_SH3_2 | 155 | 160 | PF14604 | 0.469 |
LIG_SH3_2 | 596 | 601 | PF14604 | 0.384 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.524 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.530 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.624 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.370 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.505 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.541 |
LIG_SH3_CIN85_PxpxPR_1 | 596 | 601 | PF14604 | 0.386 |
LIG_SUMO_SIM_anti_2 | 142 | 148 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 679 | 685 | PF11976 | 0.421 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.482 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.405 |
LIG_TYR_ITIM | 346 | 351 | PF00017 | 0.548 |
LIG_TYR_ITSM | 316 | 323 | PF00017 | 0.387 |
LIG_WW_3 | 598 | 602 | PF00397 | 0.414 |
MOD_CDK_SPK_2 | 615 | 620 | PF00069 | 0.518 |
MOD_CDK_SPxK_1 | 615 | 621 | PF00069 | 0.513 |
MOD_CDK_SPxxK_3 | 79 | 86 | PF00069 | 0.499 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.534 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.271 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.672 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.422 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.569 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.538 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.561 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.371 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.565 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.403 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.497 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.571 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.646 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.433 |
MOD_CK2_1 | 773 | 779 | PF00069 | 0.396 |
MOD_Cter_Amidation | 641 | 644 | PF01082 | 0.277 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.632 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.452 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.622 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.594 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.544 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.467 |
MOD_GlcNHglycan | 470 | 474 | PF01048 | 0.569 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.525 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.554 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.274 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.535 |
MOD_GlcNHglycan | 772 | 776 | PF01048 | 0.349 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.426 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.582 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.568 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.687 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.551 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.481 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.498 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.383 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.543 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.542 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.375 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.327 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.529 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.527 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.574 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.392 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.504 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.503 |
MOD_N-GLC_1 | 714 | 719 | PF02516 | 0.308 |
MOD_N-GLC_1 | 841 | 846 | PF02516 | 0.315 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.362 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.507 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.512 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.501 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.409 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.433 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.537 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.477 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.532 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.673 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.422 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.549 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.520 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.402 |
MOD_PKA_1 | 522 | 528 | PF00069 | 0.627 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.594 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.482 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.402 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.581 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.586 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.477 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.528 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.577 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.370 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.362 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.527 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.423 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.387 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.315 |
MOD_Plk_1 | 722 | 728 | PF00069 | 0.306 |
MOD_Plk_1 | 841 | 847 | PF00069 | 0.320 |
MOD_Plk_1 | 849 | 855 | PF00069 | 0.328 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.520 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.319 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.404 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.298 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.504 |
MOD_Plk_4 | 814 | 820 | PF00069 | 0.363 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.349 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.437 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.632 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.558 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.529 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.499 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.510 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.544 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 733 | 736 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 592 | 595 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 660 | 662 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 756 | 759 | PF00400 | 0.313 |
TRG_NLS_MonoExtC_3 | 230 | 236 | PF00514 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 660 | 664 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 691 | 696 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 40% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 62% | 98% |
A0A3S5H4Y9 | Leishmania donovani | 38% | 87% |
A0A3S7WT86 | Leishmania donovani | 47% | 84% |
A0A3S7WWA6 | Leishmania donovani | 40% | 100% |
A0A451EJD9 | Leishmania donovani | 41% | 100% |
A0A451EJF4 | Leishmania donovani | 61% | 97% |
A0A451EJF6 | Leishmania donovani | 96% | 100% |
A0A451EJF8 | Leishmania donovani | 56% | 100% |
A4H3A9 | Leishmania braziliensis | 53% | 97% |
A4H3B4 | Leishmania braziliensis | 51% | 96% |
A4H3B6 | Leishmania braziliensis | 50% | 97% |
A4H3B7 | Leishmania braziliensis | 42% | 100% |
A4H3B8 | Leishmania braziliensis | 60% | 100% |
A4H3B9 | Leishmania braziliensis | 39% | 100% |
A4H4W8 | Leishmania braziliensis | 40% | 100% |
A4HJ20 | Leishmania braziliensis | 50% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 96% |
A4HNK6 | Leishmania braziliensis | 40% | 100% |
A4HRL9 | Leishmania infantum | 66% | 100% |
A4HRM0 | Leishmania infantum | 56% | 99% |
A4HRM1 | Leishmania infantum | 95% | 100% |
A4HRS1 | Leishmania infantum | 98% | 100% |
A4HRS3 | Leishmania infantum | 38% | 87% |
A4HRS5 | Leishmania infantum | 55% | 100% |
A4HZM0 | Leishmania infantum | 40% | 100% |
A4I7C7 | Leishmania infantum | 41% | 100% |
A4IAQ2 | Leishmania infantum | 39% | 100% |
E9AC91 | Leishmania major | 68% | 100% |
E9AC92 | Leishmania major | 72% | 100% |
E9AC94 | Leishmania major | 38% | 73% |
E9AC95 | Leishmania major | 54% | 100% |
E9AC96 | Leishmania major | 88% | 100% |
E9AC98 | Leishmania major | 38% | 87% |
E9AEH8 | Leishmania major | 41% | 100% |
E9AHA6 | Leishmania infantum | 40% | 100% |
E9AIP8 | Leishmania braziliensis | 41% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 99% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 98% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 87% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 98% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4Q5T6 | Leishmania major | 40% | 100% |
Q4QCL8 | Leishmania major | 41% | 100% |
Q4QFJ3 | Leishmania major | 42% | 100% |
Q4QIG9 | Leishmania major | 41% | 100% |
Q7YXU9 | Leishmania major | 40% | 100% |
Q7YXV1 | Leishmania major | 40% | 100% |
Q7YXV2 | Leishmania major | 39% | 100% |