Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate BWI76_RS20495 BWI76_RS20495 alanine transaminase
Query= BRENDA::D2Z0I0 (402 letters) >FitnessBrowser__Koxy:BWI76_RS20495 Length = 412 Score = 453 bits (1165), Expect = e-132 Identities = 222/391 (56%), Positives = 286/391 (73%), Gaps = 5/391 (1%) Query: 2 SEEWMFPKVKKLPKYVFAMVNELKYQLRREGEDIVDLGMGNPDIPPSQHIIDKLCEVANR 61 S E F ++ +LP YVF + ELK RR GEDI+D MGNPD HI++KLC VA R Sbjct: 5 SPERRFTRIDRLPPYVFNITAELKMAARRRGEDIIDFSMGNPDGATPPHIVEKLCTVAQR 64 Query: 62 PNVHGYSASKGIPRLRKAICDFYKRRYGVELDPERNAIMTIGAKEGYSHLMLAMLEPGDT 121 P+ HGYS S+GIPRLR+AI +Y+ RY VE+DPE AI+TIG+KEG +HLMLA L+ GDT Sbjct: 65 PDTHGYSTSRGIPRLRRAISRWYQERYNVEIDPESEAIVTIGSKEGLAHLMLATLDHGDT 124 Query: 122 VIVPNPTYPIHYYAPIICGGDAISVPILPEEDFPEVFLRRLYDLIKTSFRKPKAVVLSFP 181 V+VPNP+YPIH Y +I G SVP++ DF L I+ S+ KPK ++L FP Sbjct: 125 VLVPNPSYPIHIYGAVIAGAQVRSVPLVEGVDF----FNELERAIRESYPKPKMMILGFP 180 Query: 182 HNPTTLCVDLEFFQEVVKLAKQEGIWIVHDFAYADLGFDGYTPPSILQVEGALDVAVELY 241 NPT CV+LEFF++VV LAK+ + +VHD AYAD+ +DG+ PSI+QV GA DVAVE + Sbjct: 181 SNPTAQCVELEFFEKVVALAKRYDVLVVHDLAYADIVYDGWKAPSIMQVPGARDVAVEFF 240 Query: 242 SMSKGFSMAGWRVAFVVGNEMLIKNLAHLKSYLDYGVFTPIQVASIIALESPYEVVEKNR 301 ++SK ++MAGWR+ F+VGN+ L+ LA +KSY DYG FTP+QVA+I ALE + V Sbjct: 241 TLSKSYNMAGWRIGFMVGNKTLVNALARIKSYHDYGTFTPLQVAAIAALEGDQQCVRDIA 300 Query: 302 EIYRRRRDVLVEGLNRVGWEVKKPKGSMFVWAKVPEE-VGMNSLDFSLFLLREAKVAVSP 360 E Y+RRRDVLV+GL+ GW V+ PK SM+VWAK+PE+ M SL+F+ LL++AKV VSP Sbjct: 301 EQYKRRRDVLVKGLHEAGWMVECPKASMYVWAKIPEQYAAMGSLEFAKKLLQDAKVCVSP 360 Query: 361 GIGFGEYGEGYVRFALVENEHRIRQAVRGIK 391 GIGFG+YG+ +VRFAL+EN RIRQAVRGIK Sbjct: 361 GIGFGDYGDTHVRFALIENRDRIRQAVRGIK 391 Lambda K H 0.322 0.141 0.425 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: 548 Number of extensions: 29 Number of successful extensions: 3 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: 402 Length of database: 412 Length adjustment: 31 Effective length of query: 371 Effective length of database: 381 Effective search space: 141351 Effective search space used: 141351 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 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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