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: 120 |
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: 45, no: 5 |
NetGPI | no | yes: 0, no: 50 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 51 |
GO:0016020 | membrane | 2 | 28 |
GO:0042995 | cell projection | 2 | 51 |
GO:0043226 | organelle | 2 | 51 |
GO:0043227 | membrane-bounded organelle | 3 | 51 |
GO:0110165 | cellular anatomical entity | 1 | 51 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 51 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: Q4QGJ9
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 | 277 | 279 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.645 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.720 |
DEG_SCF_FBW7_1 | 474 | 480 | PF00400 | 0.414 |
DEG_SCF_FBW7_2 | 515 | 520 | PF00400 | 0.448 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.581 |
DEG_SPOP_SBC_1 | 477 | 481 | PF00917 | 0.429 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.562 |
DEG_SPOP_SBC_1 | 495 | 499 | PF00917 | 0.461 |
DOC_CKS1_1 | 474 | 479 | PF01111 | 0.413 |
DOC_CYCLIN_RxL_1 | 107 | 115 | PF00134 | 0.265 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.647 |
DOC_CYCLIN_RxL_1 | 374 | 385 | PF00134 | 0.258 |
DOC_MAPK_gen_1 | 278 | 285 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 326 | 333 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.293 |
DOC_PP1_RVXF_1 | 132 | 138 | PF00149 | 0.230 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.369 |
DOC_PP1_RVXF_1 | 228 | 235 | PF00149 | 0.283 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.410 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.382 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 278 | 285 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 201 | 216 | PF00022 | 0.254 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.257 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.312 |
LIG_deltaCOP1_diTrp_1 | 62 | 69 | PF00928 | 0.385 |
LIG_EVH1_1 | 473 | 477 | PF00568 | 0.411 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.277 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.351 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.235 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.299 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.372 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.474 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.422 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.423 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.422 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.446 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.461 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.394 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.362 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.403 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 231 | 242 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.365 |
LIG_NRBOX | 279 | 285 | PF00104 | 0.228 |
LIG_NRBOX | 327 | 333 | PF00104 | 0.325 |
LIG_PDZ_Class_2 | 582 | 587 | PF00595 | 0.269 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.251 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.531 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.658 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.496 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.454 |
LIG_Sin3_3 | 571 | 578 | PF02671 | 0.255 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.323 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.473 |
LIG_UBA3_1 | 108 | 116 | PF00899 | 0.229 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.437 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.336 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.360 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.342 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.351 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.301 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.341 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.356 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.403 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.394 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.332 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.293 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.424 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.426 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.476 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.462 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.432 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.449 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.597 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.540 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.596 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.570 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.576 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.498 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.566 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.730 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.554 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.504 |
MOD_GlcNHglycan | 297 | 301 | PF01048 | 0.515 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.611 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.606 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.581 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.560 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.490 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.561 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.564 |
