Align asparagine synthetase B, glutamine-hydrolyzing; EC 6.3.5.4 (characterized)
to candidate Ga0059261_3119 Ga0059261_3119 asparagine synthase (glutamine-hydrolyzing)
Query= CharProtDB::CH_002444 (554 letters) >FitnessBrowser__Korea:Ga0059261_3119 Length = 616 Score = 139 bits (351), Expect = 2e-37 Identities = 121/374 (32%), Positives = 188/374 (50%), Gaps = 62/374 (16%) Query: 28 MRHRGPDWSGIYASDNAI--LAHERLSIVDVNAGA-QPLYNQQKTHVLAVNGEIYNHQAL 84 + HRGPD +G + S + LA RL+I+D++ G QP++ + + NGEIYN + L Sbjct: 26 LHHRGPDDTGQWWSPDGRVGLAQARLAIIDLSPGGHQPMHREADRLSVVFNGEIYNFRDL 85 Query: 85 RAEY-GDRYQFQTGSDCEVILALYQEKGPEFLDDLQGMFAFALYDSEKDAYLIGRDHLGI 143 RAE G + F++ SD EV+LA Y + G L L GMFAFA++D+ + RD G Sbjct: 86 RAELEGLGHVFRSHSDTEVLLAAYAQWGIGCLTRLNGMFAFAIFDARANKVYFARDRAGE 145 Query: 144 IPLYMGYDEHGQLYVASEMKALVP---VCRTIKEFPAGSYLWSQ----DGEIRSYY---- 192 PL+ + +G ++ ASE+K L+ + R I YL + DG I + Y Sbjct: 146 KPLFY-HAANGTIHFASELKTLLADPTLPRVIDPAALDGYLLTGYVPGDGCILAGYRKLP 204 Query: 193 -------------HRDWF-----DYDAVKDNVTDK-NELRQALEDSVKSHLMSDVPYGVL 233 HR W DY V+D+ EL LED+V L++DVP GVL Sbjct: 205 PGHAMELDLSSGAHRVWRYWNLPDYAPVEDDDAGLLGELEALLEDAVGRQLVADVPVGVL 264 Query: 234 LSGGLDSSIISAITKKYAARRVEDQERSEAWWPQLHSFAVGLPGS---PDLKAAQEVANH 290 LSGG+DSS+I+A+ + AA+ + +F +G G+ +++ A+ +A+H Sbjct: 265 LSGGVDSSLITAMAVRNAAK--------------VRTFTIGFAGAGPLNEIEHARLIADH 310 Query: 291 LGTVHHEI--HFTVQEGLDAIRDVIYHIETYDVTTIRAST-PMYLMSRKIKAMGIKMVLS 347 GT E+ TV E L + +D +S P +++S ++ + L Sbjct: 311 FGTEQVELMAEPTVAELLPRL------AAQFDEPMADSSMFPTFMVSELVR-QHCTVALG 363 Query: 348 GEGSDEVFGGYLYF 361 G+G DE+FGGY ++ Sbjct: 364 GDGGDELFGGYGHY 377 Score = 26.2 bits (56), Expect = 0.004 Identities = 19/97 (19%), Positives = 41/97 (42%), Gaps = 3/97 (3%) Query: 360 YFHKAPNAKELHEETVRKLLALHMYD--CARANKAMSAWGVEARVPFLDKKFLDVAMRIN 417 Y + P +L + R ++ + + ++ +E R PFLD + ++ A Sbjct: 455 YRSRIPAMDDLLQRATRTDFGTYLSEDILVKVDRTSMLTSLEVRAPFLDHRLIEFAFGKV 514 Query: 418 PQDKMCGNGKMEKHILRECFEAYLPASVAWRQKEQFS 454 P ++ +K +L++ LP ++K+ FS Sbjct: 515 P-SRLKATASDKKILLKQLAARVLPPQFDRQRKQGFS 550 Lambda K H 0.319 0.135 0.407 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 745 Number of extensions: 39 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 554 Length of database: 616 Length adjustment: 36 Effective length of query: 518 Effective length of database: 580 Effective search space: 300440 Effective search space used: 300440 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory