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: 110 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 39, no: 8 |
NetGPI | no | yes: 0, no: 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 48 |
GO:0042995 | cell projection | 2 | 48 |
GO:0043226 | organelle | 2 | 48 |
GO:0043227 | membrane-bounded organelle | 3 | 48 |
GO:0110165 | cellular anatomical entity | 1 | 48 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 48 |
GO:0016020 | membrane | 2 | 25 |
GO:0005886 | plasma membrane | 3 | 6 |
Related structures:
AlphaFold database: E9AGG7
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 | 123 | 127 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.754 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.286 |
DEG_SCF_FBW7_2 | 555 | 560 | PF00400 | 0.457 |
DEG_SPOP_SBC_1 | 456 | 460 | PF00917 | 0.584 |
DEG_SPOP_SBC_1 | 464 | 468 | PF00917 | 0.627 |
DEG_SPOP_SBC_1 | 474 | 478 | PF00917 | 0.437 |
DEG_SPOP_SBC_1 | 482 | 486 | PF00917 | 0.581 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.428 |
DEG_SPOP_SBC_1 | 500 | 504 | PF00917 | 0.401 |
DEG_SPOP_SBC_1 | 508 | 512 | PF00917 | 0.496 |
DEG_SPOP_SBC_1 | 518 | 522 | PF00917 | 0.431 |
DEG_SPOP_SBC_1 | 526 | 530 | PF00917 | 0.412 |
DEG_SPOP_SBC_1 | 534 | 538 | PF00917 | 0.441 |
DOC_AGCK_PIF_2 | 69 | 74 | PF00069 | 0.271 |
DOC_CKS1_1 | 115 | 120 | PF01111 | 0.230 |
DOC_CYCLIN_RxL_1 | 105 | 117 | PF00134 | 0.274 |
DOC_CYCLIN_RxL_1 | 184 | 196 | PF00134 | 0.300 |
DOC_CYCLIN_RxL_1 | 254 | 264 | PF00134 | 0.240 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.273 |
DOC_MAPK_gen_1 | 153 | 163 | PF00069 | 0.250 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 276 | 283 | PF00149 | 0.233 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.233 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.228 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.252 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.240 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.260 |
LIG_Actin_WH2_2 | 249 | 264 | PF00022 | 0.353 |
LIG_Actin_WH2_2 | 71 | 89 | PF00022 | 0.225 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.685 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_2 | 70 | 76 | PF00533 | 0.233 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.233 |
LIG_DLG_GKlike_1 | 278 | 285 | PF00625 | 0.217 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.291 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.366 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.301 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.397 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.416 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.346 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.298 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.279 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.403 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.416 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.432 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.417 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.616 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.411 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.447 |
LIG_GBD_Chelix_1 | 617 | 625 | PF00786 | 0.182 |
LIG_LIR_Apic_2 | 113 | 118 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 126 | 134 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.347 |
LIG_NRBOX | 182 | 188 | PF00104 | 0.240 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.370 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.592 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.386 |
LIG_SUMO_SIM_anti_2 | 350 | 356 | PF11976 | 0.256 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 616 | 622 | PF11976 | 0.186 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.457 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.356 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.330 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.364 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.307 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.343 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.313 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.351 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.391 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.349 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.380 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.543 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.252 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.611 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.563 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.604 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.624 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.705 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.633 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.625 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.575 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.571 |
MOD_GlcNHglycan | 385 | 389 | PF01048 | 0.559 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.482 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.566 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.599 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.653 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.415 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.583 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.377 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.290 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.371 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.379 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.379 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.338 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.277 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.368 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.322 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.354 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.431 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.350 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.411 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.366 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.479 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.539 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.490 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.533 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.520 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.459 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.476 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.519 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.458 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.478 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.452 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.574 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.565 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.405 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.457 |
MOD_N-GLC_2 | 435 | 437 | PF02516 | 0.572 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.673 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.345 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.318 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.313 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.357 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.625 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.293 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.368 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.361 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.424 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.448 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.358 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.401 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.369 |
MOD_PK_1 | 165 | 171 | PF00069 | 0.249 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.375 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.393 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.354 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.408 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.345 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.407 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.362 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.353 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.349 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.359 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.225 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.255 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 427 | 433 | PF00179 | 0.299 |
TRG_DiLeu_BaEn_1 | 591 | 596 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.226 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I661 | Leptomonas seymouri | 35% | 100% |
A0A0S4IRQ2 | Bodo saltans | 29% | 73% |
A0A0S4IU91 | Bodo saltans | 24% | 71% |
A0A0S4IVQ8 | Bodo saltans | 32% | 100% |
A0A0S4IWB9 | Bodo saltans | 29% | 76% |
A0A0S4J014 | Bodo saltans | 27% | 88% |
A0A0S4J6M1 | Bodo saltans | 29% | 68% |
A0A0S4JAQ3 | Bodo saltans | 25% | 70% |
A0A0S4JAW7 | Bodo saltans | 25% | 100% |
A0A0S4JBI6 | Bodo saltans | 24% | 74% |
A0A0S4JTM6 | Bodo saltans | 29% | 85% |
A0A0S4KEG2 | Bodo saltans | 25% | 75% |
A0A0S4KF94 | Bodo saltans | 24% | 72% |
A0A0S4KIR5 | Bodo saltans | 24% | 75% |
A0A3Q8IC27 | Leishmania donovani | 32% | 100% |
A0A3S5H6M3 | Leishmania donovani | 59% | 91% |
A0A3S5H6M4 | Leishmania donovani | 47% | 95% |
A0A3S7WS66 | Leishmania donovani | 51% | 95% |
A4HBX3 | Leishmania braziliensis | 31% | 100% |
A4HM88 | Leishmania braziliensis | 26% | 73% |
A4HZ93 | Leishmania infantum | 32% | 100% |
C0LGE4 | Arabidopsis thaliana | 24% | 71% |
D1GJ51 | Leishmania infantum | 57% | 100% |
E9AGG2 | Leishmania infantum | 54% | 100% |
E9AGG5 | Leishmania infantum | 41% | 94% |
E9AGG9 | Leishmania infantum | 57% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 89% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 90% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 95% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4JTU7 | Arabidopsis thaliana | 23% | 77% |
Q1PEN0 | Arabidopsis thaliana | 23% | 87% |
Q4QC79 | Leishmania major | 34% | 100% |
Q4QGI0 | Leishmania major | 57% | 100% |
Q4QGI2 | Leishmania major | 59% | 100% |
Q4QGI4 | Leishmania major | 59% | 100% |
Q4QGI6 | Leishmania major | 59% | 100% |
Q4QGI8 | Leishmania major | 59% | 82% |
Q4QGJ0 | Leishmania major | 53% | 100% |
Q4QGJ2 | Leishmania major | 54% | 100% |
Q4QGJ9 | Leishmania major | 58% | 100% |
Q4QGK0 | Leishmania major | 61% | 100% |
Q4QGK1 | Leishmania major | 57% | 89% |
Q4QGK2 | Leishmania major | 57% | 100% |
Q4QGK4 | Leishmania major | 49% | 100% |
Q4QGK8 | Leishmania major | 54% | 100% |
Q4QGL2 | Leishmania major | 54% | 100% |
Q4QGL8 | Leishmania major | 58% | 100% |
Q4QGM1 | Leishmania major | 59% | 81% |
Q9C9H6 | Arabidopsis thaliana | 21% | 80% |
Q9SHI3 | Arabidopsis thaliana | 23% | 86% |
Q9SVM3 | Arabidopsis thaliana | 21% | 74% |