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)
Glycosylation, Phosphoglycan beta 1,3 galactosyltransferase SCGR5
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 | 13 |
GO:0031090 | organelle membrane | 3 | 13 |
GO:0098588 | bounding membrane of organelle | 4 | 13 |
Related structures:
AlphaFold database: A4HRM0
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 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.569 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 655 | 657 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 699 | 701 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 725 | 727 | PF00082 | 0.527 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 585 | 591 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.534 |
CLV_Separin_Metazoa | 280 | 284 | PF03568 | 0.463 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.618 |
DEG_SCF_FBW7_1 | 377 | 384 | PF00400 | 0.501 |
DOC_CKS1_1 | 207 | 212 | PF01111 | 0.358 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.464 |
DOC_CKS1_1 | 378 | 383 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 370 | 380 | PF00134 | 0.313 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.397 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.693 |
DOC_MAPK_gen_1 | 516 | 524 | PF00069 | 0.314 |
DOC_MAPK_JIP1_4 | 18 | 24 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 16 | 24 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 439 | 446 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.544 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.404 |
DOC_USP7_UBL2_3 | 721 | 725 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.368 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 516 | 520 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 571 | 580 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 676 | 684 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 173 | 189 | PF00022 | 0.402 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.352 |
LIG_EH1_1 | 529 | 537 | PF00400 | 0.273 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.268 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.561 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.529 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.358 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.341 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.454 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.308 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.401 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.436 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.475 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.388 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.301 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.312 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.367 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.319 |
LIG_GBD_Chelix_1 | 26 | 34 | PF00786 | 0.247 |
LIG_IRF3_LxIS_1 | 24 | 31 | PF10401 | 0.241 |
LIG_LIR_Apic_2 | 380 | 386 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 238 | 243 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 605 | 613 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 62 | 69 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 622 | 628 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.299 |
LIG_NRBOX | 579 | 585 | PF00104 | 0.308 |
LIG_REV1ctd_RIR_1 | 640 | 649 | PF16727 | 0.307 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.270 |
LIG_SH2_GRB2like | 715 | 718 | PF00017 | 0.327 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.433 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.364 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.391 |
LIG_SH2_SRC | 638 | 641 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.342 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.470 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.351 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.514 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.373 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.352 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.305 |
LIG_SUMO_SIM_anti_2 | 551 | 556 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 551 | 556 | PF11976 | 0.355 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.374 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.570 |
LIG_TYR_ITSM | 207 | 214 | PF00017 | 0.405 |
LIG_UBA3_1 | 39 | 44 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.388 |
MOD_CDK_SPxxK_3 | 345 | 352 | PF00069 | 0.355 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.720 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.386 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.352 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.532 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.516 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.590 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.662 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.414 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.469 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.502 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.392 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.365 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.645 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.657 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.461 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.482 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.418 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.476 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.572 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.397 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.468 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.483 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.503 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.571 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.519 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.509 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.443 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.501 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.341 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.416 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.448 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.521 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.417 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.450 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.337 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.414 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.361 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.460 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.391 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.508 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.361 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.463 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.501 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.378 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.706 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.396 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.577 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.399 |
MOD_PKA_1 | 416 | 422 | PF00069 | 0.685 |
MOD_PKA_1 | 655 | 661 | PF00069 | 0.381 |
MOD_PKA_1 | 675 | 681 | PF00069 | 0.408 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.578 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.610 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.412 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.598 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.634 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.323 |
MOD_PKA_2 | 655 | 661 | PF00069 | 0.406 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.422 |
MOD_PKB_1 | 569 | 577 | PF00069 | 0.290 |
MOD_PKB_1 | 88 | 96 | PF00069 | 0.460 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.444 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.415 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.446 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.395 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.426 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.492 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.350 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.447 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.395 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.344 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.531 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.448 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.459 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.584 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.640 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.548 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.568 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.368 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 531 | 536 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 579 | 584 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 568 | 571 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.624 |
TRG_NLS_MonoExtC_3 | 484 | 489 | PF00514 | 0.371 |
TRG_NLS_MonoExtC_3 | 654 | 659 | PF00514 | 0.407 |
TRG_NLS_MonoExtN_4 | 655 | 660 | PF00514 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 571 | 576 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 582 | 587 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 40% | 91% |
A0A3S5H4Y6 | Leishmania donovani | 88% | 91% |
A0A3S5H4Y9 | Leishmania donovani | 35% | 74% |
A0A3S7WT86 | Leishmania donovani | 43% | 72% |
A0A3S7WWA6 | Leishmania donovani | 40% | 91% |
A0A451EJD9 | Leishmania donovani | 39% | 90% |
A0A451EJF4 | Leishmania donovani | 74% | 90% |
A0A451EJF6 | Leishmania donovani | 63% | 100% |
A0A451EJF8 | Leishmania donovani | 75% | 95% |
A0A451EJF9 | Leishmania donovani | 56% | 85% |
A4H3A9 | Leishmania braziliensis | 64% | 100% |
A4H3B4 | Leishmania braziliensis | 61% | 100% |
A4H3B5 | Leishmania braziliensis | 63% | 100% |
A4H3B6 | Leishmania braziliensis | 65% | 100% |
A4H3B8 | Leishmania braziliensis | 54% | 100% |
A4H3B9 | Leishmania braziliensis | 41% | 100% |
A4H4W8 | Leishmania braziliensis | 36% | 100% |
A4HJ20 | Leishmania braziliensis | 65% | 100% |
A4HNK3 | Leishmania braziliensis | 39% | 99% |
A4HNK6 | Leishmania braziliensis | 37% | 100% |
A4HRL9 | Leishmania infantum | 74% | 100% |
A4HRM1 | Leishmania infantum | 62% | 100% |
A4HRS1 | Leishmania infantum | 56% | 85% |
A4HRS3 | Leishmania infantum | 35% | 74% |
A4HRS5 | Leishmania infantum | 75% | 95% |
A4HZM0 | Leishmania infantum | 38% | 100% |
A4I7C7 | Leishmania infantum | 39% | 90% |
A4IAQ2 | Leishmania infantum | 38% | 100% |
E9AC91 | Leishmania major | 70% | 100% |
E9AC92 | Leishmania major | 69% | 100% |
E9AC95 | Leishmania major | 71% | 100% |
E9AC96 | Leishmania major | 57% | 100% |
E9AC98 | Leishmania major | 35% | 100% |
E9AEH8 | Leishmania major | 38% | 100% |
E9AHA6 | Leishmania infantum | 39% | 90% |
E9AIP8 | Leishmania braziliensis | 38% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AJI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4Q5T6 | Leishmania major | 39% | 100% |
Q4QCL8 | Leishmania major | 39% | 100% |
Q4QFJ3 | Leishmania major | 44% | 100% |
Q4QIG9 | Leishmania major | 39% | 100% |
Q7YXU9 | Leishmania major | 39% | 100% |
Q7YXV1 | Leishmania major | 38% | 100% |
Q7YXV2 | Leishmania major | 40% | 100% |