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. | yes | yes: 140 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 7 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 69, no: 14 |
| NetGPI | no | yes: 0, no: 83 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005886 | plasma membrane | 3 | 7 |
| GO:0005929 | cilium | 4 | 84 |
| GO:0016020 | membrane | 2 | 33 |
| GO:0042995 | cell projection | 2 | 84 |
| GO:0043226 | organelle | 2 | 84 |
| GO:0043227 | membrane-bounded organelle | 3 | 84 |
| GO:0110165 | cellular anatomical entity | 1 | 84 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 84 |
Related structures:
AlphaFold database: Q4QGL2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 4 |
| GO:0004672 | protein kinase activity | 3 | 4 |
| GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
| GO:0016301 | kinase activity | 4 | 4 |
| GO:0016740 | transferase activity | 2 | 4 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 4 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.541 |
| CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.227 |
| CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.744 |
| CLV_PCSK_FUR_1 | 255 | 259 | PF00082 | 0.223 |
| CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.220 |
| CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.744 |
| CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.450 |
| CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.429 |
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.495 |
| CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.534 |
| CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.465 |
| CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.714 |
| DEG_APCC_DBOX_1 | 446 | 454 | PF00400 | 0.275 |
| DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.321 |
| DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.734 |
| DOC_CYCLIN_RxL_1 | 326 | 336 | PF00134 | 0.233 |
| DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.496 |
| DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.238 |
| DOC_MAPK_gen_1 | 257 | 266 | PF00069 | 0.261 |
| DOC_MAPK_MEF2A_6 | 468 | 476 | PF00069 | 0.481 |
| DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.309 |
| DOC_PP1_RVXF_1 | 396 | 403 | PF00149 | 0.235 |
| DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.474 |
| DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.445 |
| DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.506 |
| DOC_USP7_MATH_2 | 247 | 253 | PF00917 | 0.368 |
| DOC_USP7_MATH_2 | 295 | 301 | PF00917 | 0.327 |
| DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.756 |
| DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.574 |
| LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.331 |
| LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.538 |
| LIG_14-3-3_CanoR_1 | 492 | 496 | PF00244 | 0.726 |
| LIG_Actin_WH2_2 | 273 | 288 | PF00022 | 0.565 |
| LIG_Actin_WH2_2 | 297 | 312 | PF00022 | 0.414 |
| LIG_Actin_WH2_2 | 321 | 336 | PF00022 | 0.268 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.685 |
| LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.377 |
| LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.392 |
| LIG_Clathr_ClatBox_1 | 354 | 358 | PF01394 | 0.369 |
| LIG_Clathr_ClatBox_1 | 473 | 477 | PF01394 | 0.313 |
| LIG_deltaCOP1_diTrp_1 | 176 | 179 | PF00928 | 0.462 |
| LIG_deltaCOP1_diTrp_1 | 200 | 206 | PF00928 | 0.517 |
| LIG_deltaCOP1_diTrp_1 | 297 | 303 | PF00928 | 0.405 |
| LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.550 |
| LIG_FHA_1 | 168 | 174 | PF00498 | 0.450 |
| LIG_FHA_1 | 183 | 189 | PF00498 | 0.353 |
