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: 60 |
| 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: 29, no: 1 |
| NetGPI | no | yes: 0, no: 30 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005929 | cilium | 4 | 31 |
| GO:0042995 | cell projection | 2 | 31 |
| GO:0043226 | organelle | 2 | 31 |
| GO:0043227 | membrane-bounded organelle | 3 | 31 |
| GO:0110165 | cellular anatomical entity | 1 | 31 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 31 |
| GO:0016020 | membrane | 2 | 10 |
| GO:0005886 | plasma membrane | 3 | 2 |
Related structures:
AlphaFold database: A0A3Q8IFC2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 1 |
| GO:0004672 | protein kinase activity | 3 | 1 |
| GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
| GO:0016301 | kinase activity | 4 | 1 |
| GO:0016740 | transferase activity | 2 | 1 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.275 |
| CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.478 |
| CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.509 |
| CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.651 |
| CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.478 |
| CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.506 |
| CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.651 |
| CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.552 |
| CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.553 |
| CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.531 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.471 |
| DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.481 |
| DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.468 |
| DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.449 |
| DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.467 |
| DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.465 |
| DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.460 |
| DEG_SPOP_SBC_1 | 336 | 340 | PF00917 | 0.468 |
| DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.473 |
| DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.468 |
| DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.460 |
| DOC_MAPK_gen_1 | 264 | 272 | PF00069 | 0.337 |
| DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.266 |
| DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.252 |
| DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.243 |
| DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.279 |
| DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.265 |
| DOC_USP7_MATH_2 | 212 | 218 | PF00917 | 0.285 |
| DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.433 |
| LIG_14-3-3_CanoR_1 | 171 | 176 | PF00244 | 0.300 |
| LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.314 |
| LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.335 |
| LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.297 |
| LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.347 |
| LIG_Actin_WH2_2 | 156 | 173 | PF00022 | 0.255 |
| LIG_BIR_III_2 | 47 | 51 | PF00653 | 0.335 |
| LIG_deltaCOP1_diTrp_1 | 261 | 268 | PF00928 | 0.298 |
| LIG_eIF4E_1 | 92 | 98 | PF01652 | 0.246 |
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.251 |
| LIG_FHA_1 | 197 | 203 | PF00498 | 0.290 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.335 |
| LIG_FHA_1 | 60 | 66 | PF00498 | 0.380 |
| LIG_FHA_1 | 9 | 15 | PF00498 | 0.435 |
| LIG_FHA_2 | 106 | 112 | PF00498 | 0.450 |
| LIG_FHA_2 | 290 | 296 | PF00498 | 0.445 |
| LIG_FHA_2 | 298 | 304 | PF00498 | 0.443 |
| LIG_FHA_2 | 306 | 312 | PF00498 | 0.431 |
| LIG_FHA_2 | 314 | 320 | PF00498 | 0.449 |
| LIG_FHA_2 | 322 | 328 | PF00498 | 0.460 |
| LIG_FHA_2 | 330 | 336 | PF00498 | 0.455 |
| LIG_FHA_2 | 338 | 344 | PF00498 | 0.462 |
| LIG_FHA_2 | 346 | 352 | PF00498 | 0.459 |
| LIG_FHA_2 | 354 | 360 | PF00498 | 0.458 |
| LIG_FHA_2 | 362 | 368 | PF00498 | 0.460 |
| LIG_FHA_2 | 384 | 390 | PF00498 | 0.306 |
| LIG_LIR_Gen_1 | 117 | 126 | PF02991 | 0.290 |
| LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.374 |
| LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.291 |
| LIG_LIR_Gen_1 | 238 | 245 | PF02991 | 0.306 |
| LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.295 |
| LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.347 |
| LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.317 |
| LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.298 |
| LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.318 |
| LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.318 |
| LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.272 |
| LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.259 |
| LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.270 |
| LIG_SH3_3 | 107 | 113 | PF00018 | 0.344 |
| LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.259 |
| LIG_TYR_ITIM | 116 | 121 | PF00017 | 0.360 |
| MOD_CK1_1 | 101 | 107 | PF00069 | 0.329 |
| MOD_CK1_1 | 133 | 139 | PF00069 | 0.303 |
| MOD_CK1_1 | 166 | 172 | PF00069 | 0.415 |
| MOD_CK1_1 | 190 | 196 | PF00069 | 0.383 |
| MOD_CK1_1 | 217 | 223 | PF00069 | 0.351 |
