A large and likely artifical grouping of protease domain carrying proteins related to proteasomal proteases. Only a tiny subgroup (the AFG3-related mitochondrail proteins) seem to have a TM segment.. Localization: Cytoplasmic (by homology) / Mitochondrial (by homology)
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. | no | yes: 12 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0005874 | microtubule | 6 | 12 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0000815 | ESCRT III complex | 3 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036452 | ESCRT complex | 2 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0015630 | microtubule cytoskeleton | 6 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: E9AZK1
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 12 |
GO:0006996 | organelle organization | 4 | 13 |
GO:0007010 | cytoskeleton organization | 5 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0051013 | microtubule severing | 4 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0006810 | transport | 3 | 1 |
GO:0007033 | vacuole organization | 5 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0010506 | regulation of autophagy | 6 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008017 | microtubule binding | 5 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0008568 | microtubule severing ATPase activity | 2 | 12 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140776 | protein-containing complex destabilizing activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.285 |
CLV_MEL_PAP_1 | 182 | 188 | PF00089 | 0.481 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.219 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.219 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.287 |
DEG_APCC_KENBOX_2 | 490 | 494 | PF00400 | 0.365 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.404 |
DOC_CYCLIN_RxL_1 | 336 | 343 | PF00134 | 0.270 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 413 | 424 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 439 | 449 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 534 | 541 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.270 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.219 |
DOC_PP2B_PxIxI_1 | 114 | 120 | PF00149 | 0.448 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.504 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.232 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.311 |
DOC_USP7_UBL2_3 | 220 | 224 | PF12436 | 0.502 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.331 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.235 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.219 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 185 | 195 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 53 | 58 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.700 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.421 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.270 |
LIG_CtBP_PxDLS_1 | 505 | 509 | PF00389 | 0.222 |
LIG_deltaCOP1_diTrp_1 | 531 | 537 | PF00928 | 0.219 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.365 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.219 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.339 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.354 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.303 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.264 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.481 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.377 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.373 |
LIG_Integrin_RGD_1 | 331 | 333 | PF01839 | 0.232 |
LIG_LIR_Gen_1 | 164 | 174 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 255 | 262 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 446 | 456 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.465 |
LIG_LYPXL_S_1 | 274 | 278 | PF13949 | 0.300 |
LIG_LYPXL_yS_3 | 275 | 278 | PF13949 | 0.304 |
LIG_MYND_1 | 276 | 280 | PF01753 | 0.314 |
LIG_NRBOX | 451 | 457 | PF00104 | 0.250 |
LIG_PDZ_Class_2 | 536 | 541 | PF00595 | 0.511 |
LIG_Pex14_1 | 533 | 537 | PF04695 | 0.219 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.658 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.418 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.268 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 421 | 424 | PF00017 | 0.270 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.271 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.459 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.529 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.601 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.558 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.339 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.338 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.370 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.295 |
LIG_UBA3_1 | 433 | 439 | PF00899 | 0.321 |
LIG_UBA3_1 | 475 | 483 | PF00899 | 0.291 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.656 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.659 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.553 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.711 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.592 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.493 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.561 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.281 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.419 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.652 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.377 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.466 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.683 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.676 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.675 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.560 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.614 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.604 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.367 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.696 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.600 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.586 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.468 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.541 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.589 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.296 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.495 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.502 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.228 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.222 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.541 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.483 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.625 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.478 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.457 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.270 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.379 |
MOD_NEK2_2 | 314 | 319 | PF00069 | 0.219 |
MOD_NEK2_2 | 474 | 479 | PF00069 | 0.219 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.344 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.362 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.654 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.362 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.678 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.505 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.275 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.301 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.250 |
MOD_Plk_2-3 | 486 | 492 | PF00069 | 0.250 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.285 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.276 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.268 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.238 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.468 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.509 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.493 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.219 |
MOD_SUMO_rev_2 | 258 | 268 | PF00179 | 0.320 |
TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.327 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.524 |
TRG_DiLeu_LyEn_5 | 264 | 269 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.270 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.219 |
TRG_NLS_MonoCore_2 | 112 | 117 | PF00514 | 0.646 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.548 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.247 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRH8 | Leptomonas seymouri | 69% | 99% |
A0A0S4IUM1 | Bodo saltans | 51% | 91% |
A0A1X0NYV7 | Trypanosomatidae | 56% | 96% |
A0A1X0P983 | Trypanosomatidae | 42% | 100% |
A0A3Q8IHU1 | Leishmania donovani | 32% | 100% |
A0A3Q8IJS0 | Leishmania donovani | 32% | 100% |
A0A3S7X163 | Leishmania donovani | 92% | 100% |
A0A3S7X2R4 | Leishmania donovani | 42% | 100% |
A0A422P1K0 | Trypanosoma rangeli | 56% | 97% |
A4H6T6 | Leishmania braziliensis | 36% | 100% |
A4HG81 | Leishmania braziliensis | 83% | 95% |
A4HME8 | Leishmania braziliensis | 34% | 100% |
A4HPV3 | Leishmania braziliensis | 35% | 100% |
A4I3C0 | Leishmania infantum | 93% | 90% |
A4I4W4 | Leishmania infantum | 42% | 100% |
A4IB20 | Leishmania infantum | 32% | 100% |
A4IE38 | Leishmania infantum | 32% | 100% |
B2RYN7 | Rattus norvegicus | 38% | 93% |
B3M301 | Drosophila ananassae | 40% | 70% |
B3P8A3 | Drosophila erecta | 40% | 71% |
B4HGG6 | Drosophila sechellia | 40% | 71% |
B4NBP4 | Drosophila willistoni | 41% | 70% |
B4PL32 | Drosophila yakuba | 40% | 71% |
B4QSF0 | Drosophila simulans | 40% | 71% |
C9ZK16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 66% |
D0A833 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 98% |
E9AEB2 | Leishmania major | 42% | 100% |
E9AEU9 | Leishmania major | 32% | 100% |
E9ALH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9ATM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B605 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O75449 | Homo sapiens | 41% | 100% |
Q05AS3 | Xenopus tropicalis | 38% | 90% |
Q0IIR9 | Xenopus tropicalis | 41% | 100% |
Q1HGK7 | Gallus gallus | 42% | 100% |
Q4Q0X8 | Leishmania major | 32% | 100% |
Q4Q8N0 | Leishmania major | 94% | 100% |
Q5ZK92 | Gallus gallus | 40% | 88% |
Q6AZT2 | Xenopus laevis | 39% | 90% |
Q6NW58 | Danio rerio | 39% | 95% |
Q8I0P1 | Drosophila melanogaster | 40% | 71% |
Q9ERZ6 | Mus musculus | 30% | 71% |
Q9PUL2 | Xenopus laevis | 42% | 100% |
Q9SEX2 | Arabidopsis thaliana | 41% | 100% |
V5B0U7 | Trypanosoma cruzi | 56% | 97% |