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:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
GO:0000139 | Golgi membrane | 5 | 13 |
GO:0031090 | organelle membrane | 3 | 13 |
GO:0098588 | bounding membrane of organelle | 4 | 13 |
Related structures:
AlphaFold database: E9AJI5
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:0016740 | transferase activity | 2 | 54 |
GO:0016757 | glycosyltransferase activity | 3 | 54 |
GO:0016758 | hexosyltransferase activity | 4 | 54 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.421 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.527 |
CLV_PCSK_PC7_1 | 333 | 339 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 597 | 603 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.468 |
CLV_PCSK_PC7_1 | 730 | 736 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.605 |
DEG_APCC_DBOX_1 | 578 | 586 | PF00400 | 0.355 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.641 |
DEG_SCF_FBW7_1 | 377 | 384 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.414 |
DOC_ANK_TNKS_1 | 493 | 500 | PF00023 | 0.437 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.397 |
DOC_CKS1_1 | 207 | 212 | PF01111 | 0.400 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.496 |
DOC_CKS1_1 | 275 | 280 | PF01111 | 0.502 |
DOC_CKS1_1 | 378 | 383 | PF01111 | 0.543 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.575 |
DOC_MAPK_gen_1 | 16 | 22 | PF00069 | 0.728 |
DOC_MAPK_gen_1 | 576 | 584 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 734 | 742 | PF00069 | 0.330 |
DOC_MAPK_JIP1_4 | 18 | 24 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 16 | 24 | PF00069 | 0.745 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.421 |
DOC_MAPK_RevD_3 | 324 | 338 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 439 | 446 | PF00149 | 0.486 |
DOC_PP1_RVXF_1 | 599 | 606 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.574 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.288 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 532 | 537 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 596 | 601 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 735 | 741 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.418 |
LIG_Actin_WH2_2 | 173 | 189 | PF00022 | 0.428 |
LIG_Actin_WH2_2 | 29 | 46 | PF00022 | 0.266 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 637 | 642 | PF00928 | 0.303 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.292 |
LIG_eIF4E_1 | 296 | 302 | PF01652 | 0.375 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.579 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.559 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.400 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.470 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.344 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.373 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.427 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.419 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.396 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.467 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.508 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.528 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.387 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.391 |
LIG_Integrin_isoDGR_2 | 629 | 631 | PF01839 | 0.534 |
LIG_LIR_Apic_2 | 380 | 386 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 427 | 433 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 238 | 243 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 637 | 647 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 654 | 660 | PF02991 | 0.419 |
LIG_LIR_LC3C_4 | 321 | 326 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 599 | 603 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 637 | 642 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 765 | 770 | PF02991 | 0.358 |
LIG_Pex14_1 | 638 | 642 | PF04695 | 0.305 |
LIG_RPA_C_Fungi | 561 | 573 | PF08784 | 0.355 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.453 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.317 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.561 |
LIG_SH2_CRK | 600 | 604 | PF00017 | 0.389 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.332 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 749 | 752 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.565 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.459 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 749 | 753 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.525 |
LIG_SH3_1 | 150 | 156 | PF00018 | 0.444 |
LIG_SH3_2 | 278 | 283 | PF14604 | 0.577 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.433 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.458 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.597 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.589 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.442 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.668 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 31 | 37 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 502 | 508 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 738 | 744 | PF11976 | 0.384 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.466 |
LIG_TRAF2_1 | 689 | 692 | PF00917 | 0.469 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.427 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.603 |
LIG_TYR_ITIM | 598 | 603 | PF00017 | 0.340 |
LIG_TYR_ITSM | 207 | 214 | PF00017 | 0.449 |
LIG_UBA3_1 | 39 | 44 | PF00899 | 0.432 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.412 |
LIG_WW_3 | 205 | 209 | PF00397 | 0.486 |
LIG_WW_3 | 490 | 494 | PF00397 | 0.498 |
