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: 145 |
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: 64, no: 8 |
NetGPI | no | yes: 0, no: 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 7 |
GO:0005929 | cilium | 4 | 73 |
GO:0016020 | membrane | 2 | 34 |
GO:0042995 | cell projection | 2 | 73 |
GO:0043226 | organelle | 2 | 73 |
GO:0043227 | membrane-bounded organelle | 3 | 73 |
GO:0110165 | cellular anatomical entity | 1 | 73 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 73 |
Related structures:
AlphaFold database: Q4QGK2
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 | 0.502 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.742 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.694 |
DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.325 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.700 |
DOC_CYCLIN_yCln2_LP_2 | 290 | 296 | PF00134 | 0.253 |
DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 254 | 261 | PF00069 | 0.240 |
DOC_MAPK_gen_1 | 281 | 290 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 254 | 261 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.523 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.458 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.539 |
DOC_USP7_MATH_2 | 247 | 253 | PF00917 | 0.277 |
DOC_USP7_MATH_2 | 271 | 277 | PF00917 | 0.262 |
DOC_USP7_MATH_2 | 319 | 325 | PF00917 | 0.548 |
DOC_USP7_MATH_2 | 439 | 445 | PF00917 | 0.364 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.277 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 468 | 477 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.761 |
LIG_Actin_WH2_1 | 105 | 121 | PF00022 | 0.226 |
LIG_Actin_WH2_2 | 297 | 312 | PF00022 | 0.553 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
LIG_Clathr_ClatBox_1 | 352 | 356 | PF01394 | 0.401 |
LIG_Clathr_ClatBox_1 | 521 | 525 | PF01394 | 0.310 |
LIG_deltaCOP1_diTrp_1 | 176 | 179 | PF00928 | 0.483 |
LIG_deltaCOP1_diTrp_1 | 200 | 206 | PF00928 | 0.264 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.547 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.451 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.343 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.424 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.554 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.413 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.424 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.353 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.583 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.509 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.364 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.351 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.460 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.505 |
LIG_GBD_Chelix_1 | 349 | 357 | PF00786 | 0.230 |
LIG_LIR_Gen_1 | 126 | 134 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 200 | 207 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 321 | 328 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 441 | 448 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 465 | 472 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.418 |
LIG_PCNA_PIPBox_1 | 229 | 238 | PF02747 | 0.273 |
LIG_PCNA_PIPBox_1 | 253 | 262 | PF02747 | 0.230 |
LIG_PCNA_PIPBox_1 | 397 | 406 | PF02747 | 0.312 |
LIG_PCNA_PIPBox_1 | 421 | 430 | PF02747 | 0.262 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.355 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.424 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.406 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.470 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.518 |
LIG_SUMO_SIM_anti_2 | 135 | 141 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 305 | 312 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.396 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.469 |
LIG_UBA3_1 | 520 | 529 | PF00899 | 0.311 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.419 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.445 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.392 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.434 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.405 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.510 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.409 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.505 |
