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: 120 |
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: 63, no: 10 |
NetGPI | no | yes: 0, no: 73 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 74 |
GO:0016020 | membrane | 2 | 30 |
GO:0042995 | cell projection | 2 | 74 |
GO:0043226 | organelle | 2 | 74 |
GO:0043227 | membrane-bounded organelle | 3 | 74 |
GO:0110165 | cellular anatomical entity | 1 | 74 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 74 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: Q4QGL8
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_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.365 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.718 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.671 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.615 |
DOC_MAPK_gen_1 | 130 | 139 | PF00069 | 0.175 |
DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.184 |
DOC_MAPK_MEF2A_6 | 516 | 523 | PF00069 | 0.301 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.220 |
DOC_PP1_RVXF_1 | 131 | 137 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.190 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.220 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.333 |
LIG_14-3-3_CanoR_1 | 421 | 428 | PF00244 | 0.213 |
LIG_Actin_WH2_2 | 272 | 287 | PF00022 | 0.193 |
LIG_Actin_WH2_2 | 344 | 359 | PF00022 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.622 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.194 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.375 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.294 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.425 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.185 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.263 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.344 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.377 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.269 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.272 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.224 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.471 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.332 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.337 |
LIG_LIR_Gen_1 | 126 | 136 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 151 | 158 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 440 | 448 | PF02991 | 0.224 |
LIG_LIR_Gen_1 | 487 | 497 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.228 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.293 |
LIG_NRBOX | 422 | 428 | PF00104 | 0.239 |
LIG_PDZ_Class_2 | 605 | 610 | PF00595 | 0.207 |
LIG_PTAP_UEV_1 | 538 | 543 | PF05743 | 0.285 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.247 |
LIG_SH3_1 | 536 | 542 | PF00018 | 0.290 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.390 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.386 |
LIG_Sin3_3 | 594 | 601 | PF02671 | 0.190 |
LIG_SUMO_SIM_anti_2 | 135 | 141 | PF11976 | 0.179 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.200 |
LIG_SUMO_SIM_anti_2 | 278 | 283 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.245 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 208 | 215 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.423 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.407 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.200 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.278 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.298 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.269 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.262 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.253 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.358 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.284 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.301 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.266 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.283 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.258 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.275 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.310 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.327 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.303 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.322 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.212 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.269 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.467 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.379 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.530 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.494 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.566 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.509 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.457 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.490 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.675 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.621 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.491 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.512 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.518 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.510 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.484 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.549 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.455 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.441 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.510 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.493 |
