Publication identifier(s): 9566492
These leucine-rich repeat proteins bear a signal peptide but most lack a TM segment. They belong to the broader PSA/GP46/bodonin family. Localization: Cell surface (experimental)
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. | no | yes: 65 |
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: 9 |
NetGPI | no | yes: 0, no: 44 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 5 |
GO:0005929 | cilium | 4 | 45 |
GO:0016020 | membrane | 2 | 23 |
GO:0042995 | cell projection | 2 | 45 |
GO:0043226 | organelle | 2 | 45 |
GO:0043227 | membrane-bounded organelle | 3 | 45 |
GO:0110165 | cellular anatomical entity | 1 | 45 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 45 |
Related structures:
AlphaFold database: Q4QGM1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004672 | protein kinase activity | 3 | 1 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.653 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.623 |
DEG_APCC_DBOX_1 | 710 | 718 | PF00400 | 0.252 |
DOC_CYCLIN_RxL_1 | 185 | 196 | PF00134 | 0.252 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.677 |
DOC_MAPK_gen_1 | 635 | 645 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.207 |
DOC_MAPK_MEF2A_6 | 732 | 740 | PF00069 | 0.566 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.268 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.393 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.272 |
DOC_USP7_MATH_2 | 295 | 301 | PF00917 | 0.426 |
DOC_USP7_MATH_2 | 391 | 397 | PF00917 | 0.290 |
DOC_USP7_MATH_2 | 463 | 469 | PF00917 | 0.307 |
DOC_USP7_MATH_2 | 535 | 541 | PF00917 | 0.322 |
DOC_WW_Pin1_4 | 762 | 767 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 345 | 352 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 441 | 448 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 513 | 520 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 585 | 592 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 635 | 641 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 684 | 693 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 756 | 760 | PF00244 | 0.694 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.209 |
LIG_Clathr_ClatBox_1 | 737 | 741 | PF01394 | 0.272 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.491 |
LIG_DLG_GKlike_1 | 203 | 210 | PF00625 | 0.221 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.332 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.380 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.468 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.256 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.345 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.286 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.265 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.243 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.244 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.526 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.350 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.227 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.242 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.251 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.471 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.347 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.391 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.481 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.448 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.504 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.274 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.277 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.307 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.377 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.487 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 225 | 232 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 465 | 472 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 537 | 544 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 681 | 688 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 705 | 714 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.327 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.211 |
LIG_PCNA_PIPBox_1 | 613 | 622 | PF02747 | 0.366 |
LIG_PCNA_PIPBox_1 | 637 | 646 | PF02747 | 0.316 |
LIG_SH2_SRC | 620 | 623 | PF00017 | 0.433 |
LIG_SH2_SRC | 644 | 647 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.338 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.211 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.238 |
