Align [LysW]-aminoadipate semialdehyde transaminase; EC 2.6.1.- (uncharacterized)
to candidate CCNA_02326 CCNA_02326 acetylornithine aminotransferase/succinyldiaminopimelate aminotransferase
Query= curated2:Q5SHH5 (395 letters) >lcl|FitnessBrowser__Caulo:CCNA_02326 CCNA_02326 acetylornithine aminotransferase/succinyldiaminopimelate aminotransferase Length = 405 Score = 236 bits (601), Expect = 1e-66 Identities = 149/392 (38%), Positives = 210/392 (53%), Gaps = 21/392 (5%) Query: 22 GVYNKHDLLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMP 81 GVYN+ L RG+GAR+ EG EY+DCV G LGH +P +VE +K QAE L + Sbjct: 16 GVYNRAPLAFERGRGARLISTEGEEYLDCVAGIATNGLGHAHPALVEVLKAQAEKLWHVS 75 Query: 82 QTLPTPMRGEFYRTLTAILPPELNRVFPVNSGTEANEAALKFARAHTG------RKKFVA 135 P + E L A ++ VF NSGTEA E ALK AR + R Sbjct: 76 NIYRIPEQEELADALCANSFADV--VFFTNSGTEAVECALKTARKYHSANGQPERIDIYG 133 Query: 136 AMRGFSGRTMGSLSVTWEPKYREPFLPLVEPVEFIPYNDVEALKRAV-DEETAAVILEPV 194 F GRT +++ + P Y + F P + + + D +A+K A+ TAA+I+EPV Sbjct: 134 FDGSFHGRTYAAVNASGNPSYVDGFGPRLPGYSQLTFGDHDAIKAAIASPTTAAIIVEPV 193 Query: 195 QGEGGVRPATPEFLRAAREITQEKGALLILDEIQTGMGRTGKRFAFEHF-GIVPDILTLA 253 QGEGG R + L R++ E G LLI DE+Q GMGRTGK FA+E G P I+ +A Sbjct: 194 QGEGGARSIPTQCLVGLRQLCDEHGVLLIYDEVQCGMGRTGKLFAYEWAEGGEPHIMAVA 253 Query: 254 KALGGGVPLGAAVMREEVARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAEL 313 KALGGG P+GA + E A+ M HG+TFGGNPLAMA G AA+ ++ + + Sbjct: 254 KALGGGFPIGACLATTEAAKGMTVAAHGSTFGGNPLAMAVGKAALEIIKSPETLDNVKTV 313 Query: 314 GPWFMEKLRAIPS---PKIREVRGMGLMVGLELKEKAAPYIARLEKEHRVLALQAGPTVI 370 +F ++L + I +VRG G+++G++L ++ L ++ ++L G + Sbjct: 314 SGFFTQQLNGLKDRFPDVIVDVRGKGMLIGVKLIPNNRDFMV-LARDEKLLIAGGGDNCV 372 Query: 371 RFLPPLVIEKED-------LERVVEAVRAVLA 395 R LPPL + E+ LE+ EA RA A Sbjct: 373 RLLPPLNLTIEEASEAIAKLEKACEAARAKAA 404 Lambda K H 0.319 0.137 0.402 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: 378 Number of extensions: 23 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: 395 Length of database: 405 Length adjustment: 31 Effective length of query: 364 Effective length of database: 374 Effective search space: 136136 Effective search space used: 136136 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 (21.7 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