Publication identifier(s): 8702946
A surface coat protein involved in immune evasion in Leishmaniids. Extremely fast evolving, almost completely disordered mucin-like protein. . Localization: Cell surface (experimental)
                
                    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: 130 | 
| 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: 14 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 50, no: 8 | 
| NetGPI | no | yes: 0, no: 58 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005929 | cilium | 4 | 59 | 
| GO:0016020 | membrane | 2 | 17 | 
| GO:0042995 | cell projection | 2 | 59 | 
| GO:0043226 | organelle | 2 | 59 | 
| GO:0043227 | membrane-bounded organelle | 3 | 59 | 
| GO:0110165 | cellular anatomical entity | 1 | 59 | 
| GO:0120025 | plasma membrane bounded cell projection | 3 | 59 | 
| GO:0005886 | plasma membrane | 3 | 3 | 
Related structures:
AlphaFold database: Q4QGK6
| 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_NRD_NRD_1 | 6 | 8 | PF00675 | 0.678 | 
| CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.678 | 
| CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.679 | 
| DEG_SCF_FBW7_1 | 272 | 278 | PF00400 | 0.470 | 
| DEG_SCF_FBW7_2 | 313 | 318 | PF00400 | 0.465 | 
| DEG_SPOP_SBC_1 | 275 | 279 | PF00917 | 0.480 | 
| DEG_SPOP_SBC_1 | 281 | 285 | PF00917 | 0.482 | 
| DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.475 | 
| DOC_CKS1_1 | 272 | 277 | PF01111 | 0.470 | 
| DOC_CYCLIN_RxL_1 | 105 | 116 | PF00134 | 0.300 | 
| DOC_CYCLIN_RxL_1 | 182 | 193 | PF00134 | 0.299 | 
| DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.503 | 
| DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.373 | 
| DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.302 | 
| DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.317 | 
| DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.276 | 
| DOC_USP7_MATH_2 | 151 | 157 | PF00917 | 0.323 | 
| DOC_USP7_UBL2_3 | 350 | 354 | PF12436 | 0.324 | 
| DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.311 | 
| DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.483 | 
| DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.470 | 
| DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.496 | 
| DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.472 | 
| DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.314 | 
| LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.473 | 
| LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.341 | 
| LIG_Actin_WH2_2 | 153 | 168 | PF00022 | 0.305 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 | 
| LIG_deltaCOP1_diTrp_1 | 62 | 69 | PF00928 | 0.345 | 
| LIG_EVH1_1 | 271 | 275 | PF00568 | 0.468 | 
| LIG_FHA_1 | 263 | 269 | PF00498 | 0.492 | 
| LIG_FHA_1 | 277 | 283 | PF00498 | 0.475 | 
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.362 | 
| LIG_FHA_2 | 131 | 137 | PF00498 | 0.326 | 
| LIG_FHA_2 | 275 | 281 | PF00498 | 0.476 | 
| LIG_FHA_2 | 283 | 289 | PF00498 | 0.476 | 
| LIG_FHA_2 | 293 | 299 | PF00498 | 0.468 | 
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.409 | 
| LIG_FHA_2 | 92 | 98 | PF00498 | 0.377 | 
| LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.329 | 
| LIG_LIR_Gen_1 | 128 | 135 | PF02991 | 0.352 | 
| LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.369 | 
| LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.329 | 
| LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.352 | 
| LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.370 | 
| LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.345 | 
| LIG_PDZ_Class_2 | 380 | 385 | PF00595 | 0.285 | 
| LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.329 | 
| LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.326 | 
| LIG_SH3_3 | 269 | 275 | PF00018 | 0.468 | 
| LIG_SH3_3 | 287 | 293 | PF00018 | 0.470 | 
| LIG_SH3_3 | 297 | 303 | PF00018 | 0.479 | 
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.384 | 
| LIG_Sin3_3 | 369 | 376 | PF02671 | 0.263 | 
| LIG_SUMO_SIM_anti_2 | 158 | 164 | PF11976 | 0.292 | 
| LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.317 | 
| LIG_SUMO_SIM_par_1 | 232 | 238 | PF11976 | 0.340 | 
| LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.358 | 
| MOD_CDK_SPK_2 | 271 | 276 | PF00069 | 0.470 | 
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.439 | 
| MOD_CK1_1 | 156 | 162 | PF00069 | 0.342 | 
| MOD_CK1_1 | 179 | 185 | PF00069 | 0.351 | 
| MOD_CK1_1 | 197 | 203 | PF00069 | 0.315 | 
| MOD_CK1_1 | 259 | 265 | PF00069 | 0.466 | 
| MOD_CK1_1 | 85 | 91 | PF00069 | 0.335 | 
| MOD_CK2_1 | 130 | 136 | PF00069 | 0.291 | 
| MOD_CK2_1 | 274 | 280 | PF00069 | 0.475 | 
| MOD_CK2_1 | 282 | 288 | PF00069 | 0.477 | 
| MOD_CK2_1 | 292 | 298 | PF00069 | 0.469 | 
| MOD_CK2_1 | 316 | 322 | PF00069 | 0.433 | 
| MOD_CK2_1 | 91 | 97 | PF00069 | 0.387 | 
| MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.599 | 
| MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.538 | 
| MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.658 | 
| MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.557 | 
| MOD_GlcNHglycan | 193 | 197 | PF01048 | 0.566 | 
| MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.522 | 
| MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.650 | 
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.649 | 
| MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.563 | 
| MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.294 | 
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.528 | 
| MOD_GSK3_1 | 121 | 128 | PF00069 | 0.452 | 
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.447 | 
| MOD_GSK3_1 | 142 | 149 | PF00069 | 0.329 | 
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.472 | 
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.306 | 
| MOD_GSK3_1 | 249 | 256 | PF00069 | 0.448 | 
| MOD_GSK3_1 | 258 | 265 | PF00069 | 0.488 | 
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.473 | 
| MOD_GSK3_1 | 280 | 287 | PF00069 | 0.472 | 
| MOD_GSK3_1 | 301 | 308 | PF00069 | 0.490 | 
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.513 | 
| MOD_GSK3_1 | 344 | 351 | PF00069 | 0.352 | 
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.341 | 
| MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.666 | 
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.510 | 
| MOD_NEK2_1 | 121 | 126 | PF00069 | 0.419 | 
| MOD_NEK2_1 | 165 | 170 | PF00069 | 0.314 | 
| MOD_NEK2_1 | 194 | 199 | PF00069 | 0.339 | 
| MOD_NEK2_1 | 207 | 212 | PF00069 | 0.302 | 
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.497 | 
| MOD_NEK2_1 | 282 | 287 | PF00069 | 0.477 | 
| MOD_PK_1 | 142 | 148 | PF00069 | 0.309 | 
| MOD_PKA_2 | 165 | 171 | PF00069 | 0.294 | 
| MOD_PKA_2 | 275 | 281 | PF00069 | 0.472 | 
| MOD_Plk_1 | 348 | 354 | PF00069 | 0.357 | 
| MOD_Plk_2-3 | 136 | 142 | PF00069 | 0.288 | 
| MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.318 | 
| MOD_Plk_4 | 158 | 164 | PF00069 | 0.329 | 
| MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.485 | 
| MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.471 | 
| MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.494 | 
| MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.311 | 
| MOD_SUMO_rev_2 | 224 | 230 | PF00179 | 0.328 | 
| MOD_SUMO_rev_2 | 342 | 351 | PF00179 | 0.335 | 
| TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.381 | 
| TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.566 | 
| TRG_Pf-PMV_PEXEL_1 | 185 | 190 | PF00026 | 0.497 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1HZ17 | Leptomonas seymouri | 32% | 100% | 
| A0A0S4JEJ4 | Bodo saltans | 24% | 100% | 
| A0A3Q8I9A6 | Leishmania donovani | 55% | 100% | 
| A0A3Q8I9D0 | Leishmania donovani | 56% | 100% | 
| A0A3Q8IFC2 | Leishmania donovani | 40% | 100% | 
| A0A3Q8IIJ9 | Leishmania donovani | 31% | 100% | 
| A0A3S5H6D6 | Leishmania donovani | 32% | 100% | 
| A0A3S5H6L9 | Leishmania donovani | 57% | 66% | 
| A0A3S7WP69 | Leishmania donovani | 21% | 100% | 
| A0A3S7WPB2 | Leishmania donovani | 30% | 100% | 
| A0A3S7X4J4 | Leishmania donovani | 31% | 100% | 
| A4H4D2 | Leishmania braziliensis | 23% | 100% | 
| A4H4G6 | Leishmania braziliensis | 29% | 100% | 
| A4H5P0 | Leishmania braziliensis | 32% | 100% | 
| A4HBX3 | Leishmania braziliensis | 31% | 85% | 
| A4HJC8 | Leishmania braziliensis | 30% | 100% | 
| A4HJX1 | Leishmania braziliensis | 37% | 100% | 
| A4HSL2 | Leishmania infantum | 21% | 100% | 
| A4HTX9 | Leishmania infantum | 32% | 100% | 
| A4HVB0 | Leishmania infantum | 51% | 96% | 
| A4I6S4 | Leishmania infantum | 31% | 100% | 
| D1GJ51 | Leishmania infantum | 49% | 83% | 
| E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 87% | 
| E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% | 
| E9ACQ0 | Leishmania major | 30% | 100% | 
| E9AG65 | Leishmania infantum | 30% | 100% | 
| E9AGG5 | Leishmania infantum | 56% | 92% | 
| E9AGG9 | Leishmania infantum | 57% | 71% | 
| E9AGH0 | Leishmania infantum | 55% | 100% | 
| E9AKJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% | 
| E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% | 
| E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% | 
| E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% | 
| E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 98% | 
| E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 75% | 
| E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% | 
| E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 92% | 
| E9B1U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 85% | 
| E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% | 
| E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 92% | 
| E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% | 
| P21978 | Leishmania amazonensis | 52% | 81% | 
| Q25331 | Leishmania major | 100% | 100% | 
| Q4Q6B6 | Leishmania major | 29% | 100% | 
| Q4Q6B7 | Leishmania major | 29% | 100% | 
| Q4QC79 | Leishmania major | 29% | 84% | 
| Q4QGI0 | Leishmania major | 60% | 76% | 
| Q4QGI2 | Leishmania major | 46% | 69% | 
| Q4QGI4 | Leishmania major | 47% | 72% | 
| Q4QGI6 | Leishmania major | 72% | 70% | 
| Q4QGJ4 | Leishmania major | 99% | 100% | 
| Q4QGJ6 | Leishmania major | 51% | 67% | 
| Q4QGJ7 | Leishmania major | 94% | 97% | 
| Q4QGK0 | Leishmania major | 56% | 68% | 
| Q4QGK2 | Leishmania major | 52% | 69% | 
| Q4QGL4 | Leishmania major | 60% | 97% | 
| Q4QHW6 | Leishmania major | 33% | 100% | 
| Q4QJB2 | Leishmania major | 21% | 100% |