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_091518683.1 BM253_RS02725 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_900115115.1:WP_091518683.1 Length = 432 Score = 204 bits (519), Expect = 5e-57 Identities = 129/423 (30%), Positives = 211/423 (49%), Gaps = 5/423 (1%) Query: 56 QSGFEAWRKVPAHERAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIE 115 QS F WR +R + ++ + + A +T + KP+ A EV A + + Sbjct: 14 QSSFLKWRDFSLDDRISVLKNIKEKLLQNKRDYAYAITTDMNKPIKLAIAEVEKCAYLCD 73 Query: 116 WFADEGRRVYGRIVPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSF 175 ++ + + G + + P+G + PWNFP QV R + +L TG F Sbjct: 74 YYIENAAQFLEDQEVKTGWG-KSYITFRPLGVLLGVMPWNFPFWQVFRFVIPSLLTGNVF 132 Query: 176 LVKAPEETPASPAALLRAFVDAGVPAGVIGLVYGDPAEISSYLIPHPVIRKVTFTGSTPV 235 +VK P S AL F + + + +E+++ +I +P+I+ V+ TGS Sbjct: 133 VVKHASNVPLSAKALEDVFNVDTIDFPIYKDLSIKSSEVAN-VIANPIIKAVSLTGSEHA 191 Query: 236 GKQLASLAGLHMKRATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLV 295 G+ +A AG H+K+ +ELGG IV DAD+ A + A A+ +NAGQ CI+ RFL+ Sbjct: 192 GRSVAETAGKHLKKCVLELGGSNAFIVLNDADLNCAAEKAVNARMQNAGQSCIASKRFLI 251 Query: 296 HNSIRDEFTRALVKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETG 355 H ++ ++F + L +G+ +E T G++A + + ++ + GA+I G Sbjct: 252 HEAVYNQFVDLFKQKLSTLILGDKYDETVTFGSMAREDLAVELENQLEKSVAKGATIIAG 311 Query: 356 GERIGSEGNFFAPTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGY 415 G+R FF PT++ NV +D VF E FGP+AAI F ++EAI +N+ FGL Sbjct: 312 GKR---NRAFFEPTLVTNVTVDMPVFAEETFGPLAAIIPFKTIDEAIELSNKSNFGLGAS 368 Query: 416 AFTRSFANVHLLTQRLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKS 475 FT + + + G L+IN+ P +PFGG+K+SGYG E AL + ++ Sbjct: 369 IFTDNPQQLDNYLHLFDEGALFINEMIVSDPHLPFGGIKNSGYGRELSHFALYEFANIQT 428 Query: 476 VTV 478 V + Sbjct: 429 VVI 431 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: 412 Number of extensions: 20 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: 432 Length adjustment: 33 Effective length of query: 448 Effective length of database: 399 Effective search space: 178752 Effective search space used: 178752 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