| 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: 15 |
| NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: A4I2H8
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006468 | protein phosphorylation | 5 | 16 |
| GO:0006793 | phosphorus metabolic process | 3 | 16 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
| GO:0008152 | metabolic process | 1 | 16 |
| GO:0009987 | cellular process | 1 | 16 |
| GO:0016310 | phosphorylation | 5 | 16 |
| GO:0019538 | protein metabolic process | 3 | 16 |
| GO:0036211 | protein modification process | 4 | 16 |
| GO:0043170 | macromolecule metabolic process | 3 | 16 |
| GO:0043412 | macromolecule modification | 4 | 16 |
| GO:0044237 | cellular metabolic process | 2 | 16 |
| GO:0044238 | primary metabolic process | 2 | 16 |
| GO:0071704 | organic substance metabolic process | 2 | 16 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 16 |
| GO:0003824 | catalytic activity | 1 | 16 |
| GO:0004672 | protein kinase activity | 3 | 16 |
| GO:0004674 | protein serine/threonine kinase activity | 4 | 11 |
| GO:0005488 | binding | 1 | 16 |
| GO:0005524 | ATP binding | 5 | 16 |
| GO:0016301 | kinase activity | 4 | 16 |
| GO:0016740 | transferase activity | 2 | 16 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 16 |
| GO:0017076 | purine nucleotide binding | 4 | 16 |
| GO:0030554 | adenyl nucleotide binding | 5 | 16 |
| GO:0032553 | ribonucleotide binding | 3 | 16 |
| GO:0032555 | purine ribonucleotide binding | 4 | 16 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
| GO:0036094 | small molecule binding | 2 | 16 |
| GO:0043167 | ion binding | 2 | 16 |
| GO:0043168 | anion binding | 3 | 16 |
| GO:0097159 | organic cyclic compound binding | 2 | 16 |
| GO:0097367 | carbohydrate derivative binding | 2 | 16 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
| GO:1901265 | nucleoside phosphate binding | 3 | 16 |
| GO:1901363 | heterocyclic compound binding | 2 | 16 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.537 |
| CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.548 |
| CLV_MEL_PAP_1 | 195 | 201 | PF00089 | 0.411 |
| CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.290 |
| CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.469 |
| CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.317 |
| CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.347 |
| CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.383 |
| CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.367 |
| CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.420 |
| CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.262 |
| CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.283 |
| CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.332 |
| CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.348 |
| CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.513 |
| CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.472 |
| CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.262 |
| DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.547 |
| DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.232 |
| DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.470 |
| DOC_CKS1_1 | 1 | 6 | PF01111 | 0.633 |
| DOC_CKS1_1 | 199 | 204 | PF01111 | 0.280 |
| DOC_CYCLIN_RxL_1 | 10 | 19 | PF00134 | 0.438 |
| DOC_CYCLIN_yCln2_LP_2 | 298 | 304 | PF00134 | 0.363 |
| DOC_MAPK_DCC_7 | 125 | 134 | PF00069 | 0.262 |
| DOC_MAPK_FxFP_2 | 46 | 49 | PF00069 | 0.228 |
| DOC_MAPK_gen_1 | 125 | 134 | PF00069 | 0.262 |
| DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.299 |
| DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.433 |
| DOC_MAPK_MEF2A_6 | 125 | 134 | PF00069 | 0.405 |
| DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.336 |
| DOC_PP4_FxxP_1 | 46 | 49 | PF00568 | 0.228 |
| DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.454 |
| DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.736 |
| DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.401 |
| DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.280 |
| DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.445 |
| DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.590 |
| LIG_14-3-3_CanoR_1 | 241 | 249 | PF00244 | 0.327 |
| LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.429 |
| LIG_14-3-3_CanoR_1 | 288 | 296 | PF00244 | 0.319 |
| LIG_14-3-3_CanoR_1 | 297 | 301 | PF00244 | 0.305 |
| LIG_14-3-3_CanoR_1 | 372 | 381 | PF00244 | 0.567 |
| LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.466 |
| LIG_APCC_ABBA_1 | 311 | 316 | PF00400 | 0.457 |
| LIG_APCC_ABBAyCdc20_2 | 152 | 158 | PF00400 | 0.418 |
| LIG_APCC_ABBAyCdc20_2 | 250 | 256 | PF00400 | 0.375 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.652 |
| LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.535 |
| LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.535 |
| LIG_BIR_III_4 | 342 | 346 | PF00653 | 0.686 |
| LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.376 |
| LIG_deltaCOP1_diTrp_1 | 404 | 409 | PF00928 | 0.380 |
| LIG_EH1_1 | 381 | 389 | PF00400 | 0.338 |
| LIG_FHA_1 | 189 | 195 | PF00498 | 0.241 |
| LIG_FHA_1 | 263 | 269 | PF00498 | 0.324 |
| LIG_FHA_1 | 297 | 303 | PF00498 | 0.324 |
| LIG_FHA_1 | 369 | 375 | PF00498 | 0.417 |
| LIG_FHA_1 | 393 | 399 | PF00498 | 0.551 |
| LIG_FHA_2 | 215 | 221 | PF00498 | 0.269 |
| LIG_FHA_2 | 280 | 286 | PF00498 | 0.278 |
| LIG_FHA_2 | 288 | 294 | PF00498 | 0.212 |
| LIG_FHA_2 | 61 | 67 | PF00498 | 0.262 |
| LIG_GBD_Chelix_1 | 273 | 281 | PF00786 | 0.262 |
| LIG_HCF-1_HBM_1 | 81 | 84 | PF13415 | 0.262 |
| LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.280 |
| LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.388 |
| LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.245 |
| LIG_LIR_Gen_1 | 29 | 39 | PF02991 | 0.262 |
| LIG_LIR_Gen_1 | 290 | 298 | PF02991 | 0.228 |
| LIG_LIR_Gen_1 | 413 | 424 | PF02991 | 0.356 |
| LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.245 |
| LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.262 |
| LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.228 |
| LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.370 |
| LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.293 |
| LIG_NRBOX | 369 | 375 | PF00104 | 0.353 |
| LIG_NRBOX | 401 | 407 | PF00104 | 0.369 |
| LIG_SH2_CRK | 182 | 186 | PF00017 | 0.262 |
| LIG_SH2_CRK | 292 | 296 | PF00017 | 0.282 |
| LIG_SH2_CRK | 309 | 313 | PF00017 | 0.348 |
| LIG_SH2_CRK | 427 | 431 | PF00017 | 0.369 |
| LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.375 |
| LIG_SH2_SRC | 309 | 312 | PF00017 | 0.329 |
| LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.309 |
| LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.282 |
| LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.325 |
| LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.316 |
| LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.275 |
| LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.262 |
| LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.300 |
| LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.363 |
| LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.288 |
| LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.234 |
| LIG_SH3_1 | 309 | 315 | PF00018 | 0.486 |
| LIG_SH3_2 | 312 | 317 | PF14604 | 0.377 |
| LIG_SH3_3 | 196 | 202 | PF00018 | 0.280 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.582 |
| LIG_SH3_3 | 309 | 315 | PF00018 | 0.503 |
| LIG_SH3_3 | 321 | 327 | PF00018 | 0.614 |
| LIG_SUMO_SIM_anti_2 | 418 | 426 | PF11976 | 0.343 |
| LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.370 |
| LIG_WW_3 | 323 | 327 | PF00397 | 0.728 |
| MOD_CDC14_SPxK_1 | 323 | 326 | PF00782 | 0.552 |
| MOD_CDK_SPxK_1 | 320 | 326 | PF00069 | 0.535 |
| MOD_CK1_1 | 216 | 222 | PF00069 | 0.303 |
| MOD_CK1_1 | 223 | 229 | PF00069 | 0.322 |
| MOD_CK1_1 | 300 | 306 | PF00069 | 0.262 |
| MOD_CK1_1 | 392 | 398 | PF00069 | 0.392 |
| MOD_CK2_1 | 279 | 285 | PF00069 | 0.316 |
| MOD_DYRK1A_RPxSP_1 | 198 | 202 | PF00069 | 0.280 |
| MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.228 |
| MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.379 |
| MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.244 |
| MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.258 |
| MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.595 |
| MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.546 |
| MOD_GSK3_1 | 164 | 171 | PF00069 | 0.299 |
| MOD_GSK3_1 | 184 | 191 | PF00069 | 0.302 |
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.262 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.231 |
| MOD_GSK3_1 | 264 | 271 | PF00069 | 0.475 |
| MOD_GSK3_1 | 296 | 303 | PF00069 | 0.295 |
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.303 |
| MOD_GSK3_1 | 368 | 375 | PF00069 | 0.359 |
| MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.241 |
| MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.393 |
| MOD_NEK2_1 | 146 | 151 | PF00069 | 0.245 |
| MOD_NEK2_1 | 168 | 173 | PF00069 | 0.381 |
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.275 |
| MOD_NEK2_1 | 194 | 199 | PF00069 | 0.217 |
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.280 |
| MOD_NEK2_2 | 264 | 269 | PF00069 | 0.232 |
| MOD_PKA_1 | 361 | 367 | PF00069 | 0.358 |
| MOD_PKA_2 | 287 | 293 | PF00069 | 0.246 |
| MOD_PKA_2 | 296 | 302 | PF00069 | 0.313 |
| MOD_PKA_2 | 368 | 374 | PF00069 | 0.356 |
| MOD_Plk_1 | 44 | 50 | PF00069 | 0.418 |
| MOD_Plk_4 | 200 | 206 | PF00069 | 0.375 |
| MOD_Plk_4 | 223 | 229 | PF00069 | 0.245 |
| MOD_Plk_4 | 264 | 270 | PF00069 | 0.232 |
| MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.280 |
| MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.440 |
| MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.595 |
| TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.431 |
| TRG_DiLeu_BaEn_1 | 418 | 423 | PF01217 | 0.335 |
| TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.262 |
| TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.262 |
| TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.466 |
| TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.262 |
| TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.418 |
| TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.241 |
| TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.375 |
| TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.370 |
| TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.351 |
| TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.649 |
| TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.335 |
| TRG_Pf-PMV_PEXEL_1 | 14 | 19 | PF00026 | 0.451 |
| TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.356 |
| TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.262 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HT76 | Leptomonas seymouri | 26% | 97% |
| A0A0N1HZW6 | Leptomonas seymouri | 51% | 98% |
| A0A0N1IM47 | Leptomonas seymouri | 27% | 100% |
| A0A0S4IX86 | Bodo saltans | 28% | 100% |
| A0A0S4J3Y5 | Bodo saltans | 26% | 100% |
| A0A0S4JF22 | Bodo saltans | 25% | 100% |
| A0A0S4JNA1 | Bodo saltans | 29% | 87% |
| A0A0S4JP91 | Bodo saltans | 29% | 72% |
| A0A0S4KN74 | Bodo saltans | 24% | 100% |
| A0A1X0NIA0 | Trypanosomatidae | 28% | 100% |
| A0A1X0NJV4 | Trypanosomatidae | 25% | 84% |
| A0A1X0NVR3 | Trypanosomatidae | 25% | 100% |
| A0A1X0NWR7 | Trypanosomatidae | 24% | 84% |
| A0A1X0NY93 | Trypanosomatidae | 24% | 100% |
| A0A1X0P1A2 | Trypanosomatidae | 25% | 94% |
| A0A1X0P3P4 | Trypanosomatidae | 26% | 89% |
| A0A1X0P765 | Trypanosomatidae | 45% | 80% |
| A0A1X0P919 | Trypanosomatidae | 29% | 100% |
| A0A1X0P994 | Trypanosomatidae | 29% | 87% |
| A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 27% | 82% |
| A0A3Q8IAQ1 | Leishmania donovani | 28% | 100% |
| A0A3Q8IIG1 | Leishmania donovani | 33% | 100% |
| A0A3Q8IPJ5 | Leishmania donovani | 100% | 100% |
| A0A3R7M848 | Trypanosoma rangeli | 39% | 92% |
| A0A3R7NLI6 | Trypanosoma rangeli | 29% | 100% |
| A0A3S5H4Z4 | Leishmania donovani | 26% | 82% |
