Align 2-aminomuconate semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate 3607686 Dshi_1095 aldehyde dehydrogenase (RefSeq)
Query= metacyc::MONOMER-13349 (490 letters) >FitnessBrowser__Dino:3607686 Length = 506 Score = 343 bits (879), Expect = 1e-98 Identities = 195/488 (39%), Positives = 275/488 (56%), Gaps = 17/488 (3%) Query: 3 QYRNYINGEWVE--SARRFDDVNPVDGTVVAQVHEADREAVDSAIRAGHAAVRGAWGRTT 60 +Y N+I G++V R FD+V P+ G VV Q+ + V+ A+ A HAA + AWG+T+ Sbjct: 18 RYDNFIGGKFVPPVEGRYFDNVTPITGEVVGQIARSSAADVELALDAAHAA-KDAWGKTS 76 Query: 61 VAERAAILCRIADEIDRRYDDFLAAEIADTGKPVAMASTIDIPRGAANFRVFADILKTAP 120 V ERA I+ +IAD I+ D AE D GKP+ + DIP +FR FA +L+ Sbjct: 77 VTERANIVLKIADRIEENLDIIAKAETWDNGKPIRETTLADIPLAVDHFRYFAGVLRGQE 136 Query: 121 LDTFQTDLPDGARALNYAVRKPLGVVGVISPWNLPLLLLTWKIAPALACGNAVVAKPSEE 180 + D A Y +PLGVVG I PWN +L+ WK+APA+A GN +V KP+E+ Sbjct: 137 GSMSEIDNDTVA----YHFHEPLGVVGQIIPWNFSILMAAWKLAPAIAAGNCIVLKPAEQ 192 Query: 181 TPGTATLLAEVMHTVGVPPGVFNLVHGFGPDSAGEFITTNDDIDAITFTGESRTGSAIMR 240 TP +L E++ + +P GV N+V+G+G + G + T+D I I FTG + TG IM Sbjct: 193 TPAAIMVLVELISDL-LPAGVLNIVNGYGGE-VGAALATSDRIAKIAFTGSTATGRKIME 250 Query: 241 AAATHVKPVSFELGGKNAAIIFADCDFE------KMIDGMMRAVFLHSGQVCLCAERVYV 294 AA ++ PV+ ELGGK+ I F D E K ++G + F + G+VC C R + Sbjct: 251 AATVNLIPVTLELGGKSPNIFFKDVMAEDDAFLDKAVEGFVLFAF-NQGEVCTCPSRALI 309 Query: 295 ERPIYNRFLDAFVERVKALKLGWPQDGTTGMGPLISAEHRDKVLSYFKLAREEGAQVLVG 354 IY F+ + RVKA+ G P+ T +G S E +DK+LSYF++ EEGA+VL G Sbjct: 310 HEDIYEEFIARAIARVKAIVQGDPRKMETMVGAQASKEQKDKILSYFQIGVEEGAEVLTG 369 Query: 355 GGVPKFGDARDAGFWVEPTIITGLPQTARCIKEEVFGPICHVSPFDTEAEAIALANDTKY 414 G V D GF++EPTI+ G R +EE+FGP+ V+ F TE EA+ LANDT Y Sbjct: 370 GKVADVSDDLKDGFYIEPTILKG-HNKMRVFQEEIFGPVVSVTTFKTEEEALELANDTMY 428 Query: 415 GLSATTWTGNLNRGHRVSEAMRVGLSWVNSWFLRDLRTPFGGVGLSGIGREGGMHSLNFY 474 GL A W+ + N +R ++ G WVN++ FGG SGIGRE L+ Y Sbjct: 429 GLGAGVWSRDQNTCYRFGRGVQAGRVWVNNYHAYPAHAAFGGYKQSGIGRENHKMMLDHY 488 Query: 475 SELTNVCV 482 + N+ V Sbjct: 489 QQTKNMLV 496 Lambda K H 0.321 0.137 0.420 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: 567 Number of extensions: 21 Number of successful extensions: 7 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: 490 Length of database: 506 Length adjustment: 34 Effective length of query: 456 Effective length of database: 472 Effective search space: 215232 Effective search space used: 215232 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 (21.8 bits) S2: 52 (24.6 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:
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