MOD_GlcNHglycan | 480 | 484 | PF01048 | 0.536 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.562 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.666 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.450 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.319 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.295 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.295 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.275 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.310 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.357 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.254 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.299 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.271 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.513 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.289 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.333 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.285 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.240 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.247 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.318 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.270 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.364 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.441 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.452 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.288 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.509 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.288 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.489 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.341 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.282 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.276 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.328 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.216 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.354 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.281 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.252 |
MOD_NEK2_2 | 496 | 501 | PF00069 | 0.349 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.256 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.232 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.331 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.387 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.416 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.407 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.364 |
MOD_PK_1 | 165 | 171 | PF00069 | 0.204 |
MOD_PK_1 | 277 | 283 | PF00069 | 0.185 |
MOD_PK_1 | 285 | 291 | PF00069 | 0.193 |
MOD_PKA_1 | 421 | 427 | PF00069 | 0.186 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.253 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.287 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.308 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.209 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.233 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.443 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.319 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.184 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.378 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.298 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.270 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.248 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.268 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.277 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.213 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.272 |
MOD_SUMO_rev_2 | 511 | 517 | PF00179 | 0.230 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.226 |
TRG_DiLeu_BaEn_1 | 574 | 579 | PF01217 | 0.250 |
TRG_DiLeu_BaEn_2 | 131 | 137 | PF01217 | 0.173 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 28% | 96% |
A0A0N1I121 | Leptomonas seymouri | 27% | 100% |
A0A0N1I661 | Leptomonas seymouri | 37% | 100% |
A0A0S4IHI7 | Bodo saltans | 29% | 79% |
A0A0S4IJN2 | Bodo saltans | 30% | 91% |
A0A0S4IN27 | Bodo saltans | 39% | 100% |
A0A0S4IQE4 | Bodo saltans | 26% | 100% |
A0A0S4IRQ2 | Bodo saltans | 33% | 71% |
A0A0S4ISU4 | Bodo saltans | 35% | 93% |
A0A0S4IT62 | Bodo saltans | 38% | 82% |
A0A0S4ITE7 | Bodo saltans | 37% | 68% |
A0A0S4IU73 | Bodo saltans | 38% | 100% |
A0A0S4IU91 | Bodo saltans | 28% | 69% |
A0A0S4IVQ8 | Bodo saltans | 34% | 100% |
A0A0S4IW93 | Bodo saltans | 28% | 100% |
