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: A4I7C7
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 | 180 | 184 | PF00656 | 0.355 |
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.349 |
CLV_C14_Caspase3-7 | 743 | 747 | PF00656 | 0.315 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.470 |
CLV_PCSK_FUR_1 | 91 | 95 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 769 | 771 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.540 |
CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.342 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.683 |
DEG_SCF_FBW7_1 | 452 | 459 | PF00400 | 0.432 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.321 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.482 |
DOC_CYCLIN_yCln2_LP_2 | 633 | 639 | PF00134 | 0.317 |
DOC_MAPK_DCC_7 | 572 | 581 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.414 |
DOC_MAPK_HePTP_8 | 104 | 116 | PF00069 | 0.438 |
DOC_MAPK_JIP1_4 | 298 | 304 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 106 | 114 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 480 | 487 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 628 | 635 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 659 | 668 | PF00069 | 0.275 |
DOC_MAPK_NFAT4_5 | 480 | 488 | PF00069 | 0.331 |
DOC_MAPK_NFAT4_5 | 628 | 636 | PF00069 | 0.273 |
DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.444 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.389 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.489 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.357 |
DOC_PP2B_LxvP_1 | 633 | 636 | PF13499 | 0.288 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.340 |
DOC_SPAK_OSR1_1 | 107 | 111 | PF12202 | 0.413 |
DOC_SPAK_OSR1_1 | 128 | 132 | PF12202 | 0.372 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 811 | 815 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 492 | 496 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 733 | 737 | PF12436 | 0.335 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 323 | 327 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 563 | 570 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 659 | 665 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 678 | 685 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 803 | 808 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 91 | 100 | PF00244 | 0.668 |
LIG_Actin_WH2_2 | 664 | 680 | PF00022 | 0.313 |
LIG_Actin_WH2_2 | 754 | 771 | PF00022 | 0.335 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.278 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.626 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.328 |
LIG_EH_1 | 619 | 623 | PF12763 | 0.320 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.463 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.455 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.352 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.391 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.350 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.380 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.383 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.385 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.274 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.343 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.380 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.333 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.326 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.305 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.407 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.444 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.377 |
LIG_FHA_2 | 762 | 768 | PF00498 | 0.354 |
LIG_FHA_2 | 804 | 810 | PF00498 | 0.340 |
LIG_Integrin_RGD_1 | 778 | 780 | PF01839 | 0.568 |
LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.362 |
LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 504 | 508 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 155 | 161 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 634 | 645 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 699 | 710 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 643 | 648 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.377 |
LIG_NRBOX | 111 | 117 | PF00104 | 0.308 |
LIG_NRBOX | 628 | 634 | PF00104 | 0.320 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.337 |
LIG_Pex14_2 | 722 | 726 | PF04695 | 0.266 |
LIG_PTB_Apo_2 | 208 | 215 | PF02174 | 0.348 |
LIG_PTB_Apo_2 | 639 | 646 | PF02174 | 0.298 |
LIG_PTB_Phospho_1 | 208 | 214 | PF10480 | 0.344 |
LIG_PTB_Phospho_1 | 639 | 645 | PF10480 | 0.271 |
LIG_SH2_CRK | 645 | 649 | PF00017 | 0.296 |
LIG_SH2_CRK | 709 | 713 | PF00017 | 0.276 |
LIG_SH2_GRB2like | 595 | 598 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.378 |
LIG_SH2_NCK_1 | 709 | 713 | PF00017 | 0.275 |
LIG_SH2_NCK_1 | 796 | 800 | PF00017 | 0.321 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.290 |
LIG_SH2_SRC | 796 | 799 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 645 | 649 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 796 | 800 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.376 |
LIG_SH3_1 | 709 | 715 | PF00018 | 0.271 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.459 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.374 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.383 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.298 |
LIG_SH3_3 | 687 | 693 | PF00018 | 0.335 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.304 |
LIG_SH3_4 | 492 | 499 | PF00018 | 0.367 |
LIG_SUMO_SIM_par_1 | 628 | 634 | PF11976 | 0.311 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.444 |
MOD_CDC14_SPxK_1 | 27 | 30 | PF00782 | 0.623 |
MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.624 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.426 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.337 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.456 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.489 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.300 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.382 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.705 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.328 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.330 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.408 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.665 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.465 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.657 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.319 |
MOD_CK2_1 | 803 | 809 | PF00069 | 0.301 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.579 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.623 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.507 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.494 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.521 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.627 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.645 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.510 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.497 |