LIG_SUMO_SIM_par_1 | 665 | 670 | PF11976 | 0.349 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.532 |
LIG_UBA3_1 | 736 | 745 | PF00899 | 0.278 |
LIG_WW_3 | 342 | 346 | PF00397 | 0.238 |
LIG_WW_3 | 438 | 442 | PF00397 | 0.237 |
LIG_WW_3 | 510 | 514 | PF00397 | 0.239 |
LIG_WW_3 | 582 | 586 | PF00397 | 0.245 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.322 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.376 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.389 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.298 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.311 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.285 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.303 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.258 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.260 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.284 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.239 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.242 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.233 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.232 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.260 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.257 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.336 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.341 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.347 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.229 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.264 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.240 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.302 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.314 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.406 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.459 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.390 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.267 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.342 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.352 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.393 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.583 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.344 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.333 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.377 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.325 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.282 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.276 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.268 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.298 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.263 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.272 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.269 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.313 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.268 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.374 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.403 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.474 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.433 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.397 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.319 |
MOD_GlcNHglycan | 697 | 701 | PF01048 | 0.405 |
MOD_GlcNHglycan | 705 | 709 | PF01048 | 0.382 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.338 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.267 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.344 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.405 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.325 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.320 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.325 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.597 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.371 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.303 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.286 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.319 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.261 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.260 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.284 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.387 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.386 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.348 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.688 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.713 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.354 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.456 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.294 |
