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: 115 |
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: 55, no: 11 |
NetGPI | no | yes: 0, no: 66 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 67 |
GO:0042995 | cell projection | 2 | 67 |
GO:0043226 | organelle | 2 | 67 |
GO:0043227 | membrane-bounded organelle | 3 | 67 |
GO:0110165 | cellular anatomical entity | 1 | 67 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 67 |
GO:0016020 | membrane | 2 | 24 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: E9AVA1
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 | 51 | 53 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.658 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.453 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 174 | 183 | PF00134 | 0.166 |
DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.204 |
DOC_MAPK_gen_1 | 237 | 247 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 192 | 199 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.591 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.544 |
DOC_USP7_MATH_2 | 160 | 166 | PF00917 | 0.253 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 42 | 49 | PF00244 | 0.535 |
LIG_AP2alpha_1 | 54 | 58 | PF02296 | 0.229 |
LIG_APCC_ABBA_1 | 363 | 368 | PF00400 | 0.205 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.407 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.407 |
LIG_deltaCOP1_diTrp_1 | 235 | 238 | PF00928 | 0.392 |
LIG_deltaCOP1_diTrp_1 | 283 | 289 | PF00928 | 0.472 |
LIG_DLG_GKlike_1 | 214 | 221 | PF00625 | 0.187 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.381 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.277 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.317 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.292 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.341 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.308 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.405 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.521 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.456 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 265 | 276 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 283 | 290 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.407 |
LIG_LIR_LC3C_4 | 167 | 171 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.345 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.229 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.452 |
LIG_SUMO_SIM_anti_2 | 167 | 173 | PF11976 | 0.265 |
LIG_SUMO_SIM_anti_2 | 193 | 198 | PF11976 | 0.178 |
LIG_SUMO_SIM_par_1 | 193 | 198 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.281 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.509 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.364 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.344 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.271 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.474 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.517 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.459 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.412 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.311 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.404 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.423 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.390 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.387 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.310 |
MOD_GlcNHglycan | 251 | 255 | PF01048 | 0.363 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.350 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.346 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.350 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.444 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.497 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.440 |
MOD_GlcNHglycan | 450 | 454 | PF01048 | 0.539 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.433 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.553 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.376 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.377 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.329 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.316 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.314 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.305 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.309 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.551 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.529 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.459 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.520 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.371 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.484 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.334 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.469 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.448 |
