Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_009547631.1 CCE_RS15270 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000017845.1:WP_009547631.1 Length = 490 Score = 427 bits (1099), Expect = e-124 Identities = 216/475 (45%), Positives = 307/475 (64%), Gaps = 3/475 (0%) Query: 21 RLFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSP 80 +L IN E+ +A + FET++P T + +A + D+D+A+ AAR F +GDW S Sbjct: 17 QLLINNEWIESASGKRFETINPTTGEVICDVAEADATDVDKAVKAARNAFNQGDWPNLSA 76 Query: 81 AKRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYG 140 ++R +L KLADL+EA+ EELA LETLD GKP + SL D+ R+YA DK+ G Sbjct: 77 SQRGQLLYKLADLIEANIEELARLETLDNGKPYQDSLNADLQLVIACYRYYAGWADKIQG 136 Query: 141 EVATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSA 200 + + EPVGV+ I+PWNFPLL+ WKL PALAAGN+V++K +E++PLSA Sbjct: 137 KTIPINGPYFCYTRHEPVGVVGQIIPWNFPLLMQAWKLAPALAAGNTVVMKTAEQTPLSA 196 Query: 201 IRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSN 260 R+ L EAG P GV+N+++G+G AGQA++RH+DID +AFTGST G +++ A +N Sbjct: 197 FRVGELIIEAGFPPGVVNLLSGYGPTAGQAIARHHDIDKVAFTGSTEVGHLIMEAAAQTN 256 Query: 261 MKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLA 320 +KRV LE GGKS NIVFAD +L QA G+F+NQGQ C AG+RL +EE DEF+A Sbjct: 257 LKRVTLELGGKSPNIVFADA-NLDQAIEGAHFGLFFNQGQCCCAGSRLFVEEKCYDEFVA 315 Query: 321 LLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLL--DGRNAGLAAA 378 ++A+ G P D TT G +D D V +I G+ +G LL GR Sbjct: 316 KSVERAKQRIVGDPFDDHTTQGPQVDKTQFDKVMEYIESGQREGAKLLCGGGRVGDRGYF 375 Query: 379 IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAH 438 I PT+F DV + +++EEIFGPV+ + +F ++ +Q AND+ YGL AAVWT+D+S+ H Sbjct: 376 IEPTVFADVQDDMKIAQEEIFGPVMSIIKFKDMDEVIQRANDTMYGLAAAVWTQDISKGH 435 Query: 439 RMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISL 493 ++ L+AG+V+VN Y+ D PFGG+KQSG GR+ + L+++TE+KT+ + L Sbjct: 436 AIANALRAGTVWVNCYDVFDAAAPFGGFKQSGMGRELGEYGLQQYTEIKTVTVKL 490 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: 565 Number of extensions: 24 Number of successful extensions: 3 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: 490 Length adjustment: 34 Effective length of query: 461 Effective length of database: 456 Effective search space: 210216 Effective search space used: 210216 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 Apr 09 2024. 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