MOD_N-GLC_2 | 753 | 755 | PF02516 | 0.488 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.502 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.322 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.248 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.265 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.355 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.473 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.309 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.337 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.393 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.346 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.337 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.303 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.285 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.238 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.287 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.245 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.240 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.283 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.247 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.245 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.438 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.357 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.405 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.447 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.530 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.335 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.299 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.480 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.281 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.437 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.533 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.413 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.450 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.466 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.394 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.384 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.278 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.333 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.270 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.302 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.328 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.341 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.366 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.480 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.487 |
MOD_PIKK_1 | 621 | 627 | PF00454 | 0.417 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.455 |
MOD_PIKK_1 | 669 | 675 | PF00454 | 0.432 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.298 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.365 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.295 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.293 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.320 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.326 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.730 |
MOD_PKB_1 | 157 | 165 | PF00069 | 0.224 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.288 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.349 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.440 |
MOD_Plk_1 | 680 | 686 | PF00069 | 0.410 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.486 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.380 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.499 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.392 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.337 |
MOD_ProDKin_1 | 762 | 768 | PF00069 | 0.495 |
MOD_SUMO_rev_2 | 251 | 256 | PF00179 | 0.247 |
MOD_SUMO_rev_2 | 323 | 328 | PF00179 | 0.248 |
MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.249 |
MOD_SUMO_rev_2 | 419 | 424 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 443 | 448 | PF00179 | 0.237 |
MOD_SUMO_rev_2 | 491 | 496 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 515 | 520 | PF00179 | 0.235 |
MOD_SUMO_rev_2 | 563 | 568 | PF00179 | 0.252 |
MOD_SUMO_rev_2 | 587 | 592 | PF00179 | 0.247 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.265 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.234 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.250 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.293 |