MOD_N-GLC_2 | 402 | 404 | PF02516 | 0.543 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.350 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.361 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.365 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.276 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.262 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.330 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.302 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.274 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.290 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.286 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.357 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.291 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.285 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.387 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.350 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.323 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.178 |
MOD_OFUCOSY | 75 | 82 | PF10250 | 0.358 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.499 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.328 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.429 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.446 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.447 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.515 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.325 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.315 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.243 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.288 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.255 |
MOD_Plk_2-3 | 162 | 168 | PF00069 | 0.358 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.353 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.287 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.232 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.599 |
TRG_NES_CRM1_1 | 189 | 200 | PF08389 | 0.149 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 37% | 72% |
A0A0N1I121 | Leptomonas seymouri | 29% | 92% |
A0A0N1I661 | Leptomonas seymouri | 31% | 81% |
A0A0N1I7S5 | Leptomonas seymouri | 31% | 91% |
A0A0N1II82 | Leptomonas seymouri | 33% | 67% |
A0A0S4IIK7 | Bodo saltans | 28% | 100% |
A0A0S4IJN2 | Bodo saltans | 30% | 68% |
A0A0S4IN27 | Bodo saltans | 36% | 85% |
A0A0S4IQP4 | Bodo saltans | 35% | 100% |
A0A0S4IR61 | Bodo saltans | 35% | 100% |
A0A0S4ISU4 | Bodo saltans | 38% | 70% |
A0A0S4IU23 | Bodo saltans | 26% | 78% |
A0A0S4IU73 | Bodo saltans | 39% | 92% |
A0A0S4IV96 | Bodo saltans | 37% | 76% |
A0A0S4IVN7 | Bodo saltans | 40% | 100% |
A0A0S4IVQ8 | Bodo saltans | 34% | 77% |
A0A0S4IW93 | Bodo saltans | 31% | 76% |
A0A0S4IY44 | Bodo saltans | 28% | 69% |
A0A0S4IZC7 | Bodo saltans | 29% | 100% |
A0A0S4J206 | Bodo saltans | 34% | 75% |
A0A0S4J2H8 | Bodo saltans | 30% | 79% |
A0A0S4J3T7 | Bodo saltans | 34% | 100% |
A0A0S4J5A0 | Bodo saltans | 34% | 81% |
A0A0S4JAQ6 | Bodo saltans | 28% | 90% |
A0A0S4JAW7 | Bodo saltans | 28% | 90% |
A0A0S4JB95 | Bodo saltans | 27% | 76% |
A0A0S4JBV9 | Bodo saltans | 30% | 94% |
A0A0S4JCG7 | Bodo saltans | 39% | 100% |
A0A0S4JD35 | Bodo saltans | 30% | 77% |
A0A0S4JDT0 | Bodo saltans | 36% | 70% |
A0A0S4JEK1 | Bodo saltans | 30% | 100% |
A0A0S4JEP2 | Bodo saltans | 27% | 79% |
A0A0S4JFC9 | Bodo saltans | 36% | 96% |
A0A0S4JFY5 | Bodo saltans | 38% | 100% |
A0A0S4JHM1 | Bodo saltans | 31% | 100% |
A0A0S4JL29 | Bodo saltans | 30% | 91% |
A0A0S4JP43 | Bodo saltans | 38% | 100% |
A0A0S4JQW3 | Bodo saltans | 28% | 100% |
A0A0S4JS89 | Bodo saltans | 29% | 100% |
A0A0S4JSB8 | Bodo saltans | 38% | 83% |
A0A0S4KGV4 | Bodo saltans | 25% | 85% |
A0A0S4KH41 | Bodo saltans | 29% | 66% |
A0A0S4KJA7 | Bodo saltans | 29% | 69% |
A0A0S4KK37 | Bodo saltans | 33% | 79% |
A0A0S4KMV2 | Bodo saltans | 31% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 32% | 100% |
A0A3Q8IC27 | Leishmania donovani | 77% | 97% |
A0A3S5H6M3 | Leishmania donovani | 38% | 67% |
A0A3S5H6M4 | Leishmania donovani | 30% | 70% |
A0A3S7WS66 | Leishmania donovani | 30% | 70% |
A4HBX3 | Leishmania braziliensis | 56% | 100% |
A4HVB0 | Leishmania infantum | 29% | 100% |
A4HZ93 | Leishmania infantum | 77% | 97% |
A7PW81 | Vitis vinifera | 29% | 100% |
D1GJ51 | Leishmania infantum | 35% | 100% |
E9AGG2 | Leishmania infantum | 34% | 69% |
E9AGG5 | Leishmania infantum | 36% | 100% |
E9AGG7 | Leishmania infantum | 32% | 74% |
E9AGG9 | Leishmania infantum | 35% | 85% |
E9AGH0 | Leishmania infantum | 35% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 99% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 66% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P35858 | Homo sapiens | 24% | 76% |
Q05091 | Pyrus communis | 30% | 100% |
Q4QC79 | Leishmania major | 70% | 100% |
Q4QGI0 | Leishmania major | 35% | 100% |
Q4QGI2 | Leishmania major | 35% | 82% |
Q4QGI4 | Leishmania major | 35% | 100% |
Q4QGI6 | Leishmania major | 36% | 84% |
Q4QGJ0 | Leishmania major | 32% | 73% |
Q4QGJ2 | Leishmania major | 34% | 100% |
Q4QGJ6 | Leishmania major | 36% | 81% |
Q4QGJ9 | Leishmania major | 34% | 100% |
Q4QGK0 | Leishmania major | 33% | 100% |
Q4QGK2 | Leishmania major | 35% | 100% |
Q4QGK4 | Leishmania major | 34% | 69% |
Q4QGK8 | Leishmania major | 35% | 100% |
Q4QGL2 | Leishmania major | 34% | 100% |
Q4QGL4 | Leishmania major | 36% | 100% |
Q4QGL5 | Leishmania major | 32% | 100% |
Q4QGL8 | Leishmania major | 37% | 76% |
Q5ZLN0 | Gallus gallus | 24% | 76% |
Q940E8 | Zea mays | 26% | 75% |
Q9CRC8 | Mus musculus | 27% | 77% |
Q9M5J9 | Arabidopsis thaliana | 27% | 100% |
Q9SKK5 | Arabidopsis thaliana | 23% | 69% |