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: 155 |
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: 59, no: 9 |
NetGPI | no | yes: 0, no: 68 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 8 |
GO:0005929 | cilium | 4 | 69 |
GO:0016020 | membrane | 2 | 31 |
GO:0042995 | cell projection | 2 | 69 |
GO:0043226 | organelle | 2 | 69 |
GO:0043227 | membrane-bounded organelle | 3 | 69 |
GO:0110165 | cellular anatomical entity | 1 | 69 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 69 |
Related structures:
AlphaFold database: Q4QGI4
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 | 0.494 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 470 | 478 | PF00400 | 0.255 |
DOC_CYCLIN_RxL_1 | 185 | 196 | PF00134 | 0.490 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 395 | 405 | PF00069 | 0.234 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 492 | 500 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.281 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.442 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.409 |
DOC_USP7_MATH_2 | 295 | 301 | PF00917 | 0.253 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 345 | 352 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 444 | 453 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 516 | 520 | PF00244 | 0.642 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.697 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.371 |
LIG_Clathr_ClatBox_1 | 497 | 501 | PF01394 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.529 |
LIG_DLG_GKlike_1 | 203 | 210 | PF00625 | 0.217 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.387 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.354 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.344 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.289 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.362 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.530 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.320 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.557 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.358 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.419 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.454 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.398 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.400 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.449 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.486 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 225 | 232 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 441 | 448 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 465 | 474 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.343 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.368 |
LIG_PCNA_PIPBox_1 | 373 | 382 | PF02747 | 0.322 |
LIG_PCNA_PIPBox_1 | 397 | 406 | PF02747 | 0.303 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.312 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.293 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.378 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 425 | 430 | PF11976 | 0.328 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.528 |
LIG_UBA3_1 | 496 | 505 | PF00899 | 0.282 |
LIG_WW_3 | 342 | 346 | PF00397 | 0.248 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.459 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.360 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.370 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.342 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.414 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.288 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.357 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.305 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.402 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.450 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.413 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.398 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.363 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.432 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.401 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.405 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.392 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.380 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.703 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.409 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.370 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.422 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.456 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.441 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.365 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.339 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.406 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.360 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.351 |
MOD_GlcNHglycan | 465 | 469 | PF01048 | 0.422 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.350 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.342 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.365 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.382 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.335 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.335 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.340 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.659 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.371 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.349 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.328 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.446 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.649 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.670 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.419 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.559 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.330 |
