Nuclear proteins, nucleolar RNA helicase II
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HSE3
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.378 |
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.168 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.168 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.203 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.369 |
DOC_CKS1_1 | 596 | 601 | PF01111 | 0.431 |
DOC_CYCLIN_RxL_1 | 144 | 153 | PF00134 | 0.471 |
DOC_CYCLIN_RxL_1 | 340 | 350 | PF00134 | 0.368 |
DOC_CYCLIN_RxL_1 | 398 | 409 | PF00134 | 0.400 |
DOC_MAPK_DCC_7 | 401 | 410 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 203 | 213 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 386 | 394 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 432 | 442 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 453 | 462 | PF00069 | 0.350 |
DOC_MAPK_HePTP_8 | 398 | 410 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 206 | 213 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 250 | 257 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 435 | 442 | PF00069 | 0.285 |
DOC_MAPK_NFAT4_5 | 250 | 258 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.378 |
DOC_PP1_RVXF_1 | 341 | 348 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 599 | 606 | PF00149 | 0.471 |
DOC_PP1_SILK_1 | 556 | 561 | PF00149 | 0.368 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.379 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.368 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.283 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.378 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 34 | 38 | PF12436 | 0.718 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 309 | 317 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 490 | 497 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 51 | 60 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 601 | 606 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.312 |
LIG_APCC_ABBAyCdc20_2 | 225 | 231 | PF00400 | 0.434 |
LIG_BIR_III_2 | 506 | 510 | PF00653 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 285 | 292 | PF00928 | 0.447 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.472 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.394 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.368 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.363 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.368 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.368 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.301 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 116 | 121 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 227 | 238 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 387 | 398 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 536 | 544 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 604 | 613 | PF02991 | 0.471 |
LIG_LIR_LC3C_4 | 184 | 189 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 116 | 120 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 604 | 608 | PF02991 | 0.471 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.368 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 198 | 201 | PF00017 | 0.471 |
LIG_SH2_PTP2 | 539 | 542 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 198 | 201 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.421 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 207 | 213 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 251 | 258 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 508 | 515 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 573 | 580 | PF11976 | 0.368 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.368 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.389 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.415 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.600 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.739 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.600 |
LIG_UBA3_1 | 244 | 250 | PF00899 | 0.368 |
LIG_UBA3_1 | 329 | 335 | PF00899 | 0.264 |
LIG_WRC_WIRS_1 | 382 | 387 | PF05994 | 0.403 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.368 |
MOD_CDK_SPxK_1 | 595 | 601 | PF00069 | 0.434 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.368 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.395 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.273 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.666 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.202 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.405 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.348 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.572 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.481 |
MOD_Cter_Amidation | 433 | 436 | PF01082 | 0.282 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.168 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.192 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.165 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.202 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.693 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.331 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.340 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.448 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.621 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.520 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.369 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.331 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.693 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.368 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.378 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.368 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.353 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.434 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.203 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.368 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.178 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.271 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.633 |
