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:0000139 | Golgi membrane | 5 | 15 |
GO:0016020 | membrane | 2 | 53 |
GO:0031090 | organelle membrane | 3 | 15 |
GO:0098588 | bounding membrane of organelle | 4 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 53 |
Related structures:
AlphaFold database: Q7YXV1
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:0008194 | UDP-glycosyltransferase activity | 4 | 15 |
GO:0016740 | transferase activity | 2 | 53 |
GO:0016757 | glycosyltransferase activity | 3 | 53 |
GO:0016758 | hexosyltransferase activity | 4 | 53 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.555 |
CLV_PCSK_FUR_1 | 137 | 141 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 706 | 708 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 762 | 764 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 828 | 834 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.498 |
CLV_Separin_Metazoa | 301 | 305 | PF03568 | 0.336 |
DEG_Kelch_Keap1_1 | 324 | 329 | PF01344 | 0.409 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.597 |
DEG_SCF_FBW7_1 | 17 | 23 | PF00400 | 0.626 |
DEG_SCF_FBW7_1 | 484 | 491 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 470 | 474 | PF00917 | 0.331 |
DOC_CKS1_1 | 17 | 22 | PF01111 | 0.624 |
DOC_CKS1_1 | 485 | 490 | PF01111 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.329 |
DOC_CYCLIN_yCln2_LP_2 | 482 | 488 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 56 | 59 | PF00134 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 664 | 670 | PF00134 | 0.323 |
DOC_MAPK_DCC_7 | 46 | 56 | PF00069 | 0.660 |
DOC_MAPK_DCC_7 | 604 | 613 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 137 | 146 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 330 | 339 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 528 | 535 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 593 | 601 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 671 | 679 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 725 | 734 | PF00069 | 0.271 |
DOC_MAPK_JIP1_4 | 330 | 336 | PF00069 | 0.357 |
DOC_MAPK_JIP1_4 | 593 | 599 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 512 | 519 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 568 | 577 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 593 | 601 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 604 | 613 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 674 | 681 | PF00069 | 0.288 |
DOC_MAPK_NFAT4_5 | 332 | 340 | PF00069 | 0.274 |
DOC_MAPK_NFAT4_5 | 512 | 520 | PF00069 | 0.333 |
DOC_MAPK_NFAT4_5 | 674 | 682 | PF00069 | 0.279 |
DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 620 | 626 | PF00149 | 0.311 |
DOC_PP1_RVXF_1 | 726 | 732 | PF00149 | 0.310 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.270 |
DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 575 | 578 | PF13499 | 0.297 |
DOC_PP4_FxxP_1 | 738 | 741 | PF00568 | 0.259 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 524 | 528 | PF12436 | 0.355 |
DOC_USP7_UBL2_3 | 752 | 756 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 125 | 132 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 459 | 463 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 595 | 600 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 622 | 628 | PF00244 | 0.274 |
LIG_Actin_WH2_2 | 570 | 587 | PF00022 | 0.257 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.407 |
LIG_EH_1 | 650 | 654 | PF12763 | 0.326 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.457 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.632 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.481 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.479 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.352 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.369 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.701 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.401 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.348 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.381 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.669 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.410 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.453 |
LIG_FHA_2 | 771 | 777 | PF00498 | 0.310 |
LIG_FHA_2 | 813 | 819 | PF00498 | 0.340 |
LIG_IBAR_NPY_1 | 666 | 668 | PF08397 | 0.295 |
LIG_Integrin_RGD_1 | 807 | 809 | PF01839 | 0.559 |
LIG_LIR_Apic_2 | 448 | 454 | PF02991 | 0.348 |
LIG_LIR_Apic_2 | 534 | 540 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 186 | 193 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 238 | 249 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 514 | 520 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 654 | 664 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 673 | 683 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 730 | 738 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 654 | 659 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 730 | 734 | PF02991 | 0.356 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.308 |
LIG_NRBOX | 659 | 665 | PF00104 | 0.330 |
LIG_NRP_CendR_1 | 845 | 846 | PF00754 | 0.581 |
LIG_PCNA_yPIPBox_3 | 657 | 671 | PF02747 | 0.278 |
LIG_Pex14_2 | 801 | 805 | PF04695 | 0.274 |
LIG_PTB_Apo_2 | 240 | 247 | PF02174 | 0.372 |
LIG_PTB_Phospho_1 | 240 | 246 | PF10480 | 0.368 |
LIG_RPA_C_Fungi | 710 | 722 | PF08784 | 0.304 |
LIG_SH2_NCK_1 | 408 | 412 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 814 | 818 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 825 | 829 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 746 | 749 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.460 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.581 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.415 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.449 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.457 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.335 |
LIG_SH3_4 | 524 | 531 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 171 | 178 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 730 | 736 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 609 | 615 | PF11976 | 0.364 |
LIG_TRAF2_1 | 773 | 776 | PF00917 | 0.390 |
LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.542 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.520 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.512 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.500 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.550 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.641 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.241 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.611 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.553 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.518 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.490 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.581 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.577 |
MOD_CK2_1 | 770 | 776 | PF00069 | 0.415 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.368 |
MOD_CMANNOS | 307 | 310 | PF00535 | 0.299 |
MOD_Cter_Amidation | 843 | 846 | PF01082 | 0.360 |
