by homology
Contact email: handman@wehi.edu.au
Publication title: A Leucine-Rich Repeat Motif of Leishmania Parasite Surface Antigen 2 Binds to Macrophages through the Complement Receptor 3
Publication 1st author(s): Kedzierski
Publication Identifier(s): 15067069
Host organism: -1
Interaction detection method(s): fluorescence activated cell sorting
Interaction type: physical association
Identification method participant A: identification by antibody
Identification method participant B: identification by antibody
ID(s) interactor A: P11215
ID(s) interactor B: E9AGG4
Taxid interactor A: Homo sapiens
Taxid interactor B: Leishmania infantum
Biological role(s) interactor A: unspecified role
Biological role(s) interactor B: unspecified role
Experimental role(s) interactor A: unspecified role
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: 110 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 44, no: 7 |
NetGPI | no | yes: 0, no: 51 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 52 |
GO:0016020 | membrane | 2 | 28 |
GO:0042995 | cell projection | 2 | 52 |
GO:0043226 | organelle | 2 | 52 |
GO:0043227 | membrane-bounded organelle | 3 | 52 |
GO:0110165 | cellular anatomical entity | 1 | 52 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 52 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: A0A3S7WS66
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004252 | serine-type endopeptidase activity | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008236 | serine-type peptidase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0017171 | serine hydrolase activity | 3 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:0004672 | protein kinase activity | 3 | 3 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0016301 | kinase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.704 |
DEG_SCF_FBW7_2 | 586 | 591 | PF00400 | 0.431 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.377 |
DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.448 |
DEG_SPOP_SBC_1 | 534 | 538 | PF00917 | 0.460 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 550 | 554 | PF00917 | 0.393 |
DEG_SPOP_SBC_1 | 564 | 568 | PF00917 | 0.590 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.249 |
DOC_CYCLIN_RxL_1 | 107 | 116 | PF00134 | 0.247 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.693 |
DOC_CYCLIN_RxL_1 | 348 | 357 | PF00134 | 0.203 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.224 |
DOC_MAPK_gen_1 | 228 | 238 | PF00069 | 0.201 |
DOC_MAPK_gen_1 | 351 | 358 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 626 | 636 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 494 | 501 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 629 | 638 | PF00069 | 0.157 |
DOC_MAPK_MEF2A_6 | 79 | 86 | PF00069 | 0.204 |
DOC_MAPK_NFAT4_5 | 231 | 239 | PF00069 | 0.193 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.295 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.291 |
DOC_PP1_RVXF_1 | 349 | 356 | PF00149 | 0.201 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.398 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.340 |
DOC_USP7_MATH_2 | 248 | 254 | PF00917 | 0.360 |
DOC_USP7_MATH_2 | 320 | 326 | PF00917 | 0.341 |
DOC_USP7_MATH_2 | 368 | 374 | PF00917 | 0.340 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.218 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.240 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.182 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.694 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.208 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.434 |
LIG_eIF4E_1 | 237 | 243 | PF01652 | 0.188 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.260 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.299 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.302 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.338 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.197 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.347 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.488 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.320 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.395 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.616 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.566 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.531 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.368 |
LIG_HCF-1_HBM_1 | 306 | 309 | PF13415 | 0.191 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 128 | 135 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 232 | 243 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 250 | 257 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 370 | 377 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 393 | 403 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 418 | 425 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 466 | 475 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 152 | 156 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.329 |
LIG_NRBOX | 328 | 334 | PF00104 | 0.225 |
LIG_PDZ_Class_2 | 653 | 658 | PF00595 | 0.255 |
LIG_PTAP_UEV_1 | 561 | 566 | PF05743 | 0.375 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.242 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.203 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.323 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.390 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.430 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.411 |
LIG_Sin3_3 | 642 | 649 | PF02671 | 0.252 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.197 |