MOD_N-GLC_2 | 79 | 81 | PF02516 | 0.572 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.434 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.471 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.368 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.368 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.661 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.305 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.471 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.368 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.421 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.600 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.379 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.539 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.389 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.421 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.644 |
MOD_PKB_1 | 570 | 578 | PF00069 | 0.378 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.279 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.368 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.368 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.395 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.345 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.311 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.368 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.292 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.301 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.368 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.368 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.369 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.412 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.433 |
MOD_SUMO_rev_2 | 384 | 391 | PF00179 | 0.368 |
MOD_SUMO_rev_2 | 7 | 14 | PF00179 | 0.622 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.245 |
TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 676 | 678 | PF00400 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 170 | 175 | PF00026 | 0.168 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKV7 | Leptomonas seymouri | 87% | 99% |
A0A0S4IWD0 | Bodo saltans | 31% | 100% |
A0A0S4JPY9 | Bodo saltans | 75% | 100% |
A0A1D6GDY8 | Zea mays | 38% | 91% |
A0A1D6LAB7 | Zea mays | 37% | 91% |
A0A1X0P2M8 | Trypanosomatidae | 79% | 100% |
A0A3Q8ID91 | Leishmania donovani | 32% | 100% |
A0A3S5H5G1 | Leishmania donovani | 100% | 100% |
A0A3S7XAT8 | Leishmania donovani | 32% | 100% |
A0A422NYD5 | Trypanosoma rangeli | 78% | 100% |
A0R8U6 | Bacillus thuringiensis (strain Al Hakam) | 34% | 100% |
A1C5V3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 30% | 100% |
A4H460 | Leishmania braziliensis | 93% | 100% |
A4HGR1 | Leishmania braziliensis | 32% | 100% |
A4HP48 | Leishmania braziliensis | 30% | 100% |
A4HP49 | Leishmania braziliensis | 32% | 100% |
A4HT33 | Leishmania infantum | 33% | 100% |
A4HZF8 | Leishmania infantum | 27% | 100% |
A4I3T6 | Leishmania infantum | 32% | 100% |
A4IDF6 | Leishmania infantum | 32% | 100% |
A7F4L5 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 32% | 85% |
C9ZPX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 81% | 100% |
D0A6Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9AJG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AKB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9ASV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ASV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B304 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 88% |
P0A4D7 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 31% | 100% |
P0A4D8 | Streptococcus pneumoniae (strain ATCC BAA-255 / R6) | 31% | 100% |
P33906 | Klebsiella pneumoniae | 33% | 100% |
P57453 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 33% | 100% |
P96614 | Bacillus subtilis (strain 168) | 34% | 100% |
Q0DM51 | Oryza sativa subsp. japonica | 38% | 89% |
Q2FF45 | Staphylococcus aureus (strain USA300) | 30% | 100% |
Q2FWH5 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 30% | 100% |
Q2YUH3 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 30% | 100% |
Q39189 | Arabidopsis thaliana | 38% | 100% |
Q3B8Q1 | Rattus norvegicus | 40% | 87% |
Q41382 | Spinacia oleracea | 40% | 99% |
Q49Z29 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 32% | 100% |
Q4L7W0 | Staphylococcus haemolyticus (strain JCSC1435) | 31% | 100% |
Q4Q1N9 | Leishmania major | 31% | 100% |
Q4Q1P0 | Leishmania major | 31% | 100% |
Q4Q858 | Leishmania major | 32% | 100% |
Q4QJI9 | Leishmania major | 96% | 100% |
Q5AWA6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 31% | 100% |
Q5HEB9 | Staphylococcus aureus (strain COL) | 30% | 100% |
Q5HME0 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 31% | 100% |
Q5L3G9 | Geobacillus kaustophilus (strain HTA426) | 36% | 100% |
Q63GX5 | Bacillus cereus (strain ZK / E33L) | 34% | 100% |
Q650T9 | Oryza sativa subsp. japonica | 40% | 97% |
Q6G7M9 | Staphylococcus aureus (strain MSSA476) | 30% | 100% |
Q6GEZ3 | Staphylococcus aureus (strain MRSA252) | 31% | 100% |
Q6HPE6 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 34% | 100% |
Q6NZQ2 | Mus musculus | 31% | 99% |
Q73EU1 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 34% | 100% |
Q7A0D2 | Staphylococcus aureus (strain MW2) | 30% | 100% |
Q7A4G0 | Staphylococcus aureus (strain N315) | 30% | 100% |
Q81IT9 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 34% | 100% |
Q81VG0 | Bacillus anthracis | 34% | 100% |
Q8CRP6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 31% | 100% |
Q8K9H6 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 34% | 100% |
Q8L7S8 | Arabidopsis thaliana | 36% | 91% |
Q8Y8N0 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 36% | 100% |
Q99MJ9 | Mus musculus | 40% | 92% |
Q99SH6 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 30% | 100% |
Q9BQ39 | Homo sapiens | 38% | 92% |
Q9DF35 | Xenopus laevis | 38% | 89% |
Q9DF36 | Xenopus laevis | 38% | 85% |
Q9JIK5 | Mus musculus | 40% | 80% |
Q9NR30 | Homo sapiens | 39% | 87% |
Q9Z6C9 | Limosilactobacillus reuteri | 33% | 100% |
V5BDT6 | Trypanosoma cruzi | 26% | 100% |
V5BEY7 | Trypanosoma cruzi | 73% | 100% |