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: 160 |
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: 71, no: 14 |
NetGPI | no | yes: 0, no: 85 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 86 |
GO:0042995 | cell projection | 2 | 86 |
GO:0043226 | organelle | 2 | 86 |
GO:0043227 | membrane-bounded organelle | 3 | 86 |
GO:0110165 | cellular anatomical entity | 1 | 86 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 86 |
GO:0016020 | membrane | 2 | 34 |
GO:0005886 | plasma membrane | 3 | 7 |
Related structures:
AlphaFold database: E9AP05
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 | 124 | 128 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.766 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.752 |
DEG_SPOP_SBC_1 | 499 | 503 | PF00917 | 0.476 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.333 |
DOC_CYCLIN_RxL_1 | 185 | 197 | PF00134 | 0.351 |
DOC_CYCLIN_RxL_1 | 399 | 409 | PF00134 | 0.245 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.695 |
DOC_MAPK_gen_1 | 469 | 477 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 469 | 477 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.369 |
DOC_MAPK_NFAT4_5 | 482 | 490 | PF00069 | 0.299 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.360 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.688 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.439 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.515 |
DOC_USP7_MATH_2 | 344 | 350 | PF00917 | 0.291 |
DOC_USP7_MATH_2 | 368 | 374 | PF00917 | 0.262 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.282 |
LIG_14-3-3_CanoR_1 | 258 | 263 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 311 | 319 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 504 | 512 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 298 | 313 | PF00022 | 0.526 |
LIG_Actin_WH2_2 | 346 | 361 | PF00022 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.566 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.500 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.353 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.471 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.395 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.404 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.362 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.375 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.556 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.353 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.445 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.555 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.440 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.510 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.534 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 201 | 208 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 346 | 355 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 71 | 79 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 346 | 350 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.420 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.529 |
LIG_PCNA_PIPBox_1 | 156 | 165 | PF02747 | 0.501 |
LIG_PCNA_PIPBox_1 | 230 | 239 | PF02747 | 0.422 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.543 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.310 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.511 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 240 | 244 | PF00017 | 0.239 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.558 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 328 | 333 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 375 | 381 | PF11976 | 0.515 |
LIG_SUMO_SIM_anti_2 | 423 | 429 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.314 |
LIG_SxIP_EBH_1 | 439 | 450 | PF03271 | 0.250 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.570 |
LIG_TYR_ITIM | 238 | 243 | PF00017 | 0.498 |
LIG_TYR_ITIM | 382 | 387 | PF00017 | 0.563 |
LIG_UBA3_1 | 331 | 338 | PF00899 | 0.502 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.479 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.453 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.380 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.405 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.517 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.336 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.402 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.321 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.491 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.544 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.447 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.492 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.389 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.408 