Align Ketoglutarate semialdehyde dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_068173703.1 HTA01S_RS16100 aldehyde dehydrogenase (NADP(+))
Query= reanno::WCS417:GFF2159 (526 letters) >NCBI__GCF_001592305.1:WP_068173703.1 Length = 491 Score = 364 bits (934), Expect = e-105 Identities = 208/482 (43%), Positives = 282/482 (58%), Gaps = 4/482 (0%) Query: 22 LQSVDATSGEALPQHFYQATPQEVDAAAKAAAQAYPAYRALSAARRAQFLDAVADELDAL 81 LQS +A +G P+ ++ Q++D + +AA QA+ + + S A+RA L A+A+ L+A Sbjct: 5 LQSFNARTGAPHPEALSASSSQDIDDSVRAAHQAFEVWGSSSGAQRAALLRALAEALEAD 64 Query: 82 GDEFVELVCRETALPAARIKGERGRTSGQMRLFATVLRRGDFYGARIDKALPDRQPMPRP 141 D V ETAL A R+ GE RT Q+R FA + RG + D A+ P+ P Sbjct: 65 RDALVPWADLETALGAVRLSGELDRTCFQLRRFADLAERGVPFETLDDPAVAGAPPVGHP 124 Query: 142 DLRQYRIGLGPVAVFGASNFPLAFSTAGGDTAAALAAGCPVVFKAHSGHMATAERVADAI 201 + + R+ LGPVA+F ASNFP AFS GGDTA+ALAAGCPVV KAH GH + RV I Sbjct: 125 AMVRQRVPLGPVAMFAASNFPFAFSVLGGDTASALAAGCPVVVKAHPGHPLLSRRVFGLI 184 Query: 202 IRAAEATEMPAGVFNMIFGGG--VGEALVKHPAIQAVGFTGSLKGGRALCDMAAARPQPI 259 + +A +PAG+ M+ G G VG AL++HP I A FTGS +GG AL A ARP+PI Sbjct: 185 QQVLQAQGLPAGLVGMVQGAGVDVGVALIRHPLIAAGAFTGSTRGGAALQAEANARPRPI 244 Query: 260 PVFAEMSSINPVIVLPQALKARAESVARDLTASVVQGCGQFCTNPGLVIGVASPEFTAFT 319 P + E+ SINPV+ LP+AL AR +A L S+ GCGQFCTNPGL++ + PE AF Sbjct: 245 PFYGELGSINPVLALPKALAARGAELATTLAGSIALGCGQFCTNPGLIVLLDDPESDAFI 304 Query: 320 QQVAQLIGDQPAQTMLNAGTLSSYGKGLEKLLAHPGIQHLAGSQQAGNQAQPQLFKADVR 379 +Q+ + + Q ML AG S++ G+ +++ G L +Q A P L + Sbjct: 305 EQLTRALAAQKPHPMLTAGMKSAFDAGVRQMM-DQGALALLAAQGAAPAPGPHLLQVSAA 363 Query: 380 LLIDGDEVLQEEVFGPTTVFVEVADQAQLSAALHGLHGQLTATIIGEPADLQQFAELTPL 439 I+ L+EEVFGP ++ V A QA+L A L + G LT T+ G D + L Sbjct: 364 RFIE-RAALREEVFGPASLIVRAASQAELLAVLAAVGGSLTVTLWGADDDTPENQALVRA 422 Query: 440 LEQKVGRILLNGYPTGVEVCDSMVHGGPYPATSDARGTSVGTLAIDRFLRPVCFQNYPDS 499 GR+L +G PTGV V + HGGP+PA+S TSVG A+DRFLRP+C Q+ P Sbjct: 423 ATAIAGRVLFSGVPTGVAVTAAQQHGGPWPASSAPMTTSVGDAALDRFLRPICLQDAPAW 482 Query: 500 LL 501 LL Sbjct: 483 LL 484 Lambda K H 0.319 0.135 0.392 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: 643 Number of extensions: 23 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: 526 Length of database: 491 Length adjustment: 34 Effective length of query: 492 Effective length of database: 457 Effective search space: 224844 Effective search space used: 224844 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 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