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: A0A451EJF4
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 | 62 | 66 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 564 | 566 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 733 | 735 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 753 | 755 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 777 | 779 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 412 | 418 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 663 | 669 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.525 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.368 |
DEG_APCC_DBOX_1 | 369 | 377 | PF00400 | 0.395 |
DEG_SCF_FBW7_1 | 455 | 462 | PF00400 | 0.464 |
DEG_SCF_FBW7_2 | 424 | 431 | PF00400 | 0.310 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.346 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.612 |
DOC_CYCLIN_yCln2_LP_2 | 453 | 459 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 483 | 490 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 507 | 516 | PF00069 | 0.323 |
DOC_PP1_RVXF_1 | 481 | 488 | PF00149 | 0.325 |
DOC_PP1_RVXF_1 | 517 | 524 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.360 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.411 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 776 | 781 | PF00397 | 0.346 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.208 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 435 | 440 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 754 | 762 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 803 | 808 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.645 |
LIG_Actin_WH2_2 | 175 | 190 | PF00022 | 0.376 |
LIG_Actin_WH2_2 | 254 | 270 | PF00022 | 0.370 |
LIG_Actin_WH2_2 | 653 | 669 | PF00022 | 0.287 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.616 |
LIG_EH1_1 | 607 | 615 | PF00400 | 0.249 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.661 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.369 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.537 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.484 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.345 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.640 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.373 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.425 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.279 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.652 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.309 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.403 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.496 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.335 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.283 |
LIG_FHA_2 | 755 | 761 | PF00498 | 0.331 |
LIG_FHA_2 | 764 | 770 | PF00498 | 0.291 |
LIG_FHA_2 | 803 | 809 | PF00498 | 0.323 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.365 |
LIG_LIR_Apic_2 | 505 | 511 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 319 | 324 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 525 | 536 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 683 | 691 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 700 | 706 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 700 | 704 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 713 | 717 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 808 | 814 | PF02991 | 0.322 |
LIG_NRBOX | 656 | 662 | PF00104 | 0.274 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.373 |
LIG_PTB_Apo_2 | 596 | 603 | PF02174 | 0.257 |
LIG_REV1ctd_RIR_1 | 718 | 727 | PF16727 | 0.279 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.377 |
LIG_SH2_CRK | 811 | 815 | PF00017 | 0.325 |
LIG_SH2_GRB2like | 793 | 796 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.373 |
LIG_SH2_PTP2 | 545 | 548 | PF00017 | 0.302 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.332 |
LIG_SH2_SRC | 526 | 529 | PF00017 | 0.363 |
LIG_SH2_SRC | 716 | 719 | PF00017 | 0.265 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 797 | 801 | PF00017 | 0.364 |
LIG_SH2_STAT3 | 50 | 53 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.429 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.458 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.478 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.307 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.341 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.326 |
LIG_SUMO_SIM_anti_2 | 113 | 119 | PF11976 | 0.263 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.343 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.435 |
LIG_TYR_ITSM | 288 | 295 | PF00017 | 0.338 |
LIG_UBA3_1 | 145 | 149 | PF00899 | 0.383 |
LIG_WW_3 | 78 | 82 | PF00397 | 0.606 |
MOD_CDC14_SPxK_1 | 185 | 188 | PF00782 | 0.388 |
MOD_CDC14_SPxK_1 | 78 | 81 | PF00782 | 0.605 |
MOD_CDK_SPxK_1 | 182 | 188 | PF00069 | 0.386 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.611 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.626 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.536 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.655 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.357 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.675 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.438 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.400 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.468 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.514 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.366 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.410 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.310 |
