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
Plasma membrane, surface antigen 2 LINJ.12.0666
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: 155 |
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: 62, no: 8 |
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 | 25 |
GO:0005886 | plasma membrane | 3 | 3 |
Related structures:
AlphaFold database: E9AGG5
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 | 277 | 279 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.732 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.748 |
DEG_SCF_FBW7_2 | 345 | 350 | PF00400 | 0.444 |
DEG_SPOP_SBC_1 | 303 | 307 | PF00917 | 0.643 |
DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.433 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 277 | 284 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 277 | 284 | PF00069 | 0.359 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.475 |
DOC_USP7_MATH_2 | 199 | 205 | PF00917 | 0.349 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.346 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.294 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.511 |
LIG_Actin_WH2_2 | 177 | 192 | PF00022 | 0.274 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.336 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.336 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.438 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.321 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.436 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.457 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.327 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.382 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.502 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 128 | 136 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 153 | 160 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.358 |
LIG_PCNA_PIPBox_1 | 132 | 141 | PF02747 | 0.264 |
LIG_PDZ_Class_2 | 412 | 417 | PF00595 | 0.283 |
LIG_Pex14_1 | 72 | 76 | PF04695 | 0.245 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.481 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.268 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.376 |
LIG_SH3_1 | 298 | 304 | PF00018 | 0.387 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.393 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.581 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 206 | 212 | PF11976 | 0.277 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 280 | 285 | PF11976 | 0.321 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.351 |
LIG_UBA3_1 | 210 | 217 | PF00899 | 0.296 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.413 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.486 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.385 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.351 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.363 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.426 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.351 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.459 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.445 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.355 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.544 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.415 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.588 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.583 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.551 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.633 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.641 |
MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.605 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.571 |
MOD_GlcNHglycan | 241 | 245 | PF01048 | 0.526 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.764 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.561 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.554 |
MOD_GlcNHglycan | 362 | 367 | PF01048 | 0.724 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.290 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.591 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.435 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.374 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.456 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.367 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.324 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.354 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.403 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.353 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.508 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.483 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.475 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.627 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.521 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.448 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.591 |
MOD_N-GLC_2 | 297 | 299 | PF02516 | 0.686 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.528 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.444 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.410 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.341 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.420 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.528 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.317 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.365 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.361 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.363 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.252 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.326 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.311 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.431 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.295 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.444 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.281 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.439 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.357 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.445 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.372 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.365 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.573 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I121 | Leptomonas seymouri | 30% | 83% |
A0A0N1I7S5 | Leptomonas seymouri | 30% | 82% |
A0A0S4IZC7 | Bodo saltans | 25% | 100% |
A0A0S4J206 | Bodo saltans | 31% | 68% |
A0A0S4JB17 | Bodo saltans | 29% | 67% |
A0A0S4JEP2 | Bodo saltans | 21% | 72% |
A0A0S4KK37 | Bodo saltans | 25% | 72% |
A0A0S4KMS7 | Bodo saltans | 27% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 81% | 100% |
A0A3Q8I9B4 | Leishmania donovani | 59% | 67% |
A0A3Q8I9D0 | Leishmania donovani | 60% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 59% | 66% |
A0A3Q8IFC2 | Leishmania donovani | 38% | 96% |
A0A3Q8IIJ9 | Leishmania donovani | 30% | 100% |
A0A3S5H6D6 | Leishmania donovani | 30% | 100% |
A0A3S5H6L9 | Leishmania donovani | 59% | 72% |
A0A3S7WP69 | Leishmania donovani | 24% | 100% |
A0A3S7WPB2 | Leishmania donovani | 24% | 100% |
A0A3S7X4J4 | Leishmania donovani | 33% | 100% |
A4H4D2 | Leishmania braziliensis | 23% | 100% |
A4H4G6 | Leishmania braziliensis | 24% | 100% |
A4H5P0 | Leishmania braziliensis | 29% | 100% |
A4HBX3 | Leishmania braziliensis | 31% | 92% |
A4HJC8 | Leishmania braziliensis | 34% | 100% |
A4HSL2 | Leishmania infantum | 24% | 100% |
A4HTX9 | Leishmania infantum | 28% | 100% |
A4HVB0 | Leishmania infantum | 53% | 100% |
A4I6S2 | Leishmania infantum | 35% | 100% |
A4I6S3 | Leishmania infantum | 39% | 83% |
A4I6S4 | Leishmania infantum | 32% | 100% |
D1GJ51 | Leishmania infantum | 53% | 90% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 94% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ACQ0 | Leishmania major | 24% | 100% |
E9AG65 | Leishmania infantum | 24% | 100% |
E9AGG7 | Leishmania infantum | 41% | 67% |
E9AGG9 | Leishmania infantum | 44% | 77% |
E9AGH0 | Leishmania infantum | 76% | 100% |
E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 86% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 93% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 81% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 87% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 90% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q25331 | Leishmania major | 56% | 89% |
Q4Q6B6 | Leishmania major | 34% | 100% |
Q4Q6B7 | Leishmania major | 33% | 100% |
Q4Q6B8 | Leishmania major | 35% | 79% |
Q4QGI0 | Leishmania major | 47% | 82% |
Q4QGI2 | Leishmania major | 48% | 74% |
Q4QGI4 | Leishmania major | 46% | 78% |
Q4QGI6 | Leishmania major | 61% | 76% |
Q4QGJ0 | Leishmania major | 52% | 66% |
Q4QGJ4 | Leishmania major | 56% | 89% |
Q4QGJ6 | Leishmania major | 49% | 73% |
Q4QGJ7 | Leishmania major | 57% | 89% |
Q4QGJ9 | Leishmania major | 51% | 71% |
Q4QGK2 | Leishmania major | 51% | 74% |
Q4QGK6 | Leishmania major | 56% | 89% |
Q4QGL4 | Leishmania major | 55% | 90% |
Q4QGL5 | Leishmania major | 49% | 76% |
Q4QGL8 | Leishmania major | 56% | 68% |
Q4QHW6 | Leishmania major | 29% | 100% |
Q4QJB2 | Leishmania major | 21% | 100% |