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: A4H3B4
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 | 398 | 402 | PF00656 | 0.339 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 626 | 628 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 735 | 737 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 777 | 779 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 412 | 418 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 663 | 669 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 369 | 377 | PF00400 | 0.361 |
DEG_SCF_FBW7_1 | 455 | 462 | PF00400 | 0.434 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.436 |
DOC_CYCLIN_RxL_1 | 370 | 380 | PF00134 | 0.299 |
DOC_CYCLIN_RxL_1 | 83 | 91 | PF00134 | 0.583 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.315 |
DOC_CYCLIN_yCln2_LP_2 | 27 | 30 | PF00134 | 0.617 |
DOC_CYCLIN_yCln2_LP_2 | 453 | 459 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 370 | 377 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.614 |
DOC_MAPK_HePTP_8 | 107 | 119 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 370 | 377 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 483 | 490 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 507 | 516 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.610 |
DOC_MAPK_NFAT4_5 | 110 | 118 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 166 | 172 | PF00149 | 0.318 |
DOC_PP1_RVXF_1 | 481 | 488 | PF00149 | 0.321 |
DOC_PP1_RVXF_1 | 517 | 524 | PF00149 | 0.415 |
DOC_PP1_RVXF_1 | 675 | 681 | PF00149 | 0.261 |
DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.617 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.299 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 776 | 781 | PF00397 | 0.362 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 576 | 580 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 663 | 667 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 754 | 758 | PF00244 | 0.328 |
LIG_Actin_WH2_2 | 254 | 270 | PF00022 | 0.364 |
LIG_Actin_WH2_2 | 653 | 669 | PF00022 | 0.286 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.622 |
LIG_BIR_III_2 | 765 | 769 | PF00653 | 0.285 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.617 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.653 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.493 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.449 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.660 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.485 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.641 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.346 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.349 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.413 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.281 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.593 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.359 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.442 |
LIG_FHA_2 | 803 | 809 | PF00498 | 0.305 |
LIG_GBD_Chelix_1 | 113 | 121 | PF00786 | 0.221 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 506 | 511 | PF02991 | 0.440 |
LIG_LIR_Apic_2 | 809 | 815 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 724 | 730 | PF02991 | 0.274 |
LIG_LIR_LC3C_4 | 5 | 10 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 724 | 729 | PF02991 | 0.300 |
LIG_MYND_1 | 347 | 351 | PF01753 | 0.382 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.300 |
LIG_NRBOX | 609 | 615 | PF00104 | 0.232 |
LIG_NRBOX | 656 | 662 | PF00104 | 0.272 |
LIG_Pex14_1 | 800 | 804 | PF04695 | 0.271 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 596 | 603 | PF02174 | 0.255 |
LIG_REV1ctd_RIR_1 | 718 | 727 | PF16727 | 0.280 |
LIG_RPA_C_Fungi | 412 | 424 | PF08784 | 0.320 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.496 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.260 |
LIG_SH2_CRK | 726 | 730 | PF00017 | 0.325 |
LIG_SH2_CRK | 812 | 816 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 782 | 786 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 812 | 816 | PF00017 | 0.334 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.384 |
LIG_SH2_SRC | 526 | 529 | PF00017 | 0.399 |
LIG_SH2_SRC | 716 | 719 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 726 | 730 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.529 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.521 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.513 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.327 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.557 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.423 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.362 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.507 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.405 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.526 |
LIG_WW_3 | 286 | 290 | PF00397 | 0.401 |
MOD_CDC14_SPxK_1 | 367 | 370 | PF00782 | 0.395 |
MOD_CDK_SPxK_1 | 364 | 370 | PF00069 | 0.428 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.472 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.521 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.657 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.564 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.483 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.486 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.403 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.535 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.478 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.471 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.426 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.569 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.380 |
MOD_Cter_Amidation | 733 | 736 | PF01082 | 0.369 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.494 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.425 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.497 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.546 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.523 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.358 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.419 |