TRG_NES_CRM1_1 | 252 | 262 | PF08389 | 0.244 |
TRG_NES_CRM1_1 | 324 | 334 | PF08389 | 0.243 |
TRG_NES_CRM1_1 | 348 | 358 | PF08389 | 0.236 |
TRG_NES_CRM1_1 | 420 | 430 | PF08389 | 0.232 |
TRG_NES_CRM1_1 | 444 | 454 | PF08389 | 0.233 |
TRG_NES_CRM1_1 | 492 | 502 | PF08389 | 0.233 |
TRG_NES_CRM1_1 | 516 | 526 | PF08389 | 0.233 |
TRG_NES_CRM1_1 | 564 | 574 | PF08389 | 0.245 |
TRG_NES_CRM1_1 | 588 | 598 | PF08389 | 0.242 |
TRG_NES_CRM1_1 | 612 | 622 | PF08389 | 0.241 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.226 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.236 |
TRG_Pf-PMV_PEXEL_1 | 305 | 310 | PF00026 | 0.230 |
TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 401 | 406 | PF00026 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 473 | 478 | PF00026 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 521 | 526 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 545 | 550 | PF00026 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 665 | 670 | PF00026 | 0.247 |
TRG_Pf-PMV_PEXEL_1 | 684 | 689 | PF00026 | 0.248 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A5 | Leptomonas seymouri | 30% | 100% |
A0A0R0HPY5 | Glycine max | 29% | 79% |
A0A0S4IH88 | Bodo saltans | 40% | 70% |
A0A0S4IIQ2 | Bodo saltans | 25% | 71% |
A0A0S4IJN2 | Bodo saltans | 25% | 100% |
A0A0S4ISU4 | Bodo saltans | 40% | 100% |
A0A0S4IT62 | Bodo saltans | 37% | 100% |
A0A0S4ITE7 | Bodo saltans | 38% | 87% |
A0A0S4ITR1 | Bodo saltans | 35% | 71% |
A0A0S4IU23 | Bodo saltans | 30% | 100% |
A0A0S4IU91 | Bodo saltans | 29% | 88% |
A0A0S4IVQ8 | Bodo saltans | 33% | 100% |
A0A0S4IW93 | Bodo saltans | 27% | 100% |
A0A0S4IZD9 | Bodo saltans | 26% | 69% |
A0A0S4J014 | Bodo saltans | 27% | 100% |
A0A0S4J021 | Bodo saltans | 26% | 67% |
A0A0S4J0N5 | Bodo saltans | 25% | 90% |
A0A0S4J0Q7 | Bodo saltans | 26% | 81% |
A0A0S4J0S0 | Bodo saltans | 25% | 71% |
A0A0S4J0Z0 | Bodo saltans | 27% | 72% |
A0A0S4J1D6 | Bodo saltans | 30% | 79% |
A0A0S4J360 | Bodo saltans | 35% | 72% |
A0A0S4J5I5 | Bodo saltans | 27% | 77% |
A0A0S4J8U4 | Bodo saltans | 35% | 73% |
A0A0S4J954 | Bodo saltans | 25% | 100% |
A0A0S4J985 | Bodo saltans | 39% | 78% |
A0A0S4JAS1 | Bodo saltans | 36% | 100% |
A0A0S4JDT0 | Bodo saltans | 34% | 100% |
A0A0S4JG17 | Bodo saltans | 25% | 67% |
A0A0S4JJG7 | Bodo saltans | 28% | 75% |
A0A0S4JL76 | Bodo saltans | 28% | 66% |
A0A0S4JMQ7 | Bodo saltans | 43% | 77% |
A0A0S4JNU2 | Bodo saltans | 43% | 95% |
A0A0S4JQZ4 | Bodo saltans | 36% | 77% |
A0A0S4JTM6 | Bodo saltans | 33% | 100% |
A0A0S4JU35 | Bodo saltans | 26% | 82% |
A0A0S4JV99 | Bodo saltans | 27% | 73% |
A0A0S4JVI0 | Bodo saltans | 26% | 100% |
A0A0S4KEC2 | Bodo saltans | 35% | 88% |
A0A0S4KEG2 | Bodo saltans | 28% | 92% |
A0A0S4KF94 | Bodo saltans | 26% | 89% |
A0A0S4KJA7 | Bodo saltans | 25% | 100% |
A0A0S4KLY4 | Bodo saltans | 28% | 73% |
A0A1P8ATR9 | Arabidopsis thaliana | 25% | 83% |
A0A1X0ND37 | Trypanosomatidae | 25% | 82% |
A0A3Q8I9B4 | Leishmania donovani | 37% | 100% |
A0A3Q8I9D9 | Leishmania donovani | 37% | 100% |
A0A3S5H6L9 | Leishmania donovani | 42% | 100% |
A0A3S5H6M3 | Leishmania donovani | 52% | 100% |
A0A3S5H6M4 | Leishmania donovani | 53% | 100% |
A0A3S7WS66 | Leishmania donovani | 53% | 100% |
A4H6Y8 | Leishmania braziliensis | 51% | 85% |
A4HM85 | Leishmania braziliensis | 31% | 77% |
A4HM88 | Leishmania braziliensis | 28% | 90% |
C0LGF5 | Arabidopsis thaliana | 29% | 72% |
C0LGJ1 | Arabidopsis thaliana | 25% | 70% |
C0LGP4 | Arabidopsis thaliana | 25% | 77% |
C0LGQ9 | Arabidopsis thaliana | 29% | 74% |
C0LGR3 | Arabidopsis thaliana | 27% | 71% |
C0LGS2 | Arabidopsis thaliana | 29% | 68% |
C0LGT6 | Arabidopsis thaliana | 24% | 75% |
C0LGV1 | Arabidopsis thaliana | 27% | 68% |
C0LGW6 | Arabidopsis thaliana | 27% | 80% |
C0LGX3 | Arabidopsis thaliana | 26% | 78% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AGG2 | Leishmania infantum | 54% | 100% |
E9AGG7 | Leishmania infantum | 59% | 100% |
E9AGG9 | Leishmania infantum | 60% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9Q7T7 | Mus musculus | 23% | 100% |
F4HTV4 | Arabidopsis thaliana | 23% | 80% |
F4I9S3 | Arabidopsis thaliana | 24% | 83% |
F4IUU1 | Arabidopsis thaliana | 26% | 96% |
F4J7T6 | Arabidopsis thaliana | 25% | 88% |
F4J8G2 | Arabidopsis thaliana | 26% | 89% |
F4J9A8 | Arabidopsis thaliana | 24% | 82% |
F4JGB6 | Arabidopsis thaliana | 26% | 96% |
F4JTU7 | Arabidopsis thaliana | 24% | 95% |
F4K4T3 | Arabidopsis thaliana | 26% | 82% |
F4K6B8 | Arabidopsis thaliana | 26% | 71% |
F4KHA2 | Arabidopsis thaliana | 24% | 98% |
G7JIK2 | Medicago truncatula | 28% | 80% |
