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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 50, no: 2 |
NetGPI | no | yes: 0, no: 52 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 53 |
GO:0016020 | membrane | 2 | 28 |
GO:0042995 | cell projection | 2 | 53 |
GO:0043226 | organelle | 2 | 53 |
GO:0043227 | membrane-bounded organelle | 3 | 53 |
GO:0110165 | cellular anatomical entity | 1 | 53 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 53 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: Q4QGK0
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 | 0.426 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.719 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.719 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.737 |
DEG_SCF_FBW7_2 | 498 | 503 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.477 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.457 |
DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.456 |
DEG_SPOP_SBC_1 | 468 | 472 | PF00917 | 0.579 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.580 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.292 |
DOC_CYCLIN_RxL_1 | 105 | 116 | PF00134 | 0.305 |
DOC_CYCLIN_RxL_1 | 235 | 243 | PF00134 | 0.241 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.584 |
DOC_CYCLIN_yCln2_LP_2 | 221 | 224 | PF00134 | 0.263 |
DOC_CYCLIN_yCln2_LP_2 | 242 | 248 | PF00134 | 0.243 |
DOC_MAPK_gen_1 | 157 | 164 | PF00069 | 0.248 |
DOC_MAPK_MEF2A_6 | 397 | 404 | PF00069 | 0.433 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.326 |
DOC_PP2B_LxvP_1 | 221 | 224 | PF13499 | 0.404 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.429 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.438 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.424 |
DOC_USP7_MATH_2 | 295 | 301 | PF00917 | 0.358 |
DOC_USP7_MATH_2 | 319 | 325 | PF00917 | 0.262 |
DOC_USP7_MATH_2 | 367 | 373 | PF00917 | 0.359 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 377 | 382 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.363 |
LIG_Actin_WH2_2 | 180 | 195 | PF00022 | 0.300 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.251 |
LIG_Actin_WH2_2 | 297 | 312 | PF00022 | 0.245 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.666 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 62 | 69 | PF00928 | 0.422 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.275 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.403 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.405 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.309 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.295 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.480 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.341 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.356 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.439 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.448 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.507 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.569 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.640 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.444 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.445 |
LIG_FXI_DFP_1 | 164 | 168 | PF00024 | 0.437 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 127 | 135 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 201 | 208 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 225 | 232 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 369 | 376 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.377 |
LIG_PDZ_Class_2 | 565 | 570 | PF00595 | 0.333 |
LIG_SH2_STAT3 | 334 | 337 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.400 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.251 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.440 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.432 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.431 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.426 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.483 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.481 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.464 |
LIG_Sin3_3 | 554 | 561 | PF02671 | 0.299 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.373 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.410 |
LIG_TYR_ITIM | 256 | 261 | PF00017 | 0.224 |
LIG_TYR_ITIM | 328 | 333 | PF00017 | 0.234 |
LIG_TYR_ITIM | 357 | 362 | PF00017 | 0.360 |
MOD_CDK_SPxK_1 | 429 | 435 | PF00069 | 0.431 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.344 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.375 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.433 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.425 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.468 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.440 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.435 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.433 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.435 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.620 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.607 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.459 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.696 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.624 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.582 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.567 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.763 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.541 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.524 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.624 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.595 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.551 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.542 |
