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: 7 |
NetGPI | no | yes: 0, no: 42 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 43 |
GO:0016020 | membrane | 2 | 28 |
GO:0042995 | cell projection | 2 | 43 |
GO:0043226 | organelle | 2 | 43 |
GO:0043227 | membrane-bounded organelle | 3 | 43 |
GO:0110165 | cellular anatomical entity | 1 | 43 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 43 |
GO:0005886 | plasma membrane | 3 | 7 |
Related structures:
AlphaFold database: Q4QGI8
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 | 0.343 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.761 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.722 |
DEG_APCC_DBOX_1 | 494 | 502 | PF00400 | 0.433 |
DEG_SCF_FBW7_2 | 688 | 693 | PF00400 | 0.490 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 556 | 560 | PF00917 | 0.590 |
DEG_SPOP_SBC_1 | 566 | 570 | PF00917 | 0.550 |
DEG_SPOP_SBC_1 | 576 | 580 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 587 | 591 | PF00917 | 0.450 |
DEG_SPOP_SBC_1 | 596 | 600 | PF00917 | 0.443 |
DEG_SPOP_SBC_1 | 607 | 611 | PF00917 | 0.530 |
DEG_SPOP_SBC_1 | 616 | 620 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 646 | 650 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 667 | 671 | PF00917 | 0.501 |
DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.322 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.635 |
DOC_MAPK_gen_1 | 419 | 429 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 517 | 524 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.415 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.446 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 468 | 477 | PF00244 | 0.382 |
LIG_Actin_WH2_2 | 417 | 432 | PF00022 | 0.231 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.435 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 176 | 183 | PF00928 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 61 | 69 | PF00928 | 0.434 |
LIG_DLG_GKlike_1 | 203 | 210 | PF00625 | 0.251 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.361 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.362 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.377 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.316 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.357 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.343 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.318 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.310 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.357 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.443 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.362 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.419 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.408 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.449 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.539 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.520 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.358 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.420 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.404 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.387 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.503 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.482 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.442 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 465 | 472 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.349 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.357 |
LIG_PCNA_PIPBox_1 | 397 | 406 | PF02747 | 0.324 |
LIG_PDZ_Class_2 | 755 | 760 | PF00595 | 0.298 |
LIG_Pex14_1 | 179 | 183 | PF04695 | 0.228 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 730 | 733 | PF00017 | 0.542 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.624 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.419 |
LIG_Sin3_3 | 744 | 751 | PF02671 | 0.298 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.377 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.446 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.367 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.374 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.363 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.240 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.320 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.348 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.379 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.334 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.347 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.260 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.338 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.381 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.267 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.427 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.431 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.502 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.487 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.443 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.597 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.550 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.543 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.577 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.545 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.545 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.736 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.588 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.557 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.567 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.568 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.462 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.601 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.571 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.580 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.604 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.584 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.586 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.647 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.706 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.433 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.383 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.320 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.328 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.371 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.345 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.346 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.355 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.594 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.355 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.353 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.367 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.398 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.378 