MOD_Cter_Amidation | 334 | 337 | PF01082 | 0.304 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.409 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.446 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.632 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.511 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.416 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.405 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.480 |
MOD_GlcNHglycan | 409 | 413 | PF01048 | 0.410 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.475 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.554 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.491 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.455 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.430 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.563 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.369 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.400 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.417 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.581 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.475 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.358 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.479 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.524 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.721 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.752 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.450 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.338 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.390 |
MOD_N-GLC_2 | 537 | 539 | PF02516 | 0.479 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.631 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.545 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.343 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.429 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.566 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.404 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.561 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.374 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.451 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.436 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.318 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.488 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.489 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.348 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.459 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.317 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.591 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.581 |
MOD_PKA_1 | 336 | 342 | PF00069 | 0.266 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.364 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.567 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.773 |
MOD_PKB_1 | 157 | 165 | PF00069 | 0.260 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.454 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.382 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.480 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.460 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.510 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.551 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.443 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.505 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.368 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.370 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.443 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.390 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.312 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.572 |
MOD_SUMO_rev_2 | 395 | 400 | PF00179 | 0.268 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.319 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.740 |
TRG_NES_CRM1_1 | 396 | 409 | PF08389 | 0.280 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.268 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 29% | 88% |
A0A0N1I121 | Leptomonas seymouri | 28% | 100% |
A0A0N1I661 | Leptomonas seymouri | 34% | 98% |
A0A0N1I7S5 | Leptomonas seymouri | 32% | 100% |
A0A0N1II82 | Leptomonas seymouri | 31% | 81% |
A0A0S4IHI7 | Bodo saltans | 28% | 72% |
A0A0S4IJN2 | Bodo saltans | 25% | 83% |
A0A0S4ILC9 | Bodo saltans | 34% | 100% |
A0A0S4IN27 | Bodo saltans | 38% | 100% |
A0A0S4IQE4 | Bodo saltans | 26% | 99% |
A0A0S4ISU4 | Bodo saltans | 41% | 85% |
A0A0S4IT62 | Bodo saltans | 36% | 76% |
A0A0S4IU23 | Bodo saltans | 27% | 95% |
A0A0S4IU73 | Bodo saltans | 38% | 100% |