MOD_GlcNHglycan | 34 | 38 | PF01048 | 0.608 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.557 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.603 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.531 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.490 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.531 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.293 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.554 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.449 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.525 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.506 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.567 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.474 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.450 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.571 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.587 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.393 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.510 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.449 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.432 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.504 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.504 |
MOD_N-GLC_1 | 640 | 645 | PF02516 | 0.324 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.451 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.535 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.519 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.465 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.535 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.342 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.403 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.494 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.442 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.548 |
MOD_NEK2_2 | 590 | 595 | PF00069 | 0.302 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.429 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.344 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.525 |
MOD_PK_1 | 417 | 423 | PF00069 | 0.347 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.502 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.616 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.532 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.574 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.567 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.425 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.324 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.366 |
MOD_PKB_1 | 176 | 184 | PF00069 | 0.421 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.458 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.494 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.361 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.449 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.316 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.402 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.434 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.539 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.483 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.387 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.361 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.311 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.498 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.510 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.443 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.592 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.489 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.512 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.550 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.344 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.545 |
MOD_ProDKin_1 | 776 | 782 | PF00069 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 726 | 729 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.415 |
TRG_NLS_MonoExtC_3 | 498 | 504 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 496 | 503 | PF00514 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 500 | 504 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 42% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 59% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 39% | 82% |
A0A3S7WT86 | Leishmania donovani | 40% | 79% |
A0A3S7WWA6 | Leishmania donovani | 42% | 100% |
A0A451EJD9 | Leishmania donovani | 40% | 100% |
A0A451EJF4 | Leishmania donovani | 67% | 100% |
A0A451EJF6 | Leishmania donovani | 60% | 100% |
A0A451EJF8 | Leishmania donovani | 54% | 100% |
A0A451EJF9 | Leishmania donovani | 51% | 95% |
A4H3A9 | Leishmania braziliensis | 79% | 100% |
A4H3B6 | Leishmania braziliensis | 79% | 100% |
A4H3B8 | Leishmania braziliensis | 72% | 99% |
A4H3B9 | Leishmania braziliensis | 39% | 92% |
A4H4W8 | Leishmania braziliensis | 38% | 100% |
A4HJ20 | Leishmania braziliensis | 70% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 100% |
A4HNK6 | Leishmania braziliensis | 38% | 100% |
A4HRL9 | Leishmania infantum | 68% | 100% |
A4HRM0 | Leishmania infantum | 61% | 100% |
A4HRM1 | Leishmania infantum | 61% | 100% |
A4HRS1 | Leishmania infantum | 52% | 95% |
A4HRS3 | Leishmania infantum | 39% | 82% |
A4HRS5 | Leishmania infantum | 55% | 100% |
A4HZM0 | Leishmania infantum | 41% | 100% |
A4I7C7 | Leishmania infantum | 42% | 100% |
A4IAQ2 | Leishmania infantum | 40% | 100% |
E9AC91 | Leishmania major | 67% | 100% |
E9AC92 | Leishmania major | 70% | 100% |
E9AC94 | Leishmania major | 39% | 69% |
E9AC95 | Leishmania major | 54% | 100% |
E9AC96 | Leishmania major | 58% | 100% |
E9AC98 | Leishmania major | 39% | 82% |
E9AEH8 | Leishmania major | 40% | 100% |
E9AHA6 | Leishmania infantum | 40% | 100% |
E9AIP8 | Leishmania braziliensis | 39% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 83% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
Q4Q5T6 | Leishmania major | 41% | 100% |
Q4QCL8 | Leishmania major | 41% | 100% |
Q4QFJ3 | Leishmania major | 40% | 79% |
Q4QIG9 | Leishmania major | 39% | 100% |
Q7YXU9 | Leishmania major | 42% | 100% |
Q7YXV1 | Leishmania major | 41% | 100% |
Q7YXV2 | Leishmania major | 41% | 100% |