Align asparagine synthetase B, glutamine-hydrolyzing; EC 6.3.5.4 (characterized)
to candidate WP_012631017.1 MNOD_RS38500 asparagine synthase (glutamine-hydrolyzing)
Query= CharProtDB::CH_002444 (554 letters) >NCBI__GCF_000022085.1:WP_012631017.1 Length = 654 Score = 141 bits (355), Expect = 9e-38 Identities = 116/372 (31%), Positives = 172/372 (46%), Gaps = 53/372 (14%) Query: 28 MRHRGPDWSGIYASDNA--ILAHERLSIVDVNAGAQPLYNQQKTHVLAVNGEIYNHQALR 85 +RHRGPD I+ A L H RLSI+ ++ G QP+ +Q L VNGE Y+ + +R Sbjct: 27 IRHRGPDERDIWLDPEAGVALGHTRLSIIGLSNGRQPIASQDGALQLIVNGEFYDFERIR 86 Query: 86 AEYGDR-YQFQTGSDCEVILALYQEKGPEFLDDLQGMFAFALYDSEKDAYLIGRDHLGII 144 AE R F+T SD E+ L LY+E G L L+G FA LYD+ + ++ RD GI Sbjct: 87 AELQARGCVFRTQSDSEIALHLYREFGTAGLGRLRGEFALVLYDAVERQLVVMRDRFGIK 146 Query: 145 PLYMGYDEHGQLYVASEMKALV-----------------------PVCRTIKEFPAGSYL 181 PL++ + G L+V SE+KALV + + I+ G L Sbjct: 147 PLFVA-EHDGALWVGSEIKALVAAGVPAFWDLDAYVSRGFYLGNRTLFQGIRSLAPGHLL 205 Query: 182 WSQDGEI--RSYYHRDWFDYDAVKDNVTDKNE----LRQALEDSVKSHLMSDVPYGVLLS 235 + G I R+Y+ D+ A+ D+ E LR + ++V L +DVP V LS Sbjct: 206 IASPGHIRERAYWDLDFPAAAALDSAAIDEAEAVEGLRAEILEAVGLRLRADVPIAVYLS 265 Query: 236 GGLDSSIISAITKKYAARRVEDQERSEAWWPQLHSFAVGLPGSPDL---KAAQEVANHLG 292 GG+DSS + + L +F + D + A E A+ G Sbjct: 266 GGIDSSAMLGCATRLRG-------------TPLDAFTLSFTDDGDYDERRFAAEAASFNG 312 Query: 293 TVHHEIHFTVQEGLDAIRDVIYHIETYDVTTIRA-STPMYLMSRKIKAMGIKMVLSGEGS 351 H I T + D + ++H E V A Y +SR + K+V++GEG+ Sbjct: 313 ARFHPIPVTQDDLADDFEEALWHNE---VPFFNAHGVAKYRLSRVVAQARFKVVITGEGA 369 Query: 352 DEVFGGYLYFHK 363 DE+F GY +F + Sbjct: 370 DEIFAGYPHFRR 381 Score = 37.7 bits (86), Expect = 1e-06 Identities = 26/87 (29%), Positives = 41/87 (47%), Gaps = 3/87 (3%) Query: 398 VEARVPFLDKKFLDVAMRINPQDKMCGNGKMEKHILRECFEAYLPASVAWRQKEQFSDGV 457 +E RVP LD + A R+ K+ G EKH+ RE +LP ++ R+K F Sbjct: 509 IEGRVPLLDHHVAEYAARLPVWLKI--RGATEKHVFREAMRPFLPEALYRRKKHYFRAPP 566 Query: 458 GYS-WIDTLKEVAAQQVSDQQLETARF 483 S + L ++ A ++ + LE F Sbjct: 567 AMSAQRNRLAQLVADTLASRHLEDLPF 593 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: 813 Number of extensions: 50 Number of successful extensions: 6 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: 654 Length adjustment: 37 Effective length of query: 517 Effective length of database: 617 Effective search space: 318989 Effective search space used: 318989 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