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. | yes | 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:0000139 | Golgi membrane | 5 | 14 |
GO:0016020 | membrane | 2 | 54 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0098588 | bounding membrane of organelle | 4 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
Related structures:
AlphaFold database: E9AC95
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:0008194 | UDP-glycosyltransferase activity | 4 | 14 |
GO:0016740 | transferase activity | 2 | 54 |
GO:0016757 | glycosyltransferase activity | 3 | 54 |
GO:0016758 | hexosyltransferase activity | 4 | 54 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.623 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.555 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.475 |
CLV_PCSK_PC7_1 | 730 | 736 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.537 |
CLV_Separin_Metazoa | 280 | 284 | PF03568 | 0.476 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.329 |
DEG_APCC_DBOX_1 | 578 | 586 | PF00400 | 0.349 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.632 |
DEG_SCF_FBW7_1 | 377 | 384 | PF00400 | 0.517 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.476 |
DOC_CKS1_1 | 378 | 383 | PF01111 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.420 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.730 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 576 | 584 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 90 | 99 | PF00069 | 0.395 |
DOC_MAPK_JIP1_4 | 18 | 24 | PF00069 | 0.627 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.742 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 581 | 589 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.414 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 439 | 446 | PF00149 | 0.464 |
DOC_PP1_RVXF_1 | 599 | 606 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.436 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.281 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 487 | 492 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 595 | 603 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 60 | 64 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 704 | 713 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 735 | 741 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 173 | 189 | PF00022 | 0.406 |
LIG_Actin_WH2_2 | 29 | 46 | PF00022 | 0.249 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.360 |
LIG_BIR_III_4 | 73 | 77 | PF00653 | 0.373 |
LIG_CaM_IQ_9 | 696 | 712 | PF13499 | 0.312 |
LIG_deltaCOP1_diTrp_1 | 637 | 642 | PF00928 | 0.290 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.275 |
LIG_eIF4E_1 | 296 | 302 | PF01652 | 0.331 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.536 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.532 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.448 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.491 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.434 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.336 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.407 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.455 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.484 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.372 |
LIG_FHA_2 | 737 | 743 | PF00498 | 0.390 |
LIG_Integrin_isoDGR_2 | 629 | 631 | PF01839 | 0.514 |
LIG_LIR_Apic_2 | 380 | 386 | PF02991 | 0.407 |
LIG_LIR_Apic_2 | 427 | 433 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 238 | 243 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 522 | 531 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 62 | 69 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 637 | 647 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 654 | 660 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 522 | 527 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 637 | 642 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 765 | 770 | PF02991 | 0.341 |
LIG_NRBOX | 29 | 35 | PF00104 | 0.313 |
LIG_Pex14_1 | 638 | 642 | PF04695 | 0.293 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.289 |
LIG_RPA_C_Fungi | 561 | 573 | PF08784 | 0.331 |
LIG_RPA_C_Fungi | 591 | 603 | PF08784 | 0.334 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.511 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.541 |
LIG_SH2_CRK | 600 | 604 | PF00017 | 0.380 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.315 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 524 | 527 | PF00017 | 0.518 |
LIG_SH2_GRB2like | 749 | 752 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 524 | 528 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.392 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.454 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.460 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 749 | 753 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.511 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.566 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.410 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.647 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.402 |
LIG_Sin3_3 | 20 | 27 | PF02671 | 0.244 |
LIG_SUMO_SIM_anti_2 | 31 | 37 | PF11976 | 0.304 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.461 |
LIG_TRAF2_1 | 689 | 692 | PF00917 | 0.433 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.594 |
LIG_UBA3_1 | 39 | 44 | PF00899 | 0.449 |
MOD_CDK_SPxxK_3 | 345 | 352 | PF00069 | 0.358 |
MOD_CDK_SPxxK_3 | 525 | 532 | PF00069 | 0.505 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.731 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.540 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.603 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.467 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.449 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.513 |
