Align Alpha-ketoglutaric semialdehyde dehydrogenase; alphaKGSA dehydrogenase; 2,5-dioxovalerate dehydrogenase; EC 1.2.1.26 (characterized)
to candidate WP_104913346.1 C3B54_RS03975 aldehyde dehydrogenase family protein
Query= SwissProt::P42236 (488 letters) >NCBI__GCF_002950575.1:WP_104913346.1 Length = 486 Score = 275 bits (702), Expect = 3e-78 Identities = 165/470 (35%), Positives = 260/470 (55%), Gaps = 18/470 (3%) Query: 3 VITEQNTYLNFINGEWVKSQSGDMVKVENPADVNDIVGYVQNSTAEDVERAVTAANEA-K 61 +++ + Y FINGE+ + G + +PA +++ ++ EDV+ A+ A A Sbjct: 15 IVSLADEYGLFINGEFRPGRGGVFDSI-SPA-TEEVLTRFSEASEEDVDYAIGQARAAYD 72 Query: 62 TAWRKLTGAERGQYLYKTADIMEQRLEEIAACATREMGKTLPEAKGETARGIAILRYYAG 121 W K+ G ER +YL++ A I+++R E+A T + GK + E + +A +Y Sbjct: 73 KVWSKMPGRERSKYLFRIARIVQERSRELAIAETMDNGKPIKETRDVDIPLVAAWFFYYA 132 Query: 122 EGMRKTGDVIPSTDKDALMFTTRVPLGVVGVISPWNFPVAIPIWKMAPALVYGNTVVIKP 181 K + S A GVVG + PWNFP+ + WK+APAL GNTVV+KP Sbjct: 133 GWADKLEEATGSHQPHAW--------GVVGQVIPWNFPLMMLAWKVAPALAAGNTVVLKP 184 Query: 182 ATETAVTCAKIIACFEEAGLPAGVINLVTGPGSVVGQGLAEHDGVNAVTFTGSNQVGKII 241 A T+VT ++AG+PAGV+N+VTG G+ G+ L H G++ V FTGS VG+ I Sbjct: 185 AETTSVTAMLFAEICQQAGVPAGVVNIVTGAGAT-GRALVSHAGIDKVAFTGSTPVGREI 243 Query: 242 GQAALARGAKYQLEMGGKNPVIVADDADLEAAAEAVITGAFRSTGQKCTATSRVIVQSGI 301 + R LE+GGK IV DDA ++ A E +I+G F + G C A SR++VQ + Sbjct: 244 AKTLAGRPTALTLELGGKGANIVFDDAAMDEAVEGIISGIFFNQGHVCCAGSRLLVQENV 303 Query: 302 YERFKEKLLQRTKDITIGDSLKEDVWMGPIASKNQLDNCLSYIEKGKQEGASLLIGGEKL 361 ++ +L R + + +GD L ++ +G I S+ QLD + + G EGAS+ L Sbjct: 304 HDELLARLTSRIQTLRLGDPLDKNTDIGAINSRAQLDTISTLTQSGVDEGASIWQSDCAL 363 Query: 362 ENGKYQNGYYVQPAIFDNVTSEMTIAQEEIFGPVIALIKVDSIEEALNIANDVKFGLSAS 421 + G++ P +F +V++ IAQ+EIFGPV++++ + +EA+ AN+ +GLSA Sbjct: 364 P----ERGFWFPPTVFTDVSTSHRIAQDEIFGPVLSVLTFRTPDEAVAKANNTPYGLSAG 419 Query: 422 IFTENIGRMLSFIDEIDAGLVRINAESAGVELQAPFGGMKQSSSHSREQG 471 ++TE RML+ +D + AG+V N + + +PFGG Q S + RE G Sbjct: 420 VWTEKASRMLAVVDRLRAGVVWSNTFNK-FDPTSPFGGY-QESGYGREGG 467 Lambda K H 0.315 0.132 0.374 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: 572 Number of extensions: 32 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: 488 Length of database: 486 Length adjustment: 34 Effective length of query: 454 Effective length of database: 452 Effective search space: 205208 Effective search space used: 205208 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 (21.5 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