| MOD_CK1_1 | 274 | 280 | PF00069 | 0.383 |
| MOD_CK1_1 | 413 | 419 | PF00069 | 0.430 |
| MOD_CK1_1 | 53 | 59 | PF00069 | 0.365 |
| MOD_CK2_1 | 289 | 295 | PF00069 | 0.450 |
| MOD_CK2_1 | 297 | 303 | PF00069 | 0.451 |
| MOD_CK2_1 | 305 | 311 | PF00069 | 0.436 |
| MOD_CK2_1 | 313 | 319 | PF00069 | 0.449 |
| MOD_CK2_1 | 321 | 327 | PF00069 | 0.458 |
| MOD_CK2_1 | 329 | 335 | PF00069 | 0.445 |
| MOD_CK2_1 | 337 | 343 | PF00069 | 0.461 |
| MOD_CK2_1 | 345 | 351 | PF00069 | 0.464 |
| MOD_CK2_1 | 353 | 359 | PF00069 | 0.463 |
| MOD_CK2_1 | 361 | 367 | PF00069 | 0.476 |
| MOD_CK2_1 | 43 | 49 | PF00069 | 0.355 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.550 |
| MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.546 |
| MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.512 |
| MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.556 |
| MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.544 |
| MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.609 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.334 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.368 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.350 |
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.286 |
| MOD_GSK3_1 | 183 | 190 | PF00069 | 0.335 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.388 |
| MOD_GSK3_1 | 213 | 220 | PF00069 | 0.341 |
| MOD_GSK3_1 | 231 | 238 | PF00069 | 0.335 |
| MOD_GSK3_1 | 264 | 271 | PF00069 | 0.330 |
| MOD_GSK3_1 | 283 | 290 | PF00069 | 0.421 |
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.477 |
| MOD_GSK3_1 | 299 | 306 | PF00069 | 0.487 |
| MOD_GSK3_1 | 307 | 314 | PF00069 | 0.561 |
| MOD_GSK3_1 | 315 | 322 | PF00069 | 0.553 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.467 |
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.467 |
| MOD_GSK3_1 | 339 | 346 | PF00069 | 0.473 |
| MOD_GSK3_1 | 347 | 354 | PF00069 | 0.475 |
| MOD_GSK3_1 | 355 | 362 | PF00069 | 0.497 |
| MOD_GSK3_1 | 363 | 370 | PF00069 | 0.452 |
| MOD_GSK3_1 | 410 | 417 | PF00069 | 0.537 |
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.373 |
| MOD_N-GLC_2 | 254 | 256 | PF02516 | 0.517 |
| MOD_N-GLC_2 | 285 | 287 | PF02516 | 0.578 |
| MOD_NEK2_1 | 122 | 127 | PF00069 | 0.351 |
| MOD_NEK2_1 | 154 | 159 | PF00069 | 0.262 |
| MOD_NEK2_1 | 202 | 207 | PF00069 | 0.271 |
| MOD_NEK2_1 | 231 | 236 | PF00069 | 0.318 |
| MOD_NEK2_1 | 98 | 103 | PF00069 | 0.312 |
| MOD_NEK2_2 | 87 | 92 | PF00069 | 0.248 |
| MOD_OFUCOSY | 281 | 287 | PF10250 | 0.508 |
| MOD_OFUCOSY | 84 | 91 | PF10250 | 0.483 |
| MOD_PIKK_1 | 202 | 208 | PF00454 | 0.266 |
| MOD_PIKK_1 | 271 | 277 | PF00454 | 0.280 |
| MOD_PK_1 | 85 | 91 | PF00069 | 0.287 |
| MOD_PKA_1 | 246 | 252 | PF00069 | 0.271 |
| MOD_PKA_1 | 264 | 270 | PF00069 | 0.289 |
| MOD_PKA_1 | 405 | 411 | PF00069 | 0.378 |
| MOD_PKA_2 | 246 | 252 | PF00069 | 0.340 |
| MOD_PKA_2 | 264 | 270 | PF00069 | 0.290 |
| MOD_PKA_2 | 405 | 411 | PF00069 | 0.378 |
| MOD_PKA_2 | 43 | 49 | PF00069 | 0.366 |
| MOD_PKA_2 | 50 | 56 | PF00069 | 0.304 |
| MOD_Plk_1 | 116 | 122 | PF00069 | 0.349 |
| MOD_Plk_1 | 213 | 219 | PF00069 | 0.283 |
| MOD_Plk_2-3 | 367 | 373 | PF00069 | 0.381 |
| MOD_Plk_4 | 171 | 177 | PF00069 | 0.270 |
| MOD_Plk_4 | 196 | 202 | PF00069 | 0.300 |
| MOD_Plk_4 | 246 | 252 | PF00069 | 0.311 |
| MOD_Plk_4 | 92 | 98 | PF00069 | 0.298 |
| MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.434 |
| TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.403 |
| TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.561 |
| TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.367 |
| TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.288 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I121 | Leptomonas seymouri | 27% | 87% |
| A0A3Q8IIJ9 | Leishmania donovani | 33% | 100% |
| A0A3S7X4J4 | Leishmania donovani | 33% | 100% |
| A4H4D2 | Leishmania braziliensis | 26% | 100% |
| A4HJC8 | Leishmania braziliensis | 32% | 100% |
| A4HJX1 | Leishmania braziliensis | 66% | 100% |
| A4HVB0 | Leishmania infantum | 36% | 100% |
| A4I6S4 | Leishmania infantum | 33% | 100% |
| D1GJ51 | Leishmania infantum | 32% | 94% |
| E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
| E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
| E9AEF4 | Leishmania major | 86% | 100% |
| E9AGG5 | Leishmania infantum | 38% | 100% |
| E9AGH0 | Leishmania infantum | 38% | 100% |
| E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
| E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
| E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
| E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 96% |
| E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
| Q25331 | Leishmania major | 40% | 100% |
| Q4Q6B6 | Leishmania major | 32% | 100% |
| Q4Q6B7 | Leishmania major | 32% | 100% |
| Q4QGI2 | Leishmania major | 32% | 78% |
| Q4QGI4 | Leishmania major | 32% | 81% |
| Q4QGJ4 | Leishmania major | 40% | 100% |
| Q4QGJ6 | Leishmania major | 36% | 76% |
| Q4QGK6 | Leishmania major | 40% | 100% |
| Q4QGL4 | Leishmania major | 40% | 100% |
| Q4QGL5 | Leishmania major | 34% | 80% |