Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
GO:0016282 | eukaryotic 43S preinitiation complex | 4 | 6 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0033290 | eukaryotic 48S preinitiation complex | 4 | 6 |
GO:0070993 | translation preinitiation complex | 3 | 6 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HNN3
Term | Name | Level | Count |
---|---|---|---|
GO:0001732 | formation of cytoplasmic translation initiation complex | 7 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 6 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.595 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.601 |
CLV_MEL_PAP_1 | 229 | 235 | PF00089 | 0.408 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.329 |
CLV_PCSK_PC7_1 | 24 | 30 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.396 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.529 |
DEG_COP1_1 | 147 | 156 | PF00400 | 0.417 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.608 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.412 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 295 | 304 | PF00134 | 0.608 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 386 | 393 | PF00134 | 0.608 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 262 | 269 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 58 | 65 | PF00069 | 0.464 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.515 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.602 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.668 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 107 | 116 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 446 | 461 | PF00022 | 0.694 |
LIG_AP2alpha_1 | 327 | 331 | PF02296 | 0.559 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.572 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.318 |
LIG_BRCT_BRCA1_2 | 82 | 88 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_1 | 393 | 397 | PF01394 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 103 | 113 | PF00928 | 0.366 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.520 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.580 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.590 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.608 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.580 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.632 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.617 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.608 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.565 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.535 |
LIG_Integrin_isoDGR_2 | 270 | 272 | PF01839 | 0.390 |
LIG_LIR_Apic_2 | 118 | 122 | PF02991 | 0.590 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 14 | 22 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 192 | 203 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 247 | 254 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 335 | 343 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 430 | 437 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.380 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.565 |
LIG_NRBOX | 389 | 395 | PF00104 | 0.590 |
LIG_PCNA_yPIPBox_3 | 166 | 174 | PF02747 | 0.608 |
LIG_PCNA_yPIPBox_3 | 202 | 211 | PF02747 | 0.535 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.512 |
LIG_REV1ctd_RIR_1 | 16 | 24 | PF16727 | 0.455 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.590 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.616 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.515 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.565 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.605 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.374 |
LIG_SH2_GRB2like | 382 | 385 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.590 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.608 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.529 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.623 |
LIG_SUMO_SIM_anti_2 | 439 | 447 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 391 | 398 | PF11976 | 0.512 |
LIG_TYR_ITIM | 139 | 144 | PF00017 | 0.590 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.457 |
LIG_UBA3_1 | 112 | 117 | PF00899 | 0.608 |
LIG_UBA3_1 | 169 | 174 | PF00899 | 0.577 |
LIG_UBA3_1 | 372 | 380 | PF00899 | 0.590 |
LIG_UBA3_1 | 403 | 407 | PF00899 | 0.529 |
LIG_UBA3_1 | 457 | 462 | PF00899 | 0.681 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.389 |
MOD_CDK_SPK_2 | 332 | 337 | PF00069 | 0.504 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.556 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.582 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.590 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.574 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.574 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.590 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.539 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.535 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.608 |
MOD_CMANNOS | 124 | 127 | PF00535 | 0.315 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.390 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.375 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.173 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.590 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.585 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.590 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.315 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.602 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.534 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.505 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.492 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.565 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.482 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.637 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.515 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.548 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.590 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.554 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.565 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.527 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.577 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.521 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.511 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.529 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.515 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.389 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.597 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.504 |
TRG_DiLeu_BaEn_1 | 155 | 160 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.417 |
TRG_DiLeu_LyEn_5 | 155 | 160 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.547 |
TRG_NES_CRM1_1 | 128 | 142 | PF08389 | 0.515 |
TRG_NES_CRM1_1 | 371 | 383 | PF08389 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 411 | 416 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA7 | Leptomonas seymouri | 81% | 87% |
A0A0S4KNQ8 | Bodo saltans | 34% | 100% |
A0A1X0P8D7 | Trypanosomatidae | 53% | 95% |
A0A3Q8IIN0 | Leishmania donovani | 97% | 86% |
A0A3R7KQY4 | Trypanosoma rangeli | 53% | 96% |
A1C690 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 23% | 98% |
A1DGW6 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 98% |
A2R7S7 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 23% | 98% |
A4ICW2 | Leishmania infantum | 97% | 86% |
A5A6M4 | Pan troglodytes | 24% | 83% |
A6S1A3 | Botryotinia fuckeliana (strain B05.10) | 24% | 98% |
A7E5J5 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 24% | 98% |
A7SDW5 | Nematostella vectensis | 24% | 89% |
A8PHP4 | Brugia malayi | 23% | 85% |
A8X419 | Caenorhabditis briggsae | 24% | 87% |
A9VCY6 | Monosiga brevicollis | 25% | 91% |
B0WR18 | Culex quinquefasciatus | 23% | 87% |
B0XS74 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 23% | 98% |
B3M7W0 | Drosophila ananassae | 24% | 87% |
B3NH71 | Drosophila erecta | 25% | 87% |
B4GR63 | Drosophila persimilis | 25% | 86% |
B4HFJ3 | Drosophila sechellia | 25% | 87% |
B4IWN1 | Drosophila grimshawi | 24% | 86% |
B4KZ45 | Drosophila mojavensis | 24% | 87% |
B4LEJ0 | Drosophila virilis | 24% | 87% |
B4MX71 | Drosophila willistoni | 24% | 87% |
B4PG99 | Drosophila yakuba | 25% | 87% |
B4QR64 | Drosophila simulans | 25% | 87% |
D0A2I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 96% |
E9ASE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 86% |
L7HXG6 | Magnaporthe oryzae (strain Y34) | 23% | 99% |
P0CN56 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 23% | 74% |
P0CN57 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 23% | 74% |
P0CT08 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 99% |
Q0CPA8 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 23% | 98% |
Q0UIU6 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 23% | 96% |
Q16FL6 | Aedes aegypti | 23% | 87% |
Q1DZB0 | Coccidioides immitis (strain RS) | 22% | 97% |
Q2H9N4 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 22% | 99% |
Q2M0S3 | Drosophila pseudoobscura pseudoobscura | 25% | 86% |
Q2U041 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 98% |
Q3ZCK1 | Bos taurus | 25% | 83% |
Q4PF85 | Ustilago maydis (strain 521 / FGSC 9021) | 22% | 70% |
Q4Q253 | Leishmania major | 96% | 100% |
Q4X1D2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 98% |
Q5B0H6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 98% |
Q5F428 | Gallus gallus | 25% | 83% |
Q6CAE9 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 25% | 90% |
Q6P878 | Xenopus tropicalis | 24% | 83% |
Q7Q5Y8 | Anopheles gambiae | 23% | 87% |
Q7SB62 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 99% |
Q7T2A5 | Danio rerio | 25% | 81% |
Q86LA2 | Dictyostelium discoideum | 26% | 76% |
Q8AVJ0 | Xenopus laevis | 24% | 83% |
Q8QZY1 | Mus musculus | 25% | 83% |
Q95QW0 | Caenorhabditis elegans | 23% | 87% |
Q9VTU4 | Drosophila melanogaster | 25% | 87% |
Q9Y262 | Homo sapiens | 25% | 83% |
V5BV76 | Trypanosoma cruzi | 53% | 96% |