Align Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized)
to candidate WP_052123206.1 Q763_RS03145 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_000769915.1:WP_052123206.1 Length = 451 Score = 223 bits (569), Expect = 8e-63 Identities = 135/431 (31%), Positives = 215/431 (49%), Gaps = 5/431 (1%) Query: 48 LDRALAAAQSGFEAWRKVPAHERAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEV 107 +++ L +Q F W K P +R ++ ++ ++ +A+ +QE GKPL +A EV Sbjct: 24 VNQMLEISQKSFRKWGKTPLKKRVKFIKNLIFVLTKKQHLLAEKCSQEMGKPLKQAIAEV 83 Query: 108 LSAADIIEWFADEGRRVYGRIVPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSA 167 + + E++ + + + G + V EP+G + PWNFP QV R Sbjct: 84 KKCSLLCEFYLEHAEKFLQDEKISSDAG-ESFVTHEPLGVILGVMPWNFPYWQVFRFAIP 142 Query: 168 ALATGCSFLVKAPEETPASPAALLRAFVDAGVPAGVIGLVYGDPAEISSYLIPHPVIRKV 227 A+ G + +VK L F +A P + + +++ + +I +P+I+ V Sbjct: 143 AIIAGNTVVVKHASNVAECAQLLEELFKEAEFPEMIYQNLQISGSQVKN-VIENPIIKGV 201 Query: 228 TFTGSTPVGKQLASLAGLHMKRATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVC 287 + TGS G +AS A +K++ +ELGG IV EDAD+ AV A A+ +N GQ C Sbjct: 202 SLTGSEKAGATVASTAANLIKKSVLELGGSNAFIVLEDADLDKAVPVAVTARMQNTGQSC 261 Query: 288 ISPTRFLVHNSIRDEFTRALVKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARK 347 I+ RFLVH+S+ DEF + + LK GN ++E T +G LA + ++ + Sbjct: 262 IAAKRFLVHSSLYDEFLKRFTTEVKKLKSGNPMDEDTDIGPLARVDLAEDIEKQVNKSVD 321 Query: 348 VGASIETGGERIGSEGNFFAPTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANR 407 +GA + GG R F+ PT++ NV D +FN E FGPVA + FD EEA+ +N Sbjct: 322 MGAKVIIGGRR---NNAFYEPTIVVNVTSDMPLFNEEVFGPVAPVIAFDSFEEAVKLSNY 378 Query: 408 LPFGLAGYAFTRSFANVHLLTQRLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEAL 467 FGL FT + E G ++IN P +PFGGVK SG+G E + Sbjct: 379 SDFGLGVNIFTEDIEGIKEKISLFEEGAVFINAMVKSDPALPFGGVKKSGFGRELAENGI 438 Query: 468 EPYLVTKSVTV 478 + ++ K+V + Sbjct: 439 KEFVNVKTVYI 449 Lambda K H 0.318 0.134 0.393 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: 428 Number of extensions: 17 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: 481 Length of database: 451 Length adjustment: 33 Effective length of query: 448 Effective length of database: 418 Effective search space: 187264 Effective search space used: 187264 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: 51 (24.3 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