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: 150 |
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: 58, no: 13 |
NetGPI | no | yes: 0, no: 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 8 |
GO:0005929 | cilium | 4 | 72 |
GO:0016020 | membrane | 2 | 32 |
GO:0042995 | cell projection | 2 | 72 |
GO:0043226 | organelle | 2 | 72 |
GO:0043227 | membrane-bounded organelle | 3 | 72 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 72 |
Related structures:
AlphaFold database: Q4QGI2
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 | 0.457 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.574 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.693 |
DEG_APCC_DBOX_1 | 494 | 502 | PF00400 | 0.255 |
DOC_CYCLIN_RxL_1 | 185 | 196 | PF00134 | 0.463 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.704 |
DOC_MAPK_gen_1 | 419 | 429 | PF00069 | 0.263 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.210 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.278 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.400 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.746 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 468 | 477 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.659 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.618 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.202 |
LIG_Clathr_ClatBox_1 | 521 | 525 | PF01394 | 0.296 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.476 |
LIG_DLG_GKlike_1 | 203 | 210 | PF00625 | 0.220 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.390 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.328 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.387 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.261 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.342 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.224 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.414 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.553 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.336 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.467 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.522 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.489 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.421 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.237 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.413 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.438 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 225 | 232 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 465 | 472 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.357 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.210 |
LIG_PCNA_PIPBox_1 | 397 | 406 | PF02747 | 0.327 |
LIG_PCNA_PIPBox_1 | 421 | 430 | PF02747 | 0.293 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.423 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.290 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.204 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.361 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.548 |
LIG_UBA3_1 | 520 | 529 | PF00899 | 0.336 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.349 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.401 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.348 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.357 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.240 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.308 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.321 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.352 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.521 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.510 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.361 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.245 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.474 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.405 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.494 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.498 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.413 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.443 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.625 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.473 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.420 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.252 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.257 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.409 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.407 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.448 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.406 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.429 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.389 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.374 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.393 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.448 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.460 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.394 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.392 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.324 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.375 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.359 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.540 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.246 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.428 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.304 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.377 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.436 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.649 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.616 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.384 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.528 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.280 |
MOD_N-GLC_2 | 537 | 539 | PF02516 | 0.459 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.568 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.378 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.469 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.295 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.399 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.506 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.334 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.502 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.399 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.247 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.238 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.363 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.396 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.325 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.383 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.412 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.388 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.283 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.238 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.429 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.363 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.573 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.500 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.249 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.241 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.561 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.502 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.483 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.456 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.537 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.306 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.432 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.721 |