MOD_CDK_SPxxK_3 | 345 | 352 | PF00069 | 0.400 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.387 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.752 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.453 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.456 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.481 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.544 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.549 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.628 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.689 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.458 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.518 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.452 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.527 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.465 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.652 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.680 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.504 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.583 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.604 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.378 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.515 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.528 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.545 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.577 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.380 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.333 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.766 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.570 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.505 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.495 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.533 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.451 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.502 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.383 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.542 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.481 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.449 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.393 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.399 |
MOD_N-GLC_1 | 730 | 735 | PF02516 | 0.428 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.481 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.408 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.414 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.471 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.511 |
MOD_NEK2_1 | 718 | 723 | PF00069 | 0.396 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.723 |
MOD_NEK2_2 | 544 | 549 | PF00069 | 0.360 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.454 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.444 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.602 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.444 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.365 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.494 |
MOD_PKA_1 | 416 | 422 | PF00069 | 0.670 |
MOD_PKA_1 | 596 | 602 | PF00069 | 0.338 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.531 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.585 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.631 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.467 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.639 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.620 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.379 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.320 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.541 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.476 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.481 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.390 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.446 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.390 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.459 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.536 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.549 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.472 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.395 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.568 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.385 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.490 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.457 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.496 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.623 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.627 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.680 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.613 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.645 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 596 | 598 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 600 | 602 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 662 | 665 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.609 |
TRG_NLS_Bipartite_1 | 579 | 599 | PF00514 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 422 | 426 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 768 | 772 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 38% | 95% |
A0A3S5H4Y6 | Leishmania donovani | 62% | 96% |
A0A3S5H4Y9 | Leishmania donovani | 33% | 78% |
A0A3S7WT86 | Leishmania donovani | 40% | 75% |
A0A3S7WWA6 | Leishmania donovani | 38% | 95% |
A0A451EJD9 | Leishmania donovani | 38% | 95% |
A0A451EJF4 | Leishmania donovani | 59% | 95% |
A0A451EJF6 | Leishmania donovani | 59% | 100% |
A0A451EJF8 | Leishmania donovani | 87% | 100% |
A0A451EJF9 | Leishmania donovani | 54% | 90% |
A4H3A9 | Leishmania braziliensis | 57% | 100% |
A4H3B4 | Leishmania braziliensis | 55% | 100% |
A4H3B5 | Leishmania braziliensis | 55% | 95% |
A4H3B6 | Leishmania braziliensis | 60% | 95% |
A4H3B7 | Leishmania braziliensis | 42% | 100% |
A4H3B8 | Leishmania braziliensis | 66% | 100% |
A4H3B9 | Leishmania braziliensis | 38% | 100% |
A4H4W8 | Leishmania braziliensis | 37% | 100% |
A4HJ20 | Leishmania braziliensis | 59% | 100% |
A4HNK3 | Leishmania braziliensis | 38% | 95% |
A4HNK6 | Leishmania braziliensis | 36% | 100% |
A4HRL9 | Leishmania infantum | 56% | 95% |
A4HRM0 | Leishmania infantum | 69% | 100% |
A4HRM1 | Leishmania infantum | 60% | 100% |
A4HRS1 | Leishmania infantum | 54% | 90% |
A4HRS3 | Leishmania infantum | 33% | 78% |
A4HRS5 | Leishmania infantum | 87% | 100% |
A4HZM0 | Leishmania infantum | 38% | 95% |
A4I7C7 | Leishmania infantum | 39% | 95% |
A4IAQ2 | Leishmania infantum | 38% | 95% |
E9AC91 | Leishmania major | 54% | 100% |
E9AC92 | Leishmania major | 54% | 100% |
E9AC95 | Leishmania major | 84% | 100% |
E9AC96 | Leishmania major | 54% | 100% |
E9AC98 | Leishmania major | 35% | 100% |
E9AEH8 | Leishmania major | 39% | 100% |
E9AHA6 | Leishmania infantum | 38% | 95% |
E9AIP8 | Leishmania braziliensis | 36% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 95% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 95% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 95% |
Q4Q5T6 | Leishmania major | 39% | 100% |
Q4QCL8 | Leishmania major | 37% | 100% |
Q4QFJ3 | Leishmania major | 40% | 100% |
Q4QIG9 | Leishmania major | 38% | 100% |
Q7YXU9 | Leishmania major | 38% | 100% |
Q7YXV1 | Leishmania major | 36% | 100% |
Q7YXV2 | Leishmania major | 39% | 100% |