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
Plasma membrane, surface antigen 2 PSA-50S
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: 61, no: 7 |
NetGPI | no | yes: 0, no: 68 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 69 |
GO:0042995 | cell projection | 2 | 69 |
GO:0043226 | organelle | 2 | 69 |
GO:0043227 | membrane-bounded organelle | 3 | 69 |
GO:0110165 | cellular anatomical entity | 1 | 69 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 69 |
GO:0016020 | membrane | 2 | 30 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: D1GJ51
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 | 124 | 128 | PF00656 | 0.298 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.742 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.706 |
DEG_SPOP_SBC_1 | 372 | 376 | PF00917 | 0.569 |
DOC_CYCLIN_RxL_1 | 107 | 115 | PF00134 | 0.267 |
DOC_CYCLIN_RxL_1 | 203 | 212 | PF00134 | 0.236 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 154 | 164 | PF00069 | 0.234 |
DOC_MAPK_HePTP_8 | 431 | 443 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 157 | 164 | PF00069 | 0.211 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 434 | 443 | PF00069 | 0.179 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.296 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.369 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.303 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.361 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.694 |
LIG_Clathr_ClatBox_1 | 258 | 262 | PF01394 | 0.216 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.355 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.368 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.282 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.444 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.455 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.312 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.458 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.309 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.595 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.548 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.400 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 127 | 135 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 177 | 184 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 225 | 234 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 321 | 328 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.397 |
LIG_PCNA_PIPBox_1 | 156 | 165 | PF02747 | 0.326 |
LIG_PCNA_PIPBox_1 | 277 | 286 | PF02747 | 0.218 |
LIG_PDZ_Class_2 | 458 | 463 | PF00595 | 0.516 |
LIG_PTB_Apo_2 | 300 | 307 | PF02174 | 0.225 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.385 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.413 |
LIG_Sin3_3 | 447 | 454 | PF02671 | 0.272 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.247 |
LIG_SUMO_SIM_anti_2 | 254 | 260 | PF11976 | 0.281 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 209 | 216 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 257 | 262 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 437 | 442 | PF11976 | 0.180 |
LIG_SUMO_SIM_par_1 | 44 | 51 | PF11976 | 0.209 |
LIG_SUMO_SIM_par_1 | 97 | 103 | PF11976 | 0.413 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.461 |
LIG_UBA3_1 | 234 | 241 | PF00899 | 0.280 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.368 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.330 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.357 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.310 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.363 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.350 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.427 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.409 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.618 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.407 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.592 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.495 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.549 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.597 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.518 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.688 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.575 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.548 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.590 |
MOD_GlcNHglycan | 313 | 317 | PF01048 | 0.593 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.626 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.646 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.379 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.296 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.324 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.338 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.361 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.324 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.360 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.269 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.329 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.515 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.586 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.552 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.480 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.363 |
MOD_N-GLC_2 | 363 | 365 | PF02516 | 0.665 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.549 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.310 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.335 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.314 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.542 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.333 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.305 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.418 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.375 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.279 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.387 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.444 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.417 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.386 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.320 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.355 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.344 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.328 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.337 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.365 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.353 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.376 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.395 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.263 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.295 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.625 |
MOD_SUMO_rev_2 | 355 | 361 | PF00179 | 0.288 |
TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.296 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 35% | 73% |
A0A0N1I661 | Leptomonas seymouri | 40% | 81% |
A0A0N1I7S5 | Leptomonas seymouri | 33% | 91% |
A0A0N1II82 | Leptomonas seymouri | 36% | 67% |
A0A0S4ISU4 | Bodo saltans | 36% | 70% |
A0A0S4IVN7 | Bodo saltans | 34% | 100% |
A0A0S4IVQ8 | Bodo saltans | 36% | 77% |
A0A0S4IZC7 | Bodo saltans | 27% | 100% |
A0A0S4J3T7 | Bodo saltans | 30% | 100% |
A0A0S4J7Q5 | Bodo saltans | 28% | 100% |
A0A0S4JAQ6 | Bodo saltans | 25% | 90% |
A0A0S4JAS1 | Bodo saltans | 28% | 73% |
A0A0S4JB95 | Bodo saltans | 26% | 76% |
A0A0S4JD35 | Bodo saltans | 29% | 77% |
A0A0S4JDT0 | Bodo saltans | 28% | 70% |
A0A0S4JEK1 | Bodo saltans | 26% | 100% |
A0A0S4JMF9 | Bodo saltans | 34% | 100% |
A0A0S4JP43 | Bodo saltans | 35% | 100% |
A0A0S4KGV4 | Bodo saltans | 24% | 85% |
A0A0S4KH41 | Bodo saltans | 28% | 67% |
A0A0S4KJA7 | Bodo saltans | 25% | 69% |
A0A0S4KK37 | Bodo saltans | 27% | 79% |
A0A0S4KMV2 | Bodo saltans | 27% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 51% | 100% |
A0A3Q8IC27 | Leishmania donovani | 34% | 97% |
A0A3Q8IFC2 | Leishmania donovani | 32% | 100% |
A0A3S5H6M3 | Leishmania donovani | 59% | 67% |
A0A3S5H6M4 | Leishmania donovani | 55% | 70% |
A0A3S7WS66 | Leishmania donovani | 55% | 70% |
A4HBX3 | Leishmania braziliensis | 38% | 100% |
A4HJX1 | Leishmania braziliensis | 31% | 100% |
A4HVB0 | Leishmania infantum | 47% | 85% |
A4HZ93 | Leishmania infantum | 34% | 100% |
A4I6S3 | Leishmania infantum | 32% | 100% |
E9AEF4 | Leishmania major | 32% | 100% |
E9AGG2 | Leishmania infantum | 60% | 70% |
E9AGG5 | Leishmania infantum | 53% | 85% |
E9AGG7 | Leishmania infantum | 57% | 74% |
E9AGG9 | Leishmania infantum | 63% | 86% |
E9AGH0 | Leishmania infantum | 56% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 78% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 84% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 66% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 79% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 85% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q25331 | Leishmania major | 49% | 76% |
Q4QC79 | Leishmania major | 34% | 100% |
Q4QGI0 | Leishmania major | 62% | 100% |
Q4QGI2 | Leishmania major | 54% | 83% |
Q4QGI4 | Leishmania major | 54% | 86% |
Q4QGI6 | Leishmania major | 61% | 100% |
Q4QGJ0 | Leishmania major | 50% | 74% |
Q4QGJ2 | Leishmania major | 51% | 100% |
Q4QGJ4 | Leishmania major | 49% | 76% |
Q4QGJ6 | Leishmania major | 61% | 81% |
Q4QGJ7 | Leishmania major | 50% | 76% |
Q4QGJ9 | Leishmania major | 55% | 100% |
Q4QGK0 | Leishmania major | 55% | 100% |
Q4QGK2 | Leishmania major | 54% | 83% |
Q4QGK4 | Leishmania major | 51% | 69% |
Q4QGK6 | Leishmania major | 49% | 76% |
Q4QGK8 | Leishmania major | 55% | 100% |
Q4QGL2 | Leishmania major | 55% | 100% |
Q4QGL4 | Leishmania major | 60% | 85% |
Q4QGL5 | Leishmania major | 58% | 100% |
Q4QGL8 | Leishmania major | 63% | 76% |
Q8W3M4 | Arabidopsis thaliana | 23% | 100% |
Q9SSD1 | Arabidopsis thaliana | 26% | 93% |