MOD_N-GLC_2 | 513 | 515 | PF02516 | 0.571 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.557 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.325 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.344 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.291 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.424 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.453 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.332 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.376 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.432 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.436 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.370 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.357 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.426 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.505 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.499 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.421 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.394 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.441 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.440 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.368 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.428 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.466 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.404 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.498 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.440 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.436 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.349 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.442 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.313 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.366 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.468 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.680 |
MOD_PKB_1 | 157 | 165 | PF00069 | 0.223 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.266 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.347 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.299 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.538 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.490 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.377 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.441 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.287 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.302 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 251 | 256 | PF00179 | 0.248 |
MOD_SUMO_rev_2 | 323 | 328 | PF00179 | 0.250 |
MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.250 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.243 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.559 |
TRG_NES_CRM1_1 | 252 | 262 | PF08389 | 0.402 |
TRG_NES_CRM1_1 | 324 | 334 | PF08389 | 0.246 |
TRG_NES_CRM1_1 | 348 | 358 | PF08389 | 0.245 |
TRG_NES_CRM1_1 | 372 | 382 | PF08389 | 0.239 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.234 |
TRG_Pf-PMV_PEXEL_1 | 305 | 310 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 425 | 430 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 444 | 449 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 29% | 84% |
A0A0N1I661 | Leptomonas seymouri | 38% | 94% |
A0A0N1I7S5 | Leptomonas seymouri | 35% | 100% |
A0A0N1II82 | Leptomonas seymouri | 27% | 78% |
A0A0S4IHI7 | Bodo saltans | 29% | 69% |
A0A0S4IJN2 | Bodo saltans | 29% | 80% |
A0A0S4ILC9 | Bodo saltans | 38% | 97% |
A0A0S4IN27 | Bodo saltans | 42% | 99% |
A0A0S4IQE4 | Bodo saltans | 26% | 95% |
A0A0S4ISU4 | Bodo saltans | 38% | 81% |
A0A0S4IT62 | Bodo saltans | 37% | 72% |
A0A0S4IU23 | Bodo saltans | 29% | 91% |
A0A0S4IU73 | Bodo saltans | 38% | 100% |
A0A0S4IV96 | Bodo saltans | 37% | 88% |
A0A0S4IVQ8 | Bodo saltans | 34% | 89% |
A0A0S4IW93 | Bodo saltans | 28% | 88% |
A0A0S4IY44 | Bodo saltans | 27% | 80% |
A0A0S4J014 | Bodo saltans | 29% | 75% |
A0A0S4J206 | Bodo saltans | 36% | 87% |
A0A0S4J2H8 | Bodo saltans | 28% | 92% |
A0A0S4J4L7 | Bodo saltans | 27% | 73% |
A0A0S4J5A0 | Bodo saltans | 37% | 94% |
A0A0S4J954 | Bodo saltans | 24% | 72% |
A0A0S4JAQ6 | Bodo saltans | 26% | 100% |
A0A0S4JAS1 | Bodo saltans | 38% | 85% |
A0A0S4JB95 | Bodo saltans | 23% | 88% |
A0A0S4JBV9 | Bodo saltans | 30% | 100% |
A0A0S4JD35 | Bodo saltans | 29% | 90% |
A0A0S4JDS1 | Bodo saltans | 26% | 100% |
A0A0S4JDT0 | Bodo saltans | 36% | 81% |
A0A0S4JEK1 | Bodo saltans | 25% | 100% |
A0A0S4JFY5 | Bodo saltans | 33% | 100% |
A0A0S4JL29 | Bodo saltans | 34% | 100% |
A0A0S4JQZ0 | Bodo saltans | 26% | 71% |
A0A0S4JS89 | Bodo saltans | 27% | 100% |
A0A0S4JTM6 | Bodo saltans | 33% | 73% |
A0A0S4JTQ7 | Bodo saltans | 40% | 100% |
A0A0S4JU95 | Bodo saltans | 35% | 71% |
A0A0S4JVI0 | Bodo saltans | 27% | 75% |
A0A0S4KGV4 | Bodo saltans | 26% | 99% |
A0A0S4KH41 | Bodo saltans | 31% | 77% |
A0A0S4KJA7 | Bodo saltans | 25% | 80% |
A0A0S4KK37 | Bodo saltans | 31% | 92% |
A0A3Q8I9A6 | Leishmania donovani | 48% | 100% |
A0A3Q8IC27 | Leishmania donovani | 36% | 100% |
A0A3Q8IFC2 | Leishmania donovani | 32% | 100% |
A0A3S5H6M3 | Leishmania donovani | 52% | 78% |
A0A3S5H6M4 | Leishmania donovani | 58% | 82% |
A0A3S7WS66 | Leishmania donovani | 58% | 81% |
A4HBX3 | Leishmania braziliensis | 33% | 100% |
A4HVB0 | Leishmania infantum | 50% | 100% |
A4HZ93 | Leishmania infantum | 35% | 100% |
A4I6S3 | Leishmania infantum | 31% | 100% |
A7SFP1 | Nematostella vectensis | 26% | 93% |
B4LXW1 | Drosophila virilis | 23% | 87% |
D1GJ51 | Leishmania infantum | 54% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 70% |
E9AGG2 | Leishmania infantum | 52% | 81% |
E9AGG5 | Leishmania infantum | 46% | 100% |
E9AGG7 | Leishmania infantum | 59% | 85% |
E9AGG9 | Leishmania infantum | 65% | 99% |
E9AGH0 | Leishmania infantum | 48% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 76% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 77% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
F4IUU1 | Arabidopsis thaliana | 26% | 66% |
F4JGB6 | Arabidopsis thaliana | 26% | 66% |
F4KHA2 | Arabidopsis thaliana | 24% | 68% |
O48851 | Arabidopsis thaliana | 26% | 70% |
O49325 | Arabidopsis thaliana | 24% | 69% |
O49328 | Arabidopsis thaliana | 22% | 67% |
O80809 | Arabidopsis thaliana | 29% | 74% |
Q1PEN0 | Arabidopsis thaliana | 23% | 75% |
Q25331 | Leishmania major | 47% | 100% |
Q4QC79 | Leishmania major | 36% | 100% |
Q4QGI0 | Leishmania major | 64% | 98% |
Q4QGI2 | Leishmania major | 88% | 100% |
Q4QGI6 | Leishmania major | 56% | 98% |
Q4QGI8 | Leishmania major | 89% | 71% |
Q4QGJ0 | Leishmania major | 53% | 85% |
Q4QGJ2 | Leishmania major | 51% | 83% |
Q4QGJ4 | Leishmania major | 47% | 100% |
Q4QGJ7 | Leishmania major | 47% | 100% |
Q4QGJ9 | Leishmania major | 57% | 91% |
Q4QGK0 | Leishmania major | 62% | 94% |
Q4QGK1 | Leishmania major | 53% | 76% |
Q4QGK2 | Leishmania major | 75% | 96% |
Q4QGK4 | Leishmania major | 50% | 80% |
Q4QGK6 | Leishmania major | 47% | 100% |
Q4QGK8 | Leishmania major | 73% | 100% |
Q4QGL2 | Leishmania major | 73% | 100% |
Q4QGL4 | Leishmania major | 52% | 100% |
Q4QGL8 | Leishmania major | 64% | 88% |
Q4QGM1 | Leishmania major | 88% | 69% |
Q5F4C4 | Gallus gallus | 27% | 100% |
Q7FZR1 | Arabidopsis thaliana | 24% | 66% |
Q80VQ1 | Mus musculus | 25% | 100% |
Q940E8 | Zea mays | 28% | 87% |
Q9BTT6 | Homo sapiens | 26% | 100% |
Q9C9H6 | Arabidopsis thaliana | 24% | 68% |
Q9LJW7 | Arabidopsis thaliana | 25% | 75% |
Q9LS79 | Arabidopsis thaliana | 24% | 68% |
Q9MA83 | Arabidopsis thaliana | 26% | 68% |
Q9SHI3 | Arabidopsis thaliana | 23% | 74% |
Q9SHI4 | Arabidopsis thaliana | 24% | 71% |
Q9SKK5 | Arabidopsis thaliana | 22% | 80% |
Q9SVN2 | Arabidopsis thaliana | 24% | 67% |