Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_003471449.1 J416_RS11040 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000359605.1:WP_003471449.1 Length = 473 Score = 277 bits (708), Expect = 7e-79 Identities = 170/482 (35%), Positives = 265/482 (54%), Gaps = 25/482 (5%) Query: 22 LFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPA 81 L+ING + ET + +D +Q A +A+ +D A+S+A + + S P Sbjct: 6 LYINGGWVET--EETIDVLDKYSQTTYATVAKASREHVDEAISSATKAYRKNQLS---PY 60 Query: 82 KRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGE 141 +R +L ++ LM+ + EELA T + GKP++ + R +I +A AE +++GE Sbjct: 61 QRFEILRNVSTLMKNNKEELAYTITKEAGKPLKQA-RTEIDRSAETFLLAAEEAKRIHGE 119 Query: 142 -----VATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKS 196 A S H +A ++ PVGV+ AI P+NFPL L K+ PALAAGN+V+LKP+ K+ Sbjct: 120 GVPVEAAPGSEHRMAFTIKVPVGVVGAISPFNFPLNLVAHKVAPALAAGNAVVLKPASKT 179 Query: 197 PLSAIRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDA 256 PL++++LA L +EAGLP G+L VV G G GQ + ID FTGS G QL ++ Sbjct: 180 PLASLKLAKLLEEAGLPKGLLQVVVGSGSVVGQQMMDDERIDLYTFTGSAEVGLQLKQNT 239 Query: 257 GDSNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIAD 316 G + R+ LE G S IV + D+ AA A F GQVCI+ R+ + ESI + Sbjct: 240 G---LNRLILELGNNSPVIVDKEA-DIDHAAKTLAGQSFAFAGQVCISVQRVYVHESIQE 295 Query: 317 EFLALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKG-QLLLDGRNAGL 375 FL +Q + G P D T +G +I + A+ ++I E KG +++L G+ G Sbjct: 296 RFLETFSEQIKQLLVGDPTDATTDVGPMISVSEAERAETWIHEAVDKGAKVVLGGKREG- 354 Query: 376 AAAIGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLS 435 A + PTI DV P + EEIF PV+ V +T + ++ N S YGL ++T+++ Sbjct: 355 -ALLEPTILTDVKPEMRVVCEEIFAPVVSVIAYTDLDSCIEEVNQSVYGLQGGIFTQNID 413 Query: 436 RAHRMSRRLKAGSVFVNNYNDGDM----TVPFGGYKQSGNGRDKSLHALEKFTELKTIWI 491 A+ ++R++ G + NDG +P+GG K SGNG++ +++E+ TE + I + Sbjct: 414 TAYYAAKRVEVGGFMI---NDGSQYRVDLMPYGGVKDSGNGKEGPKYSIEEMTEERLIVM 470 Query: 492 SL 493 +L Sbjct: 471 NL 472 Lambda K H 0.317 0.133 0.389 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: 460 Number of extensions: 26 Number of successful extensions: 5 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: 495 Length of database: 473 Length adjustment: 34 Effective length of query: 461 Effective length of database: 439 Effective search space: 202379 Effective search space used: 202379 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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