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: 60, no: 7 |
NetGPI | no | yes: 0, no: 67 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 68 |
GO:0016020 | membrane | 2 | 32 |
GO:0042995 | cell projection | 2 | 68 |
GO:0043226 | organelle | 2 | 68 |
GO:0043227 | membrane-bounded organelle | 3 | 68 |
GO:0110165 | cellular anatomical entity | 1 | 68 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 68 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: Q4QGI6
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 | 97 | 101 | PF00656 | 0.310 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.775 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.738 |
DEG_SCF_FBW7_2 | 475 | 480 | PF00400 | 0.480 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.504 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.280 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.705 |
DOC_MAPK_gen_1 | 419 | 427 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 133 | 140 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 419 | 427 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 131 | 138 | PF00149 | 0.228 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.509 |
DOC_USP7_MATH_2 | 270 | 276 | PF00917 | 0.398 |
DOC_USP7_MATH_2 | 390 | 396 | PF00917 | 0.354 |
DOC_USP7_UBL2_3 | 512 | 516 | PF12436 | 0.288 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 444 | 452 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 152 | 167 | PF00022 | 0.225 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.683 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.238 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.432 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.284 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.432 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.280 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.384 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.476 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.310 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.416 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.610 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.481 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.559 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.416 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.406 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 134 | 145 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 392 | 399 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.362 |
LIG_PCNA_PIPBox_1 | 324 | 333 | PF02747 | 0.229 |
LIG_PDZ_Class_2 | 542 | 547 | PF00595 | 0.499 |
LIG_PTB_Apo_2 | 136 | 143 | PF02174 | 0.210 |
LIG_PTB_Apo_2 | 184 | 191 | PF02174 | 0.315 |
LIG_PTB_Phospho_1 | 136 | 142 | PF10480 | 0.212 |
LIG_PTB_Phospho_1 | 184 | 190 | PF10480 | 0.216 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.472 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.300 |
LIG_SH2_GRB2like | 190 | 193 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.216 |
LIG_SH2_PTP2 | 190 | 193 | PF00017 | 0.228 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.499 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.609 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.630 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.446 |
LIG_Sin3_3 | 531 | 538 | PF02671 | 0.294 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.291 |
LIG_SUMO_SIM_anti_2 | 208 | 215 | PF11976 | 0.233 |
LIG_SUMO_SIM_anti_2 | 254 | 259 | PF11976 | 0.305 |
LIG_SUMO_SIM_anti_2 | 280 | 287 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 349 | 355 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 232 | 239 | PF11976 | 0.427 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.471 |
LIG_TYR_ITIM | 140 | 145 | PF00017 | 0.302 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.271 |
LIG_UBA3_1 | 136 | 144 | PF00899 | 0.213 |
LIG_UBA3_1 | 257 | 264 | PF00899 | 0.237 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.315 |
LIG_UBA3_1 | 353 | 360 | PF00899 | 0.257 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.243 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.366 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.275 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.366 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.391 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.336 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.325 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.304 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.331 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.403 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.411 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.661 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.576 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.450 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.680 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.565 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.475 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.545 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.594 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.553 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.739 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.580 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.539 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.535 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.564 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.603 |
MOD_GlcNHglycan | 368 | 372 | PF01048 | 0.603 |