MOD_CK2_1 | 763 | 769 | PF00069 | 0.297 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.407 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.710 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.702 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.687 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.648 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.497 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.592 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.659 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.625 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.640 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.512 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.578 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.484 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.445 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.393 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.412 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.470 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.542 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.445 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.402 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.400 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.325 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.666 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.686 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.336 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.630 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.598 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.606 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.633 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.659 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.532 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.478 |
MOD_N-GLC_1 | 697 | 702 | PF02516 | 0.500 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.385 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.472 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.349 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.367 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.625 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.393 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.630 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.295 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.310 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.367 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.548 |
MOD_NEK2_2 | 590 | 595 | PF00069 | 0.268 |
MOD_NEK2_2 | 88 | 93 | PF00069 | 0.611 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.386 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.604 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.432 |
MOD_PK_1 | 110 | 116 | PF00069 | 0.208 |
MOD_PK_1 | 803 | 809 | PF00069 | 0.271 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.609 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.357 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.485 |
MOD_PKA_1 | 733 | 739 | PF00069 | 0.328 |
MOD_PKA_1 | 753 | 759 | PF00069 | 0.321 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.659 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.471 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.461 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.402 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.437 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.451 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.289 |
MOD_PKA_2 | 733 | 739 | PF00069 | 0.346 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.331 |
MOD_PKA_2 | 802 | 808 | PF00069 | 0.321 |
MOD_PKB_1 | 84 | 92 | PF00069 | 0.614 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.365 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.330 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.299 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.340 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.310 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.396 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.345 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.278 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.407 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.404 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.380 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.620 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.493 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.436 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.295 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.641 |
MOD_ProDKin_1 | 776 | 782 | PF00069 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 811 | 814 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.666 |
TRG_NES_CRM1_1 | 136 | 152 | PF08389 | 0.377 |
TRG_NLS_MonoExtC_3 | 562 | 567 | PF00514 | 0.297 |
TRG_NLS_MonoExtC_3 | 732 | 737 | PF00514 | 0.347 |
TRG_NLS_MonoExtN_4 | 733 | 738 | PF00514 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 812 | 816 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 39% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 74% | 99% |
A0A3S5H4Y9 | Leishmania donovani | 34% | 100% |
A0A3S7WT86 | Leishmania donovani | 44% | 100% |
A0A3S7WWA6 | Leishmania donovani | 39% | 100% |
A0A451EJD9 | Leishmania donovani | 38% | 100% |
A0A451EJF6 | Leishmania donovani | 75% | 100% |
A0A451EJF8 | Leishmania donovani | 58% | 100% |
A0A451EJF9 | Leishmania donovani | 61% | 95% |
A4H3A9 | Leishmania braziliensis | 65% | 100% |
A4H3B4 | Leishmania braziliensis | 67% | 100% |
A4H3B6 | Leishmania braziliensis | 64% | 100% |
A4H3B8 | Leishmania braziliensis | 61% | 100% |
A4H3B9 | Leishmania braziliensis | 40% | 100% |
A4H4W8 | Leishmania braziliensis | 38% | 100% |
A4HJ20 | Leishmania braziliensis | 63% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 100% |
A4HNK6 | Leishmania braziliensis | 37% | 100% |
A4HRL9 | Leishmania infantum | 98% | 100% |
A4HRM0 | Leishmania infantum | 74% | 100% |
A4HRM1 | Leishmania infantum | 75% | 100% |
A4HRS1 | Leishmania infantum | 61% | 100% |
A4HRS3 | Leishmania infantum | 34% | 100% |
A4HRS5 | Leishmania infantum | 58% | 100% |
A4HZM0 | Leishmania infantum | 38% | 100% |
A4I7C7 | Leishmania infantum | 39% | 100% |
A4IAQ2 | Leishmania infantum | 37% | 100% |
E9AC91 | Leishmania major | 87% | 100% |
E9AC92 | Leishmania major | 80% | 100% |
E9AC94 | Leishmania major | 34% | 100% |
E9AC95 | Leishmania major | 60% | 100% |
E9AC96 | Leishmania major | 65% | 100% |
E9AC98 | Leishmania major | 35% | 100% |
E9AEH8 | Leishmania major | 41% | 100% |
E9AHA6 | Leishmania infantum | 38% | 100% |
E9AIP8 | Leishmania braziliensis | 40% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4Q5T6 | Leishmania major | 41% | 100% |
Q4QCL8 | Leishmania major | 41% | 100% |
Q4QFJ3 | Leishmania major | 43% | 100% |
Q4QIG9 | Leishmania major | 41% | 100% |
Q7YXU9 | Leishmania major | 40% | 100% |
Q7YXV1 | Leishmania major | 41% | 100% |
Q7YXV2 | Leishmania major | 41% | 100% |