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: 120 |
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: 58, no: 12 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 71 |
GO:0042995 | cell projection | 2 | 71 |
GO:0043226 | organelle | 2 | 71 |
GO:0043227 | membrane-bounded organelle | 3 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 71 |
GO:0016020 | membrane | 2 | 29 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: A4HZ93
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 | 447 | 451 | PF00656 | 0.415 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.505 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.228 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.391 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 121 | 127 | PF00134 | 0.421 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 142 | 151 | PF00134 | 0.224 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 166 | 175 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 206 | 215 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 229 | 239 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 300 | 306 | PF00149 | 0.504 |
DOC_PP2B_LxvP_1 | 17 | 20 | PF13499 | 0.582 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.496 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.358 |
LIG_AP2alpha_1 | 46 | 50 | PF02296 | 0.230 |
LIG_APCC_ABBA_1 | 379 | 384 | PF00400 | 0.219 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.287 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.223 |
LIG_Clathr_ClatBox_1 | 285 | 289 | PF01394 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 227 | 230 | PF00928 | 0.424 |
LIG_deltaCOP1_diTrp_1 | 299 | 305 | PF00928 | 0.477 |
LIG_DLG_GKlike_1 | 206 | 213 | PF00625 | 0.485 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.263 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.336 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.359 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.346 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.322 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.338 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.333 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.223 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.446 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.474 |
LIG_Integrin_isoDGR_2 | 119 | 121 | PF01839 | 0.325 |
LIG_IRF3_LxIS_1 | 329 | 336 | PF10401 | 0.446 |
LIG_LIR_Gen_1 | 251 | 258 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 299 | 306 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.503 |
LIG_NRBOX | 281 | 287 | PF00104 | 0.187 |
LIG_PCNA_TLS_4 | 44 | 51 | PF02747 | 0.203 |
LIG_Pex14_1 | 396 | 400 | PF04695 | 0.464 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.388 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.472 |
LIG_PTB_Apo_2 | 374 | 381 | PF02174 | 0.220 |
LIG_PTB_Phospho_1 | 374 | 380 | PF10480 | 0.227 |
LIG_SH2_NCK_1 | 35 | 39 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 400 | 403 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.388 |
LIG_SUMO_SIM_anti_2 | 185 | 190 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 211 | 217 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.409 |
LIG_TYR_ITIM | 378 | 383 | PF00017 | 0.429 |
LIG_UBA3_1 | 133 | 139 | PF00899 | 0.249 |
MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.269 |
MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.298 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.356 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.338 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.425 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.393 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.358 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.545 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.567 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.498 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.542 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.343 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.365 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.423 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.211 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.461 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.417 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.437 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.363 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.313 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.404 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.434 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.341 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.394 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.393 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.422 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.531 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.561 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.367 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.372 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.352 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.286 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.337 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.338 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.375 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.292 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.355 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.345 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.392 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.605 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.621 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.589 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.403 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.373 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.275 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.308 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.421 |
