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: 120 |
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: 48, no: 7 |
NetGPI | no | yes: 0, no: 55 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 56 |
GO:0016020 | membrane | 2 | 30 |
GO:0042995 | cell projection | 2 | 56 |
GO:0043226 | organelle | 2 | 56 |
GO:0043227 | membrane-bounded organelle | 3 | 56 |
GO:0110165 | cellular anatomical entity | 1 | 56 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 56 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: Q4QGJ0
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_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.696 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.714 |
DEG_SCF_FBW7_1 | 520 | 527 | PF00400 | 0.409 |
DEG_SCF_FBW7_2 | 557 | 562 | PF00400 | 0.478 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.612 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.442 |
DEG_SPOP_SBC_1 | 505 | 509 | PF00917 | 0.524 |
DEG_SPOP_SBC_1 | 524 | 528 | PF00917 | 0.443 |
DEG_SPOP_SBC_1 | 537 | 541 | PF00917 | 0.477 |
DOC_CKS1_1 | 521 | 526 | PF01111 | 0.412 |
DOC_CYCLIN_RxL_1 | 105 | 115 | PF00134 | 0.425 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 228 | 238 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 240 | 249 | PF00069 | 0.237 |
DOC_MAPK_gen_1 | 351 | 358 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 182 | 191 | PF00069 | 0.232 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 446 | 453 | PF00069 | 0.428 |
DOC_MAPK_NFAT4_5 | 231 | 239 | PF00069 | 0.224 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.314 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.390 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.449 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.373 |
DOC_USP7_MATH_2 | 224 | 230 | PF00917 | 0.405 |
DOC_USP7_MATH_2 | 320 | 326 | PF00917 | 0.261 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.247 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.351 |
LIG_Actin_WH2_2 | 201 | 216 | PF00022 | 0.246 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.464 |
LIG_deltaCOP1_diTrp_1 | 62 | 69 | PF00928 | 0.426 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.341 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.357 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.316 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.354 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.464 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.499 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.349 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.237 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.318 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.438 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.352 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.475 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.459 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.401 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.421 |
LIG_GSK3_LRP6_1 | 520 | 526 | PF00069 | 0.408 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 127 | 135 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 232 | 243 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 250 | 257 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 297 | 305 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 370 | 378 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 370 | 374 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.365 |
LIG_NRBOX | 352 | 358 | PF00104 | 0.361 |
LIG_PCNA_PIPBox_1 | 326 | 335 | PF02747 | 0.216 |
LIG_PDZ_Class_2 | 624 | 629 | PF00595 | 0.309 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.552 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.437 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.409 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.641 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.461 |
LIG_Sin3_3 | 613 | 620 | PF02671 | 0.286 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.465 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.398 |
LIG_TYR_ITIM | 233 | 238 | PF00017 | 0.360 |
LIG_UBA3_1 | 108 | 116 | PF00899 | 0.218 |
LIG_UBA3_1 | 233 | 240 | PF00899 | 0.212 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.395 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.339 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.344 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.320 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.360 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.316 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.323 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.336 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.314 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.373 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.385 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.381 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.379 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.341 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.450 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.410 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.632 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.628 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.448 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.593 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.526 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.569 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.598 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.720 |
MOD_GlcNHglycan | 290 | 294 | PF01048 | 0.525 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.527 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.558 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.547 |
MOD_GlcNHglycan | 370 | 374 | PF01048 | 0.539 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.619 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.658 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.624 |