A0A0S4IY44 | Bodo saltans | 26% | 92% |
A0A0S4J014 | Bodo saltans | 27% | 85% |
A0A0S4J0N5 | Bodo saltans | 26% | 71% |
A0A0S4J2H8 | Bodo saltans | 28% | 100% |
A0A0S4J542 | Bodo saltans | 27% | 67% |
A0A0S4J5A0 | Bodo saltans | 39% | 100% |
A0A0S4J7S2 | Bodo saltans | 26% | 67% |
A0A0S4J954 | Bodo saltans | 25% | 82% |
A0A0S4JAQ6 | Bodo saltans | 28% | 100% |
A0A0S4JAS1 | Bodo saltans | 37% | 96% |
A0A0S4JB95 | Bodo saltans | 26% | 100% |
A0A0S4JD35 | Bodo saltans | 31% | 100% |
A0A0S4JDT0 | Bodo saltans | 34% | 93% |
A0A0S4JJV0 | Bodo saltans | 29% | 71% |
A0A0S4JL29 | Bodo saltans | 34% | 100% |
A0A0S4JNU2 | Bodo saltans | 41% | 74% |
A0A0S4JQZ0 | Bodo saltans | 26% | 81% |
A0A0S4JTM6 | Bodo saltans | 35% | 83% |
A0A0S4JTQ7 | Bodo saltans | 42% | 100% |
A0A0S4JVI0 | Bodo saltans | 30% | 86% |
A0A0S4KEC2 | Bodo saltans | 39% | 69% |
A0A0S4KEG2 | Bodo saltans | 31% | 73% |
A0A0S4KF94 | Bodo saltans | 25% | 70% |
A0A0S4KGV4 | Bodo saltans | 25% | 100% |
A0A0S4KH41 | Bodo saltans | 27% | 88% |
A0A0S4KIR5 | Bodo saltans | 27% | 73% |
A0A0S4KJA7 | Bodo saltans | 28% | 91% |
A0A0S4KK37 | Bodo saltans | 30% | 100% |
A0A3Q8I9B4 | Leishmania donovani | 42% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 41% | 99% |
A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
A0A3S5H6L9 | Leishmania donovani | 44% | 100% |
A0A3S5H6M3 | Leishmania donovani | 54% | 89% |
A0A3S5H6M4 | Leishmania donovani | 54% | 93% |
A0A3S7WS66 | Leishmania donovani | 54% | 93% |
A4H6Y8 | Leishmania braziliensis | 50% | 67% |
A4HBX3 | Leishmania braziliensis | 36% | 100% |
A4HM88 | Leishmania braziliensis | 31% | 71% |
A4HVB0 | Leishmania infantum | 53% | 100% |
A4HZ93 | Leishmania infantum | 36% | 100% |
A6QLV3 | Bos taurus | 23% | 100% |
D1GJ51 | Leishmania infantum | 63% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 80% |
E9AGG2 | Leishmania infantum | 54% | 92% |
E9AGG5 | Leishmania infantum | 56% | 100% |
E9AGG7 | Leishmania infantum | 58% | 97% |
E9AGG9 | Leishmania infantum | 59% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 86% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 88% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
F4IUU1 | Arabidopsis thaliana | 24% | 75% |
F4J7T6 | Arabidopsis thaliana | 25% | 69% |
F4J8G2 | Arabidopsis thaliana | 24% | 70% |
F4JGB6 | Arabidopsis thaliana | 24% | 75% |
F4JTU7 | Arabidopsis thaliana | 24% | 75% |
F4KHA2 | Arabidopsis thaliana | 23% | 77% |
O22938 | Arabidopsis thaliana | 25% | 69% |
O48849 | Arabidopsis thaliana | 20% | 69% |
O48851 | Arabidopsis thaliana | 24% | 79% |
O49325 | Arabidopsis thaliana | 23% | 78% |
O49328 | Arabidopsis thaliana | 22% | 76% |
O49329 | Arabidopsis thaliana | 23% | 71% |
O49879 | Solanum lycopersicum | 24% | 72% |
O80809 | Arabidopsis thaliana | 25% | 85% |
O88520 | Mus musculus | 23% | 100% |
P0DO05 | Solanum pimpinellifolium | 25% | 71% |
P0DO06 | Solanum pimpinellifolium | 25% | 71% |
P35859 | Rattus norvegicus | 21% | 100% |
P70389 | Mus musculus | 20% | 100% |
Q1L8Y7 | Danio rerio | 23% | 100% |
Q1PEN0 | Arabidopsis thaliana | 24% | 85% |
Q22875 | Caenorhabditis elegans | 23% | 100% |
Q40235 | Solanum pimpinellifolium | 26% | 71% |
Q4QC79 | Leishmania major | 35% | 100% |
Q4QGI0 | Leishmania major | 64% | 93% |
Q4QGI2 | Leishmania major | 60% | 98% |
Q4QGI4 | Leishmania major | 64% | 98% |
Q4QGI6 | Leishmania major | 59% | 85% |
Q4QGI8 | Leishmania major | 65% | 100% |
Q4QGJ0 | Leishmania major | 51% | 100% |
Q4QGJ2 | Leishmania major | 48% | 100% |
Q4QGJ9 | Leishmania major | 64% | 100% |
Q4QGK0 | Leishmania major | 51% | 89% |
Q4QGK1 | Leishmania major | 50% | 100% |
Q4QGK2 | Leishmania major | 57% | 98% |
Q4QGK4 | Leishmania major | 50% | 100% |
Q4QGK8 | Leishmania major | 59% | 94% |
Q4QGL2 | Leishmania major | 59% | 94% |
Q4QGM1 | Leishmania major | 60% | 79% |
Q5MR23 | Solanum pimpinellifolium | 26% | 71% |
Q5RAV5 | Pongo abelii | 23% | 100% |
Q5ZLN0 | Gallus gallus | 24% | 100% |
Q6AYI5 | Rattus norvegicus | 23% | 100% |
Q7FZR1 | Arabidopsis thaliana | 24% | 75% |
Q7SXW3 | Danio rerio | 24% | 100% |
Q8AVI4 | Xenopus laevis | 24% | 100% |
Q8C0R9 | Mus musculus | 22% | 72% |
Q8RX63 | Arabidopsis thaliana | 26% | 71% |
Q93YT3 | Arabidopsis thaliana | 25% | 68% |
Q9C9H6 | Arabidopsis thaliana | 23% | 78% |
Q9C9H7 | Arabidopsis thaliana | 25% | 72% |
Q9FL51 | Arabidopsis thaliana | 24% | 70% |
Q9FYK0 | Arabidopsis thaliana | 22% | 69% |
Q9LJS0 | Arabidopsis thaliana | 23% | 69% |
Q9LJS2 | Arabidopsis thaliana | 27% | 69% |
Q9LJW7 | Arabidopsis thaliana | 25% | 86% |
Q9LRW9 | Arabidopsis thaliana | 23% | 69% |
Q9LS79 | Arabidopsis thaliana | 23% | 78% |
Q9LS80 | Arabidopsis thaliana | 25% | 73% |
Q9M9X0 | Arabidopsis thaliana | 24% | 70% |
Q9MA83 | Arabidopsis thaliana | 25% | 78% |
Q9SHI3 | Arabidopsis thaliana | 25% | 84% |
Q9SHI4 | Arabidopsis thaliana | 23% | 81% |
Q9SKK5 | Arabidopsis thaliana | 21% | 91% |
Q9SVM3 | Arabidopsis thaliana | 25% | 72% |
Q9SVN2 | Arabidopsis thaliana | 24% | 76% |
Q9UQ13 | Homo sapiens | 23% | 100% |
Q9ZUK7 | Arabidopsis thaliana | 25% | 74% |