G9LZD7 | Oryza sativa subsp. japonica | 30% | 67% |
I1Z695 | Oryza sativa subsp. japonica | 26% | 79% |
O15455 | Homo sapiens | 24% | 86% |
O48849 | Arabidopsis thaliana | 22% | 87% |
O48851 | Arabidopsis thaliana | 24% | 100% |
O49318 | Arabidopsis thaliana | 28% | 69% |
O49325 | Arabidopsis thaliana | 23% | 100% |
O49328 | Arabidopsis thaliana | 23% | 97% |
O49329 | Arabidopsis thaliana | 23% | 90% |
O49545 | Arabidopsis thaliana | 28% | 77% |
O49879 | Solanum lycopersicum | 23% | 92% |
O65440 | Arabidopsis thaliana | 28% | 78% |
O80809 | Arabidopsis thaliana | 26% | 100% |
O82318 | Arabidopsis thaliana | 27% | 81% |
P0DL10 | Zea mays | 28% | 78% |
P0DO05 | Solanum pimpinellifolium | 23% | 90% |
P0DO06 | Solanum pimpinellifolium | 23% | 90% |
P47735 | Arabidopsis thaliana | 27% | 78% |
P93194 | Ipomoea nil | 27% | 70% |
Q1MX30 | Oryza sativa subsp. indica | 27% | 76% |
Q1PEN0 | Arabidopsis thaliana | 22% | 100% |
Q2R2D5 | Oryza sativa subsp. japonica | 26% | 75% |
Q40235 | Solanum pimpinellifolium | 24% | 90% |
Q42371 | Arabidopsis thaliana | 26% | 80% |
Q4QGI2 | Leishmania major | 83% | 100% |
Q4QGI4 | Leishmania major | 88% | 100% |
Q4QGI6 | Leishmania major | 57% | 100% |
Q4QGI8 | Leishmania major | 83% | 100% |
Q4QGJ0 | Leishmania major | 56% | 100% |
Q4QGJ2 | Leishmania major | 56% | 100% |
Q4QGJ9 | Leishmania major | 54% | 100% |
Q4QGK0 | Leishmania major | 62% | 100% |
Q4QGK2 | Leishmania major | 69% | 100% |
Q4QGK4 | Leishmania major | 55% | 100% |
Q4QGL8 | Leishmania major | 60% | 100% |
Q5MR23 | Solanum pimpinellifolium | 23% | 90% |
Q5Z9N5 | Oryza sativa subsp. japonica | 29% | 78% |
Q69SP5 | Oryza sativa subsp. japonica | 27% | 79% |
Q6JN46 | Solanum lycopersicum | 25% | 76% |
Q6JN47 | Solanum lycopersicum | 26% | 75% |
Q6K7R2 | Oryza sativa subsp. japonica | 25% | 100% |
Q6R5N8 | Mus musculus | 24% | 78% |
Q70CT4 | Arabidopsis thaliana | 25% | 74% |
Q7FZR1 | Arabidopsis thaliana | 22% | 96% |
Q7G768 | Oryza sativa subsp. japonica | 27% | 70% |
Q7TQ62 | Mus musculus | 22% | 100% |
Q7Z5L7 | Homo sapiens | 22% | 100% |
Q8C0R9 | Mus musculus | 24% | 91% |
Q8GRU6 | Lotus japonicus | 28% | 79% |
Q8LPB4 | Daucus carota | 25% | 76% |
Q8RX63 | Arabidopsis thaliana | 26% | 90% |
Q8VZG8 | Arabidopsis thaliana | 27% | 74% |
Q93YT3 | Arabidopsis thaliana | 24% | 87% |
Q942F3 | Oryza sativa subsp. japonica | 25% | 69% |
Q9C637 | Arabidopsis thaliana | 22% | 78% |
Q9C699 | Arabidopsis thaliana | 24% | 80% |
Q9C6A6 | Arabidopsis thaliana | 25% | 73% |
Q9C6A8 | Arabidopsis thaliana | 24% | 80% |
Q9C7S5 | Arabidopsis thaliana | 25% | 71% |
Q9C9H6 | Arabidopsis thaliana | 24% | 99% |
Q9C9H7 | Arabidopsis thaliana | 23% | 92% |
Q9FII5 | Arabidopsis thaliana | 25% | 75% |
Q9FL28 | Arabidopsis thaliana | 26% | 66% |
Q9FN37 | Arabidopsis thaliana | 24% | 75% |
Q9FRS6 | Arabidopsis thaliana | 25% | 75% |
Q9FZ59 | Arabidopsis thaliana | 27% | 71% |
Q9LHP4 | Arabidopsis thaliana | 28% | 68% |
Q9LJF3 | Arabidopsis thaliana | 26% | 67% |
Q9LJS0 | Arabidopsis thaliana | 23% | 87% |
Q9LJS2 | Arabidopsis thaliana | 25% | 88% |
Q9LJW7 | Arabidopsis thaliana | 25% | 100% |
Q9LNV9 | Arabidopsis thaliana | 26% | 72% |
Q9LP24 | Arabidopsis thaliana | 27% | 69% |
Q9LRT1 | Arabidopsis thaliana | 29% | 76% |
Q9LRW9 | Arabidopsis thaliana | 22% | 88% |
Q9LS79 | Arabidopsis thaliana | 23% | 99% |
Q9LS80 | Arabidopsis thaliana | 23% | 93% |
Q9LVP0 | Arabidopsis thaliana | 27% | 70% |
Q9LZV7 | Arabidopsis thaliana | 27% | 80% |
Q9M0G7 | Arabidopsis thaliana | 28% | 77% |
Q9M2Z1 | Arabidopsis thaliana | 28% | 77% |
Q9M6A7 | Glycine max | 29% | 79% |
Q9M9X0 | Arabidopsis thaliana | 25% | 89% |
Q9MA83 | Arabidopsis thaliana | 27% | 99% |
Q9S7I6 | Arabidopsis thaliana | 25% | 67% |
Q9S9U3 | Arabidopsis thaliana | 25% | 81% |
Q9SD62 | Arabidopsis thaliana | 26% | 76% |
Q9SGP2 | Arabidopsis thaliana | 27% | 78% |
Q9SHI2 | Arabidopsis thaliana | 25% | 70% |
Q9SHI3 | Arabidopsis thaliana | 24% | 100% |
Q9SHI4 | Arabidopsis thaliana | 25% | 100% |
Q9SKK2 | Arabidopsis thaliana | 25% | 79% |
Q9SLI6 | Arabidopsis thaliana | 24% | 77% |
Q9SRL2 | Arabidopsis thaliana | 24% | 81% |
Q9SRL7 | Arabidopsis thaliana | 24% | 82% |
Q9SSL9 | Arabidopsis thaliana | 28% | 69% |
Q9SVM3 | Arabidopsis thaliana | 24% | 92% |
Q9SVN2 | Arabidopsis thaliana | 24% | 97% |
Q9SYQ8 | Arabidopsis thaliana | 26% | 79% |
Q9ZPS9 | Arabidopsis thaliana | 26% | 68% |
Q9ZUI0 | Arabidopsis thaliana | 25% | 79% |
Q9ZUK3 | Arabidopsis thaliana | 23% | 79% |
Q9ZUK7 | Arabidopsis thaliana | 23% | 94% |
Q9ZVR7 | Arabidopsis thaliana | 23% | 77% |
Q9ZWC8 | Arabidopsis thaliana | 26% | 67% |