Align tyrosine transaminase (EC 2.6.1.5) (characterized)
to candidate Synpcc7942_0645 Synpcc7942_0645 glutamate-1-semialdehyde aminotransferase
Query= BRENDA::H8WR05 (434 letters) >lcl|FitnessBrowser__SynE:Synpcc7942_0645 Synpcc7942_0645 glutamate-1-semialdehyde aminotransferase Length = 453 Score = 218 bits (555), Expect = 3e-61 Identities = 150/417 (35%), Positives = 208/417 (49%), Gaps = 25/417 (5%) Query: 24 SQRQFEAQARYMPGANSRSVLFYAPF---PLTIARGEGAALWDADGHRYADFIAEYTAGV 80 S F A + MPG S V + P+ R + A WD DG+RY D++ + + Sbjct: 32 SDEIFAAAQKLMPGGVSSPVRAFKSVGGQPIVFDRVKDAYAWDVDGNRYIDYVGTWGPAI 91 Query: 81 YGHSAPEIRDAVIEAMQGGINLTGHNLLEGRLARLICERFPQIEQLRFTNSGTEANLMAL 140 GH+ PE+ +A+ AM+ G + LE LA ++ + P IE +RF NSGTEA + L Sbjct: 92 CGHAHPEVIEALKVAMEKGTSFGAPCALENVLAEMVIDAVPSIEMVRFVNSGTEACMAVL 151 Query: 141 TAALHFTGRRKIVVFSGGYHG-----------GVLGFGARPS---PTTVPFDFLVLPYND 186 +TGR KI+ F G YHG GV G S P + + L PYND Sbjct: 152 RLMRAYTGRDKIIKFEGCYHGHADMFLVKAGSGVATLGLPDSPGVPKSTTANTLTAPYND 211 Query: 187 AQTARAQIERHGPEIAVVLVEPMQGASGCIPGQPDFLQALRESATQVGALLVFDEVMTS- 245 + +A + EIA V++EP+ G SG I FL+ LRE + ALLVFDEVMT Sbjct: 212 LEAVKALFAENPGEIAGVILEPIVGNSGFIVPDAGFLEGLREITLEHDALLVFDEVMTGF 271 Query: 246 RLAPHGLANKLGIRSDLTTLGKYIGGGMSFGAFGGRADVMALFDPRTGPLAHSGTFNNNV 305 R+A G+ K G+ DLTTLGK IGGG+ GA+GG+ ++M L P GP+ +GT + N Sbjct: 272 RIAYGGVQEKFGVTPDLTTLGKIIGGGLPVGAYGGKREIMQLVAP-AGPMYQAGTLSGNP 330 Query: 306 MTMAAGYAGLTKLFTPEAAGALAERGEALRARLNALCANEGVAMQFTGIGSLMNAHFVQG 365 + M AG L L P L + + L L A+ G A + + F +G Sbjct: 331 LAMTAGIKTLELLRQPGTYEYLDQITKRLSDGLLAIAQETGHAACGGQVSGMFGFFFTEG 390 Query: 366 DVRSSEDLAAVDGRLRQLLFFH--LLNEDIYSSPRGFVV--LSLPLTDADIDRYVAA 418 V + ED D L++ FH +L + IY +P F SL T+ DID +AA Sbjct: 391 PVHNYEDAKKSD--LQKFSRFHRGMLEQGIYLAPSQFEAGFTSLAHTEEDIDATLAA 445 Lambda K H 0.322 0.138 0.408 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: 454 Number of extensions: 21 Number of successful extensions: 4 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: 434 Length of database: 453 Length adjustment: 32 Effective length of query: 402 Effective length of database: 421 Effective search space: 169242 Effective search space used: 169242 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: 51 (24.3 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