MOD_GlcNHglycan | 385 | 389 | PF01048 | 0.599 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.563 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.628 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.470 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.550 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.399 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.388 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.326 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.367 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.332 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.331 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.552 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.362 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.368 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.345 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.568 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.608 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.588 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.483 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.501 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.535 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.489 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.342 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.532 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.351 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.360 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.336 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.559 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.345 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.358 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.294 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.359 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.334 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.376 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.408 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.349 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.347 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.523 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.486 |
MOD_NEK2_2 | 401 | 406 | PF00069 | 0.268 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.466 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.322 |
MOD_PK_1 | 166 | 172 | PF00069 | 0.267 |
MOD_PK_1 | 214 | 220 | PF00069 | 0.251 |
MOD_PKA_1 | 278 | 284 | PF00069 | 0.238 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.250 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.359 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.345 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.386 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.319 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.284 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.293 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.345 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.540 |
MOD_Plk_2-3 | 160 | 166 | PF00069 | 0.439 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.320 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.278 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.341 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.335 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.350 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.324 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.286 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.297 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.611 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.600 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 416 | 422 | PF00179 | 0.295 |
TRG_DiLeu_BaEn_1 | 551 | 556 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I661 | Leptomonas seymouri | 37% | 100% |
A0A0S4IHI7 | Bodo saltans | 28% | 76% |
A0A0S4IN27 | Bodo saltans | 37% | 100% |
A0A0S4IRQ2 | Bodo saltans | 31% | 69% |
A0A0S4ISU4 | Bodo saltans | 36% | 89% |
A0A0S4IT62 | Bodo saltans | 36% | 79% |
A0A0S4IU91 | Bodo saltans | 26% | 67% |
A0A0S4IW93 | Bodo saltans | 30% | 97% |
A0A0S4IWB9 | Bodo saltans | 32% | 71% |
A0A0S4J014 | Bodo saltans | 29% | 82% |
A0A0S4J2H8 | Bodo saltans | 25% | 100% |
A0A0S4J4L7 | Bodo saltans | 25% | 80% |
A0A0S4J954 | Bodo saltans | 25% | 79% |
A0A0S4JB95 | Bodo saltans | 28% | 97% |
A0A0S4JNU2 | Bodo saltans | 36% | 71% |
A0A0S4KEC2 | Bodo saltans | 36% | 67% |
A0A0S4KEG2 | Bodo saltans | 26% | 70% |
A0A0S4KF94 | Bodo saltans | 24% | 67% |
A0A0S4KK37 | Bodo saltans | 31% | 100% |
A0A3Q8IC27 | Leishmania donovani | 35% | 100% |
A0A3S5H6M3 | Leishmania donovani | 61% | 86% |
A0A3S5H6M4 | Leishmania donovani | 57% | 89% |
A0A3S7WS66 | Leishmania donovani | 57% | 89% |
A4HBX3 | Leishmania braziliensis | 37% | 100% |
A4HVB0 | Leishmania infantum | 44% | 90% |
A4HZ93 | Leishmania infantum | 34% | 100% |
D1GJ51 | Leishmania infantum | 55% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 77% |
E9AGG2 | Leishmania infantum | 62% | 88% |
E9AGG5 | Leishmania infantum | 51% | 100% |
E9AGG7 | Leishmania infantum | 58% | 94% |
E9AGG9 | Leishmania infantum | 59% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 83% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 88% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 84% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
F4J7T6 | Arabidopsis thaliana | 22% | 66% |
F4J8G2 | Arabidopsis thaliana | 27% | 67% |
F4JTU7 | Arabidopsis thaliana | 24% | 72% |
Q1PEN0 | Arabidopsis thaliana | 23% | 82% |
Q40235 | Solanum pimpinellifolium | 22% | 68% |
Q4QC79 | Leishmania major | 36% | 100% |
Q4QGI0 | Leishmania major | 57% | 100% |
Q4QGI2 | Leishmania major | 58% | 100% |
Q4QGI4 | Leishmania major | 57% | 100% |
Q4QGI6 | Leishmania major | 60% | 100% |
Q4QGI8 | Leishmania major | 49% | 100% |
Q4QGJ0 | Leishmania major | 64% | 100% |
Q4QGJ2 | Leishmania major | 67% | 100% |
Q4QGJ6 | Leishmania major | 55% | 100% |
Q4QGK0 | Leishmania major | 63% | 100% |
Q4QGK1 | Leishmania major | 68% | 83% |
Q4QGK2 | Leishmania major | 51% | 100% |
Q4QGK4 | Leishmania major | 55% | 88% |
Q4QGK8 | Leishmania major | 54% | 100% |
Q4QGL2 | Leishmania major | 54% | 100% |
Q4QGL4 | Leishmania major | 68% | 100% |
Q4QGL8 | Leishmania major | 64% | 96% |
Q4QGM1 | Leishmania major | 54% | 76% |
Q8RX63 | Arabidopsis thaliana | 26% | 68% |
Q8TF66 | Homo sapiens | 22% | 100% |
Q9C9H6 | Arabidopsis thaliana | 24% | 75% |
Q9C9H7 | Arabidopsis thaliana | 24% | 69% |
Q9FYK0 | Arabidopsis thaliana | 23% | 66% |
Q9LS79 | Arabidopsis thaliana | 21% | 75% |
Q9LS80 | Arabidopsis thaliana | 24% | 70% |
Q9M9X0 | Arabidopsis thaliana | 25% | 68% |
Q9SHI3 | Arabidopsis thaliana | 22% | 81% |
Q9SVM3 | Arabidopsis thaliana | 24% | 70% |
Q9SVN2 | Arabidopsis thaliana | 22% | 73% |