MOD_Cter_Amidation | 94 | 97 | PF01082 | 0.577 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.544 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.548 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.495 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.565 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.595 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.498 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.517 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.531 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.632 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.614 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.400 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.646 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.463 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.512 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.569 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.510 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.618 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.499 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.542 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.596 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.515 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.495 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.405 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.638 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.403 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.638 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.622 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.461 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.502 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.396 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.419 |
MOD_N-GLC_1 | 776 | 781 | PF02516 | 0.444 |
MOD_N-GLC_2 | 119 | 121 | PF02516 | 0.529 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.561 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.449 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.530 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.473 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.430 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.358 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.601 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.448 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.552 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.523 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.575 |
MOD_PIKK_1 | 776 | 782 | PF00454 | 0.421 |
MOD_PIKK_1 | 785 | 791 | PF00454 | 0.379 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.478 |
MOD_PKA_1 | 523 | 529 | PF00069 | 0.593 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.556 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.532 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.442 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.611 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.560 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.574 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.616 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.501 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.437 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.596 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.561 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.461 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.433 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.343 |
MOD_Plk_2-3 | 385 | 391 | PF00069 | 0.501 |
MOD_Plk_2-3 | 770 | 776 | PF00069 | 0.347 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.507 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.524 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.491 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.448 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.371 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.255 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.478 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.372 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.543 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.510 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.532 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.612 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 518 | 526 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 754 | 764 | PF00179 | 0.343 |
TRG_DiLeu_BaEn_1 | 760 | 765 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 641 | 646 | PF01217 | 0.398 |
TRG_DiLeu_LyEn_5 | 760 | 765 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 676 | 679 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 714 | 716 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 831 | 834 | PF00400 | 0.415 |
TRG_NLS_MonoExtN_4 | 525 | 532 | PF00514 | 0.439 |
TRG_NLS_MonoExtN_4 | 704 | 709 | PF00514 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 643 | 647 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 763 | 767 | PF00026 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 83% | 100% |
A0A3S5H4Y6 | Leishmania donovani | 40% | 100% |
A0A3S5H4Y9 | Leishmania donovani | 33% | 85% |
A0A3S7WT86 | Leishmania donovani | 36% | 82% |
A0A3S7WWA6 | Leishmania donovani | 83% | 100% |
A0A451EJD9 | Leishmania donovani | 74% | 100% |
A0A451EJF4 | Leishmania donovani | 41% | 100% |
A0A451EJF6 | Leishmania donovani | 40% | 100% |
A0A451EJF8 | Leishmania donovani | 37% | 100% |
A0A451EJF9 | Leishmania donovani | 40% | 98% |
A4H3A9 | Leishmania braziliensis | 42% | 100% |
A4H3B4 | Leishmania braziliensis | 41% | 100% |
A4H3B6 | Leishmania braziliensis | 39% | 100% |
A4H3B8 | Leishmania braziliensis | 40% | 100% |
A4H3B9 | Leishmania braziliensis | 33% | 95% |
A4H4W8 | Leishmania braziliensis | 63% | 100% |
A4HJ20 | Leishmania braziliensis | 39% | 100% |
A4HNK3 | Leishmania braziliensis | 71% | 100% |
A4HNK6 | Leishmania braziliensis | 62% | 100% |
A4HRL9 | Leishmania infantum | 42% | 100% |
A4HRM0 | Leishmania infantum | 38% | 100% |
A4HRM1 | Leishmania infantum | 40% | 100% |
A4HRS1 | Leishmania infantum | 40% | 98% |
A4HRS3 | Leishmania infantum | 32% | 85% |
A4HRS5 | Leishmania infantum | 37% | 100% |
A4HZM0 | Leishmania infantum | 74% | 100% |
A4I7C7 | Leishmania infantum | 75% | 100% |
A4IAQ2 | Leishmania infantum | 72% | 100% |
E9AC91 | Leishmania major | 43% | 100% |
E9AC92 | Leishmania major | 43% | 100% |
E9AC94 | Leishmania major | 32% | 72% |
E9AC95 | Leishmania major | 38% | 100% |
E9AC96 | Leishmania major | 41% | 100% |
E9AC98 | Leishmania major | 33% | 100% |
E9AEH8 | Leishmania major | 81% | 100% |
E9AHA6 | Leishmania infantum | 74% | 100% |
E9AIP8 | Leishmania braziliensis | 64% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 86% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q5T6 | Leishmania major | 84% | 100% |
Q4QCL8 | Leishmania major | 95% | 100% |
Q4QFJ3 | Leishmania major | 37% | 82% |
Q4QIG9 | Leishmania major | 96% | 100% |
Q7YXU9 | Leishmania major | 94% | 100% |
Q7YXV2 | Leishmania major | 93% | 100% |