MOD_CK2_1 | 736 | 742 | PF00069 | 0.422 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.633 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.655 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.461 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.451 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.504 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.554 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.588 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.530 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.410 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.492 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.577 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.745 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.537 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.484 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.544 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.446 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.449 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.411 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.364 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.440 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.398 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.377 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.507 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.378 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.438 |
MOD_N-GLC_1 | 730 | 735 | PF02516 | 0.431 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.445 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.303 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.391 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.575 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.379 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.367 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.504 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.471 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.439 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.668 |
MOD_NEK2_2 | 544 | 549 | PF00069 | 0.340 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.427 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.577 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.404 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.343 |
MOD_PKA_1 | 416 | 422 | PF00069 | 0.647 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.579 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.620 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.433 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.596 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.548 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.373 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.316 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.517 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.430 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.283 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.391 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.506 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.403 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.444 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.485 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.319 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.403 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.406 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.373 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.554 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.382 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.419 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.602 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.641 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.536 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.596 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.506 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 579 | 582 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 600 | 602 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 662 | 665 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.621 |
TRG_NLS_MonoExtN_4 | 15 | 20 | PF00514 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 422 | 426 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 768 | 772 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 37% | 95% |
A0A3S5H4Y6 | Leishmania donovani | 64% | 96% |
A0A3S5H4Y9 | Leishmania donovani | 34% | 78% |
A0A3S7WT86 | Leishmania donovani | 40% | 75% |
A0A3S7WWA6 | Leishmania donovani | 37% | 95% |
A0A451EJD9 | Leishmania donovani | 38% | 95% |
A0A451EJF4 | Leishmania donovani | 60% | 95% |
A0A451EJF6 | Leishmania donovani | 60% | 100% |
A0A451EJF8 | Leishmania donovani | 90% | 100% |
A0A451EJF9 | Leishmania donovani | 54% | 90% |
A4H3A9 | Leishmania braziliensis | 54% | 100% |
A4H3B4 | Leishmania braziliensis | 54% | 95% |
A4H3B5 | Leishmania braziliensis | 51% | 100% |
A4H3B6 | Leishmania braziliensis | 56% | 100% |
A4H3B7 | Leishmania braziliensis | 46% | 72% |
A4H3B8 | Leishmania braziliensis | 66% | 93% |
A4H3B9 | Leishmania braziliensis | 38% | 87% |
A4H4W8 | Leishmania braziliensis | 35% | 95% |
A4HJ20 | Leishmania braziliensis | 55% | 95% |
A4HNK3 | Leishmania braziliensis | 38% | 100% |
A4HNK6 | Leishmania braziliensis | 37% | 98% |
A4HRL9 | Leishmania infantum | 60% | 95% |
A4HRM0 | Leishmania infantum | 71% | 100% |
A4HRM1 | Leishmania infantum | 61% | 100% |
A4HRS1 | Leishmania infantum | 54% | 90% |
A4HRS3 | Leishmania infantum | 33% | 78% |
A4HRS5 | Leishmania infantum | 91% | 100% |
A4HZM0 | Leishmania infantum | 37% | 95% |
A4I7C7 | Leishmania infantum | 38% | 95% |
A4IAQ2 | Leishmania infantum | 37% | 95% |
E9AC91 | Leishmania major | 60% | 100% |
E9AC92 | Leishmania major | 56% | 100% |
E9AC96 | Leishmania major | 57% | 90% |
E9AC98 | Leishmania major | 34% | 78% |
E9AEH8 | Leishmania major | 39% | 95% |
E9AHA6 | Leishmania infantum | 37% | 95% |
E9AIP8 | Leishmania braziliensis | 36% | 98% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 94% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 97% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 78% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 95% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 95% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 95% |
Q4Q5T6 | Leishmania major | 39% | 95% |
Q4QCL8 | Leishmania major | 39% | 95% |
Q4QFJ3 | Leishmania major | 40% | 75% |
Q4QIG9 | Leishmania major | 38% | 95% |
Q7YXU9 | Leishmania major | 37% | 95% |
Q7YXV1 | Leishmania major | 38% | 91% |
Q7YXV2 | Leishmania major | 39% | 95% |