Align aspartate ammonia-lyase (EC 4.3.1.1) (characterized)
to candidate 6936634 Sama_0822 fumarate hydratase (RefSeq)
Query= BRENDA::Q9HTD7 (474 letters) >FitnessBrowser__SB2B:6936634 Length = 457 Score = 316 bits (810), Expect = 9e-91 Identities = 196/461 (42%), Positives = 264/461 (57%), Gaps = 19/461 (4%) Query: 7 SRIEKDLLGTLEVPADAYYGIQTLRAVNNFRLSGVPLSHYPKLVVALAMVKQAAADANRQ 66 SRIE D +G + VPA+A YG QT RA+NNF + G P+ + L ++K AAA AN Q Sbjct: 3 SRIETDSMGEVLVPAEALYGAQTQRALNNFAIGGQPMPR--AFIETLLLIKAAAARANSQ 60 Query: 67 LGHLPEDKHAAISEACARLIRGD-FHEQFVVDMIQGGAGTSTNMNANEVIANIALEAMGH 125 LG L D AI+EA L + + F VD+ Q G+GTS+NMNANEV+A + E++G Sbjct: 61 LGVLASDCGQAITEAALSLRQDKALMQHFPVDVFQTGSGTSSNMNANEVLARLTSESLGR 120 Query: 126 TKGEYKYLHPNNDVNMAQSTNDAYPTAIRL---GLLLGHDTLLASLDSLIQAFAAKGVEF 182 + N++VN+ QS+ND P+ I++ G+L TLL +L L K Sbjct: 121 A------VSANDEVNLGQSSNDVIPSCIQIASAGVLT--KTLLPALTHLKSCIRTKAASV 172 Query: 183 AGVLKMGRTQLQDAVPMTLGQEFHAFATTLGEDLDRLRRLAPELLT--EVNLGGTAIGTG 240 GV+K GRT L DA+P+ L Q +A+ L R +L +L++ ++ GGTA+GTG Sbjct: 173 KGVVKTGRTHLMDAMPVRLSQSLETWASQLDA---RELQLQSQLISLWQLPQGGTAVGTG 229 Query: 241 INADPGYQKLAVERLAAISGQPLKPAADLIEATSDMGAFVLFSGMLKRTAVKLSKICNDL 300 +NA PG+ + L ++G +PA L + V SG LK AV L KI NDL Sbjct: 230 VNAAPGFPQAFCHELNLLTGLAFQPAPHLFTGIASQDTAVALSGELKALAVTLMKIANDL 289 Query: 301 RLLSSGPRTGINEINLPPRQPGSSIMPGKVNPVIPEAVNQVAFEVIGNDLALTLAAEGGQ 360 R ++SGP G+ EI LP QPGSSIMPGKVNPVIPEAV +VIGND +T+A + G Sbjct: 290 RWMNSGPLAGLGEIRLPALQPGSSIMPGKVNPVIPEAVAMACAQVIGNDACITVAGQSGN 349 Query: 361 LQLNVMEPLIAYKIFDSIRLLQRAMDMLREHCITGITANVERCHELVEHSIGLVTALNPY 420 +LNVM P+IA + S+RLL AM L + I G R + + + LVTALNP Sbjct: 350 FELNVMLPVIADNLLSSLRLLTNAMMALADKAIDGFEVCEGRMAKELSRNPILVTALNPI 409 Query: 421 IGYENSTRIAKTALESGRGVLELVREEKLLDEATLADILLP 461 +GY + IAK A GR VLE+ E +D LA +L P Sbjct: 410 VGYAKAADIAKRAYAEGRPVLEVALEMTDIDAEELARLLDP 450 Lambda K H 0.318 0.135 0.380 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: 519 Number of extensions: 22 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 474 Length of database: 457 Length adjustment: 33 Effective length of query: 441 Effective length of database: 424 Effective search space: 186984 Effective search space used: 186984 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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