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
Plasma membrane, surface antigen LINJ.12.0671
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: 150 |
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: 66, no: 12 |
NetGPI | no | yes: 0, no: 78 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 79 |
GO:0042995 | cell projection | 2 | 79 |
GO:0043226 | organelle | 2 | 79 |
GO:0043227 | membrane-bounded organelle | 3 | 79 |
GO:0110165 | cellular anatomical entity | 1 | 79 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 79 |
GO:0016020 | membrane | 2 | 34 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: E9AGG9
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
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 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.697 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.650 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.264 |
DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.681 |
DOC_CYCLIN_RxL_1 | 107 | 116 | PF00134 | 0.283 |
DOC_CYCLIN_RxL_1 | 187 | 197 | PF00134 | 0.284 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.691 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 286 | 295 | PF00134 | 0.440 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 454 | 463 | PF00134 | 0.251 |
DOC_MAPK_gen_1 | 154 | 164 | PF00069 | 0.232 |
DOC_MAPK_gen_1 | 43 | 49 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 494 | 501 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.315 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.524 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.440 |
DOC_USP7_MATH_2 | 224 | 230 | PF00917 | 0.416 |
DOC_USP7_MATH_2 | 296 | 302 | PF00917 | 0.393 |
DOC_USP7_MATH_2 | 344 | 350 | PF00917 | 0.281 |
DOC_USP7_MATH_2 | 368 | 374 | PF00917 | 0.342 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 418 | 423 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 298 | 313 | PF00022 | 0.532 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.660 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.423 |
LIG_DLG_GKlike_1 | 418 | 425 | PF00625 | 0.230 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.262 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.340 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.370 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.335 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.338 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.355 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.295 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.537 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.422 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.425 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.254 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.555 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.445 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.542 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 176 | 184 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 201 | 208 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 226 | 233 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 346 | 355 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 455 | 464 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 466 | 473 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.268 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.453 |
LIG_PCNA_PIPBox_1 | 156 | 165 | PF02747 | 0.419 |
LIG_PCNA_PIPBox_1 | 230 | 239 | PF02747 | 0.484 |
LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.307 |
LIG_PTB_Phospho_1 | 426 | 432 | PF10480 | 0.350 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.539 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.267 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.383 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.238 |
LIG_SH2_CRK | 456 | 460 | PF00017 | 0.255 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.244 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.242 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.235 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.409 |
LIG_SH3_2 | 96 | 101 | PF14604 | 0.253 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 327 | 333 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.361 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.566 |
LIG_TYR_ITIM | 382 | 387 | PF00017 | 0.491 |
LIG_TYR_ITIM | 430 | 435 | PF00017 | 0.367 |
LIG_TYR_ITIM | 454 | 459 | PF00017 | 0.493 |
LIG_UBA3_1 | 379 | 386 | PF00899 | 0.229 |
LIG_UBA3_1 | 427 | 434 | PF00899 | 0.224 |
LIG_WRC_WIRS_1 | 134 | 139 | PF05994 | 0.317 |
LIG_WW_3 | 415 | 419 | PF00397 | 0.239 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.466 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.392 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.359 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.376 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.299 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.323 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.331 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.344 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.363 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.293 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.350 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.358 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.308 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.455 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.422 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.494 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.259 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.586 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.403 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.265 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.431 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.419 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.376 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.395 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.345 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.604 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.360 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.391 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.401 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.416 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.362 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.331 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.437 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.409 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.431 |
MOD_GlcNHglycan | 466 | 470 | PF01048 | 0.549 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.434 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.403 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.367 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.420 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.351 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.412 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.336 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.351 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.534 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.370 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.317 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.269 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.301 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.406 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.319 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.465 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.685 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.467 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.373 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.288 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.351 |