A0A0S4IV96 | Bodo saltans | 37% | 92% |
A0A0S4IVQ8 | Bodo saltans | 36% | 93% |
A0A0S4IW93 | Bodo saltans | 28% | 92% |
A0A0S4IY44 | Bodo saltans | 27% | 84% |
A0A0S4IZC7 | Bodo saltans | 24% | 100% |
A0A0S4J014 | Bodo saltans | 26% | 78% |
A0A0S4J100 | Bodo saltans | 28% | 67% |
A0A0S4J206 | Bodo saltans | 34% | 91% |
A0A0S4J2H8 | Bodo saltans | 28% | 96% |
A0A0S4J3T7 | Bodo saltans | 33% | 100% |
A0A0S4J4L7 | Bodo saltans | 28% | 76% |
A0A0S4J5A0 | Bodo saltans | 38% | 98% |
A0A0S4J954 | Bodo saltans | 25% | 76% |
A0A0S4JAQ6 | Bodo saltans | 26% | 100% |
A0A0S4JAS1 | Bodo saltans | 38% | 88% |
A0A0S4JAW7 | Bodo saltans | 26% | 100% |
A0A0S4JB95 | Bodo saltans | 25% | 92% |
A0A0S4JBV9 | Bodo saltans | 28% | 100% |
A0A0S4JD35 | Bodo saltans | 26% | 94% |
A0A0S4JDS1 | Bodo saltans | 25% | 100% |
A0A0S4JDT0 | Bodo saltans | 34% | 85% |
A0A0S4JEK1 | Bodo saltans | 26% | 100% |
A0A0S4JL29 | Bodo saltans | 31% | 100% |
A0A0S4JMF9 | Bodo saltans | 33% | 100% |
A0A0S4JN05 | Bodo saltans | 36% | 67% |
A0A0S4JNU2 | Bodo saltans | 40% | 68% |
A0A0S4JQZ0 | Bodo saltans | 26% | 74% |
A0A0S4JS89 | Bodo saltans | 28% | 100% |
A0A0S4JSB8 | Bodo saltans | 35% | 100% |
A0A0S4JTM6 | Bodo saltans | 33% | 76% |
A0A0S4JTQ7 | Bodo saltans | 39% | 100% |
A0A0S4JVI0 | Bodo saltans | 27% | 79% |
A0A0S4KEG2 | Bodo saltans | 26% | 67% |
A0A0S4KGV4 | Bodo saltans | 24% | 100% |
A0A0S4KH41 | Bodo saltans | 29% | 80% |
A0A0S4KIR5 | Bodo saltans | 23% | 67% |
A0A0S4KJA7 | Bodo saltans | 27% | 83% |
A0A0S4KK37 | Bodo saltans | 29% | 96% |
A0A3Q8I9A6 | Leishmania donovani | 52% | 100% |
A0A3Q8I9B4 | Leishmania donovani | 38% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 38% | 100% |
A0A3Q8IC27 | Leishmania donovani | 32% | 100% |
A0A3S5H6L9 | Leishmania donovani | 43% | 100% |
A0A3S5H6M3 | Leishmania donovani | 53% | 82% |
A0A3S5H6M4 | Leishmania donovani | 53% | 85% |
A0A3S7WS66 | Leishmania donovani | 51% | 85% |
A4HBX3 | Leishmania braziliensis | 32% | 100% |
A4HVB0 | Leishmania infantum | 50% | 100% |
A4HZ93 | Leishmania infantum | 32% | 100% |
A7SFP1 | Nematostella vectensis | 25% | 97% |
D1GJ51 | Leishmania infantum | 54% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 73% |
E9AGG2 | Leishmania infantum | 54% | 84% |
E9AGG5 | Leishmania infantum | 51% | 100% |
E9AGG7 | Leishmania infantum | 57% | 89% |
E9AGG9 | Leishmania infantum | 57% | 100% |
E9AGH0 | Leishmania infantum | 51% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 79% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 80% |
E9AP05 | 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) | 35% | 100% |
F4IUU1 | Arabidopsis thaliana | 24% | 69% |
F4JGB6 | Arabidopsis thaliana | 27% | 69% |
F4JTU7 | Arabidopsis thaliana | 24% | 69% |
F4KHA2 | Arabidopsis thaliana | 24% | 71% |
O48851 | Arabidopsis thaliana | 26% | 73% |
O49325 | Arabidopsis thaliana | 25% | 72% |
O49328 | Arabidopsis thaliana | 25% | 70% |
O49879 | Solanum lycopersicum | 25% | 66% |
O80809 | Arabidopsis thaliana | 25% | 78% |
Q1PEN0 | Arabidopsis thaliana | 23% | 78% |
Q25331 | Leishmania major | 52% | 100% |
Q4QC79 | Leishmania major | 35% | 100% |
Q4QGI0 | Leishmania major | 62% | 94% |
Q4QGI2 | Leishmania major | 77% | 100% |
Q4QGI4 | Leishmania major | 75% | 99% |
Q4QGI6 | Leishmania major | 51% | 100% |
Q4QGI8 | Leishmania major | 75% | 100% |
Q4QGJ0 | Leishmania major | 54% | 100% |
Q4QGJ2 | Leishmania major | 53% | 100% |
Q4QGJ4 | Leishmania major | 53% | 100% |
Q4QGJ7 | Leishmania major | 52% | 100% |
Q4QGJ9 | Leishmania major | 51% | 100% |
Q4QGK0 | Leishmania major | 55% | 100% |
Q4QGK1 | Leishmania major | 53% | 100% |
Q4QGK4 | Leishmania major | 46% | 84% |
Q4QGK6 | Leishmania major | 52% | 100% |
Q4QGK8 | Leishmania major | 70% | 100% |
Q4QGL2 | Leishmania major | 70% | 100% |
Q4QGL4 | Leishmania major | 50% | 100% |
Q4QGL8 | Leishmania major | 57% | 92% |
Q4QGM1 | Leishmania major | 69% | 72% |
Q7FZR1 | Arabidopsis thaliana | 23% | 69% |
Q940E8 | Zea mays | 29% | 91% |
Q9C9H6 | Arabidopsis thaliana | 25% | 71% |
Q9C9H7 | Arabidopsis thaliana | 26% | 66% |
Q9LJW7 | Arabidopsis thaliana | 25% | 79% |
Q9LS79 | Arabidopsis thaliana | 24% | 71% |
Q9LS80 | Arabidopsis thaliana | 24% | 67% |
Q9MA83 | Arabidopsis thaliana | 25% | 71% |
Q9SHI3 | Arabidopsis thaliana | 25% | 77% |
Q9SHI4 | Arabidopsis thaliana | 24% | 74% |
Q9SKK5 | Arabidopsis thaliana | 20% | 83% |
Q9SVM3 | Arabidopsis thaliana | 24% | 66% |
Q9SVN2 | Arabidopsis thaliana | 24% | 70% |
Q9ZUK7 | Arabidopsis thaliana | 24% | 68% |