Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ASA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 23 |
GO:0006793 | phosphorus metabolic process | 3 | 23 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 23 |
GO:0006807 | nitrogen compound metabolic process | 2 | 23 |
GO:0008152 | metabolic process | 1 | 23 |
GO:0009987 | cellular process | 1 | 23 |
GO:0016310 | phosphorylation | 5 | 23 |
GO:0019538 | protein metabolic process | 3 | 23 |
GO:0036211 | protein modification process | 4 | 23 |
GO:0043170 | macromolecule metabolic process | 3 | 23 |
GO:0043412 | macromolecule modification | 4 | 23 |
GO:0044237 | cellular metabolic process | 2 | 23 |
GO:0044238 | primary metabolic process | 2 | 23 |
GO:0071704 | organic substance metabolic process | 2 | 23 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 23 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0046777 | protein autophosphorylation | 6 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004672 | protein kinase activity | 3 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0005524 | ATP binding | 5 | 23 |
GO:0016301 | kinase activity | 4 | 23 |
GO:0016740 | transferase activity | 2 | 23 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 23 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 23 |
GO:0017076 | purine nucleotide binding | 4 | 23 |
GO:0030554 | adenyl nucleotide binding | 5 | 23 |
GO:0032553 | ribonucleotide binding | 3 | 23 |
GO:0032555 | purine ribonucleotide binding | 4 | 23 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 23 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 23 |
GO:0036094 | small molecule binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043168 | anion binding | 3 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0097367 | carbohydrate derivative binding | 2 | 23 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 23 |
GO:1901265 | nucleoside phosphate binding | 3 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 12 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005516 | calmodulin binding | 3 | 2 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 2 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.391 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.695 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 267 | 275 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.311 |
DEG_SCF_FBW7_1 | 394 | 401 | PF00400 | 0.334 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.514 |
DOC_CYCLIN_RxL_1 | 265 | 273 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 286 | 295 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 438 | 445 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.343 |
DOC_PP1_RVXF_1 | 95 | 101 | PF00149 | 0.376 |
DOC_PP4_FxxP_1 | 404 | 407 | PF00568 | 0.276 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.644 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.299 |
DOC_USP7_UBL2_3 | 26 | 30 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 552 | 557 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 60 | 66 | PF00244 | 0.443 |
LIG_BIR_III_4 | 582 | 586 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 560 | 564 | PF00533 | 0.514 |
LIG_BRCT_MDC1_1 | 617 | 621 | PF00533 | 0.527 |
LIG_CtBP_PxDLS_1 | 442 | 446 | PF00389 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 575 | 579 | PF00928 | 0.509 |
LIG_DLG_GKlike_1 | 552 | 559 | PF00625 | 0.430 |
LIG_EVH1_1 | 361 | 365 | PF00568 | 0.247 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.424 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.305 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.456 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.421 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.306 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.451 |
LIG_GBD_Chelix_1 | 168 | 176 | PF00786 | 0.391 |
LIG_GBD_Chelix_1 | 266 | 274 | PF00786 | 0.276 |
LIG_Integrin_isoDGR_2 | 612 | 614 | PF01839 | 0.445 |
LIG_LIR_Apic_2 | 401 | 407 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 485 | 489 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 260 | 267 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 515 | 525 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 555 | 564 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 575 | 583 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 575 | 580 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.408 |
LIG_MLH1_MIPbox_1 | 137 | 141 | PF16413 | 0.311 |
LIG_MYND_1 | 359 | 363 | PF01753 | 0.227 |
LIG_Pex14_1 | 137 | 141 | PF04695 | 0.340 |
LIG_REV1ctd_RIR_1 | 138 | 148 | PF16727 | 0.329 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.476 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.334 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.247 |
LIG_SH2_NCK_1 | 531 | 535 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 237 | 240 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 329 | 332 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 493 | 496 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.633 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.472 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.272 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.419 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.611 |
LIG_SH3_3 | 491 | 497 | PF00018 | 0.259 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.428 |
LIG_SUMO_SIM_anti_2 | 262 | 267 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 441 | 447 | PF11976 | 0.466 |
LIG_SxIP_EBH_1 | 583 | 592 | PF03271 | 0.437 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.173 |
LIG_UBA3_1 | 172 | 179 | PF00899 | 0.401 |
LIG_UBA3_1 | 501 | 509 | PF00899 | 0.173 |
LIG_WW_2 | 359 | 362 | PF00397 | 0.227 |
MOD_CDC14_SPxK_1 | 352 | 355 | PF00782 | 0.192 |
MOD_CDK_SPxK_1 | 349 | 355 | PF00069 | 0.192 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.452 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.506 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.466 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.465 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.333 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.527 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.276 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.276 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.339 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.698 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.606 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.521 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.341 |
MOD_GlcNHglycan | 485 | 489 | PF01048 | 0.400 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.484 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.705 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.358 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.732 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.394 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.386 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.364 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.594 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.508 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.536 |
MOD_LATS_1 | 48 | 54 | PF00433 | 0.349 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.227 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.311 |
MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.483 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.549 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.577 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.519 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.293 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.380 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.360 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.332 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.472 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.518 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.575 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.391 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.500 |
MOD_OFUCOSY | 23 | 29 | PF10250 | 0.333 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.421 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.344 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.334 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.173 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.399 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.335 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.243 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.578 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.441 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.361 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.321 |
MOD_Plk_2-3 | 533 | 539 | PF00069 | 0.639 |
MOD_Plk_2-3 | 600 | 606 | PF00069 | 0.493 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.448 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.393 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.314 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.325 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.547 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.434 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.433 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.390 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.334 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.350 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.603 |
MOD_SUMO_for_1 | 288 | 291 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 171 | 181 | PF00179 | 0.582 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.325 |
TRG_DiLeu_BaEn_2 | 141 | 147 | PF01217 | 0.327 |
TRG_DiLeu_BaEn_2 | 271 | 277 | PF01217 | 0.247 |
TRG_DiLeu_BaEn_2 | 574 | 580 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6Q7 | Leptomonas seymouri | 25% | 100% |
A0A0N1IM89 | Leptomonas seymouri | 63% | 100% |
A0A0S4JQP0 | Bodo saltans | 23% | 100% |
A0A0S4KKJ1 | Bodo saltans | 39% | 98% |
A0A1X0P834 | Trypanosomatidae | 22% | 100% |
A0A3S5H5G0 | Leishmania donovani | 25% | 100% |
A0A3S7WVR6 | Leishmania donovani | 92% | 100% |
A0A3S7WY10 | Leishmania donovani | 25% | 100% |
A0A3S7X8Z8 | Leishmania donovani | 25% | 100% |
A4H459 | Leishmania braziliensis | 27% | 92% |
A4HA97 | Leishmania braziliensis | 82% | 100% |
A4HD79 | Leishmania braziliensis | 25% | 100% |
A4HFF3 | Leishmania braziliensis | 24% | 100% |
A4HSE2 | Leishmania infantum | 25% | 100% |
A4HYH7 | Leishmania infantum | 92% | 100% |
A4IB02 | Leishmania infantum | 25% | 100% |
C9ZTU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZX15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AET0 | Leishmania major | 26% | 100% |
E9AH34 | Leishmania infantum | 25% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
P15791 | Rattus norvegicus | 23% | 100% |
Q4QD63 | Leishmania major | 90% | 100% |
Q4QJJ0 | Leishmania major | 24% | 96% |
Q93VD3 | Arabidopsis thaliana | 24% | 100% |