MOD_N-GLC_2 | 418 | 420 | PF02516 | 0.474 |
MOD_N-GLC_2 | 65 | 67 | PF02516 | 0.291 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.379 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.370 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.347 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.352 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.333 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.316 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.344 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.284 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.339 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.333 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.340 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.315 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.332 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.340 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.397 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.385 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.565 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.307 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.535 |
MOD_NEK2_2 | 179 | 184 | PF00069 | 0.500 |
MOD_OFUCOSY | 67 | 74 | PF10250 | 0.352 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.491 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.520 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.491 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.382 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.379 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.291 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.364 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.563 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.393 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.325 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.357 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.366 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.397 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.539 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.608 |
TRG_NLS_MonoExtC_3 | 137 | 143 | PF00514 | 0.464 |
TRG_NLS_MonoExtN_4 | 135 | 142 | PF00514 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.186 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 27% | 75% |
A0A0N1I121 | Leptomonas seymouri | 28% | 95% |
A0A0N1I661 | Leptomonas seymouri | 34% | 84% |
A0A0N1I7S5 | Leptomonas seymouri | 33% | 94% |
A0A0N1II82 | Leptomonas seymouri | 34% | 69% |
A0A0S4ILC9 | Bodo saltans | 38% | 86% |
A0A0S4IN27 | Bodo saltans | 33% | 88% |
A0A0S4IQE4 | Bodo saltans | 31% | 84% |
A0A0S4IR61 | Bodo saltans | 32% | 100% |
A0A0S4ISU4 | Bodo saltans | 36% | 72% |
A0A0S4IU23 | Bodo saltans | 30% | 81% |
A0A0S4IU73 | Bodo saltans | 40% | 96% |
A0A0S4IV96 | Bodo saltans | 38% | 79% |
A0A0S4IVN7 | Bodo saltans | 39% | 100% |
A0A0S4IVQ8 | Bodo saltans | 38% | 79% |
A0A0S4IW93 | Bodo saltans | 30% | 79% |
A0A0S4IY44 | Bodo saltans | 29% | 72% |
A0A0S4IZC7 | Bodo saltans | 31% | 100% |
A0A0S4J014 | Bodo saltans | 34% | 67% |
A0A0S4J206 | Bodo saltans | 36% | 78% |
A0A0S4J2H8 | Bodo saltans | 28% | 82% |
A0A0S4J3T7 | Bodo saltans | 33% | 100% |
A0A0S4J5A0 | Bodo saltans | 35% | 83% |
A0A0S4J746 | Bodo saltans | 30% | 68% |
A0A0S4JAS1 | Bodo saltans | 36% | 75% |
A0A0S4JAW7 | Bodo saltans | 30% | 94% |
A0A0S4JB95 | Bodo saltans | 26% | 79% |
A0A0S4JD35 | Bodo saltans | 32% | 80% |
A0A0S4JDS1 | Bodo saltans | 27% | 90% |
A0A0S4JEK1 | Bodo saltans | 27% | 100% |
A0A0S4JEP2 | Bodo saltans | 27% | 82% |
A0A0S4JFC9 | Bodo saltans | 34% | 99% |
A0A0S4JL29 | Bodo saltans | 34% | 94% |
A0A0S4JQW3 | Bodo saltans | 26% | 100% |
A0A0S4JS12 | Bodo saltans | 29% | 100% |
A0A0S4JSB8 | Bodo saltans | 40% | 86% |
A0A0S4JVI0 | Bodo saltans | 28% | 67% |
A0A0S4KGV4 | Bodo saltans | 26% | 88% |
A0A0S4KH41 | Bodo saltans | 34% | 69% |
A0A0S4KJA7 | Bodo saltans | 29% | 71% |
A0A0S4KK37 | Bodo saltans | 30% | 82% |
A0A0S4KL26 | Bodo saltans | 26% | 100% |
A0A0S4KMV2 | Bodo saltans | 30% | 100% |
A0A3Q8IC27 | Leishmania donovani | 100% | 100% |
A0A3S5H6M3 | Leishmania donovani | 35% | 70% |
A0A3S5H6M4 | Leishmania donovani | 38% | 73% |
A0A3S7WS66 | Leishmania donovani | 38% | 72% |
A4HBX3 | Leishmania braziliensis | 64% | 100% |
A4HVB0 | Leishmania infantum | 36% | 100% |
D1GJ51 | Leishmania infantum | 34% | 100% |
E9AGG2 | Leishmania infantum | 34% | 72% |
E9AGG7 | Leishmania infantum | 32% | 76% |
E9AGG9 | Leishmania infantum | 37% | 88% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 67% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 68% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
O02833 | Papio hamadryas | 23% | 79% |
O80809 | Arabidopsis thaliana | 28% | 66% |
O81765 | Arabidopsis thaliana | 24% | 68% |
P35858 | Homo sapiens | 27% | 79% |
P35859 | Rattus norvegicus | 20% | 79% |
P70389 | Mus musculus | 25% | 79% |
Q00874 | Arabidopsis thaliana | 28% | 100% |
Q1PEN0 | Arabidopsis thaliana | 24% | 66% |
Q3URE9 | Mus musculus | 21% | 79% |
Q4PSE6 | Arabidopsis thaliana | 28% | 100% |
Q4QC79 | Leishmania major | 92% | 100% |
Q4QGI0 | Leishmania major | 36% | 100% |
Q4QGI2 | Leishmania major | 35% | 100% |
Q4QGI4 | Leishmania major | 35% | 100% |
Q4QGI6 | Leishmania major | 32% | 100% |
Q4QGJ0 | Leishmania major | 33% | 76% |
Q4QGJ2 | Leishmania major | 32% | 100% |
Q4QGJ6 | Leishmania major | 31% | 100% |
Q4QGJ7 | Leishmania major | 31% | 100% |
Q4QGJ9 | Leishmania major | 34% | 100% |
Q4QGK0 | Leishmania major | 32% | 100% |
Q4QGK1 | Leishmania major | 32% | 68% |
Q4QGK2 | Leishmania major | 32% | 100% |
Q4QGK4 | Leishmania major | 33% | 100% |
Q4QGK8 | Leishmania major | 35% | 100% |
Q4QGL2 | Leishmania major | 35% | 100% |
Q4QGL4 | Leishmania major | 36% | 100% |
Q4QGL5 | Leishmania major | 29% | 100% |
Q4QGL8 | Leishmania major | 36% | 78% |
Q7L985 | Homo sapiens | 21% | 79% |
Q9LJW7 | Arabidopsis thaliana | 26% | 67% |
Q9SKK5 | Arabidopsis thaliana | 26% | 71% |