Align Ketoglutarate semialdehyde dehydrogenase (EC 1.2.1.26) (characterized)
to candidate Ga0059261_0516 Ga0059261_0516 vanillin dehydrogenase (EC 1.2.1.67)
Query= reanno::Smeli:SM_b20891 (477 letters) >FitnessBrowser__Korea:Ga0059261_0516 Length = 478 Score = 257 bits (656), Expect = 7e-73 Identities = 165/461 (35%), Positives = 239/461 (51%), Gaps = 9/461 (1%) Query: 15 GDGVANINPSNTDDVVGEYARASAEDAKAAIAAAKAAFPAWSRSGILERHAILKKTADEI 74 G A +NP T +V E + + A A+ AA AAFPAWS G R A L K A+ + Sbjct: 10 GKTFARLNPV-TGEVATEAQAFTVDQANEAVEAAAAAFPAWSTLGPNARRAALNKAAEAL 68 Query: 75 LARKDELGRLLSREEGKTLAEGIGETVRAGQIFEFFAGETLRLAGEVVPSVRPGIGVEIT 134 A+ ++ ++ E G T + A + A T ++ GEV+PS +PG Sbjct: 69 AAKAEDFVEAMNGEIGATEGWARFNLMLAVSMVREAAALTTQIGGEVIPSDKPGCIAMAI 128 Query: 135 REPAGVVGIITPWNFPIAIPAWKLAPALCYGNTIVFKPAELVPGCSWAIVDILHRAGLPK 194 REP GV+ I PWN PI + +A L GNT+V K +E P I + A LPK Sbjct: 129 REPVGVMLGIAPWNAPIILGVRAVAAPLACGNTVVLKASEQCPRTHSLIAEAFDEA-LPK 187 Query: 195 GVLNLVMGKGS----VVGQAMLDSPDVQAITFTGSTATGKRVAVASVEHNRKYQLEMGGK 250 G +++V +VG A++D+P ++ I FTGSTA G+ +A + EH + LE+GGK Sbjct: 188 GAVSIVTNAPEDAPEIVG-ALIDNPHIRRINFTGSTAVGRIIAKRAAEHLKPVLLELGGK 246 Query: 251 NPFVVLDDADLSVAVEAAVNSAFFSTGQRCTASSRIIVTEGIHDRFVAAMGERIKGLVVD 310 P +VL+DADL AV+AA AF + GQ C ++ RIIV + + D FV ++ + V Sbjct: 247 APMLVLEDADLDEAVKAAAFGAFMNQGQICMSTERIIVVDAVADAFVEKFAAKVGTMPVG 306 Query: 311 DALKPGTHIGPVVDQSQLNQDTDYIAIGKQEGAKLAFGGEVISRDTPGFYLQPALFTEAT 370 D + T +G VVDQ + I GA GG V+ T G + + T Sbjct: 307 DPREGKTPLGAVVDQKTVAHVKALIGDALAAGAVQVNGGGVL-EGTGGVLMPAHVIDHVT 365 Query: 371 NEMRISREEIFGPVAAVIRVKDYDEALAVANDTPFGLSSGIATTSLKHATHFKRNAEAGM 430 +M++ R+E FGPV VIR +D A+ +ANDT +GLS+ + T R ++G+ Sbjct: 366 PDMKLFRDESFGPVVGVIRARDEAHAILLANDTEYGLSASVFTRDTARGLRVARQIKSGI 425 Query: 431 VMVNLPTAGVDFHVPFGGRKASSYGPREQGKYAAEFYTNVK 471 VN PT + +PFGG KAS YG R GK + +T ++ Sbjct: 426 CHVNGPTVHDEAQMPFGGVKASGYG-RFGGKAGIDAFTELR 465 Lambda K H 0.317 0.134 0.391 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: 564 Number of extensions: 31 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: 477 Length of database: 478 Length adjustment: 34 Effective length of query: 443 Effective length of database: 444 Effective search space: 196692 Effective search space used: 196692 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