| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q2L1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 8 |
| GO:0004497 | monooxygenase activity | 3 | 8 |
| GO:0005488 | binding | 1 | 8 |
| GO:0005506 | iron ion binding | 6 | 8 |
| GO:0016491 | oxidoreductase activity | 2 | 8 |
| GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 8 |
| GO:0020037 | heme binding | 4 | 8 |
| GO:0043167 | ion binding | 2 | 8 |
| GO:0043169 | cation binding | 3 | 8 |
| GO:0046872 | metal ion binding | 4 | 8 |
| GO:0046906 | tetrapyrrole binding | 3 | 8 |
| GO:0046914 | transition metal ion binding | 5 | 8 |
| GO:0097159 | organic cyclic compound binding | 2 | 8 |
| GO:1901363 | heterocyclic compound binding | 2 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.459 |
| CLV_MEL_PAP_1 | 129 | 135 | PF00089 | 0.339 |
| CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.280 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.259 |
| CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.355 |
| CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.480 |
| CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.280 |
| CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.260 |
| CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.339 |
| CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.402 |
| CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.402 |
| CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.339 |
| CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.339 |
| CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.462 |
| CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.280 |
| CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.339 |
| CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.324 |
| CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.327 |
| CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.343 |
| CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.582 |
| CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.425 |
| CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.280 |
| CLV_Separin_Metazoa | 362 | 366 | PF03568 | 0.355 |
| DEG_APCC_DBOX_1 | 131 | 139 | PF00400 | 0.323 |
| DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.207 |
| DEG_APCC_DBOX_1 | 200 | 208 | PF00400 | 0.280 |
| DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.339 |
| DEG_SCF_FBW7_1 | 1 | 6 | PF00400 | 0.421 |
| DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.307 |
| DOC_MAPK_gen_1 | 148 | 154 | PF00069 | 0.339 |
| DOC_MAPK_gen_1 | 213 | 222 | PF00069 | 0.339 |
| DOC_MAPK_gen_1 | 431 | 442 | PF00069 | 0.339 |
| DOC_MAPK_MEF2A_6 | 392 | 400 | PF00069 | 0.355 |
| DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.496 |
| DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.291 |
| DOC_PP1_RVXF_1 | 89 | 95 | PF00149 | 0.323 |
| DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.269 |
| DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.283 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.547 |
| DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.359 |
| LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.273 |
| LIG_14-3-3_CanoR_1 | 251 | 255 | PF00244 | 0.283 |
| LIG_14-3-3_CanoR_1 | 496 | 504 | PF00244 | 0.471 |
| LIG_Actin_WH2_2 | 228 | 245 | PF00022 | 0.355 |
| LIG_EH1_1 | 122 | 130 | PF00400 | 0.355 |
| LIG_FHA_1 | 23 | 29 | PF00498 | 0.512 |
| LIG_FHA_1 | 393 | 399 | PF00498 | 0.339 |
| LIG_FHA_1 | 484 | 490 | PF00498 | 0.385 |
| LIG_FHA_2 | 119 | 125 | PF00498 | 0.355 |
| LIG_FHA_2 | 251 | 257 | PF00498 | 0.283 |
