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: A0A3Q8IGN9
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 | 0.354 |
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 730 | 732 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.540 |
CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.335 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.682 |
DEG_SCF_FBW7_1 | 452 | 459 | PF00400 | 0.438 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.322 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.482 |
DOC_MAPK_DCC_7 | 572 | 581 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 496 | 503 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 693 | 702 | PF00069 | 0.275 |
DOC_MAPK_HePTP_8 | 104 | 116 | PF00069 | 0.435 |
DOC_MAPK_JIP1_4 | 298 | 304 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 106 | 114 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 480 | 487 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 536 | 545 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 642 | 649 | PF00069 | 0.295 |
DOC_MAPK_NFAT4_5 | 480 | 488 | PF00069 | 0.321 |
DOC_PP1_RVXF_1 | 500 | 506 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.303 |
DOC_PP1_RVXF_1 | 694 | 700 | PF00149 | 0.311 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.302 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.413 |
DOC_PP4_FxxP_1 | 706 | 709 | PF00568 | 0.258 |
DOC_SPAK_OSR1_1 | 107 | 111 | PF12202 | 0.412 |
DOC_SPAK_OSR1_1 | 128 | 132 | PF12202 | 0.375 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.646 |
DOC_USP7_UBL2_3 | 492 | 496 | PF12436 | 0.347 |
DOC_USP7_UBL2_3 | 669 | 673 | PF12436 | 0.275 |
DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.315 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 563 | 570 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 779 | 785 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 93 | 100 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 538 | 555 | PF00022 | 0.271 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.346 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.622 |
LIG_EH_1 | 618 | 622 | PF12763 | 0.323 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.458 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.388 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.459 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.460 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.341 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.353 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.365 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.431 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.340 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.379 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.355 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.395 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.434 |
LIG_FHA_2 | 781 | 787 | PF00498 | 0.334 |
LIG_IBAR_NPY_1 | 634 | 636 | PF08397 | 0.300 |
LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.338 |
LIG_LIR_Apic_2 | 504 | 508 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 155 | 161 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 622 | 632 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 643 | 651 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 622 | 627 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.350 |
LIG_NRBOX | 111 | 117 | PF00104 | 0.299 |
LIG_NRBOX | 627 | 633 | PF00104 | 0.325 |
LIG_NRP_CendR_1 | 813 | 814 | PF00754 | 0.583 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.416 |
LIG_PTB_Apo_2 | 208 | 215 | PF02174 | 0.368 |
LIG_PTB_Apo_2 | 791 | 798 | PF02174 | 0.275 |
LIG_PTB_Phospho_1 | 208 | 214 | PF10480 | 0.364 |
LIG_PTB_Phospho_1 | 791 | 797 | PF10480 | 0.270 |
LIG_RPA_C_Fungi | 678 | 690 | PF08784 | 0.313 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 782 | 786 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 644 | 647 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.415 |
LIG_SH2_STAT3 | 595 | 598 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.441 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.565 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.434 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.411 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.329 |
LIG_SH3_3 | 706 | 712 | PF00018 | 0.327 |
LIG_SH3_4 | 492 | 499 | PF00018 | 0.405 |
LIG_SUMO_SIM_anti_2 | 698 | 704 | PF11976 | 0.285 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.517 |
MOD_CDC14_SPxK_1 | 27 | 30 | PF00782 | 0.510 |
MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.516 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.516 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.504 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.544 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.623 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.371 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.457 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.600 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.449 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.470 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.557 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.553 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.536 |
MOD_CK2_1 | 780 | 786 | PF00069 | 0.366 |
