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: 105 |
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: 39, no: 6 |
NetGPI | no | yes: 0, no: 45 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 46 |
GO:0016020 | membrane | 2 | 26 |
GO:0042995 | cell projection | 2 | 46 |
GO:0043226 | organelle | 2 | 46 |
GO:0043227 | membrane-bounded organelle | 3 | 46 |
GO:0110165 | cellular anatomical entity | 1 | 46 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 46 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: A0A3S5H6M3
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_NRD_NRD_1 | 282 | 284 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.706 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.252 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.393 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.388 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.407 |
DEG_SPOP_SBC_1 | 494 | 498 | PF00917 | 0.399 |
DEG_SPOP_SBC_1 | 509 | 513 | PF00917 | 0.534 |
DEG_SPOP_SBC_1 | 524 | 528 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 532 | 536 | PF00917 | 0.544 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.384 |
DEG_SPOP_SBC_1 | 555 | 559 | PF00917 | 0.390 |
DEG_SPOP_SBC_1 | 570 | 574 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 578 | 582 | PF00917 | 0.598 |
DEG_SPOP_SBC_1 | 593 | 597 | PF00917 | 0.402 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.248 |
DOC_CYCLIN_RxL_1 | 107 | 116 | PF00134 | 0.238 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.232 |
DOC_MAPK_gen_1 | 228 | 238 | PF00069 | 0.203 |
DOC_MAPK_gen_1 | 240 | 249 | PF00069 | 0.198 |
DOC_MAPK_gen_1 | 351 | 358 | PF00069 | 0.211 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 446 | 453 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.280 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.490 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.343 |
DOC_USP7_MATH_2 | 224 | 230 | PF00917 | 0.257 |
DOC_USP7_MATH_2 | 320 | 326 | PF00917 | 0.296 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 31 | 38 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 426 | 431 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.417 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.660 |
LIG_deltaCOP1_diTrp_1 | 177 | 185 | PF00928 | 0.328 |
LIG_DLG_GKlike_1 | 209 | 216 | PF00625 | 0.202 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.250 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.319 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.312 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.364 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.323 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.435 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.451 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.387 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.222 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.566 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.569 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.408 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.394 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 128 | 136 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 232 | 243 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 370 | 378 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 418 | 427 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 152 | 156 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 370 | 374 | PF02991 | 0.273 |
LIG_NRBOX | 352 | 358 | PF00104 | 0.341 |
LIG_PCNA_PIPBox_1 | 326 | 335 | PF02747 | 0.245 |
LIG_PDZ_Class_2 | 681 | 686 | PF00595 | 0.236 |
LIG_PTAP_UEV_1 | 589 | 594 | PF05743 | 0.373 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.239 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.205 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.187 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.212 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.227 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.574 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.594 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.429 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.280 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.411 |
LIG_TYR_ITIM | 184 | 189 | PF00017 | 0.227 |
LIG_TYR_ITIM | 233 | 238 | PF00017 | 0.321 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.276 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.323 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.275 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.290 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.261 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.307 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.293 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.273 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.341 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.357 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.352 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.516 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.405 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.356 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.201 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.515 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.556 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.412 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.418 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.573 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.535 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.529 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.494 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.555 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.487 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.549 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.729 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.531 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.615 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.539 |
MOD_GlcNHglycan | 370 | 374 | PF01048 | 0.538 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.578 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.614 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.602 |
MOD_GlcNHglycan | 410 | 414 | PF01048 | 0.605 |