| LIG_FHA_2 | 320 | 326 | PF00498 | 0.307 |
| LIG_FHA_2 | 344 | 350 | PF00498 | 0.280 |
| LIG_FHA_2 | 496 | 502 | PF00498 | 0.422 |
| LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.305 |
| LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 328 | 339 | PF02991 | 0.339 |
| LIG_LIR_Gen_1 | 453 | 464 | PF02991 | 0.372 |
| LIG_LIR_Gen_1 | 506 | 516 | PF02991 | 0.484 |
| LIG_LIR_LC3C_4 | 458 | 462 | PF02991 | 0.307 |
| LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.305 |
| LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.359 |
| LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.312 |
| LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.473 |
| LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.313 |
| LIG_NRBOX | 315 | 321 | PF00104 | 0.280 |
| LIG_Pex14_1 | 79 | 83 | PF04695 | 0.280 |
| LIG_REV1ctd_RIR_1 | 91 | 95 | PF16727 | 0.280 |
| LIG_SH2_CRK | 123 | 127 | PF00017 | 0.339 |
| LIG_SH2_CRK | 32 | 36 | PF00017 | 0.564 |
| LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.507 |
| LIG_SH2_NCK_1 | 509 | 513 | PF00017 | 0.439 |
| LIG_SH2_SRC | 123 | 126 | PF00017 | 0.355 |
| LIG_SH2_SRC | 382 | 385 | PF00017 | 0.301 |
| LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.407 |
| LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.280 |
| LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.280 |
| LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.328 |
| LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.286 |
| LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.328 |
| LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.150 |
| LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.410 |
| LIG_SH3_1 | 365 | 371 | PF00018 | 0.280 |
| LIG_SH3_3 | 33 | 39 | PF00018 | 0.446 |
| LIG_SH3_3 | 365 | 371 | PF00018 | 0.280 |
| LIG_SH3_3 | 378 | 384 | PF00018 | 0.280 |
| LIG_SH3_3 | 385 | 391 | PF00018 | 0.150 |
| LIG_SH3_3 | 413 | 419 | PF00018 | 0.339 |
| LIG_SUMO_SIM_anti_2 | 258 | 263 | PF11976 | 0.264 |
| LIG_SUMO_SIM_anti_2 | 458 | 463 | PF11976 | 0.339 |
| LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.307 |
| LIG_SUMO_SIM_par_1 | 394 | 399 | PF11976 | 0.347 |
| LIG_SUMO_SIM_par_1 | 458 | 463 | PF11976 | 0.373 |
| LIG_SUMO_SIM_par_1 | 485 | 490 | PF11976 | 0.359 |
| LIG_SUMO_SIM_par_1 | 514 | 522 | PF11976 | 0.529 |
| LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.280 |
| LIG_TYR_ITIM | 454 | 459 | PF00017 | 0.283 |
| LIG_TYR_ITSM | 119 | 126 | PF00017 | 0.355 |
| LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.316 |
| LIG_WRPW_2 | 85 | 88 | PF00400 | 0.339 |
| MOD_CK1_1 | 340 | 346 | PF00069 | 0.286 |
| MOD_CK2_1 | 212 | 218 | PF00069 | 0.350 |
| MOD_CK2_1 | 250 | 256 | PF00069 | 0.339 |
| MOD_CK2_1 | 319 | 325 | PF00069 | 0.307 |
| MOD_CK2_1 | 343 | 349 | PF00069 | 0.283 |
| MOD_Cter_Amidation | 444 | 447 | PF01082 | 0.339 |
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.344 |
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.353 |
| MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.520 |
| MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.445 |
| MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.298 |
| MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.611 |
| MOD_GSK3_1 | 212 | 219 | PF00069 | 0.297 |
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.293 |
| MOD_GSK3_1 | 392 | 399 | PF00069 | 0.351 |
| MOD_GSK3_1 | 483 | 490 | PF00069 | 0.355 |
| MOD_GSK3_1 | 491 | 498 | PF00069 | 0.376 |
| MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.280 |
| MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.401 |
| MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.581 |
| MOD_NEK2_1 | 202 | 207 | PF00069 | 0.339 |
| MOD_NEK2_1 | 212 | 217 | PF00069 | 0.339 |
| MOD_NEK2_1 | 230 | 235 | PF00069 | 0.339 |
| MOD_NEK2_1 | 242 | 247 | PF00069 | 0.339 |
| MOD_NEK2_1 | 319 | 324 | PF00069 | 0.307 |
| MOD_NEK2_1 | 460 | 465 | PF00069 | 0.316 |
| MOD_NEK2_1 | 495 | 500 | PF00069 | 0.400 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.448 |
| MOD_NEK2_2 | 250 | 255 | PF00069 | 0.283 |
| MOD_OFUCOSY | 437 | 444 | PF10250 | 0.339 |
| MOD_PIKK_1 | 154 | 160 | PF00454 | 0.331 |
| MOD_PK_1 | 255 | 261 | PF00069 | 0.301 |
| MOD_PKA_2 | 212 | 218 | PF00069 | 0.312 |
| MOD_PKA_2 | 250 | 256 | PF00069 | 0.399 |
| MOD_PKA_2 | 404 | 410 | PF00069 | 0.339 |
| MOD_PKA_2 | 495 | 501 | PF00069 | 0.442 |
| MOD_Plk_1 | 255 | 261 | PF00069 | 0.357 |
| MOD_Plk_1 | 483 | 489 | PF00069 | 0.400 |
| MOD_Plk_4 | 297 | 303 | PF00069 | 0.335 |
| MOD_Plk_4 | 392 | 398 | PF00069 | 0.355 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.547 |
| MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.359 |
| MOD_SUMO_for_1 | 470 | 473 | PF00179 | 0.339 |
| MOD_SUMO_rev_2 | 82 | 88 | PF00179 | 0.358 |
| TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.339 |
| TRG_DiLeu_BaEn_4 | 425 | 431 | PF01217 | 0.339 |
| TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.280 |
| TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.354 |
| TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.280 |
| TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.339 |
| TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.150 |
| TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.443 |
| TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.452 |
| TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.339 |
| TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.280 |
| TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.339 |
| TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.339 |
| TRG_NES_CRM1_1 | 279 | 293 | PF08389 | 0.339 |
| TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.280 |
| TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.280 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0D1DMJ7 | Ustilago maydis (strain 521 / FGSC 9021) | 22% | 83% |
| A0A0D1DT62 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 100% |
| A0A0E3D8M1 | Penicillium crustosum | 23% | 100% |
| A0A0N1PC71 | Leptomonas seymouri | 75% | 97% |
| A0A0S2IHL2 | Kalopanax septemlobus | 22% | 100% |
| A0A0S4ILM5 | Bodo saltans | 26% | 100% |
| A0A0S4IUA7 | Bodo saltans | 23% | 100% |
| A0A0S4KIN8 | Bodo saltans | 23% | 100% |
| A0A140IL90 | Narcissus aff. pseudonarcissus MK-2014 | 24% | 100% |
| A0A140IL92 | Narcissus aff. pseudonarcissus MK-2014 | 24% | 100% |
| A0A140JWT9 | Penicillium simplicissimum | 23% | 100% |
| A0A1B2CTB6 | Penicillium thymicola | 23% | 100% |
| A0A1L9WVI3 | Aspergillus aculeatus (strain ATCC 16872 / CBS 172.66 / WB 5094) | 22% | 100% |
| A0A1V0QSE9 | Hericium erinaceus | 25% | 97% |
| A0A1X0NLV1 | Trypanosomatidae | 24% | 92% |
| A0A1X0P9X8 | Trypanosomatidae | 48% | 100% |
| A0A2P1DPA5 | Penicillium terrestre | 26% | 100% |
| A0A2R4SBW0 | Ganoderma lucidum | 24% | 97% |
| A0A343URW6 | Catharanthus roseus | 21% | 100% |
| A0A386KZI3 | Pseudo-nitzschia multiseries | 25% | 95% |
| A0A3G9HB50 | Alternaria alternata | 22% | 89% |
| A0A3Q8IIT3 | Leishmania donovani | 98% | 98% |
| A0A3S5HYN5 | Talaromyces variabilis | 22% | 99% |
| A0A411KZY9 | Aspergillus burnettii | 24% | 99% |