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.533 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.539 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.464 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.477 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.563 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.520 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.483 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.522 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.497 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.490 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.534 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.572 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.521 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.555 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.626 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.496 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.418 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.508 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.642 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.350 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.330 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.301 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.380 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.536 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.415 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.382 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.378 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.387 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.349 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.407 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.417 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.390 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.431 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.351 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.383 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.354 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.254 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.431 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.327 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.408 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.374 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.399 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.349 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.456 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.386 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.437 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.467 |
MOD_PK_1 | 225 | 231 | PF00069 | 0.237 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.339 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.343 |
MOD_PKB_1 | 157 | 165 | PF00069 | 0.261 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.369 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.419 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.393 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.425 |
MOD_Plk_1 | 723 | 729 | PF00069 | 0.501 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.437 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.389 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.316 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 248 | 256 | PF00179 | 0.244 |
MOD_SUMO_rev_2 | 323 | 328 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.244 |
MOD_SUMO_rev_2 | 395 | 400 | PF00179 | 0.255 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.316 |
TRG_DiLeu_BaEn_1 | 724 | 729 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.264 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.713 |
TRG_NES_CRM1_1 | 252 | 262 | PF08389 | 0.257 |
TRG_NES_CRM1_1 | 324 | 334 | PF08389 | 0.256 |
TRG_NES_CRM1_1 | 348 | 358 | PF08389 | 0.246 |
TRG_NES_CRM1_1 | 396 | 406 | PF08389 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 305 | 310 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IH88 | Bodo saltans | 34% | 68% |
A0A0S4IIQ2 | Bodo saltans | 24% | 70% |
A0A0S4IRQ2 | Bodo saltans | 30% | 89% |
A0A0S4IT62 | Bodo saltans | 38% | 100% |
A0A0S4IU23 | Bodo saltans | 28% | 100% |
A0A0S4IVU4 | Bodo saltans | 27% | 74% |
A0A0S4IZD9 | Bodo saltans | 26% | 68% |
A0A0S4J014 | Bodo saltans | 26% | 100% |
A0A0S4J0Z0 | Bodo saltans | 25% | 70% |
A0A0S4J206 | Bodo saltans | 34% | 100% |
A0A0S4J5I5 | Bodo saltans | 26% | 76% |
A0A0S4J7H0 | Bodo saltans | 29% | 76% |
A0A0S4J954 | Bodo saltans | 25% | 100% |
A0A0S4JB95 | Bodo saltans | 23% | 100% |
A0A0S4JLC0 | Bodo saltans | 31% | 73% |
A0A0S4JMQ7 | Bodo saltans | 36% | 75% |
A0A0S4JNU2 | Bodo saltans | 35% | 93% |
A0A0S4JQZ4 | Bodo saltans | 31% | 76% |
A0A0S4JTM6 | Bodo saltans | 29% | 100% |
A0A0S4JV99 | Bodo saltans | 26% | 72% |
A0A0S4KEC2 | Bodo saltans | 36% | 86% |
A0A0S4KF94 | Bodo saltans | 26% | 87% |
A0A1X0ND37 | Trypanosomatidae | 23% | 80% |
A0A3Q8I9B4 | Leishmania donovani | 41% | 100% |
A0A3S5H6M3 | Leishmania donovani | 52% | 100% |
A0A3S5H6M4 | Leishmania donovani | 54% | 100% |
A0A3S7WS66 | Leishmania donovani | 54% | 100% |
A4HM88 | Leishmania braziliensis | 27% | 100% |
E8NHG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AGG2 | Leishmania infantum | 51% | 100% |
E9AGG7 | Leishmania infantum | 59% | 100% |
E9AGG9 | Leishmania infantum | 59% | 100% |
E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
F4J8G2 | Arabidopsis thaliana | 25% | 87% |
F4JTU7 | Arabidopsis thaliana | 24% | 93% |
O65440 | Arabidopsis thaliana | 22% | 77% |
O80809 | Arabidopsis thaliana | 22% | 100% |
P93194 | Ipomoea nil | 26% | 69% |
Q1PEN0 | Arabidopsis thaliana | 22% | 100% |
Q4QGI0 | Leishmania major | 62% | 94% |
Q4QGI2 | Leishmania major | 89% | 100% |
Q4QGI4 | Leishmania major | 89% | 99% |
Q4QGI6 | Leishmania major | 57% | 100% |
Q4QGJ0 | Leishmania major | 54% | 100% |
Q4QGJ2 | Leishmania major | 53% | 100% |
Q4QGJ9 | Leishmania major | 49% | 100% |
Q4QGK0 | Leishmania major | 52% | 100% |
Q4QGK1 | Leishmania major | 52% | 100% |
Q4QGK2 | Leishmania major | 75% | 100% |
Q4QGK4 | Leishmania major | 53% | 100% |
Q4QGK8 | Leishmania major | 62% | 100% |
Q4QGL2 | Leishmania major | 62% | 100% |
Q4QGL8 | Leishmania major | 65% | 100% |
Q4QGM1 | Leishmania major | 83% | 98% |
Q5MR23 | Solanum pimpinellifolium | 22% | 88% |
Q8LPB4 | Daucus carota | 22% | 74% |
Q8RX63 | Arabidopsis thaliana | 24% | 88% |
Q93YT3 | Arabidopsis thaliana | 26% | 85% |
Q9C699 | Arabidopsis thaliana | 26% | 78% |
Q9LJW7 | Arabidopsis thaliana | 24% | 100% |
Q9LRT1 | Arabidopsis thaliana | 26% | 75% |
Q9LY03 | Arabidopsis thaliana | 26% | 79% |
Q9LZV7 | Arabidopsis thaliana | 27% | 79% |
Q9M9X0 | Arabidopsis thaliana | 25% | 88% |
Q9SD62 | Arabidopsis thaliana | 24% | 74% |
Q9SVM3 | Arabidopsis thaliana | 24% | 90% |
Q9SVN2 | Arabidopsis thaliana | 24% | 95% |
Q9ZUI0 | Arabidopsis thaliana | 24% | 78% |