MOD_PKB_1 | 157 | 165 | PF00069 | 0.221 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.245 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.358 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.334 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.364 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.379 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.377 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.437 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.340 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.337 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.736 |
MOD_SUMO_rev_2 | 251 | 256 | PF00179 | 0.248 |
MOD_SUMO_rev_2 | 299 | 304 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.251 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.250 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.270 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.230 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.243 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.568 |
TRG_NES_CRM1_1 | 252 | 262 | PF08389 | 0.246 |
TRG_NES_CRM1_1 | 300 | 310 | PF08389 | 0.387 |
TRG_NES_CRM1_1 | 348 | 358 | PF08389 | 0.247 |
TRG_NES_CRM1_1 | 372 | 382 | PF08389 | 0.562 |
TRG_NES_CRM1_1 | 396 | 406 | PF08389 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.239 |
TRG_Pf-PMV_PEXEL_1 | 329 | 334 | PF00026 | 0.227 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 29% | 88% |
A0A0N1I121 | Leptomonas seymouri | 27% | 100% |
A0A0N1I661 | Leptomonas seymouri | 37% | 98% |
A0A0N1I7S5 | Leptomonas seymouri | 36% | 100% |
A0A0S4IHI7 | Bodo saltans | 29% | 72% |
A0A0S4IJN2 | Bodo saltans | 28% | 83% |
A0A0S4ILC9 | Bodo saltans | 38% | 100% |
A0A0S4IN27 | Bodo saltans | 41% | 100% |
A0A0S4IQE4 | Bodo saltans | 26% | 99% |
A0A0S4ISU4 | Bodo saltans | 34% | 85% |
A0A0S4IT62 | Bodo saltans | 37% | 76% |
A0A0S4IU23 | Bodo saltans | 28% | 95% |
A0A0S4IU73 | Bodo saltans | 36% | 100% |
A0A0S4IV96 | Bodo saltans | 36% | 92% |
A0A0S4IVQ8 | Bodo saltans | 33% | 93% |
A0A0S4IW93 | Bodo saltans | 26% | 92% |
A0A0S4IWB9 | Bodo saltans | 32% | 68% |
A0A0S4IY44 | Bodo saltans | 26% | 84% |
A0A0S4J014 | Bodo saltans | 29% | 78% |
A0A0S4J206 | Bodo saltans | 36% | 91% |
A0A0S4J2H8 | Bodo saltans | 27% | 96% |
A0A0S4J4L7 | Bodo saltans | 27% | 76% |
A0A0S4J5A0 | Bodo saltans | 38% | 98% |
A0A0S4J954 | Bodo saltans | 24% | 76% |
A0A0S4JAQ6 | Bodo saltans | 27% | 100% |
A0A0S4JAS1 | Bodo saltans | 35% | 88% |
A0A0S4JB95 | Bodo saltans | 24% | 92% |
A0A0S4JBV9 | Bodo saltans | 30% | 100% |
A0A0S4JD35 | Bodo saltans | 26% | 94% |
A0A0S4JDS1 | Bodo saltans | 25% | 100% |
A0A0S4JDT0 | Bodo saltans | 36% | 85% |
A0A0S4JEK1 | Bodo saltans | 25% | 100% |
A0A0S4JL29 | Bodo saltans | 32% | 100% |
A0A0S4JMF9 | Bodo saltans | 34% | 100% |
A0A0S4JN05 | Bodo saltans | 36% | 67% |
A0A0S4JNU2 | Bodo saltans | 42% | 68% |
A0A0S4JQZ0 | Bodo saltans | 25% | 74% |
A0A0S4JS89 | Bodo saltans | 30% | 100% |
A0A0S4JTM6 | Bodo saltans | 32% | 76% |
A0A0S4JTQ7 | Bodo saltans | 40% | 100% |
A0A0S4JU95 | Bodo saltans | 32% | 74% |
A0A0S4JVI0 | Bodo saltans | 27% | 79% |
A0A0S4KEG2 | Bodo saltans | 27% | 67% |
A0A0S4KGV4 | Bodo saltans | 26% | 100% |
A0A0S4KIR5 | Bodo saltans | 26% | 67% |
A0A0S4KJA7 | Bodo saltans | 26% | 83% |
A0A0S4KK37 | Bodo saltans | 29% | 96% |
A0A3Q8I9A6 | Leishmania donovani | 46% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 43% | 100% |
A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
A0A3Q8IFC2 | Leishmania donovani | 32% | 100% |
A0A3S5H6L9 | Leishmania donovani | 44% | 100% |
A0A3S5H6M3 | Leishmania donovani | 54% | 82% |
A0A3S5H6M4 | Leishmania donovani | 55% | 85% |
A0A3S7WS66 | Leishmania donovani | 55% | 85% |
A4HBX3 | Leishmania braziliensis | 34% | 100% |
A4HVB0 | Leishmania infantum | 49% | 100% |
A4HZ93 | Leishmania infantum | 35% | 100% |
A4I6S3 | Leishmania infantum | 31% | 100% |
B4JTV9 | Drosophila grimshawi | 26% | 90% |
B5DX45 | Drosophila pseudoobscura pseudoobscura | 24% | 89% |
D1GJ51 | Leishmania infantum | 54% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 73% |
E9AGG2 | Leishmania infantum | 55% | 84% |
E9AGG5 | Leishmania infantum | 48% | 100% |
E9AGG7 | Leishmania infantum | 59% | 89% |
E9AGG9 | Leishmania infantum | 60% | 100% |
E9AGH0 | Leishmania infantum | 45% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 79% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 80% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
F4IUU1 | Arabidopsis thaliana | 27% | 69% |
F4JGB6 | Arabidopsis thaliana | 24% | 69% |
F4JTU7 | Arabidopsis thaliana | 24% | 69% |
F4KHA2 | Arabidopsis thaliana | 23% | 71% |
O48851 | Arabidopsis thaliana | 26% | 73% |
O49325 | Arabidopsis thaliana | 23% | 72% |
O49328 | Arabidopsis thaliana | 22% | 70% |
O49879 | Solanum lycopersicum | 24% | 66% |
O80809 | Arabidopsis thaliana | 30% | 78% |
Q1PEN0 | Arabidopsis thaliana | 21% | 78% |
Q25331 | Leishmania major | 46% | 100% |
Q4QC79 | Leishmania major | 35% | 100% |
Q4QGI0 | Leishmania major | 62% | 94% |
Q4QGI4 | Leishmania major | 88% | 100% |
Q4QGI6 | Leishmania major | 57% | 100% |
Q4QGI8 | Leishmania major | 89% | 74% |
Q4QGJ0 | Leishmania major | 56% | 89% |
Q4QGJ2 | Leishmania major | 55% | 86% |
Q4QGJ4 | Leishmania major | 46% | 100% |
Q4QGJ7 | Leishmania major | 46% | 100% |
Q4QGJ9 | Leishmania major | 58% | 95% |
Q4QGK0 | Leishmania major | 61% | 98% |
Q4QGK1 | Leishmania major | 50% | 80% |
Q4QGK2 | Leishmania major | 77% | 100% |
Q4QGK4 | Leishmania major | 54% | 84% |
Q4QGK6 | Leishmania major | 46% | 100% |
Q4QGK8 | Leishmania major | 65% | 100% |
Q4QGL2 | Leishmania major | 65% | 100% |
Q4QGL4 | Leishmania major | 52% | 100% |
Q4QGL8 | Leishmania major | 60% | 92% |
Q4QGM1 | Leishmania major | 83% | 72% |
Q5M8G4 | Xenopus tropicalis | 27% | 93% |
Q6GPJ5 | Xenopus laevis | 25% | 93% |
Q7FZR1 | Arabidopsis thaliana | 25% | 69% |
Q940E8 | Zea mays | 28% | 91% |
Q9C9H6 | Arabidopsis thaliana | 25% | 71% |
Q9C9H7 | Arabidopsis thaliana | 24% | 66% |
Q9LJW7 | Arabidopsis thaliana | 24% | 79% |
Q9LS79 | Arabidopsis thaliana | 24% | 71% |
Q9LS80 | Arabidopsis thaliana | 22% | 67% |
Q9MA83 | Arabidopsis thaliana | 25% | 71% |
Q9SHI3 | Arabidopsis thaliana | 25% | 77% |
Q9SHI4 | Arabidopsis thaliana | 25% | 74% |
Q9SKK5 | Arabidopsis thaliana | 24% | 83% |
Q9SVM3 | Arabidopsis thaliana | 23% | 66% |
Q9SVN2 | Arabidopsis thaliana | 24% | 70% |
Q9ZUK7 | Arabidopsis thaliana | 26% | 68% |