LIG_SUMO_SIM_par_1 | 632 | 637 | PF11976 | 0.160 |
LIG_SUMO_SIM_par_1 | 97 | 103 | PF11976 | 0.287 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.524 |
LIG_TYR_ITIM | 233 | 238 | PF00017 | 0.424 |
MOD_CDC14_SPxK_1 | 399 | 402 | PF00782 | 0.240 |
MOD_CDK_SPxK_1 | 396 | 402 | PF00069 | 0.239 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.409 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.397 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.328 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.347 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.350 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.305 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.276 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.403 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.783 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.255 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.277 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.500 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.499 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.784 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.532 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.493 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.235 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.497 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.366 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.429 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.408 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.390 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.344 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.367 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.696 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.413 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.407 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.408 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.473 |
MOD_GlcNHglycan | 386 | 390 | PF01048 | 0.480 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.400 |
MOD_GlcNHglycan | 418 | 422 | PF01048 | 0.401 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.506 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.451 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.432 |
MOD_GlcNHglycan | 458 | 462 | PF01048 | 0.517 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.640 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.469 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.389 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.423 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.421 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.382 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.352 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.390 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.297 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.400 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.448 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.793 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.520 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.754 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.501 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.608 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.713 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.646 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.381 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.285 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.339 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.589 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.520 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.425 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.347 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.373 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.393 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.416 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.456 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.487 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.381 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.285 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.421 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.401 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.459 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.499 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.440 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.335 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.430 |
MOD_PKB_1 | 472 | 480 | PF00069 | 0.256 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.373 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.350 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.368 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.362 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.353 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.475 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.492 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.297 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.368 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.398 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.267 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.377 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.237 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.247 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.774 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 471 | 474 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.575 |
