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: 90 |
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: 35, no: 5 |
NetGPI | no | yes: 0, no: 40 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 41 |
GO:0042995 | cell projection | 2 | 41 |
GO:0043226 | organelle | 2 | 41 |
GO:0043227 | membrane-bounded organelle | 3 | 41 |
GO:0110165 | cellular anatomical entity | 1 | 41 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 41 |
GO:0016020 | membrane | 2 | 22 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: E9AP04
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_NRD_NRD_1 | 6 | 8 | PF00675 | 0.767 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.517 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.550 |
DEG_SPOP_SBC_1 | 493 | 497 | PF00917 | 0.790 |
DEG_SPOP_SBC_1 | 502 | 506 | PF00917 | 0.711 |
DEG_SPOP_SBC_1 | 511 | 515 | PF00917 | 0.804 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.785 |
DEG_SPOP_SBC_1 | 529 | 533 | PF00917 | 0.858 |
DEG_SPOP_SBC_1 | 538 | 542 | PF00917 | 0.794 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.692 |
DEG_SPOP_SBC_1 | 556 | 560 | PF00917 | 0.811 |
DEG_SPOP_SBC_1 | 565 | 569 | PF00917 | 0.869 |
DEG_SPOP_SBC_1 | 574 | 578 | PF00917 | 0.544 |
DEG_SPOP_SBC_1 | 583 | 587 | PF00917 | 0.692 |
DEG_SPOP_SBC_1 | 592 | 596 | PF00917 | 0.811 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 610 | 614 | PF00917 | 0.733 |
DEG_SPOP_SBC_1 | 619 | 623 | PF00917 | 0.801 |
DEG_SPOP_SBC_1 | 628 | 632 | PF00917 | 0.802 |
DEG_SPOP_SBC_1 | 637 | 641 | PF00917 | 0.838 |
DEG_SPOP_SBC_1 | 646 | 650 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 655 | 659 | PF00917 | 0.797 |
DEG_SPOP_SBC_1 | 664 | 668 | PF00917 | 0.813 |
DEG_SPOP_SBC_1 | 673 | 677 | PF00917 | 0.788 |
DEG_SPOP_SBC_1 | 691 | 695 | PF00917 | 0.583 |
DOC_CYCLIN_RxL_1 | 184 | 196 | PF00134 | 0.402 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 445 | 452 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 445 | 452 | PF00069 | 0.637 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.451 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.665 |
DOC_USP7_MATH_2 | 174 | 180 | PF00917 | 0.411 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 468 | 473 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.282 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.333 |
LIG_Actin_WH2_2 | 273 | 288 | PF00022 | 0.274 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.749 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 374 | 378 | PF00533 | 0.476 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.280 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.462 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.414 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.424 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.513 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.436 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.422 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.432 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.675 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.437 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.558 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.404 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.501 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.536 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.559 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 113 | 118 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 297 | 305 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 375 | 386 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 417 | 424 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.474 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.342 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.583 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 281 | 286 | PF11976 | 0.506 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.498 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.338 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.515 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.264 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.506 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.453 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.465 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.534 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.496 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.469 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.569 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.475 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.519 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.437 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.578 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.551 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.621 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.534 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.569 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.431 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.690 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.693 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.722 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.336 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.527 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.440 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.472 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.537 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.489 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.438 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.529 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.534 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.702 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.441 |
MOD_GlcNHglycan | 297 | 301 | PF01048 | 0.432 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.521 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.471 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.421 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.450 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.501 |
MOD_GlcNHglycan | 369 | 373 | PF01048 | 0.456 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.444 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.557 |
MOD_GlcNHglycan | 409 | 413 | PF01048 | 0.461 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.443 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.444 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.384 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.462 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.360 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.471 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.396 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.435 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.369 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.459 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.665 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.471 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.499 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.388 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.409 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.710 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.713 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.662 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.676 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.692 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.684 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.696 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.649 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.653 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.606 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.613 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.611 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.563 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.599 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.603 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.608 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.414 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.640 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.727 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.675 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.667 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.724 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.651 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.730 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.680 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.670 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.635 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.394 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.518 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.441 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.421 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.423 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.594 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.367 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.501 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.410 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.465 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.456 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.463 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.523 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.458 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.504 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.572 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.441 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.393 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.299 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.665 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.288 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.264 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.487 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.431 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.465 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.336 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.500 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.497 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.362 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.483 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.443 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.369 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.416 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.384 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.467 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.386 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.704 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.272 |
MOD_SUMO_rev_2 | 306 | 315 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 454 | 464 | PF00179 | 0.424 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.765 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRQ2 | Bodo saltans | 30% | 82% |
A0A0S4IU91 | Bodo saltans | 28% | 79% |
A0A0S4IVU4 | Bodo saltans | 28% | 68% |
A0A0S4J100 | Bodo saltans | 27% | 83% |
A0A0S4J1D6 | Bodo saltans | 26% | 71% |
A0A0S4J206 | Bodo saltans | 33% | 100% |
A0A0S4J985 | Bodo saltans | 31% | 70% |
A0A0S4JB95 | Bodo saltans | 25% | 100% |
A0A0S4JDT0 | Bodo saltans | 30% | 100% |
A0A0S4JDX7 | Bodo saltans | 24% | 68% |
A0A0S4JTM6 | Bodo saltans | 28% | 94% |
A0A0S4KEC2 | Bodo saltans | 36% | 79% |
A0A1X0ND37 | Trypanosomatidae | 25% | 73% |
A0A3Q8IC27 | Leishmania donovani | 33% | 100% |
A0A3S5H6M3 | Leishmania donovani | 58% | 100% |
A0A3S5H6M4 | Leishmania donovani | 51% | 100% |
A0A3S7WS66 | Leishmania donovani | 52% | 100% |
A4HZ93 | Leishmania infantum | 33% | 100% |
D1GJ51 | Leishmania infantum | 49% | 97% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 91% |
E9AGG2 | Leishmania infantum | 58% | 100% |
E9AGG7 | Leishmania infantum | 64% | 100% |
E9AGG9 | Leishmania infantum | 55% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4JTU7 | Arabidopsis thaliana | 23% | 86% |
F4K4T3 | Arabidopsis thaliana | 23% | 74% |
Q4QGI0 | Leishmania major | 55% | 100% |
Q4QGI2 | Leishmania major | 54% | 100% |
Q4QGI4 | Leishmania major | 51% | 100% |
Q4QGI6 | Leishmania major | 52% | 100% |
Q4QGI8 | Leishmania major | 51% | 92% |
Q4QGJ0 | Leishmania major | 60% | 100% |
Q4QGJ2 | Leishmania major | 53% | 100% |
Q4QGJ9 | Leishmania major | 56% | 100% |
Q4QGK0 | Leishmania major | 54% | 100% |
Q4QGK2 | Leishmania major | 56% | 100% |
Q4QGK4 | Leishmania major | 54% | 100% |
Q4QGK8 | Leishmania major | 57% | 100% |
Q4QGL2 | Leishmania major | 57% | 100% |
Q4QGL8 | Leishmania major | 55% | 100% |
Q8LPB4 | Daucus carota | 25% | 68% |
Q9SRL2 | Arabidopsis thaliana | 24% | 73% |
Q9SVM3 | Arabidopsis thaliana | 23% | 83% |
Q9SYQ8 | Arabidopsis thaliana | 23% | 71% |