MOD_GlcNHglycan | 384 | 388 | PF01048 | 0.561 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.529 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.673 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.483 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.327 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.340 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.265 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.351 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.379 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.393 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.338 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.336 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.332 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.564 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.340 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.564 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.603 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.496 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.375 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.526 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.460 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.529 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.500 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.617 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.383 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.315 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.296 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.261 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.543 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.411 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.436 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.340 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.357 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.366 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.386 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.337 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.311 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.359 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.447 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.348 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.313 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.359 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.579 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.354 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.352 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.450 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.382 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.434 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.291 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.345 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.244 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.374 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.383 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.283 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.335 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.641 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.467 |
MOD_SUMO_rev_2 | 250 | 255 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 504 | 513 | PF00179 | 0.318 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.284 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.728 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 29% | 86% |
A0A0N1I661 | Leptomonas seymouri | 39% | 96% |
A0A0S4IHI7 | Bodo saltans | 25% | 71% |
A0A0S4ILC9 | Bodo saltans | 42% | 99% |
A0A0S4ISU4 | Bodo saltans | 36% | 83% |
A0A0S4IT62 | Bodo saltans | 42% | 74% |
A0A0S4IVQ8 | Bodo saltans | 35% | 91% |
A0A0S4IW93 | Bodo saltans | 27% | 90% |
A0A0S4IWB9 | Bodo saltans | 29% | 66% |
A0A0S4IY44 | Bodo saltans | 26% | 82% |
A0A0S4J014 | Bodo saltans | 25% | 76% |
A0A0S4J2H8 | Bodo saltans | 27% | 94% |
A0A0S4J746 | Bodo saltans | 26% | 78% |
A0A0S4JAQ6 | Bodo saltans | 26% | 100% |
A0A0S4JAS1 | Bodo saltans | 32% | 86% |
A0A0S4JB95 | Bodo saltans | 25% | 90% |
A0A0S4JDT0 | Bodo saltans | 33% | 83% |
A0A0S4JL29 | Bodo saltans | 29% | 100% |
A0A0S4JNU2 | Bodo saltans | 40% | 67% |
A0A0S4JQZ0 | Bodo saltans | 24% | 73% |
A0A0S4JTM6 | Bodo saltans | 28% | 74% |
A0A0S4JTQ7 | Bodo saltans | 40% | 100% |
A0A0S4JVI0 | Bodo saltans | 28% | 77% |
A0A0S4KJA7 | Bodo saltans | 27% | 82% |
A0A0S4KK37 | Bodo saltans | 29% | 94% |
A0A3Q8I9A6 | Leishmania donovani | 47% | 70% |
A0A3Q8IC27 | Leishmania donovani | 32% | 100% |
A0A3S5H6M3 | Leishmania donovani | 55% | 80% |
A0A3S5H6M4 | Leishmania donovani | 50% | 83% |
A0A3S7WS66 | Leishmania donovani | 49% | 83% |
A4HBX3 | Leishmania braziliensis | 34% | 100% |
A4HVB0 | Leishmania infantum | 50% | 100% |
A4HZ93 | Leishmania infantum | 32% | 100% |
D1GJ51 | Leishmania infantum | 61% | 100% |
E9AGG2 | Leishmania infantum | 54% | 82% |
E9AGG5 | Leishmania infantum | 61% | 100% |
E9AGG7 | Leishmania infantum | 59% | 87% |
E9AGG9 | Leishmania infantum | 54% | 100% |
E9AGH0 | Leishmania infantum | 48% | 69% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 77% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 71% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 78% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 74% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
F4IUU1 | Arabidopsis thaliana | 23% | 68% |
F4JGB6 | Arabidopsis thaliana | 26% | 67% |
F4JTU7 | Arabidopsis thaliana | 24% | 67% |
F4KHA2 | Arabidopsis thaliana | 24% | 69% |
O48851 | Arabidopsis thaliana | 24% | 71% |
O80809 | Arabidopsis thaliana | 23% | 76% |
Q1PEN0 | Arabidopsis thaliana | 24% | 76% |
Q25331 | Leishmania major | 72% | 100% |
Q4QC79 | Leishmania major | 33% | 100% |
Q4QGI0 | Leishmania major | 61% | 100% |
Q4QGI2 | Leishmania major | 57% | 100% |
Q4QGI4 | Leishmania major | 56% | 100% |
Q4QGI8 | Leishmania major | 57% | 72% |
Q4QGJ0 | Leishmania major | 58% | 87% |
Q4QGJ2 | Leishmania major | 58% | 84% |
Q4QGJ4 | Leishmania major | 71% | 100% |
Q4QGJ6 | Leishmania major | 54% | 100% |
Q4QGJ7 | Leishmania major | 71% | 100% |
Q4QGJ9 | Leishmania major | 60% | 93% |
Q4QGK0 | Leishmania major | 61% | 96% |
Q4QGK1 | Leishmania major | 58% | 78% |
Q4QGK2 | Leishmania major | 51% | 98% |
Q4QGK4 | Leishmania major | 57% | 82% |
Q4QGK6 | Leishmania major | 72% | 100% |
Q4QGK8 | Leishmania major | 55% | 100% |
Q4QGL2 | Leishmania major | 55% | 100% |
Q4QGL4 | Leishmania major | 65% | 100% |
Q4QGL5 | Leishmania major | 51% | 100% |
Q4QGL8 | Leishmania major | 59% | 90% |
Q4QGM1 | Leishmania major | 57% | 70% |
Q7FZR1 | Arabidopsis thaliana | 21% | 67% |
Q9C9H6 | Arabidopsis thaliana | 22% | 70% |
Q9LJW7 | Arabidopsis thaliana | 24% | 77% |
Q9LS79 | Arabidopsis thaliana | 22% | 70% |
Q9SHI3 | Arabidopsis thaliana | 24% | 75% |
Q9SVN2 | Arabidopsis thaliana | 24% | 68% |
Q9ZU46 | Arabidopsis thaliana | 26% | 76% |
Q9ZUK7 | Arabidopsis thaliana | 22% | 66% |