| A0A422N4L6 | Trypanosoma rangeli | 21% | 92% |
| A0A481NR20 | Barbarea vulgaris | 22% | 100% |
| A0A517FNC4 | Paris polyphylla | 21% | 100% |
| A0A517FNC7 | Paris polyphylla | 26% | 100% |
| A0A517FND0 | Paris polyphylla | 25% | 100% |
| A1DN29 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 97% |
| A2A974 | Mus musculus | 26% | 100% |
| A4HB52 | Leishmania braziliensis | 85% | 98% |
| A4IAA0 | Leishmania infantum | 97% | 98% |
| A7VMU4 | Alternaria alternata | 25% | 100% |
| B2RML6 | Botryotinia fuckeliana | 25% | 100% |
| B9G934 | Oryza sativa subsp. japonica | 26% | 100% |
| B9GBJ9 | Oryza sativa subsp. japonica | 25% | 100% |
| B9X287 | Oryza sativa subsp. japonica | 24% | 98% |
| C9K1X6 | Streptomyces melanosporofaciens | 25% | 100% |
| C9ZKU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 91% |
| E3W9C4 | Zingiber zerumbet | 23% | 100% |
| E9ANQ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
| E9B5C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 97% |
| E9RHV4 | Ustilago maydis | 23% | 100% |
| F1SY77 | Postia placenta (strain ATCC 44394 / Madison 698-R) | 22% | 97% |
| F1SYE5 | Postia placenta (strain ATCC 44394 / Madison 698-R) | 27% | 98% |
| F1SYG6 | Postia placenta (strain ATCC 44394 / Madison 698-R) | 26% | 98% |
| F1SYH0 | Postia placenta (strain ATCC 44394 / Madison 698-R) | 27% | 98% |
| F1SYH7 | Postia placenta (strain ATCC 44394 / Madison 698-R) | 24% | 97% |
| F4IK45 | Arabidopsis thaliana | 24% | 93% |
| G3Y420 | Aspergillus niger (strain ATCC 1015 / CBS 113.46 / FGSC A1144 / LSHB Ac4 / NCTC 3858a / NRRL 328 / USDA 3528.7) | 26% | 100% |
| H1A981 | Medicago truncatula | 24% | 100% |
| H1A988 | Glycyrrhiza uralensis | 23% | 100% |
| H2DH21 | Panax ginseng | 23% | 100% |
| I1S163 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 25% | 96% |
| M1WEN7 | Claviceps purpurea (strain 20.1) | 24% | 100% |
| O00061 | Uromyces fabae | 24% | 99% |
| O23365 | Arabidopsis thaliana | 24% | 92% |
| O35728 | Mus musculus | 24% | 100% |
| O44221 | Drosophila mettleri | 25% | 100% |
| O46054 | Drosophila melanogaster | 27% | 100% |
| O48786 | Arabidopsis thaliana | 25% | 100% |
| O48921 | Glycine max | 24% | 93% |
| O81117 | Vicia sativa | 25% | 100% |
| O88833 | Mus musculus | 25% | 100% |
| P08516 | Rattus norvegicus | 23% | 100% |
| P10611 | Oryctolagus cuniculus | 24% | 100% |
| P10615 | Candida tropicalis | 26% | 98% |
| P14579 | Oryctolagus cuniculus | 25% | 100% |
| P14580 | Oryctolagus cuniculus | 23% | 100% |
| P14581 | Oryctolagus cuniculus | 26% | 100% |
| P15128 | Oryctolagus cuniculus | 26% | 100% |
| P20816 | Rattus norvegicus | 26% | 100% |
| P20817 | Rattus norvegicus | 27% | 100% |
| P24464 | Rattus norvegicus | 26% | 100% |
| P29980 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 23% | 100% |
| P29981 | Blaberus discoidalis | 26% | 100% |
| P33274 | Rattus norvegicus | 24% | 100% |
| P51869 | Rattus norvegicus | 23% | 100% |
| P51871 | Rattus norvegicus | 26% | 99% |
| P59954 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 27% | 100% |
| P78329 | Homo sapiens | 26% | 100% |
| P82712 | Drosophila melanogaster | 25% | 100% |
| P98187 | Homo sapiens | 27% | 100% |
| P9WPN2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 100% |
| P9WPN3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 100% |
| Q02928 | Homo sapiens | 26% | 100% |
| Q05047 | Catharanthus roseus | 24% | 100% |
| Q08477 | Homo sapiens | 25% | 100% |
| Q12585 | Candida maltosa | 25% | 100% |
| Q12609 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 100% |
| Q27589 | Drosophila melanogaster | 26% | 100% |
