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: 125 |
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: 69, no: 12 |
NetGPI | no | yes: 0, no: 81 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 82 |
GO:0042995 | cell projection | 2 | 82 |
GO:0043226 | organelle | 2 | 82 |
GO:0043227 | membrane-bounded organelle | 3 | 82 |
GO:0110165 | cellular anatomical entity | 1 | 82 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 82 |
GO:0016020 | membrane | 2 | 28 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: Q4QC79
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 | 366 | 370 | PF00656 | 0.228 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.762 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.732 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 129 | 135 | PF00134 | 0.371 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 174 | 183 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 237 | 247 | PF00069 | 0.241 |
DOC_PP1_RVXF_1 | 308 | 314 | PF00149 | 0.260 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.364 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.562 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 31 | 36 | PF00244 | 0.715 |
LIG_AP2alpha_1 | 54 | 58 | PF02296 | 0.266 |
LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.244 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.256 |
LIG_Clathr_ClatBox_1 | 293 | 297 | PF01394 | 0.233 |
LIG_deltaCOP1_diTrp_1 | 235 | 238 | PF00928 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 307 | 313 | PF00928 | 0.510 |
LIG_DLG_GKlike_1 | 214 | 221 | PF00625 | 0.268 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.452 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.336 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.333 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.454 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.397 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.409 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.359 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.352 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.491 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.494 |
LIG_Integrin_isoDGR_2 | 127 | 129 | PF01839 | 0.614 |
LIG_IRF3_LxIS_1 | 337 | 344 | PF10401 | 0.459 |
LIG_LIR_Gen_1 | 259 | 266 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 267 | 276 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 306 | 314 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 331 | 340 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 405 | 416 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 92 | 101 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.585 |
LIG_NRBOX | 289 | 295 | PF00104 | 0.363 |
LIG_NRP_CendR_1 | 454 | 456 | PF00754 | 0.498 |
LIG_Pex14_1 | 404 | 408 | PF04695 | 0.293 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.499 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.329 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 408 | 411 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.434 |
LIG_SH3_2 | 4 | 9 | PF14604 | 0.468 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.619 |
LIG_SUMO_SIM_anti_2 | 193 | 198 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 195 | 200 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 23 | 30 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.430 |
LIG_UBA3_1 | 141 | 147 | PF00899 | 0.271 |
LIG_WW_2 | 4 | 7 | PF00397 | 0.471 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.428 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.344 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.342 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.489 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.609 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.471 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.404 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.393 |
MOD_Cter_Amidation | 452 | 455 | PF01082 | 0.479 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.542 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.388 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.419 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.318 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.405 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.388 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.320 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.339 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.514 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.464 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.354 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.461 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.451 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.331 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.359 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.615 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.346 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.373 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.324 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.315 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.305 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.500 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.588 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.491 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.423 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.311 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.402 |
MOD_N-GLC_2 | 426 | 428 | PF02516 | 0.362 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.402 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.332 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.460 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.355 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.316 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.377 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.279 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.330 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.339 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.339 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.326 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.289 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.279 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.328 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.405 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.363 |