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.314 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.362 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.303 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.566 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.553 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.517 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.482 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.466 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.500 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.681 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.371 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.431 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.411 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.593 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.465 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.496 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.438 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.496 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.593 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.360 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.529 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.472 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.384 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.379 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.407 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.509 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.374 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.606 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.376 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.328 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.337 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.488 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.416 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.362 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.305 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.422 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.382 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.389 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.375 |
MOD_N-GLC_2 | 490 | 492 | PF02516 | 0.589 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.495 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.407 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.461 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.531 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.335 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.362 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.423 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.496 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.556 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.413 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.447 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.344 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.575 |
MOD_OFUCOSY | 70 | 77 | PF10250 | 0.404 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.259 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.314 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.419 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.339 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.388 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.301 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.536 |
MOD_PK_1 | 258 | 264 | PF00069 | 0.390 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.462 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.482 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.293 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.298 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.418 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.284 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.552 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.362 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.537 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.346 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.381 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.349 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.401 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.360 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.491 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.402 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.361 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.247 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.759 |
TRG_Pf-PMV_PEXEL_1 | 160 | 165 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 30% | 81% |
A0A0N1I121 | Leptomonas seymouri | 26% | 100% |
A0A0N1I661 | Leptomonas seymouri | 37% | 90% |
A0A0N1I7S5 | Leptomonas seymouri | 35% | 100% |
A0A0N1II82 | Leptomonas seymouri | 30% | 75% |
A0A0S4IHI7 | Bodo saltans | 29% | 66% |
A0A0S4IIK7 | Bodo saltans | 27% | 100% |
A0A0S4IJN2 | Bodo saltans | 28% | 76% |
A0A0S4ILC9 | Bodo saltans | 41% | 93% |
A0A0S4IN27 | Bodo saltans | 41% | 95% |
A0A0S4IQE4 | Bodo saltans | 26% | 91% |
A0A0S4ISU4 | Bodo saltans | 35% | 78% |
A0A0S4IT62 | Bodo saltans | 42% | 69% |
A0A0S4IU23 | Bodo saltans | 30% | 87% |
A0A0S4IU73 | Bodo saltans | 39% | 100% |
A0A0S4IV96 | Bodo saltans | 37% | 85% |
A0A0S4IVN7 | Bodo saltans | 36% | 100% |
A0A0S4IVQ8 | Bodo saltans | 36% | 85% |
A0A0S4IW93 | Bodo saltans | 27% | 85% |
A0A0S4IY44 | Bodo saltans | 26% | 77% |
A0A0S4IZC7 | Bodo saltans | 29% | 100% |
A0A0S4J014 | Bodo saltans | 28% | 72% |
A0A0S4J1A6 | Bodo saltans | 31% | 100% |
A0A0S4J206 | Bodo saltans | 34% | 84% |
A0A0S4J2H8 | Bodo saltans | 31% | 88% |
A0A0S4J3T7 | Bodo saltans | 34% | 100% |
A0A0S4J4L7 | Bodo saltans | 24% | 70% |
A0A0S4J5A0 | Bodo saltans | 36% | 90% |
A0A0S4J746 | Bodo saltans | 27% | 74% |
A0A0S4J954 | Bodo saltans | 27% | 69% |
A0A0S4JAQ6 | Bodo saltans | 30% | 100% |
A0A0S4JAS1 | Bodo saltans | 33% | 81% |
A0A0S4JAW7 | Bodo saltans | 28% | 100% |
A0A0S4JB95 | Bodo saltans | 24% | 85% |
A0A0S4JBV9 | Bodo saltans | 28% | 100% |
A0A0S4JCG7 | Bodo saltans | 40% | 100% |
A0A0S4JD35 | Bodo saltans | 30% | 86% |
A0A0S4JDS1 | Bodo saltans | 26% | 97% |
A0A0S4JDT0 | Bodo saltans | 30% | 78% |
A0A0S4JEK1 | Bodo saltans | 28% | 100% |
A0A0S4JFY5 | Bodo saltans | 34% | 100% |
A0A0S4JGN7 | Bodo saltans | 27% | 73% |
A0A0S4JL29 | Bodo saltans | 33% | 100% |
A0A0S4JQW3 | Bodo saltans | 23% | 100% |
A0A0S4JQZ0 | Bodo saltans | 27% | 68% |
A0A0S4JS89 | Bodo saltans | 25% | 100% |
A0A0S4JSB8 | Bodo saltans | 38% | 92% |
A0A0S4JTM6 | Bodo saltans | 39% | 70% |
A0A0S4JTQ7 | Bodo saltans | 38% | 97% |
A0A0S4JU95 | Bodo saltans | 33% | 68% |
A0A0S4JVI0 | Bodo saltans | 28% | 72% |
A0A0S4KGV4 | Bodo saltans | 24% | 94% |
A0A0S4KH41 | Bodo saltans | 29% | 74% |
A0A0S4KHE4 | Bodo saltans | 30% | 100% |
A0A0S4KJA7 | Bodo saltans | 25% | 77% |
A0A0S4KK37 | Bodo saltans | 31% | 88% |
A0A3Q8I9A6 | Leishmania donovani | 49% | 100% |
A0A3Q8IC27 | Leishmania donovani | 39% | 100% |
A0A3S5H6M3 | Leishmania donovani | 52% | 75% |
A0A3S5H6M4 | Leishmania donovani | 54% | 78% |
A0A3S7WS66 | Leishmania donovani | 54% | 78% |
A0N0X6 | Bos taurus | 24% | 72% |
A4HBX3 | Leishmania braziliensis | 34% | 98% |
A4HVB0 | Leishmania infantum | 46% | 100% |
A4HZ93 | Leishmania infantum | 40% | 100% |
A7SFP1 | Nematostella vectensis | 24% | 89% |
A8XWW4 | Caenorhabditis briggsae | 25% | 92% |
D1GJ51 | Leishmania infantum | 57% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 67% |
E9AGG2 | Leishmania infantum | 53% | 77% |
E9AGG5 | Leishmania infantum | 48% | 100% |
E9AGG7 | Leishmania infantum | 58% | 82% |
E9AGG9 | Leishmania infantum | 67% | 95% |
E9AGH0 | Leishmania infantum | 48% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
O48851 | Arabidopsis thaliana | 23% | 67% |
O49325 | Arabidopsis thaliana | 23% | 66% |
O80809 | Arabidopsis thaliana | 25% | 71% |
P35859 | Rattus norvegicus | 22% | 85% |
Q1PEN0 | Arabidopsis thaliana | 23% | 72% |
Q22875 | Caenorhabditis elegans | 23% | 92% |
Q25331 | Leishmania major | 49% | 100% |
Q32Q07 | Rattus norvegicus | 23% | 72% |
Q4QC79 | Leishmania major | 37% | 100% |
Q4QGI0 | Leishmania major | 73% | 100% |
Q4QGI2 | Leishmania major | 52% | 100% |
Q4QGI4 | Leishmania major | 56% | 100% |
Q4QGI6 | Leishmania major | 53% | 100% |
Q4QGI8 | Leishmania major | 52% | 100% |
Q4QGJ0 | Leishmania major | 55% | 100% |
Q4QGJ2 | Leishmania major | 51% | 100% |
Q4QGJ4 | Leishmania major | 49% | 100% |
Q4QGJ6 | Leishmania major | 47% | 100% |
Q4QGJ7 | Leishmania major | 49% | 100% |
Q4QGJ9 | Leishmania major | 54% | 100% |
Q4QGK0 | Leishmania major | 51% | 100% |
Q4QGK1 | Leishmania major | 55% | 100% |
Q4QGK2 | Leishmania major | 49% | 100% |
Q4QGK4 | Leishmania major | 51% | 100% |
Q4QGK6 | Leishmania major | 50% | 100% |
Q4QGK8 | Leishmania major | 57% | 100% |
Q4QGL2 | Leishmania major | 57% | 100% |
Q4QGL4 | Leishmania major | 51% | 100% |
Q4QGL5 | Leishmania major | 44% | 100% |
Q4QGL8 | Leishmania major | 53% | 100% |
Q4QGM1 | Leishmania major | 57% | 66% |
Q54AX5 | Dictyostelium discoideum | 22% | 100% |
Q5F4C4 | Gallus gallus | 26% | 97% |
Q61809 | Mus musculus | 24% | 72% |
Q6P3Y9 | Mus musculus | 25% | 92% |
Q6UXK5 | Homo sapiens | 23% | 72% |
Q8AVI4 | Xenopus laevis | 25% | 89% |
Q8R5M3 | Rattus norvegicus | 23% | 89% |
Q940E8 | Zea mays | 26% | 84% |
Q9DBB9 | Mus musculus | 25% | 94% |
Q9LJW7 | Arabidopsis thaliana | 26% | 72% |
Q9SHI3 | Arabidopsis thaliana | 25% | 71% |
Q9SHI4 | Arabidopsis thaliana | 23% | 68% |
Q9SKK5 | Arabidopsis thaliana | 22% | 77% |