| LIG_FHA_1 | 207 | 213 | PF00498 | 0.397 |
| LIG_FHA_1 | 217 | 223 | PF00498 | 0.433 |
| LIG_FHA_1 | 280 | 286 | PF00498 | 0.341 |
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.571 |
| LIG_FHA_2 | 121 | 127 | PF00498 | 0.510 |
| LIG_FHA_2 | 206 | 212 | PF00498 | 0.426 |
| LIG_FHA_2 | 303 | 309 | PF00498 | 0.427 |
| LIG_FHA_2 | 63 | 69 | PF00498 | 0.485 |
| LIG_FHA_2 | 92 | 98 | PF00498 | 0.478 |
| LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.432 |
| LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.390 |
| LIG_LIR_Gen_1 | 200 | 207 | PF02991 | 0.444 |
| LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.337 |
| LIG_LIR_Gen_1 | 350 | 359 | PF02991 | 0.320 |
| LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.347 |
| LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.486 |
| LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.539 |
| LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.370 |
| LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.308 |
| LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.385 |
| LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.403 |
| LIG_PCNA_PIPBox_1 | 229 | 238 | PF02747 | 0.503 |
| LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.424 |
| LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.332 |
| LIG_SH3_3 | 266 | 272 | PF00018 | 0.464 |
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.512 |
| LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.540 |
| LIG_SUMO_SIM_par_1 | 132 | 138 | PF11976 | 0.406 |
| LIG_SUMO_SIM_par_1 | 281 | 288 | PF11976 | 0.480 |
| LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.516 |
| LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.336 |
| LIG_UBA3_1 | 472 | 481 | PF00899 | 0.335 |
| MOD_CK1_1 | 151 | 157 | PF00069 | 0.452 |
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.371 |
| MOD_CK1_1 | 299 | 305 | PF00069 | 0.335 |
| MOD_CK1_1 | 347 | 353 | PF00069 | 0.353 |
| MOD_CK1_1 | 371 | 377 | PF00069 | 0.461 |
| MOD_CK2_1 | 126 | 132 | PF00069 | 0.499 |
| MOD_CK2_1 | 205 | 211 | PF00069 | 0.424 |
| MOD_CK2_1 | 91 | 97 | PF00069 | 0.496 |
| MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.466 |
| MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.469 |
| MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.448 |
| MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.502 |
| MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.642 |
| MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.447 |
| MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.383 |
| MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.426 |
| MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.373 |
| MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.408 |
| MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.476 |
| MOD_GlcNHglycan | 433 | 437 | PF01048 | 0.411 |
| MOD_GlcNHglycan | 441 | 445 | PF01048 | 0.420 |
| MOD_GSK3_1 | 120 | 127 | PF00069 | 0.438 |
| MOD_GSK3_1 | 133 | 140 | PF00069 | 0.402 |
| MOD_GSK3_1 | 144 | 151 | PF00069 | 0.439 |
| MOD_GSK3_1 | 214 | 221 | PF00069 | 0.381 |
| MOD_GSK3_1 | 281 | 288 | PF00069 | 0.305 |
| MOD_GSK3_1 | 310 | 317 | PF00069 | 0.370 |
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.628 |
| MOD_GSK3_1 | 490 | 497 | PF00069 | 0.720 |
| MOD_GSK3_1 | 498 | 505 | PF00069 | 0.727 |
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.472 |
| MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.321 |
| MOD_N-GLC_2 | 489 | 491 | PF02516 | 0.675 |
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.607 |
| MOD_NEK2_1 | 120 | 125 | PF00069 | 0.409 |