MOD_GlcNHglycan | 410 | 414 | PF01048 | 0.628 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.588 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.514 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.585 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.386 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.317 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.364 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.346 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.368 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.315 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.327 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.374 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.315 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.588 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.362 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.393 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.366 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.527 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.581 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.553 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.575 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.473 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.535 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.579 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.555 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.512 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.395 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.569 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.367 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.396 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.345 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.314 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.376 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.548 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.329 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.348 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.370 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.417 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.352 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.413 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.421 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.447 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.372 |
MOD_PKA_1 | 351 | 357 | PF00069 | 0.231 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.438 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.311 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.370 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.355 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.344 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.422 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.527 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.305 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.359 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.269 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.433 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.387 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.323 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.318 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.248 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.511 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.620 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.453 |
MOD_SUMO_rev_2 | 441 | 447 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 586 | 595 | PF00179 | 0.333 |
TRG_DiLeu_BaEn_1 | 593 | 598 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.567 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I661 | Leptomonas seymouri | 36% | 100% |
A0A0S4IHI7 | Bodo saltans | 28% | 81% |
A0A0S4ILC9 | Bodo saltans | 34% | 100% |
A0A0S4IM54 | Bodo saltans | 29% | 70% |
A0A0S4IRQ2 | Bodo saltans | 33% | 74% |
A0A0S4IT62 | Bodo saltans | 36% | 85% |
A0A0S4IU73 | Bodo saltans | 37% | 100% |
A0A0S4IU91 | Bodo saltans | 26% | 71% |
A0A0S4IV96 | Bodo saltans | 32% | 100% |
A0A0S4IW93 | Bodo saltans | 29% | 100% |
A0A0S4J2H8 | Bodo saltans | 26% | 100% |
A0A0S4J5A0 | Bodo saltans | 33% | 100% |
A0A0S4J954 | Bodo saltans | 27% | 85% |
A0A0S4JAQ6 | Bodo saltans | 27% | 100% |
A0A0S4JNU2 | Bodo saltans | 35% | 77% |
A0A0S4JTM6 | Bodo saltans | 28% | 85% |
A0A0S4JTQ7 | Bodo saltans | 36% | 100% |
A0A0S4KEC2 | Bodo saltans | 32% | 71% |
A0A0S4KF94 | Bodo saltans | 23% | 72% |
A0A0S4KGV4 | Bodo saltans | 25% | 100% |
A0A0S4KLL4 | Bodo saltans | 27% | 67% |
A0A1P8ATR9 | Arabidopsis thaliana | 22% | 67% |
A0A1X0ND37 | Trypanosomatidae | 25% | 66% |
A0A3Q8IC27 | Leishmania donovani | 33% | 100% |
A0A3S5H6M3 | Leishmania donovani | 80% | 92% |
A0A3S5H6M4 | Leishmania donovani | 61% | 96% |
A0A3S7WS66 | Leishmania donovani | 61% | 96% |
A4HBX3 | Leishmania braziliensis | 34% | 100% |
A4HZ93 | Leishmania infantum | 33% | 100% |
D1GJ51 | Leishmania infantum | 50% | 99% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 83% |
E9AGG2 | Leishmania infantum | 82% | 95% |
E9AGG5 | Leishmania infantum | 52% | 100% |
E9AGG7 | Leishmania infantum | 53% | 100% |
E9AGG9 | Leishmania infantum | 56% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 89% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 90% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4J8G2 | Arabidopsis thaliana | 24% | 72% |
F4J9A8 | Arabidopsis thaliana | 23% | 66% |
F4JGB6 | Arabidopsis thaliana | 25% | 78% |
F4JTU7 | Arabidopsis thaliana | 23% | 77% |
F4K4T3 | Arabidopsis thaliana | 22% | 66% |
Q4QC79 | Leishmania major | 33% | 100% |
Q4QGI0 | Leishmania major | 65% | 100% |
Q4QGI2 | Leishmania major | 56% | 100% |
Q4QGI4 | Leishmania major | 53% | 100% |
Q4QGI6 | Leishmania major | 58% | 100% |
Q4QGI8 | Leishmania major | 54% | 83% |
Q4QGJ2 | Leishmania major | 66% | 97% |
Q4QGJ6 | Leishmania major | 51% | 100% |
Q4QGJ9 | Leishmania major | 64% | 100% |
Q4QGK0 | Leishmania major | 61% | 100% |
Q4QGK1 | Leishmania major | 93% | 89% |
Q4QGK2 | Leishmania major | 54% | 100% |
Q4QGK4 | Leishmania major | 55% | 94% |
Q4QGK8 | Leishmania major | 59% | 100% |
Q4QGL2 | Leishmania major | 58% | 100% |
Q4QGL5 | Leishmania major | 47% | 100% |
Q4QGL8 | Leishmania major | 51% | 100% |
Q4QGM1 | Leishmania major | 56% | 81% |
Q7FZR1 | Arabidopsis thaliana | 23% | 78% |
Q8RX63 | Arabidopsis thaliana | 23% | 73% |
Q9LJS0 | Arabidopsis thaliana | 23% | 71% |
Q9LJS2 | Arabidopsis thaliana | 22% | 71% |
Q9LS80 | Arabidopsis thaliana | 20% | 75% |
Q9SHI4 | Arabidopsis thaliana | 21% | 83% |
Q9SVM3 | Arabidopsis thaliana | 23% | 75% |
Q9SVN2 | Arabidopsis thaliana | 24% | 79% |