MOD_Cter_Amidation | 811 | 814 | PF01082 | 0.361 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.540 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.564 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.608 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.595 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.379 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.514 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.499 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.593 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.401 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.542 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.553 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.581 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.497 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.594 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.614 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.577 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.511 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.495 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.398 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.568 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.395 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.451 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.464 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.382 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.406 |
MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.330 |
MOD_N-GLC_1 | 744 | 749 | PF02516 | 0.427 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.521 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.510 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.436 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.417 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.571 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.540 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.446 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.544 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.520 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.343 |
MOD_PIKK_1 | 744 | 750 | PF00454 | 0.405 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.373 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.459 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.567 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.469 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.623 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.535 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.518 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.459 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.585 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.553 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.490 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.501 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.415 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.395 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.327 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.530 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.455 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.425 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.462 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.338 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.487 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.463 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.473 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.391 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.453 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.355 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.478 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.370 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.533 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.525 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.558 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.498 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.497 |
MOD_SUMO_rev_2 | 486 | 494 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 646 | 656 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 722 | 732 | PF00179 | 0.339 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_1 | 728 | 733 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.383 |
TRG_DiLeu_LyEn_5 | 728 | 733 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.559 |
TRG_NLS_MonoExtN_4 | 493 | 500 | PF00514 | 0.427 |
TRG_NLS_MonoExtN_4 | 672 | 677 | PF00514 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 731 | 735 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H4Y6 | Leishmania donovani | 38% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 31% | 82% |
A0A3S7WT86 | Leishmania donovani | 37% | 79% |
A0A3S7WWA6 | Leishmania donovani | 100% | 100% |
A0A451EJD9 | Leishmania donovani | 81% | 100% |
A0A451EJF4 | Leishmania donovani | 39% | 100% |
A0A451EJF6 | Leishmania donovani | 39% | 100% |
A0A451EJF8 | Leishmania donovani | 38% | 100% |
A0A451EJF9 | Leishmania donovani | 40% | 94% |
A4H3A9 | Leishmania braziliensis | 42% | 100% |
A4H3B4 | Leishmania braziliensis | 42% | 100% |
A4H3B6 | Leishmania braziliensis | 41% | 100% |
A4H3B8 | Leishmania braziliensis | 42% | 100% |
A4H3B9 | Leishmania braziliensis | 34% | 100% |
A4H4W8 | Leishmania braziliensis | 64% | 100% |
A4HJ20 | Leishmania braziliensis | 41% | 100% |
A4HNK3 | Leishmania braziliensis | 73% | 100% |
A4HNK6 | Leishmania braziliensis | 64% | 100% |
A4HRL9 | Leishmania infantum | 42% | 100% |
A4HRM0 | Leishmania infantum | 40% | 100% |
A4HRM1 | Leishmania infantum | 40% | 99% |
A4HRS1 | Leishmania infantum | 41% | 100% |
A4HRS3 | Leishmania infantum | 31% | 100% |
A4HRS5 | Leishmania infantum | 38% | 100% |
A4HZM0 | Leishmania infantum | 86% | 100% |
A4I7C7 | Leishmania infantum | 85% | 100% |
A4IAQ2 | Leishmania infantum | 77% | 100% |
E9AC91 | Leishmania major | 41% | 100% |
E9AC92 | Leishmania major | 42% | 100% |
E9AC94 | Leishmania major | 33% | 69% |
E9AC95 | Leishmania major | 37% | 100% |
E9AC96 | Leishmania major | 40% | 100% |
E9AC98 | Leishmania major | 33% | 100% |
E9AEH8 | Leishmania major | 74% | 100% |
E9AHA6 | Leishmania infantum | 81% | 100% |
E9AIP8 | Leishmania braziliensis | 64% | 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) | 38% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q5T6 | Leishmania major | 74% | 100% |
Q4QCL8 | Leishmania major | 82% | 100% |
Q4QFJ3 | Leishmania major | 37% | 100% |
Q4QIG9 | Leishmania major | 83% | 100% |
Q7YXU9 | Leishmania major | 81% | 100% |
Q7YXV1 | Leishmania major | 83% | 100% |
Q7YXV2 | Leishmania major | 82% | 100% |