| MOD_NEK2_1 | 137 | 142 | PF00069 | 0.477 |
| MOD_NEK2_1 | 169 | 174 | PF00069 | 0.304 |
| MOD_NEK2_1 | 191 | 196 | PF00069 | 0.432 |
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.598 |
| MOD_NEK2_1 | 218 | 223 | PF00069 | 0.366 |
| MOD_NEK2_1 | 285 | 290 | PF00069 | 0.367 |
| MOD_NEK2_1 | 333 | 338 | PF00069 | 0.490 |
| MOD_NEK2_1 | 357 | 362 | PF00069 | 0.398 |
| MOD_NEK2_1 | 381 | 386 | PF00069 | 0.413 |
| MOD_NEK2_1 | 405 | 410 | PF00069 | 0.354 |
| MOD_NEK2_1 | 434 | 439 | PF00069 | 0.428 |
| MOD_NEK2_1 | 86 | 91 | PF00069 | 0.454 |
| MOD_PIKK_1 | 126 | 132 | PF00454 | 0.340 |
| MOD_PIKK_1 | 357 | 363 | PF00454 | 0.482 |
| MOD_PIKK_1 | 381 | 387 | PF00454 | 0.534 |
| MOD_PIKK_1 | 405 | 411 | PF00454 | 0.433 |
| MOD_PK_1 | 310 | 316 | PF00069 | 0.554 |
| MOD_PKA_1 | 62 | 68 | PF00069 | 0.355 |
| MOD_PKA_2 | 285 | 291 | PF00069 | 0.441 |
| MOD_PKA_2 | 333 | 339 | PF00069 | 0.538 |
| MOD_PKA_2 | 491 | 497 | PF00069 | 0.739 |
| MOD_PKB_1 | 157 | 165 | PF00069 | 0.245 |
| MOD_Plk_1 | 175 | 181 | PF00069 | 0.389 |
| MOD_Plk_1 | 199 | 205 | PF00069 | 0.441 |
| MOD_Plk_1 | 296 | 302 | PF00069 | 0.353 |
| MOD_Plk_1 | 357 | 363 | PF00069 | 0.359 |
| MOD_Plk_1 | 416 | 422 | PF00069 | 0.411 |
| MOD_Plk_1 | 440 | 446 | PF00069 | 0.508 |
| MOD_Plk_1 | 86 | 92 | PF00069 | 0.405 |
| MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.240 |
| MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.504 |
| MOD_Plk_4 | 151 | 157 | PF00069 | 0.460 |
| MOD_Plk_4 | 182 | 188 | PF00069 | 0.408 |
| MOD_Plk_4 | 249 | 255 | PF00069 | 0.348 |
| MOD_Plk_4 | 299 | 305 | PF00069 | 0.374 |
| MOD_Plk_4 | 347 | 353 | PF00069 | 0.361 |
| MOD_Plk_4 | 417 | 423 | PF00069 | 0.302 |
| MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.758 |
| MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.308 |
| TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.550 |
| TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.227 |
| TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.511 |
| TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.413 |
| TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.267 |
| TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.269 |
| TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.560 |
| TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.746 |
| TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.448 |
| TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.562 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P6A5 | Leptomonas seymouri | 28% | 80% |
| A0A0N1I121 | Leptomonas seymouri | 26% | 100% |
| A0A0N1I661 | Leptomonas seymouri | 36% | 90% |
| A0A0N1I7S5 | Leptomonas seymouri | 33% | 100% |
| A0A0N1II82 | Leptomonas seymouri | 30% | 74% |
| A0A0S4IHI7 | Bodo saltans | 29% | 66% |
| A0A0S4IJN2 | Bodo saltans | 32% | 76% |
| A0A0S4ILC9 | Bodo saltans | 34% | 93% |
| A0A0S4IN27 | Bodo saltans | 41% | 95% |
| A0A0S4IQE4 | Bodo saltans | 27% | 90% |
| A0A0S4ISU4 | Bodo saltans | 39% | 78% |
| A0A0S4IT62 | Bodo saltans | 35% | 69% |
| A0A0S4IU23 | Bodo saltans | 31% | 86% |
| A0A0S4IU73 | Bodo saltans | 36% | 100% |
| A0A0S4IV96 | Bodo saltans | 39% | 84% |
| A0A0S4IVQ8 | Bodo saltans | 37% | 85% |
| A0A0S4IW93 | Bodo saltans | 26% | 84% |
| A0A0S4IY44 | Bodo saltans | 28% | 77% |
| A0A0S4IZC7 | Bodo saltans | 27% | 100% |
| A0A0S4J014 | Bodo saltans | 27% | 72% |
| A0A0S4J1A6 | Bodo saltans | 26% | 100% |
| A0A0S4J206 | Bodo saltans | 35% | 83% |
| A0A0S4J2H8 | Bodo saltans | 28% | 88% |
| A0A0S4J3T7 | Bodo saltans | 33% | 100% |
| A0A0S4J4L7 | Bodo saltans | 30% | 69% |
