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: 0 |
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 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0020023 | kinetoplast | 2 | 1 |
Related structures:
AlphaFold database: A4HM15
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000012 | single strand break repair | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0017005 | 3'-tyrosyl-DNA phosphodiesterase activity | 5 | 1 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 451 | 455 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 517 | 519 | PF00082 | 0.157 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.582 |
CLV_PCSK_PC7_1 | 671 | 677 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.157 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 317 | 321 | PF03568 | 0.509 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 308 | 316 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 562 | 570 | PF00400 | 0.279 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.417 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.456 |
DEG_SCF_FBW7_1 | 587 | 594 | PF00400 | 0.390 |
DEG_SPOP_SBC_1 | 131 | 135 | PF00917 | 0.481 |
DOC_CDC14_PxL_1 | 74 | 82 | PF14671 | 0.446 |
DOC_CKS1_1 | 580 | 585 | PF01111 | 0.295 |
DOC_CKS1_1 | 588 | 593 | PF01111 | 0.267 |
DOC_CYCLIN_yCln2_LP_2 | 149 | 155 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.334 |
DOC_MAPK_gen_1 | 372 | 380 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.357 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 475 | 478 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.357 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 161 | 176 | PF00022 | 0.538 |
LIG_Actin_WH2_2 | 60 | 77 | PF00022 | 0.357 |
LIG_AP2alpha_2 | 24 | 26 | PF02296 | 0.312 |
LIG_BIR_III_4 | 634 | 638 | PF00653 | 0.416 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 542 | 546 | PF00533 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 184 | 189 | PF00928 | 0.486 |
LIG_EH_1 | 120 | 124 | PF12763 | 0.509 |
LIG_eIF4E_1 | 581 | 587 | PF01652 | 0.367 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.552 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.469 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.473 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.256 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.475 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.426 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.366 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.649 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.496 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.503 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.469 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.357 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.428 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.530 |
LIG_LIR_Gen_1 | 24 | 34 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 543 | 554 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 55 | 66 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 582 | 592 | PF02991 | 0.305 |
LIG_LIR_LC3C_4 | 376 | 380 | PF02991 | 0.357 |
LIG_LIR_LC3C_4 | 84 | 89 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 482 | 486 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 543 | 549 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 582 | 587 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 68 | 73 | PF02991 | 0.471 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.509 |
LIG_Rb_pABgroove_1 | 528 | 536 | PF01858 | 0.503 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.435 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.347 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 567 | 571 | PF00017 | 0.373 |
LIG_SH2_PTP2 | 60 | 63 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 592 | 596 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.417 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.445 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.446 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.457 |
LIG_SUMO_SIM_anti_2 | 144 | 150 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 332 | 337 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 360 | 367 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 86 | 91 | PF11976 | 0.482 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.469 |
LIG_WW_2 | 151 | 154 | PF00397 | 0.471 |
MOD_CDK_SPxxK_3 | 302 | 309 | PF00069 | 0.357 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.488 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.486 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.473 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.469 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.458 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.486 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.509 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.348 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.467 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.428 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.426 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.516 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.407 |
MOD_CMANNOS | 391 | 394 | PF00535 | 0.269 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.351 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.257 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.157 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.242 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.450 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.288 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.224 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.228 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.310 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.422 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.612 |
MOD_GlcNHglycan | 79 | 83 | PF01048 | 0.256 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.180 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.648 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.482 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.533 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.454 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.476 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.540 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.499 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.361 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.478 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.461 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.348 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.367 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.472 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.422 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.459 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.486 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.518 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.483 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.488 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.269 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.157 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.215 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.624 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.425 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.469 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.433 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.465 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.501 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.469 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.472 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.452 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.513 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.455 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.437 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.560 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.357 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.509 |
MOD_OFUCOSY | 32 | 38 | PF10250 | 0.346 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.431 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.415 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.357 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.465 |
MOD_PKA_1 | 602 | 608 | PF00069 | 0.404 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.509 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.446 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.412 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.488 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.267 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.451 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.509 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.363 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.509 |
MOD_Plk_2-3 | 360 | 366 | PF00069 | 0.374 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.357 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.452 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.449 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.446 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.420 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.497 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.355 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.505 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.551 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.535 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.357 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.351 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.520 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.458 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 602 | 604 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 668 | 671 | PF00400 | 0.582 |
TRG_NES_CRM1_1 | 79 | 93 | PF08389 | 0.509 |
TRG_NLS_MonoExtN_4 | 514 | 520 | PF00514 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 518 | 522 | PF00026 | 0.157 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C9 | Leptomonas seymouri | 51% | 98% |
A0A0S4JE96 | Bodo saltans | 30% | 96% |
A0A1X0NRE8 | Trypanosomatidae | 35% | 100% |
A0A3Q8IMS2 | Leishmania donovani | 75% | 100% |
A0A3R7RCR4 | Trypanosoma rangeli | 34% | 100% |
A4I9E7 | Leishmania infantum | 75% | 100% |
C9ZJR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B4E6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q3N1 | Leishmania major | 73% | 100% |
Q8H1D9 | Arabidopsis thaliana | 27% | 100% |