TRG_NES_CRM1_1 | 301 | 311 | PF08389 | 0.208 |
TRG_Pf-PMV_PEXEL_1 | 354 | 359 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I121 | Leptomonas seymouri | 25% | 100% |
A0A0N1I661 | Leptomonas seymouri | 34% | 100% |
A0A0R0HPY5 | Glycine max | 25% | 67% |
A0A0S4IJN2 | Bodo saltans | 27% | 98% |
A0A0S4IM54 | Bodo saltans | 29% | 74% |
A0A0S4IRQ2 | Bodo saltans | 34% | 77% |
A0A0S4ITE7 | Bodo saltans | 36% | 74% |
A0A0S4IU91 | Bodo saltans | 26% | 75% |
A0A0S4IVQ8 | Bodo saltans | 32% | 100% |
A0A0S4IW93 | Bodo saltans | 28% | 100% |
A0A0S4J014 | Bodo saltans | 27% | 92% |
A0A0S4J1D6 | Bodo saltans | 30% | 67% |
A0A0S4J2H8 | Bodo saltans | 28% | 100% |
A0A0S4J542 | Bodo saltans | 26% | 73% |
A0A0S4J7S2 | Bodo saltans | 25% | 72% |
A0A0S4J954 | Bodo saltans | 26% | 89% |
A0A0S4J985 | Bodo saltans | 33% | 66% |
A0A0S4JB95 | Bodo saltans | 26% | 100% |
A0A0S4JL29 | Bodo saltans | 32% | 100% |
A0A0S4JNU2 | Bodo saltans | 38% | 80% |
A0A0S4JTM6 | Bodo saltans | 32% | 89% |
A0A0S4JTQ7 | Bodo saltans | 37% | 100% |
A0A0S4JVI0 | Bodo saltans | 29% | 93% |
A0A0S4KEC2 | Bodo saltans | 32% | 75% |
A0A0S4KF94 | Bodo saltans | 24% | 75% |
A0A0S4KGV4 | Bodo saltans | 26% | 100% |
A0A0S4KK37 | Bodo saltans | 30% | 100% |
A0A0S4KLL4 | Bodo saltans | 26% | 70% |
A0A1X0ND37 | Trypanosomatidae | 24% | 69% |
A0A3Q8IC27 | Leishmania donovani | 38% | 100% |
A0A3S5H6M3 | Leishmania donovani | 65% | 100% |
A0A3S5H6M4 | Leishmania donovani | 93% | 100% |
A4H6Y8 | Leishmania braziliensis | 59% | 72% |
A4HBX3 | Leishmania braziliensis | 32% | 94% |
A4HM88 | Leishmania braziliensis | 29% | 76% |
A4HZ93 | Leishmania infantum | 38% | 100% |
C0LGW6 | Arabidopsis thaliana | 26% | 68% |
C0LGX3 | Arabidopsis thaliana | 22% | 66% |
D1GJ51 | Leishmania infantum | 55% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 86% |
E9AGG2 | Leishmania infantum | 59% | 100% |
E9AGG7 | Leishmania infantum | 51% | 100% |
E9AGG9 | Leishmania infantum | 62% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 92% |
F4HTV4 | Arabidopsis thaliana | 24% | 67% |
F4I2N7 | Arabidopsis thaliana | 23% | 67% |
F4I9S3 | Arabidopsis thaliana | 25% | 71% |
F4IUU1 | Arabidopsis thaliana | 23% | 81% |
F4J7T6 | Arabidopsis thaliana | 23% | 74% |
F4J8G2 | Arabidopsis thaliana | 25% | 75% |
F4J9A8 | Arabidopsis thaliana | 24% | 69% |
F4JGB6 | Arabidopsis thaliana | 24% | 81% |
F4JTU7 | Arabidopsis thaliana | 23% | 81% |
F4K4T3 | Arabidopsis thaliana | 25% | 69% |
G7JIK2 | Medicago truncatula | 27% | 68% |
I1Z695 | Oryza sativa subsp. japonica | 26% | 67% |
O22938 | Arabidopsis thaliana | 27% | 74% |
O48849 | Arabidopsis thaliana | 21% | 74% |
O48851 | Arabidopsis thaliana | 24% | 85% |
O49328 | Arabidopsis thaliana | 21% | 82% |
O49329 | Arabidopsis thaliana | 22% | 76% |
O49879 | Solanum lycopersicum | 26% | 78% |
O65440 | Arabidopsis thaliana | 24% | 66% |
O80809 | Arabidopsis thaliana | 25% | 91% |
P0DO05 | Solanum pimpinellifolium | 23% | 76% |
P0DO06 | Solanum pimpinellifolium | 23% | 76% |
Q1PEN0 | Arabidopsis thaliana | 23% | 92% |
Q40235 | Solanum pimpinellifolium | 23% | 76% |
Q42371 | Arabidopsis thaliana | 23% | 67% |
Q4QC79 | Leishmania major | 38% | 100% |
Q4QGI0 | Leishmania major | 60% | 99% |
Q4QGI2 | Leishmania major | 55% | 100% |
Q4QGI4 | Leishmania major | 58% | 100% |
Q4QGI6 | Leishmania major | 49% | 100% |
Q4QGI8 | Leishmania major | 54% | 100% |
Q4QGJ0 | Leishmania major | 61% | 100% |
Q4QGJ2 | Leishmania major | 51% | 100% |
Q4QGJ9 | Leishmania major | 57% | 89% |
Q4QGK0 | Leishmania major | 52% | 100% |
Q4QGK1 | Leishmania major | 54% | 100% |
Q4QGK2 | Leishmania major | 51% | 100% |
Q4QGK4 | Leishmania major | 51% | 100% |
Q4QGK8 | Leishmania major | 55% | 99% |
Q4QGL2 | Leishmania major | 55% | 99% |
Q4QGL5 | Leishmania major | 49% | 100% |
Q4QGL8 | Leishmania major | 54% | 100% |
Q4QGM1 | Leishmania major | 53% | 85% |
Q5MR23 | Solanum pimpinellifolium | 23% | 76% |
Q5Z9N5 | Oryza sativa subsp. japonica | 26% | 66% |
Q658G7 | Oryza sativa subsp. japonica | 26% | 67% |
Q69SP5 | Oryza sativa subsp. japonica | 26% | 67% |
Q6XAT2 | Arabidopsis thaliana | 27% | 68% |
Q7FZR1 | Arabidopsis thaliana | 23% | 81% |
Q8AVI4 | Xenopus laevis | 25% | 100% |
Q8GRU6 | Lotus japonicus | 24% | 67% |
Q8RX63 | Arabidopsis thaliana | 24% | 77% |
Q8TF66 | Homo sapiens | 21% | 100% |
Q93YT3 | Arabidopsis thaliana | 25% | 74% |
Q940E8 | Zea mays | 28% | 100% |
Q9C637 | Arabidopsis thaliana | 23% | 66% |
Q9C699 | Arabidopsis thaliana | 25% | 68% |
Q9C6A8 | Arabidopsis thaliana | 23% | 68% |
Q9C9H6 | Arabidopsis thaliana | 23% | 84% |
Q9C9H7 | Arabidopsis thaliana | 24% | 78% |
Q9FGL5 | Arabidopsis thaliana | 26% | 68% |
Q9FL51 | Arabidopsis thaliana | 24% | 75% |
Q9FYK0 | Arabidopsis thaliana | 24% | 74% |
Q9LRW9 | Arabidopsis thaliana | 23% | 75% |
Q9LS79 | Arabidopsis thaliana | 23% | 84% |
Q9LS80 | Arabidopsis thaliana | 23% | 79% |
Q9LY03 | Arabidopsis thaliana | 25% | 68% |
Q9LZV7 | Arabidopsis thaliana | 27% | 68% |
Q9M6A7 | Glycine max | 26% | 67% |
Q9MA83 | Arabidopsis thaliana | 23% | 84% |
Q9S9U3 | Arabidopsis thaliana | 23% | 69% |
Q9SHI3 | Arabidopsis thaliana | 24% | 90% |
Q9SHI4 | Arabidopsis thaliana | 24% | 87% |
Q9SKK2 | Arabidopsis thaliana | 23% | 67% |
Q9SRL2 | Arabidopsis thaliana | 22% | 69% |
Q9SRL7 | Arabidopsis thaliana | 23% | 70% |
Q9SVM3 | Arabidopsis thaliana | 23% | 78% |
Q9SVN2 | Arabidopsis thaliana | 23% | 82% |
Q9SYQ8 | Arabidopsis thaliana | 25% | 67% |
Q9ZUI0 | Arabidopsis thaliana | 25% | 67% |
Q9ZUK3 | Arabidopsis thaliana | 23% | 67% |
Q9ZUK7 | Arabidopsis thaliana | 21% | 80% |