| A0A3S5IRC3 | Trypanosoma rangeli | 28% | 100% |
| A0A3S7X7Y2 | Leishmania donovani | 28% | 100% |
| A0A422N215 | Trypanosoma rangeli | 25% | 70% |
| A0A422NDD2 | Trypanosoma rangeli | 29% | 100% |
| A0A422NUF0 | Trypanosoma rangeli | 28% | 100% |
| A0A509AHB6 | Plasmodium berghei (strain Anka) | 27% | 83% |
| A0QNG1 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 29% | 69% |
| A2ZMH2 | Oryza sativa subsp. indica | 29% | 73% |
| A4H3C7 | Leishmania braziliensis | 27% | 100% |
| A4HCE6 | Leishmania braziliensis | 26% | 100% |
| A4HFA1 | Leishmania braziliensis | 92% | 100% |
| A4HH03 | Leishmania braziliensis | 31% | 100% |
| A4HRM6 | Leishmania infantum | 26% | 82% |
| A4HZW8 | Leishmania infantum | 28% | 100% |
| A4I435 | Leishmania infantum | 33% | 100% |
| A4I9Y5 | Leishmania infantum | 28% | 100% |
| A7MB74 | Bos taurus | 25% | 100% |
| B0LT89 | Rattus norvegicus | 27% | 100% |
| C9ZIN1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 87% |
| C9ZIZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 96% |
| C9ZX04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 93% |
| C9ZX09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 93% |
| D0A8X3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
| D3ZBE5 | Rattus norvegicus | 30% | 100% |
| E9ACA4 | Leishmania major | 26% | 82% |
| E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 80% |
| E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| E9AYN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
| E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
| E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| G5EFM9 | Caenorhabditis elegans | 27% | 100% |
| O00141 | Homo sapiens | 26% | 100% |
| O00506 | Homo sapiens | 27% | 100% |
| O61122 | Dictyostelium discoideum | 27% | 90% |
| P08458 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 88% |
| P22209 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 99% |
| P54739 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 30% | 80% |
| P54744 | Mycobacterium leprae (strain TN) | 28% | 69% |
| P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 27% | 82% |
| P62344 | Plasmodium falciparum (isolate 3D7) | 27% | 82% |
| P62345 | Plasmodium berghei (strain Anka) | 30% | 82% |
| Q06226 | Rattus norvegicus | 26% | 100% |
| Q0JI49 | Oryza sativa subsp. japonica | 27% | 86% |
| Q0VD22 | Bos taurus | 24% | 89% |
| Q10GB1 | Oryza sativa subsp. japonica | 30% | 72% |
| Q13188 | Homo sapiens | 25% | 88% |
| Q2MHE4 | Arabidopsis thaliana | 25% | 100% |
| Q2QMH1 | Oryza sativa subsp. japonica | 29% | 73% |
| Q3SWY6 | Bos taurus | 28% | 100% |
| Q4Q2Z2 | Leishmania major | 28% | 100% |
| Q4Q7W2 | Leishmania major | 33% | 100% |
| Q4Q8T4 | Leishmania major | 98% | 100% |
| Q4QBQ2 | Leishmania major | 28% | 100% |
| Q4QCR2 | Leishmania major | 26% | 100% |
| Q4R633 | Macaca fascicularis | 26% | 100% |
| Q4V3C8 | Arabidopsis thaliana | 26% | 89% |
| Q54EY4 | Dictyostelium discoideum | 29% | 77% |
| Q5Q0U5 | Fundulus heteroclitus | 25% | 100% |
| Q5QNM6 | Oryza sativa subsp. japonica | 29% | 85% |
| Q6IP06 | Xenopus laevis | 25% | 88% |
| Q7RAH3 | Plasmodium yoelii yoelii | 27% | 81% |
| Q7RJG2 | Plasmodium yoelii yoelii | 30% | 82% |
| Q802A6 | Squalus acanthias | 25% | 88% |
| Q8RX66 | Arabidopsis thaliana | 31% | 76% |
| Q8TDX7 | Homo sapiens | 29% | 100% |
| Q8W490 | Arabidopsis thaliana | 29% | 92% |
| Q94A06 | Arabidopsis thaliana | 26% | 100% |
| Q99JT2 | Mus musculus | 27% | 100% |
| Q9ES74 | Mus musculus | 30% | 100% |
| Q9LHI7 | Arabidopsis thaliana | 26% | 76% |
| Q9P289 | Homo sapiens | 27% | 100% |
| Q9WVC6 | Mus musculus | 26% | 100% |
| Q9XT18 | Oryctolagus cuniculus | 25% | 100% |
| Q9Z2W1 | Mus musculus | 27% | 100% |
| Q9ZUZ2 | Arabidopsis thaliana | 27% | 73% |
| Q9ZV15 | Arabidopsis thaliana | 28% | 74% |
| V5BCH2 | Trypanosoma cruzi | 25% | 100% |
| V5BJT8 | Trypanosoma cruzi | 29% | 100% |
| V5CI11 | Trypanosoma cruzi | 46% | 90% |
| V5D179 | Trypanosoma cruzi | 25% | 71% |
| V5D9M1 | Trypanosoma cruzi | 29% | 100% |