| A0A0S4J5A0 | Bodo saltans | 39% | 90% |
| A0A0S4J954 | Bodo saltans | 25% | 69% |
| A0A0S4JAQ6 | Bodo saltans | 27% | 99% |
| A0A0S4JAS1 | Bodo saltans | 35% | 81% |
| A0A0S4JAW7 | Bodo saltans | 25% | 100% |
| A0A0S4JB95 | Bodo saltans | 25% | 84% |
| A0A0S4JBV9 | Bodo saltans | 28% | 100% |
| A0A0S4JD35 | Bodo saltans | 29% | 86% |
| A0A0S4JDS1 | Bodo saltans | 24% | 96% |
| A0A0S4JDT0 | Bodo saltans | 35% | 78% |
| A0A0S4JEK1 | Bodo saltans | 27% | 100% |
| A0A0S4JEP2 | Bodo saltans | 25% | 88% |
| A0A0S4JL29 | Bodo saltans | 29% | 100% |
| A0A0S4JMF9 | Bodo saltans | 32% | 100% |
| A0A0S4JQZ0 | Bodo saltans | 24% | 68% |
| A0A0S4JS89 | Bodo saltans | 27% | 100% |
| A0A0S4JTM6 | Bodo saltans | 35% | 69% |
| A0A0S4JTQ7 | Bodo saltans | 35% | 97% |
| A0A0S4JU95 | Bodo saltans | 32% | 67% |
| A0A0S4JVI0 | Bodo saltans | 26% | 72% |
| A0A0S4KGV4 | Bodo saltans | 25% | 94% |
| A0A0S4KH41 | Bodo saltans | 30% | 74% |
| A0A0S4KJA7 | Bodo saltans | 28% | 76% |
| A0A0S4KK37 | Bodo saltans | 34% | 88% |
| A0A3Q8I9A6 | Leishmania donovani | 52% | 100% |
| A0A3Q8I9B4 | Leishmania donovani | 41% | 100% |
| A0A3Q8I9D9 | Leishmania donovani | 41% | 100% |
| A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
| A0A3S5H6L9 | Leishmania donovani | 42% | 100% |
| A0A3S5H6M3 | Leishmania donovani | 54% | 75% |
| A0A3S5H6M4 | Leishmania donovani | 55% | 78% |
| A0A3S7WS66 | Leishmania donovani | 55% | 78% |
| A4HBX3 | Leishmania braziliensis | 32% | 100% |
| A4HVB0 | Leishmania infantum | 47% | 100% |
| A4HZ93 | Leishmania infantum | 35% | 100% |
| D1GJ51 | Leishmania infantum | 55% | 100% |
| E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 67% |
| E9AGG2 | Leishmania infantum | 54% | 77% |
| E9AGG7 | Leishmania infantum | 54% | 82% |
| E9AGG9 | Leishmania infantum | 60% | 95% |
| E9AGH0 | Leishmania infantum | 50% | 100% |
| E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 72% |
| E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
| E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
| E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 73% |
| E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
| E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
| E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
| E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
| O48851 | Arabidopsis thaliana | 26% | 66% |
| O80809 | Arabidopsis thaliana | 24% | 71% |
| Q1PEN0 | Arabidopsis thaliana | 21% | 71% |
| Q4QC79 | Leishmania major | 36% | 100% |
| Q4QGI0 | Leishmania major | 64% | 100% |
| Q4QGI2 | Leishmania major | 65% | 100% |
| Q4QGI4 | Leishmania major | 73% | 100% |
| Q4QGI6 | Leishmania major | 55% | 100% |
| Q4QGI8 | Leishmania major | 62% | 100% |
| Q4QGJ0 | Leishmania major | 58% | 100% |
| Q4QGJ2 | Leishmania major | 56% | 100% |
| Q4QGJ6 | Leishmania major | 60% | 90% |
| Q4QGJ9 | Leishmania major | 54% | 100% |
| Q4QGK0 | Leishmania major | 55% | 100% |
| Q4QGK1 | Leishmania major | 58% | 100% |
| Q4QGK2 | Leishmania major | 70% | 100% |
| Q4QGK4 | Leishmania major | 57% | 100% |
| Q4QGK8 | Leishmania major | 100% | 100% |
| Q4QGL4 | Leishmania major | 51% | 100% |
| Q4QGL5 | Leishmania major | 60% | 94% |
| Q4QGL8 | Leishmania major | 59% | 84% |
| Q54AX5 | Dictyostelium discoideum | 24% | 100% |
| Q5M8G4 | Xenopus tropicalis | 25% | 85% |
| Q5ZLN0 | Gallus gallus | 26% | 85% |
| Q940E8 | Zea mays | 26% | 84% |
| Q9LJW7 | Arabidopsis thaliana | 25% | 72% |
| Q9SHI3 | Arabidopsis thaliana | 22% | 70% |
| Q9SHI4 | Arabidopsis thaliana | 25% | 68% |
| Q9SJH6 | Arabidopsis thaliana | 26% | 100% |
| Q9SKK5 | Arabidopsis thaliana | 23% | 76% |