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: 100 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 33, no: 2 |
NetGPI | no | yes: 0, no: 35 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 36 |
GO:0016020 | membrane | 2 | 16 |
GO:0042995 | cell projection | 2 | 36 |
GO:0043226 | organelle | 2 | 36 |
GO:0043227 | membrane-bounded organelle | 3 | 36 |
GO:0110165 | cellular anatomical entity | 1 | 36 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 36 |
GO:0005886 | plasma membrane | 3 | 2 |
Related structures:
AlphaFold database: Q4QGJ6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004672 | protein kinase activity | 3 | 2 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.319 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.701 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.672 |
DEG_SCF_FBW7_2 | 500 | 505 | PF00400 | 0.503 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.486 |
DEG_SPOP_SBC_1 | 363 | 367 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 378 | 382 | PF00917 | 0.535 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.549 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.453 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.509 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.591 |
DEG_SPOP_SBC_1 | 428 | 432 | PF00917 | 0.594 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.664 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.495 |
DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.301 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 220 | 223 | PF00134 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 241 | 247 | PF00134 | 0.291 |
DOC_MAPK_gen_1 | 156 | 163 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 205 | 212 | PF00069 | 0.287 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.275 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.264 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.291 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.373 |
DOC_USP7_MATH_2 | 174 | 180 | PF00917 | 0.394 |
DOC_USP7_MATH_2 | 198 | 204 | PF00917 | 0.265 |
DOC_USP7_MATH_2 | 222 | 228 | PF00917 | 0.337 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.272 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.358 |
LIG_14-3-3_CanoR_1 | 157 | 161 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 304 | 309 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.359 |
LIG_Actin_WH2_2 | 179 | 194 | PF00022 | 0.307 |
LIG_APCC_ABBA_1 | 208 | 213 | PF00400 | 0.256 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_deltaCOP1_diTrp_1 | 111 | 115 | PF00928 | 0.258 |
LIG_deltaCOP1_diTrp_1 | 200 | 204 | PF00928 | 0.275 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.435 |
LIG_DLG_GKlike_1 | 253 | 260 | PF00625 | 0.275 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.348 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.430 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.360 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.406 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.429 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.465 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.388 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.482 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.346 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.325 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.527 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.464 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.490 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.383 |
LIG_PDZ_Class_2 | 567 | 572 | PF00595 | 0.323 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.307 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.294 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.564 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.371 |
LIG_Sin3_3 | 556 | 563 | PF02671 | 0.291 |
LIG_SUMO_SIM_anti_2 | 254 | 259 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.340 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.364 |
LIG_UBA3_1 | 257 | 264 | PF00899 | 0.299 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.310 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.363 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.373 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.339 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.380 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.422 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.493 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.519 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.441 |
MOD_CMANNOS | 201 | 204 | PF00535 | 0.460 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.625 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.518 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.583 |
MOD_GlcNHglycan | 164 | 168 | PF01048 | 0.568 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.622 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.744 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.612 |
MOD_GlcNHglycan | 272 | 276 | PF01048 | 0.598 |
MOD_GlcNHglycan | 288 | 292 | PF01048 | 0.593 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.627 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.327 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.486 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.334 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.360 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.339 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.367 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.327 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.530 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.499 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.551 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.537 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.492 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.504 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.501 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.498 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.480 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.514 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.507 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.482 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.513 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.503 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.563 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.569 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.609 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.552 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.455 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.636 |
MOD_N-GLC_2 | 285 | 287 | PF02516 | 0.484 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.577 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.488 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.309 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.399 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.502 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.368 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.453 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.279 |
MOD_PKA_1 | 156 | 162 | PF00069 | 0.273 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.394 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.479 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.353 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.337 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.544 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.299 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.337 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.278 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.357 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.316 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.320 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.276 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.649 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.352 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.311 |
TRG_DiLeu_BaEn_1 | 536 | 541 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4ILC9 | Bodo saltans | 32% | 100% |
A0A0S4IRQ2 | Bodo saltans | 32% | 67% |
A0A0S4J206 | Bodo saltans | 32% | 93% |
A0A0S4JEE7 | Bodo saltans | 27% | 72% |
A0A3Q8I9A6 | Leishmania donovani | 50% | 100% |
A0A3Q8IC27 | Leishmania donovani | 31% | 100% |
A0A3Q8IFC2 | Leishmania donovani | 36% | 100% |
A4HBX3 | Leishmania braziliensis | 34% | 100% |
A4HJX1 | Leishmania braziliensis | 33% | 100% |
A4HVB0 | Leishmania infantum | 53% | 100% |
A4HZ93 | Leishmania infantum | 31% | 100% |
A4I6S2 | Leishmania infantum | 31% | 100% |
D1GJ51 | Leishmania infantum | 61% | 100% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AEF4 | Leishmania major | 35% | 100% |
E9AGG5 | Leishmania infantum | 49% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4Q6B8 | Leishmania major | 29% | 100% |
Q4QC79 | Leishmania major | 33% | 100% |
Q4QGI0 | Leishmania major | 63% | 100% |
Q4QGI6 | Leishmania major | 54% | 100% |
Q4QGJ0 | Leishmania major | 51% | 91% |
Q4QGJ2 | Leishmania major | 51% | 88% |
Q4QGJ9 | Leishmania major | 55% | 97% |
Q4QGK0 | Leishmania major | 61% | 100% |
Q4QGK6 | Leishmania major | 51% | 100% |
Q4QGK8 | Leishmania major | 60% | 100% |
Q4QGL2 | Leishmania major | 60% | 100% |
Q4QGL4 | Leishmania major | 69% | 100% |
Q9C9H6 | Arabidopsis thaliana | 24% | 73% |