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: 150 |
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: 59, no: 8 |
NetGPI | no | yes: 0, no: 67 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 68 |
GO:0042995 | cell projection | 2 | 68 |
GO:0043226 | organelle | 2 | 68 |
GO:0043227 | membrane-bounded organelle | 3 | 68 |
GO:0110165 | cellular anatomical entity | 1 | 68 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 68 |
GO:0016020 | membrane | 2 | 26 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: E9AP08
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 | 6 | 8 | PF00675 | 0.805 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.805 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.849 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.612 |
DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.578 |
DEG_SPOP_SBC_1 | 337 | 341 | PF00917 | 0.691 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.665 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.486 |
DOC_MAPK_gen_1 | 275 | 284 | PF00069 | 0.361 |
DOC_MAPK_HePTP_8 | 102 | 114 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 253 | 259 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.490 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.579 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.550 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.316 |
LIG_Actin_WH2_2 | 153 | 168 | PF00022 | 0.311 |
LIG_Actin_WH2_2 | 201 | 216 | PF00022 | 0.288 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.442 |
LIG_Clathr_ClatBox_1 | 186 | 190 | PF01394 | 0.276 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.391 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.479 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.366 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.322 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.330 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.487 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.415 |
LIG_LIR_Gen_1 | 128 | 136 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.352 |
LIG_LIR_LC3C_4 | 278 | 282 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.461 |
LIG_PDZ_Class_2 | 415 | 420 | PF00595 | 0.568 |
LIG_PTAP_UEV_1 | 320 | 325 | PF05743 | 0.475 |
LIG_PTAP_UEV_1 | 334 | 339 | PF05743 | 0.478 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.443 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.565 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.576 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.363 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.317 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.505 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.294 |
LIG_UBA3_1 | 135 | 142 | PF00899 | 0.284 |
LIG_UBA3_1 | 186 | 193 | PF00899 | 0.278 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.442 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.495 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.425 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.438 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.599 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.497 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.462 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.430 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.313 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.583 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.407 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.507 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.588 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.595 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.547 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.636 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.598 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.599 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.695 |
MOD_GlcNHglycan | 249 | 253 | PF01048 | 0.621 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.832 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.570 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.533 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.655 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.695 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.327 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.643 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.657 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.455 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.411 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.354 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.426 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.448 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.418 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.536 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.532 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.635 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.517 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.572 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.540 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.472 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.420 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.449 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.511 |
MOD_N-GLC_2 | 297 | 299 | PF02516 | 0.726 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.396 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.409 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.501 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.395 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.626 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.398 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.322 |
MOD_OFUCOSY | 70 | 77 | PF10250 | 0.542 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.340 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.495 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.333 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.444 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.510 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.390 |
MOD_Plk_2-3 | 377 | 383 | PF00069 | 0.340 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.402 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.312 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.294 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.350 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.466 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.539 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.580 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 286 | 296 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 377 | 386 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 97 | 107 | PF00179 | 0.311 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.747 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I121 | Leptomonas seymouri | 28% | 84% |
A0A0S4ITN5 | Bodo saltans | 25% | 100% |
A0A0S4JB17 | Bodo saltans | 27% | 67% |
A0A0S4JU20 | Bodo saltans | 35% | 100% |
A0A0S4KK37 | Bodo saltans | 28% | 72% |
A0A0S4KMS7 | Bodo saltans | 26% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 61% | 100% |
A0A3Q8I9B4 | Leishmania donovani | 59% | 68% |
A0A3Q8I9D0 | Leishmania donovani | 59% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 59% | 67% |
A0A3Q8IIJ9 | Leishmania donovani | 36% | 100% |
A0A3S5H6D6 | Leishmania donovani | 27% | 100% |
A0A3S5H6L9 | Leishmania donovani | 59% | 73% |
A0A3S7WP69 | Leishmania donovani | 25% | 100% |
A0A3S7WPB2 | Leishmania donovani | 22% | 100% |
A0A3S7X4J4 | Leishmania donovani | 36% | 100% |
A4H4D2 | Leishmania braziliensis | 26% | 100% |
A4H4G6 | Leishmania braziliensis | 23% | 100% |
A4H5P0 | Leishmania braziliensis | 27% | 100% |
A4HJC8 | Leishmania braziliensis | 32% | 100% |
A4HJX1 | Leishmania braziliensis | 38% | 100% |
A4HSL2 | Leishmania infantum | 25% | 100% |
A4HTX9 | Leishmania infantum | 27% | 100% |
A4HVB0 | Leishmania infantum | 54% | 100% |
A4I6S4 | Leishmania infantum | 36% | 100% |
D1GJ51 | Leishmania infantum | 52% | 91% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 95% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ACQ0 | Leishmania major | 25% | 100% |
E9AG65 | Leishmania infantum | 22% | 100% |
E9AGG5 | Leishmania infantum | 68% | 100% |
E9AGG7 | Leishmania infantum | 43% | 67% |
E9AGG9 | Leishmania infantum | 49% | 78% |
E9AGH0 | Leishmania infantum | 63% | 100% |
E9AKJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 86% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 93% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 82% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 87% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q25331 | Leishmania major | 54% | 89% |
Q4Q6B6 | Leishmania major | 35% | 100% |
Q4Q6B7 | Leishmania major | 35% | 100% |
Q4Q6B8 | Leishmania major | 38% | 79% |
Q4QGI0 | Leishmania major | 51% | 83% |
Q4QGI2 | Leishmania major | 48% | 75% |
Q4QGI4 | Leishmania major | 49% | 78% |
Q4QGI6 | Leishmania major | 44% | 77% |
Q4QGJ0 | Leishmania major | 51% | 67% |
Q4QGJ4 | Leishmania major | 54% | 89% |
Q4QGJ6 | Leishmania major | 53% | 73% |
Q4QGJ7 | Leishmania major | 56% | 89% |
Q4QGK2 | Leishmania major | 50% | 75% |
Q4QGK6 | Leishmania major | 54% | 89% |
Q4QGK8 | Leishmania major | 50% | 82% |
Q4QGL2 | Leishmania major | 50% | 82% |
Q4QGL4 | Leishmania major | 55% | 89% |
Q4QGL5 | Leishmania major | 49% | 77% |
Q4QGL8 | Leishmania major | 58% | 69% |
Q4QHW6 | Leishmania major | 27% | 100% |
Q4QJB2 | Leishmania major | 26% | 100% |