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: 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: E9AJI3
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 | 277 | 281 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.662 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.532 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 565 | 567 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 754 | 756 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 778 | 780 | PF00082 | 0.613 |
CLV_PCSK_PC7_1 | 413 | 419 | PF00082 | 0.598 |
CLV_PCSK_PC7_1 | 664 | 670 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 370 | 378 | PF00400 | 0.452 |
DEG_ODPH_VHL_1 | 620 | 631 | PF01847 | 0.360 |
DEG_SCF_FBW7_1 | 456 | 463 | PF00400 | 0.526 |
DEG_SCF_FBW7_2 | 425 | 432 | PF00400 | 0.368 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.661 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.380 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.395 |
DOC_CKS1_1 | 457 | 462 | PF01111 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.671 |
DOC_CYCLIN_yCln2_LP_2 | 454 | 460 | PF00134 | 0.568 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 484 | 491 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.379 |
DOC_PP1_RVXF_1 | 518 | 525 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 676 | 682 | PF00149 | 0.312 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 567 | 570 | PF13499 | 0.328 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.414 |
DOC_PP4_FxxP_1 | 462 | 465 | PF00568 | 0.414 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.710 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.397 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 371 | 379 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 436 | 441 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 664 | 668 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 755 | 763 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 804 | 812 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 86 | 96 | PF00244 | 0.728 |
LIG_Actin_WH2_2 | 175 | 190 | PF00022 | 0.427 |
LIG_Actin_WH2_2 | 254 | 270 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 654 | 670 | PF00022 | 0.339 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.401 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.661 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.657 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.637 |
LIG_BRCT_BRCA1_2 | 5 | 11 | PF00533 | 0.660 |
LIG_EH1_1 | 608 | 616 | PF00400 | 0.298 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.733 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.575 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.543 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.394 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.700 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.437 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.468 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.333 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.687 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.708 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.683 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.386 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.461 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.556 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.408 |
LIG_FHA_2 | 709 | 715 | PF00498 | 0.343 |
LIG_FHA_2 | 804 | 810 | PF00498 | 0.366 |
LIG_IRF3_LxIS_1 | 183 | 190 | PF10401 | 0.406 |
LIG_LIR_Apic_2 | 181 | 186 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 459 | 465 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 506 | 512 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 319 | 324 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 526 | 537 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 543 | 553 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 699 | 707 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 714 | 722 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 809 | 816 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 543 | 549 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 714 | 718 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 809 | 815 | PF02991 | 0.357 |
LIG_NRBOX | 657 | 663 | PF00104 | 0.325 |
LIG_Pex14_1 | 96 | 100 | PF04695 | 0.637 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.399 |
LIG_PTB_Apo_2 | 597 | 604 | PF02174 | 0.305 |
LIG_REV1ctd_RIR_1 | 719 | 728 | PF16727 | 0.334 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.427 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.385 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.292 |
LIG_SH2_CRK | 715 | 719 | PF00017 | 0.307 |
LIG_SH2_CRK | 812 | 816 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.422 |
LIG_SH2_NCK_1 | 231 | 235 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 783 | 787 | PF00017 | 0.406 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.388 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.411 |
LIG_SH2_SRC | 717 | 720 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 783 | 787 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 798 | 802 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 812 | 815 | PF00017 | 0.315 |
LIG_SH3_1 | 231 | 237 | PF00018 | 0.379 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.384 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.513 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.541 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.378 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.398 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.254 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.494 |
LIG_TYR_ITSM | 288 | 295 | PF00017 | 0.388 |
LIG_UBA3_1 | 145 | 149 | PF00899 | 0.446 |
LIG_WW_3 | 286 | 290 | PF00397 | 0.409 |
LIG_WW_3 | 78 | 82 | PF00397 | 0.664 |
MOD_CDC14_SPxK_1 | 185 | 188 | PF00782 | 0.423 |
MOD_CDC14_SPxK_1 | 78 | 81 | PF00782 | 0.663 |