MOD_NEK2_2 | 165 | 170 | PF00069 | 0.508 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.263 |
MOD_OFUCOSY | 75 | 82 | PF10250 | 0.352 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.543 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.458 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.440 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.588 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.506 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.515 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.399 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.243 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.286 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.402 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.358 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.681 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.498 |
TRG_NES_CRM1_1 | 189 | 200 | PF08389 | 0.228 |
TRG_NLS_MonoExtC_3 | 145 | 151 | PF00514 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 39% | 72% |
A0A0N1I121 | Leptomonas seymouri | 28% | 91% |
A0A0N1I661 | Leptomonas seymouri | 32% | 80% |
A0A0N1I7S5 | Leptomonas seymouri | 34% | 90% |
A0A0N1II82 | Leptomonas seymouri | 31% | 66% |
A0A0S4IIK7 | Bodo saltans | 32% | 100% |
A0A0S4IJN2 | Bodo saltans | 30% | 68% |
A0A0S4ILC9 | Bodo saltans | 35% | 83% |
A0A0S4IN27 | Bodo saltans | 38% | 84% |
A0A0S4IQP4 | Bodo saltans | 37% | 100% |
A0A0S4IR61 | Bodo saltans | 33% | 100% |
A0A0S4ISU4 | Bodo saltans | 35% | 69% |
A0A0S4IU23 | Bodo saltans | 30% | 77% |
A0A0S4IU73 | Bodo saltans | 40% | 91% |
A0A0S4IV96 | Bodo saltans | 38% | 75% |
A0A0S4IVN7 | Bodo saltans | 41% | 100% |
A0A0S4IVQ8 | Bodo saltans | 36% | 76% |
A0A0S4IW93 | Bodo saltans | 30% | 75% |
A0A0S4IY44 | Bodo saltans | 29% | 68% |
A0A0S4IZC7 | Bodo saltans | 30% | 100% |
A0A0S4J206 | Bodo saltans | 37% | 74% |
A0A0S4J2H8 | Bodo saltans | 33% | 78% |
A0A0S4J5A0 | Bodo saltans | 34% | 80% |
A0A0S4J7Q5 | Bodo saltans | 30% | 100% |
A0A0S4JAQ6 | Bodo saltans | 29% | 89% |
A0A0S4JAS1 | Bodo saltans | 36% | 72% |
A0A0S4JAW7 | Bodo saltans | 28% | 89% |
A0A0S4JB95 | Bodo saltans | 27% | 75% |
A0A0S4JD35 | Bodo saltans | 34% | 76% |
A0A0S4JDS1 | Bodo saltans | 27% | 86% |
A0A0S4JDT0 | Bodo saltans | 39% | 69% |
A0A0S4JEK1 | Bodo saltans | 30% | 100% |
A0A0S4JEP2 | Bodo saltans | 27% | 78% |
A0A0S4JFC9 | Bodo saltans | 36% | 95% |
A0A0S4JFY5 | Bodo saltans | 40% | 100% |
A0A0S4JL29 | Bodo saltans | 33% | 90% |
A0A0S4JMF9 | Bodo saltans | 34% | 100% |
A0A0S4JMG0 | Bodo saltans | 29% | 100% |
A0A0S4JP43 | Bodo saltans | 39% | 100% |
A0A0S4JQW3 | Bodo saltans | 27% | 100% |
A0A0S4JSB8 | Bodo saltans | 38% | 82% |
A0A0S4JTQ7 | Bodo saltans | 33% | 86% |
A0A0S4KGV4 | Bodo saltans | 27% | 84% |
A0A0S4KHE4 | Bodo saltans | 33% | 100% |
A0A0S4KJA7 | Bodo saltans | 31% | 68% |
A0A0S4KK37 | Bodo saltans | 29% | 78% |
A0A0S4KL26 | Bodo saltans | 29% | 100% |
A0A0S4KMV2 | Bodo saltans | 31% | 100% |
A0A3Q8IC27 | Leishmania donovani | 92% | 96% |
A0A3Q8IIJ9 | Leishmania donovani | 37% | 100% |
A0A3S5H6M3 | Leishmania donovani | 36% | 66% |
A0A3S5H6M4 | Leishmania donovani | 38% | 69% |
A0A3S7WS66 | Leishmania donovani | 38% | 69% |
A0A3S7X4J4 | Leishmania donovani | 37% | 100% |
A4HBX3 | Leishmania braziliensis | 67% | 100% |
A4HJC8 | Leishmania braziliensis | 36% | 100% |
A4HVB0 | Leishmania infantum | 36% | 100% |
A4HZ93 | Leishmania infantum | 92% | 96% |
A4I6S4 | Leishmania infantum | 37% | 100% |
A6NIV6 | Homo sapiens | 27% | 81% |
D1GJ51 | Leishmania infantum | 34% | 98% |
D3ZAL8 | Rattus norvegicus | 25% | 78% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AGG2 | Leishmania infantum | 35% | 69% |
E9AGG7 | Leishmania infantum | 34% | 73% |
E9AGG9 | Leishmania infantum | 38% | 84% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 89% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 99% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
O02833 | Papio hamadryas | 23% | 75% |
O08742 | Mus musculus | 25% | 80% |
P22792 | Homo sapiens | 25% | 84% |
P35858 | Homo sapiens | 25% | 75% |
P35859 | Rattus norvegicus | 24% | 76% |
P70389 | Mus musculus | 25% | 76% |
Q00874 | Arabidopsis thaliana | 28% | 100% |
Q05091 | Pyrus communis | 29% | 100% |
Q1L8Y7 | Danio rerio | 26% | 81% |
Q22875 | Caenorhabditis elegans | 24% | 82% |
Q25331 | Leishmania major | 29% | 100% |
Q4PSE6 | Arabidopsis thaliana | 29% | 100% |
Q4Q6B6 | Leishmania major | 38% | 100% |
Q4Q6B7 | Leishmania major | 38% | 100% |
Q4QGI0 | Leishmania major | 32% | 90% |
Q4QGI2 | Leishmania major | 35% | 81% |
Q4QGI4 | Leishmania major | 36% | 85% |
Q4QGI6 | Leishmania major | 33% | 83% |
Q4QGJ0 | Leishmania major | 33% | 72% |
Q4QGJ2 | Leishmania major | 34% | 70% |
Q4QGJ4 | Leishmania major | 29% | 100% |
Q4QGJ6 | Leishmania major | 33% | 80% |
Q4QGJ7 | Leishmania major | 29% | 100% |
Q4QGJ9 | Leishmania major | 36% | 78% |
Q4QGK0 | Leishmania major | 32% | 80% |
Q4QGK2 | Leishmania major | 35% | 81% |
Q4QGK4 | Leishmania major | 35% | 68% |
Q4QGK6 | Leishmania major | 29% | 100% |
Q4QGK8 | Leishmania major | 36% | 89% |
Q4QGL2 | Leishmania major | 36% | 89% |
Q4QGL4 | Leishmania major | 33% | 100% |
Q4QGL5 | Leishmania major | 32% | 83% |
Q4QGL8 | Leishmania major | 35% | 75% |
Q86VH5 | Homo sapiens | 25% | 78% |
Q8AVI4 | Xenopus laevis | 28% | 79% |
Q8BZ81 | Mus musculus | 25% | 78% |
Q940E8 | Zea mays | 29% | 74% |
Q9BGP6 | Macaca fascicularis | 25% | 78% |
Q9DBB9 | Mus musculus | 27% | 83% |
Q9LHF1 | Arabidopsis thaliana | 26% | 92% |
Q9M5J9 | Arabidopsis thaliana | 28% | 100% |
Q9SKK5 | Arabidopsis thaliana | 27% | 68% |
Q9SSD1 | Arabidopsis thaliana | 27% | 92% |