MOD_GlcNHglycan | 418 | 422 | PF01048 | 0.629 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.693 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.439 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.542 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.374 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.247 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.310 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.342 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.303 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.308 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.272 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.601 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.320 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.489 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.497 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.450 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.437 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.439 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.460 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.442 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.448 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.444 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.488 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.484 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.435 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.454 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.480 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.517 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.408 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.277 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.341 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.466 |
MOD_N-GLC_2 | 460 | 462 | PF02516 | 0.526 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.616 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.327 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.321 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.262 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.308 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.262 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.338 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.340 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.405 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.285 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.299 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.330 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.382 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.262 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.216 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.417 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.282 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.294 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.279 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.301 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.551 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.223 |
MOD_PKB_1 | 424 | 432 | PF00069 | 0.314 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.248 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.314 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.248 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.355 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.295 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.471 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.230 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.314 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.245 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.274 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.221 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.268 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.275 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.602 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.204 |
MOD_SUMO_rev_2 | 306 | 316 | PF00179 | 0.209 |
MOD_SUMO_rev_2 | 452 | 458 | PF00179 | 0.267 |
TRG_DiLeu_BaEn_1 | 650 | 655 | PF01217 | 0.325 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.197 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.232 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.240 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.708 |
TRG_NES_CRM1_1 | 301 | 312 | PF08389 | 0.203 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0R0HPY5 | Glycine max | 25% | 70% |
A0A0S4ILX2 | Bodo saltans | 26% | 70% |
A0A0S4IRQ2 | Bodo saltans | 33% | 80% |
A0A0S4IXY3 | Bodo saltans | 23% | 68% |
A0A0S4J014 | Bodo saltans | 26% | 96% |
A0A0S4J100 | Bodo saltans | 26% | 82% |
A0A0S4J1D6 | Bodo saltans | 25% | 70% |
A0A0S4J206 | Bodo saltans | 35% | 100% |
A0A0S4J2H8 | Bodo saltans | 26% | 100% |
A0A0S4J954 | Bodo saltans | 24% | 93% |
A0A0S4J985 | Bodo saltans | 30% | 69% |
A0A0S4JB95 | Bodo saltans | 24% | 100% |
A0A0S4JJG7 | Bodo saltans | 25% | 66% |
A0A0S4JNU2 | Bodo saltans | 34% | 84% |
A0A0S4JQZ4 | Bodo saltans | 32% | 68% |
A0A0S4JTQ7 | Bodo saltans | 35% | 100% |
A0A0S4KIR5 | Bodo saltans | 22% | 82% |
A0A1X0ND37 | Trypanosomatidae | 25% | 72% |
A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
A0A3S5H6M4 | Leishmania donovani | 65% | 100% |
A0A3S7WS66 | Leishmania donovani | 65% | 100% |
A4H6Y8 | Leishmania braziliensis | 46% | 75% |
A4HBX3 | Leishmania braziliensis | 36% | 100% |
A4HM88 | Leishmania braziliensis | 26% | 79% |
A4HZ93 | Leishmania infantum | 35% | 100% |
C0LGT6 | Arabidopsis thaliana | 22% | 67% |
D1GJ51 | Leishmania infantum | 59% | 100% |
E9AGG2 | Leishmania infantum | 91% | 100% |
E9AGG7 | Leishmania infantum | 59% | 100% |
E9AGG9 | Leishmania infantum | 54% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 97% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 98% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
F4I9S3 | Arabidopsis thaliana | 23% | 74% |
F4K4T3 | Arabidopsis thaliana | 22% | 72% |
Q4QC79 | Leishmania major | 36% | 100% |
Q4QGI0 | Leishmania major | 58% | 100% |
Q4QGI2 | Leishmania major | 54% | 100% |
Q4QGI4 | Leishmania major | 52% | 100% |
Q4QGI6 | Leishmania major | 55% | 100% |
Q4QGI8 | Leishmania major | 52% | 90% |
Q4QGJ0 | Leishmania major | 80% | 100% |
Q4QGJ2 | Leishmania major | 59% | 100% |
Q4QGJ9 | Leishmania major | 61% | 100% |
Q4QGK0 | Leishmania major | 58% | 100% |
Q4QGK1 | Leishmania major | 79% | 97% |
Q4QGK2 | Leishmania major | 53% | 100% |
Q4QGK4 | Leishmania major | 59% | 100% |
Q4QGK8 | Leishmania major | 54% | 100% |
Q4QGL2 | Leishmania major | 54% | 100% |
Q4QGL8 | Leishmania major | 54% | 100% |
Q4QGM1 | Leishmania major | 52% | 88% |
Q69SP5 | Oryza sativa subsp. japonica | 23% | 70% |
Q8LPB4 | Daucus carota | 22% | 67% |
Q9FN37 | Arabidopsis thaliana | 22% | 66% |
Q9LY03 | Arabidopsis thaliana | 25% | 71% |
Q9M0G7 | Arabidopsis thaliana | 25% | 68% |
Q9SVM3 | Arabidopsis thaliana | 21% | 81% |
Q9SVN2 | Arabidopsis thaliana | 23% | 86% |