MOD_CDK_SPxK_1 | 182 | 188 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.667 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.430 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.680 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.338 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.587 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.717 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.412 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.731 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.481 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.458 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.523 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.578 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.392 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.416 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.358 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.461 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.647 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.757 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.748 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.700 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.565 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.657 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.709 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.681 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.699 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.497 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.634 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.537 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.454 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.468 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.512 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.710 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.324 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.310 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.597 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.501 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.444 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.460 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.724 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.749 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.391 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.346 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.651 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.668 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.438 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.536 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.420 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.399 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.685 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.454 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.401 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.684 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.342 |
MOD_NEK2_1 | 726 | 731 | PF00069 | 0.363 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.581 |
MOD_NEK2_2 | 591 | 596 | PF00069 | 0.325 |
MOD_NEK2_2 | 773 | 778 | PF00069 | 0.320 |
MOD_NEK2_2 | 88 | 93 | PF00069 | 0.677 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.440 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.476 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.495 |
MOD_PKA_1 | 495 | 501 | PF00069 | 0.544 |
MOD_PKA_1 | 754 | 760 | PF00069 | 0.376 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.724 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.413 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.514 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.519 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.392 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.512 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.342 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.386 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.715 |
MOD_PKA_2 | 803 | 809 | PF00069 | 0.366 |
MOD_PKB_1 | 84 | 92 | PF00069 | 0.677 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.670 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.335 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.383 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.403 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.366 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.350 |
MOD_Plk_1 | 698 | 704 | PF00069 | 0.403 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.453 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.460 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.413 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.400 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.368 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.333 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.469 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.448 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.383 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.430 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.675 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.511 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.560 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.500 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.356 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.703 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 812 | 815 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 667 | 669 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.736 |
TRG_NES_CRM1_1 | 136 | 152 | PF08389 | 0.425 |
TRG_NLS_MonoExtN_4 | 369 | 374 | PF00514 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 613 | 617 | PF00026 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 40% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 76% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 35% | 82% |
A0A3S7WT86 | Leishmania donovani | 42% | 80% |
A0A3S7WWA6 | Leishmania donovani | 40% | 100% |
A0A451EJD9 | Leishmania donovani | 40% | 100% |
A0A451EJF4 | Leishmania donovani | 85% | 100% |
A0A451EJF6 | Leishmania donovani | 68% | 100% |
A0A451EJF8 | Leishmania donovani | 58% | 100% |
A0A451EJF9 | Leishmania donovani | 65% | 95% |
A4H3A9 | Leishmania braziliensis | 66% | 100% |
A4H3B4 | Leishmania braziliensis | 68% | 100% |
A4H3B6 | Leishmania braziliensis | 65% | 100% |
A4H3B8 | Leishmania braziliensis | 62% | 100% |
A4H3B9 | Leishmania braziliensis | 38% | 100% |
A4H4W8 | Leishmania braziliensis | 40% | 100% |
A4HJ20 | Leishmania braziliensis | 64% | 100% |
A4HNK3 | Leishmania braziliensis | 41% | 100% |
A4HNK6 | Leishmania braziliensis | 40% | 100% |
A4HRL9 | Leishmania infantum | 86% | 100% |
A4HRM0 | Leishmania infantum | 69% | 100% |
A4HRM1 | Leishmania infantum | 68% | 100% |
A4HRS1 | Leishmania infantum | 55% | 95% |
A4HRS3 | Leishmania infantum | 35% | 82% |
A4HRS5 | Leishmania infantum | 57% | 100% |
A4HZM0 | Leishmania infantum | 39% | 100% |
A4I7C7 | Leishmania infantum | 40% | 100% |
A4IAQ2 | Leishmania infantum | 39% | 100% |
E9AC91 | Leishmania major | 81% | 100% |
E9AC92 | Leishmania major | 79% | 100% |
E9AC94 | Leishmania major | 38% | 69% |
E9AC95 | Leishmania major | 58% | 100% |
E9AC96 | Leishmania major | 65% | 100% |
E9AC98 | Leishmania major | 34% | 100% |
E9AEH8 | Leishmania major | 41% | 100% |
E9AHA6 | Leishmania infantum | 39% | 100% |
E9AIP8 | Leishmania braziliensis | 41% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 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) | 40% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
Q4Q5T6 | Leishmania major | 42% | 100% |
Q4QCL8 | Leishmania major | 41% | 100% |
Q4QFJ3 | Leishmania major | 42% | 100% |
Q4QIG9 | Leishmania major | 42% | 100% |
Q7YXU9 | Leishmania major | 42% | 100% |
Q7YXV1 | Leishmania major | 42% | 100% |
Q7YXV2 | Leishmania major | 40% | 100% |