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_012536595.1 AFE_RS07230 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_000021485.1:WP_012536595.1 Length = 475 Score = 308 bits (790), Expect = 2e-88 Identities = 171/470 (36%), Positives = 268/470 (57%), Gaps = 6/470 (1%) Query: 9 TQLLIDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAH 68 T IDG W D + + +P + + V+ G + D A+ AA F AWR+ + Sbjct: 6 TAAFIDGCWTDLRARFVVQ--SPVNQQMLAEVSDCGPREADAAVQAATVAFAAWRQTTVY 63 Query: 69 ERAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRI 128 +RA + + A L++ A+ +A+L+T E GKP+ ++R E+ +A + W+A+E +RV G Sbjct: 64 QRALILSRWADLIQVHAEDLARLITWEMGKPIRQSRAEIKTAVALARWYAEECKRVTGES 123 Query: 129 VPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPA 188 +P + + + K P+GPV A TPWN PV+ VVRK++ ALA GC+ ++K E+TP S Sbjct: 124 IPSQFPDKRLQIWKVPIGPVFAITPWNSPVSMVVRKIAPALAAGCTVILKPDEQTPLSAL 183 Query: 189 ALLRAFVDAGVPAGVIG-LVYGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHM 247 L + A PAG + L DPA ++ L+ I K++FTGST VG++L + + Sbjct: 184 KLAELWAAAEGPAGTLQVLPSADPAPLAERLMADSRIAKLSFTGSTAVGQKLYAQGSPTI 243 Query: 248 KRATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRAL 307 KR ++ELGGHAPV++ DAD+ AV AKFR AGQ C++ R V +I EFT Sbjct: 244 KRLSLELGGHAPVLIFADADIDAAVAMTIHAKFRYAGQSCVAANRLYVDEAILPEFTARY 303 Query: 308 VKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFA 367 ++ LKVG+ E T +G L + + + + +A GA + GG+ ++G + + Sbjct: 304 LEAMGHLKVGDPFAEDTDIGPLVSEVAVQKFKAQLQDAMARGARLLCGGD---AQGLWCS 360 Query: 368 PTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLL 427 PT++A++ + +F+ E F P+ I+GF EA+A AN P+GLA Y +TR + + Sbjct: 361 PTLLADLDPQSRIFHEESFSPLLPIQGFRSEAEAVARANDTPYGLAAYLWTRDLGRAYRI 420 Query: 428 TQRLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKSVT 477 + L+ G++ +N A P+ PFGG K SG G+EGG LE YL + V+ Sbjct: 421 AEALQCGIVGVNDGAPATPQAPFGGSKLSGLGAEGGKWGLEEYLQLRYVS 470 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: 598 Number of extensions: 28 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: 481 Length of database: 475 Length adjustment: 34 Effective length of query: 447 Effective length of database: 441 Effective search space: 197127 Effective search space used: 197127 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 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