MOD_N-GLC_2 | 514 | 516 | PF02516 | 0.675 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.532 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.384 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.354 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.338 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.399 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.538 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.308 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.313 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.296 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.378 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.399 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.315 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.326 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.301 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.417 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.465 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.521 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.268 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.280 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.416 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.463 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.453 |
MOD_PIKK_1 | 406 | 412 | PF00454 | 0.427 |
MOD_PKA_1 | 43 | 49 | PF00069 | 0.219 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.324 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.490 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.366 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.304 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.368 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.394 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.307 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.317 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.281 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.324 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.527 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.602 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.452 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.272 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.380 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.346 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.366 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.295 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.343 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.376 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.318 |
MOD_SUMO_rev_2 | 509 | 518 | PF00179 | 0.657 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.247 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.563 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 30% | 85% |
A0A0N1I661 | Leptomonas seymouri | 38% | 95% |
A0A0N1I7S5 | Leptomonas seymouri | 34% | 100% |
A0A0S4IHI7 | Bodo saltans | 31% | 70% |
A0A0S4IJN2 | Bodo saltans | 29% | 80% |
A0A0S4ILC9 | Bodo saltans | 39% | 98% |
A0A0S4IN27 | Bodo saltans | 38% | 100% |
A0A0S4IQE4 | Bodo saltans | 26% | 95% |
A0A0S4ISU4 | Bodo saltans | 36% | 82% |
A0A0S4IT62 | Bodo saltans | 45% | 73% |
A0A0S4IU23 | Bodo saltans | 29% | 91% |
A0A0S4IU73 | Bodo saltans | 41% | 100% |
A0A0S4IV96 | Bodo saltans | 39% | 89% |
A0A0S4IVQ8 | Bodo saltans | 36% | 90% |
A0A0S4IW93 | Bodo saltans | 29% | 89% |
A0A0S4IY44 | Bodo saltans | 26% | 81% |
A0A0S4J014 | Bodo saltans | 30% | 76% |
A0A0S4J206 | Bodo saltans | 34% | 88% |
A0A0S4J2H8 | Bodo saltans | 30% | 92% |
A0A0S4J4L7 | Bodo saltans | 25% | 73% |
A0A0S4J5A0 | Bodo saltans | 39% | 95% |
A0A0S4J954 | Bodo saltans | 29% | 73% |
A0A0S4JAQ6 | Bodo saltans | 29% | 100% |
A0A0S4JAS1 | Bodo saltans | 33% | 85% |
A0A0S4JB95 | Bodo saltans | 25% | 89% |
A0A0S4JBV9 | Bodo saltans | 29% | 100% |
A0A0S4JD35 | Bodo saltans | 31% | 90% |
A0A0S4JDS1 | Bodo saltans | 26% | 100% |
A0A0S4JDT0 | Bodo saltans | 33% | 82% |
A0A0S4JEK1 | Bodo saltans | 28% | 100% |
A0A0S4JL29 | Bodo saltans | 35% | 100% |
A0A0S4JQZ0 | Bodo saltans | 25% | 72% |
A0A0S4JS89 | Bodo saltans | 27% | 100% |
A0A0S4JSD2 | Bodo saltans | 28% | 67% |
A0A0S4JTM6 | Bodo saltans | 35% | 73% |
A0A0S4JTQ7 | Bodo saltans | 37% | 100% |
A0A0S4JVI0 | Bodo saltans | 30% | 76% |
A0A0S4KGV4 | Bodo saltans | 26% | 99% |
A0A0S4KH41 | Bodo saltans | 32% | 78% |
A0A0S4KJA7 | Bodo saltans | 28% | 81% |
A0A0S4KK37 | Bodo saltans | 32% | 93% |
A0A3Q8I9A6 | Leishmania donovani | 46% | 100% |
A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
A0A3S5H6M3 | Leishmania donovani | 54% | 79% |
A0A3S5H6M4 | Leishmania donovani | 62% | 82% |
A0A3S7WS66 | Leishmania donovani | 62% | 82% |
A4HBX3 | Leishmania braziliensis | 35% | 100% |
A4HVB0 | Leishmania infantum | 49% | 100% |
A4HZ93 | Leishmania infantum | 37% | 100% |
A6QLV3 | Bos taurus | 25% | 93% |
B3LWU3 | Drosophila ananassae | 22% | 84% |
B4N9T4 | Drosophila willistoni | 23% | 84% |
B5DX45 | Drosophila pseudoobscura pseudoobscura | 21% | 86% |
D1GJ51 | Leishmania infantum | 63% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AGG2 | Leishmania infantum | 59% | 100% |
E9AGG5 | Leishmania infantum | 44% | 100% |
E9AGG7 | Leishmania infantum | 57% | 100% |
E9AGH0 | Leishmania infantum | 50% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 98% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
F4IUU1 | Arabidopsis thaliana | 23% | 67% |
F4JGB6 | Arabidopsis thaliana | 26% | 67% |
F4JTU7 | Arabidopsis thaliana | 24% | 67% |
F4KHA2 | Arabidopsis thaliana | 21% | 68% |
O48851 | Arabidopsis thaliana | 22% | 70% |
O49325 | Arabidopsis thaliana | 24% | 70% |
O49328 | Arabidopsis thaliana | 23% | 68% |
O80809 | Arabidopsis thaliana | 27% | 75% |
O88520 | Mus musculus | 25% | 93% |
Q1PEN0 | Arabidopsis thaliana | 23% | 75% |
Q25331 | Leishmania major | 56% | 100% |
Q4QC79 | Leishmania major | 38% | 100% |
Q4QGI0 | Leishmania major | 79% | 95% |
Q4QGI2 | Leishmania major | 60% | 100% |
Q4QGI4 | Leishmania major | 65% | 100% |
Q4QGI6 | Leishmania major | 54% | 100% |
Q4QGI8 | Leishmania major | 59% | 100% |
Q4QGJ0 | Leishmania major | 56% | 100% |
Q4QGJ2 | Leishmania major | 51% | 100% |
Q4QGJ4 | Leishmania major | 56% | 100% |
Q4QGJ7 | Leishmania major | 56% | 100% |
Q4QGJ9 | Leishmania major | 59% | 100% |
Q4QGK0 | Leishmania major | 60% | 100% |
Q4QGK1 | Leishmania major | 56% | 100% |
Q4QGK2 | Leishmania major | 57% | 100% |
Q4QGK4 | Leishmania major | 52% | 100% |
Q4QGK6 | Leishmania major | 57% | 100% |
Q4QGK8 | Leishmania major | 60% | 99% |
Q4QGL2 | Leishmania major | 60% | 99% |
Q4QGL4 | Leishmania major | 56% | 100% |
Q4QGL8 | Leishmania major | 59% | 100% |
Q4QGM1 | Leishmania major | 60% | 70% |
Q5RAV5 | Pongo abelii | 25% | 93% |
Q6AYI5 | Rattus norvegicus | 25% | 93% |
Q7FZR1 | Arabidopsis thaliana | 25% | 67% |
Q940E8 | Zea mays | 27% | 88% |
Q9C9H6 | Arabidopsis thaliana | 25% | 69% |
Q9LJW7 | Arabidopsis thaliana | 25% | 76% |
Q9LS79 | Arabidopsis thaliana | 22% | 69% |
Q9MA83 | Arabidopsis thaliana | 25% | 69% |
Q9SHI3 | Arabidopsis thaliana | 24% | 74% |
Q9SHI4 | Arabidopsis thaliana | 21% | 72% |
Q9SKK5 | Arabidopsis thaliana | 23% | 81% |
Q9SVN2 | Arabidopsis thaliana | 25% | 68% |
Q9UQ13 | Homo sapiens | 25% | 93% |