| Q27606 | Drosophila melanogaster | 25% | 100% |
| Q29496 | Ovis aries | 24% | 100% |
| Q2MJ19 | Medicago truncatula | 22% | 100% |
| Q2MJ21 | Medicago truncatula | 24% | 100% |
| Q2PBY6 | Claviceps purpurea | 24% | 100% |
| Q3MID2 | Rattus norvegicus | 24% | 100% |
| Q43078 | Pisum sativum | 23% | 97% |
| Q50EK0 | Picea sitchensis | 23% | 100% |
| Q50EK1 | Picea sitchensis | 22% | 100% |
| Q50EK3 | Pinus taeda | 24% | 100% |
| Q50EK5 | Pinus taeda | 23% | 100% |
| Q50LG1 | Alternaria alternata | 25% | 100% |
| Q50LH3 | Eschscholzia californica | 24% | 100% |
| Q50LH4 | Eschscholzia californica | 25% | 100% |
| Q54ZM4 | Dictyostelium discoideum | 22% | 100% |
| Q5AR55 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 100% |
| Q5TCH4 | Homo sapiens | 26% | 100% |
| Q64462 | Mus musculus | 24% | 100% |
| Q69XM6 | Oryza sativa subsp. japonica | 24% | 99% |
| Q6A152 | Mus musculus | 24% | 100% |
| Q6NKZ8 | Arabidopsis thaliana | 24% | 100% |
| Q6NT55 | Homo sapiens | 25% | 100% |
| Q6TBX7 | Arabidopsis thaliana | 22% | 99% |
| Q6Z6D6 | Oryza sativa subsp. japonica | 23% | 96% |
| Q7KR10 | Drosophila melanogaster | 25% | 100% |
| Q82IY3 | Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) | 28% | 100% |
| Q86W10 | Homo sapiens | 26% | 100% |
| Q8LIF2 | Oryza sativa subsp. japonica | 25% | 99% |
| Q8N118 | Homo sapiens | 29% | 100% |
| Q8W4T9 | Taxus cuspidata | 25% | 100% |
| Q91WL5 | Mus musculus | 27% | 100% |
| Q93Z79 | Arabidopsis thaliana | 22% | 100% |
| Q964R0 | Blattella germanica | 25% | 100% |
| Q964T1 | Blattella germanica | 28% | 100% |
| Q99N16 | Mus musculus | 24% | 100% |
| Q9EP75 | Mus musculus | 24% | 100% |
| Q9FF18 | Arabidopsis thaliana | 24% | 100% |
| Q9FMV7 | Arabidopsis thaliana | 23% | 100% |
| Q9FVS9 | Arabidopsis thaliana | 23% | 100% |
| Q9HBI6 | Homo sapiens | 23% | 100% |
| Q9HCS2 | Homo sapiens | 27% | 100% |
| Q9K498 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 23% | 100% |
| Q9LUC5 | Arabidopsis thaliana | 23% | 100% |
| Q9LUC6 | Arabidopsis thaliana | 22% | 100% |
| Q9LUC8 | Arabidopsis thaliana | 22% | 100% |
| Q9LUC9 | Arabidopsis thaliana | 23% | 100% |
| Q9PVE8 | Fundulus heteroclitus | 23% | 100% |
| Q9SMP5 | Arabidopsis thaliana | 22% | 100% |
| Q9V4T3 | Drosophila melanogaster | 23% | 100% |
| Q9V4T5 | Drosophila melanogaster | 24% | 100% |
| Q9V4U7 | Drosophila melanogaster | 21% | 100% |
| Q9V557 | Drosophila melanogaster | 25% | 100% |
| Q9V558 | Drosophila melanogaster | 26% | 100% |
| Q9V559 | Drosophila melanogaster | 26% | 100% |
| Q9V770 | Drosophila melanogaster | 24% | 100% |
| Q9V771 | Drosophila melanogaster | 24% | 100% |
| Q9V7G5 | Drosophila melanogaster | 25% | 100% |
| Q9VA27 | Drosophila melanogaster | 28% | 100% |
| Q9VG40 | Drosophila melanogaster | 21% | 100% |
| Q9VGB3 | Drosophila melanogaster | 25% | 100% |
| Q9VL92 | Drosophila melanogaster | 26% | 100% |
| Q9VMS8 | Drosophila melanogaster | 24% | 100% |
| Q9VXY0 | Drosophila melanogaster | 26% | 100% |
| Q9VYQ7 | Drosophila melanogaster | 26% | 100% |
| Q9WVK8 | Mus musculus | 25% | 100% |
| Q9Y6A2 | Homo sapiens | 25% | 100% |
| Q9Y757 | Debaryomyces hansenii | 24% | 100% |
| Q9Y758 | Debaryomyces hansenii | 24% | 100% |
| Q9ZUX1 | Arabidopsis thaliana | 23% | 100% |
| U5NDT8 | Catharanthus roseus | 24% | 100% |
| U5NE19 | Catharanthus roseus | 22% | 100% |
| V5AWA4 | Trypanosoma cruzi | 23% | 93% |
| W0FKI0 | Persicaria hydropiper | 24% | 100% |
| W7LC91 | Gibberella moniliformis (strain M3125 / FGSC 7600) | 22% | 89% |
| W8JWW3 | Catharanthus roseus | 22% | 99% |