MOD_GlcNHglycan | 741 | 745 | PF01048 | 0.538 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.538 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.454 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.444 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.445 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.501 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.466 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.427 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.710 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.481 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.424 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.412 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.325 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.715 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.678 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.293 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.303 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.333 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.364 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.556 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.538 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.552 |
MOD_N-GLC_1 | 747 | 752 | PF02516 | 0.572 |
MOD_N-GLC_1 | 772 | 777 | PF02516 | 0.522 |
MOD_N-GLC_1 | 803 | 808 | PF02516 | 0.515 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.410 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.356 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.383 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.332 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.285 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.294 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.457 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.448 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.352 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.454 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.426 |
MOD_PIKK_1 | 747 | 753 | PF00454 | 0.355 |
MOD_PIKK_1 | 756 | 762 | PF00454 | 0.345 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.583 |
MOD_PK_1 | 235 | 241 | PF00069 | 0.337 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.495 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.389 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.704 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.425 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.405 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.353 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.471 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.463 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.470 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.439 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.459 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.370 |
MOD_PKA_2 | 802 | 808 | PF00069 | 0.338 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.650 |
MOD_PKB_1 | 801 | 809 | PF00069 | 0.306 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.361 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.326 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.323 |
MOD_Plk_1 | 740 | 746 | PF00069 | 0.317 |
MOD_Plk_1 | 772 | 778 | PF00069 | 0.328 |
MOD_Plk_1 | 803 | 809 | PF00069 | 0.319 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.413 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.393 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.357 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.344 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.411 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.374 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.389 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.313 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.320 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.307 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.412 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.341 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.336 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.371 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.631 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.512 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.408 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.402 |
MOD_SUMO_for_1 | 722 | 725 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 486 | 494 | PF00179 | 0.352 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 625 | 630 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 800 | 803 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 91 | 94 | PF00400 | 0.680 |
TRG_NLS_MonoExtC_3 | 495 | 501 | PF00514 | 0.343 |
TRG_NLS_MonoExtN_4 | 493 | 500 | PF00514 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 85% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 40% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 31% | 82% |
A0A3S7WT86 | Leishmania donovani | 37% | 79% |
A0A3S7WWA6 | Leishmania donovani | 85% | 100% |
A0A451EJD9 | Leishmania donovani | 92% | 100% |
A0A451EJF4 | Leishmania donovani | 39% | 100% |
A0A451EJF6 | Leishmania donovani | 41% | 100% |
A0A451EJF8 | Leishmania donovani | 39% | 100% |
A0A451EJF9 | Leishmania donovani | 41% | 95% |
A4H3A9 | Leishmania braziliensis | 41% | 100% |
A4H3B4 | Leishmania braziliensis | 42% | 100% |
A4H3B6 | Leishmania braziliensis | 40% | 100% |
A4H3B8 | Leishmania braziliensis | 43% | 100% |
A4H3B9 | Leishmania braziliensis | 33% | 100% |
A4H4W8 | Leishmania braziliensis | 58% | 100% |
A4HJ20 | Leishmania braziliensis | 40% | 100% |
A4HNK3 | Leishmania braziliensis | 64% | 100% |
A4HNK6 | Leishmania braziliensis | 58% | 100% |
A4HRL9 | Leishmania infantum | 41% | 100% |
A4HRM0 | Leishmania infantum | 39% | 100% |
A4HRM1 | Leishmania infantum | 41% | 97% |
A4HRS1 | Leishmania infantum | 41% | 100% |
A4HRS3 | Leishmania infantum | 31% | 100% |
A4HRS5 | Leishmania infantum | 39% | 100% |
A4HZM0 | Leishmania infantum | 97% | 100% |
A4IAQ2 | Leishmania infantum | 89% | 100% |
E9AC91 | Leishmania major | 41% | 100% |
E9AC92 | Leishmania major | 41% | 100% |
E9AC94 | Leishmania major | 32% | 69% |
E9AC95 | Leishmania major | 38% | 100% |
E9AC96 | Leishmania major | 41% | 100% |
E9AC98 | Leishmania major | 33% | 100% |
E9AEH8 | Leishmania major | 85% | 100% |
E9AHA6 | Leishmania infantum | 93% | 100% |
E9AIP8 | Leishmania braziliensis | 58% | 99% |
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) | 39% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 83% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q5T6 | Leishmania major | 84% | 100% |
Q4QCL8 | Leishmania major | 74% | 100% |
Q4QFJ3 | Leishmania major | 36% | 100% |
Q4QIG9 | Leishmania major | 75% | 100% |
Q7YXU9 | Leishmania major | 73% | 100% |
Q7YXV1 | Leishmania major | 75% | 100% |
Q7YXV2 | Leishmania major | 74% | 100% |