MOD_GlcNHglycan | 361 | 365 | PF01048 | 0.643 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.594 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.733 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.453 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.477 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.395 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.389 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.371 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.353 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.307 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.333 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.324 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.579 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.372 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.508 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.580 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.629 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.469 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.381 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.554 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.492 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.436 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.364 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.597 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.352 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.338 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.417 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.399 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.378 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.253 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.426 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.368 |
MOD_PKA_1 | 157 | 163 | PF00069 | 0.241 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.441 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.254 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.373 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.329 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.350 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.474 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.494 |
MOD_Plk_2-3 | 225 | 231 | PF00069 | 0.263 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.410 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.352 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.399 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.646 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.673 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.471 |
MOD_SUMO_rev_2 | 392 | 398 | PF00179 | 0.321 |
TRG_DiLeu_BaEn_1 | 534 | 539 | PF01217 | 0.345 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I661 | Leptomonas seymouri | 32% | 100% |
A0A0S4IHI7 | Bodo saltans | 27% | 74% |
A0A0S4IJN2 | Bodo saltans | 24% | 85% |
A0A0S4IRQ2 | Bodo saltans | 30% | 67% |
A0A0S4IVQ8 | Bodo saltans | 33% | 95% |
A0A0S4IW93 | Bodo saltans | 26% | 94% |
A0A0S4J014 | Bodo saltans | 25% | 80% |
A0A0S4J2H8 | Bodo saltans | 25% | 97% |
A0A0S4J954 | Bodo saltans | 24% | 77% |
A0A0S4JAQ6 | Bodo saltans | 26% | 100% |
A0A0S4JBI6 | Bodo saltans | 24% | 67% |
A0A0S4JHE0 | Bodo saltans | 29% | 68% |
A0A0S4JL29 | Bodo saltans | 29% | 100% |
A0A0S4JTM6 | Bodo saltans | 25% | 77% |
A0A0S4JTQ7 | Bodo saltans | 36% | 100% |
A0A0S4JVI0 | Bodo saltans | 26% | 80% |
A0A0S4KEG2 | Bodo saltans | 25% | 68% |
A0A0S4KK37 | Bodo saltans | 28% | 98% |
A0A3Q8I9A6 | Leishmania donovani | 51% | 100% |
A0A3Q8I9B4 | Leishmania donovani | 48% | 100% |
A0A3Q8IC27 | Leishmania donovani | 32% | 100% |
A0A3S5H6L9 | Leishmania donovani | 48% | 100% |
A0A3S5H6M3 | Leishmania donovani | 58% | 83% |
A0A3S5H6M4 | Leishmania donovani | 53% | 87% |
A0A3S7WS66 | Leishmania donovani | 52% | 87% |
A4HBX3 | Leishmania braziliensis | 32% | 100% |
A4HVB0 | Leishmania infantum | 53% | 100% |
A4HZ93 | Leishmania infantum | 32% | 100% |
D1GJ51 | Leishmania infantum | 55% | 100% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AGG2 | Leishmania infantum | 57% | 86% |
E9AGG7 | Leishmania infantum | 61% | 91% |
E9AGG9 | Leishmania infantum | 60% | 100% |
E9AGH0 | Leishmania infantum | 53% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 81% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 82% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
F4JGB6 | Arabidopsis thaliana | 26% | 70% |
Q1PEN0 | Arabidopsis thaliana | 23% | 79% |
Q4QC79 | Leishmania major | 32% | 100% |
Q4QGI0 | Leishmania major | 64% | 100% |
Q4QGI2 | Leishmania major | 61% | 100% |
Q4QGI4 | Leishmania major | 62% | 100% |
Q4QGI6 | Leishmania major | 61% | 100% |
Q4QGI8 | Leishmania major | 52% | 75% |
Q4QGJ0 | Leishmania major | 61% | 100% |
Q4QGJ2 | Leishmania major | 68% | 100% |
Q4QGJ6 | Leishmania major | 61% | 100% |
Q4QGJ9 | Leishmania major | 63% | 100% |
Q4QGK1 | Leishmania major | 63% | 81% |
Q4QGK2 | Leishmania major | 55% | 100% |
Q4QGK4 | Leishmania major | 69% | 85% |
Q4QGK6 | Leishmania major | 56% | 100% |
Q4QGK8 | Leishmania major | 55% | 100% |
Q4QGL2 | Leishmania major | 55% | 100% |
Q4QGL4 | Leishmania major | 70% | 100% |
Q4QGL5 | Leishmania major | 62% | 100% |
Q4QGL8 | Leishmania major | 51% | 93% |
Q4QGM1 | Leishmania major | 62% | 73% |
Q9C9H6 | Arabidopsis thaliana | 22% | 73% |
Q9LJW7 | Arabidopsis thaliana | 24% | 80% |
Q9SHI4 | Arabidopsis thaliana | 22% | 75% |
Q9SVM3 | Arabidopsis thaliana | 25% | 68% |
Q9SVN2 | Arabidopsis thaliana | 26% | 71% |