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 BWI76_RS15205 BWI76_RS15205 succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >FitnessBrowser__Koxy:BWI76_RS15205 Length = 461 Score = 271 bits (694), Expect = 3e-77 Identities = 161/441 (36%), Positives = 232/441 (52%), Gaps = 18/441 (4%) Query: 29 VNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAHERAATMRKAAALVRERADAI 88 VNP TG+ + + A +D A+A A+ G+ WRKV +RA T+R A +R R++A+ Sbjct: 11 VNPTTGETLSSLPWASEQQVDSAIALAEQGYRQWRKVSVAQRATTLRNVGAAMRARSEAL 70 Query: 89 AQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRIVPPRNLGAQQTVVKE----- 143 AQ+++ E GKP+ +AR EV +A++ +W+A+ G P L + T+V++ Sbjct: 71 AQMISLEMGKPIAQARGEVAKSANLCDWYAEHG---------PAMLNTEATLVEDNKAVI 121 Query: 144 ---PVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPAALLRAFVDAGVP 200 P+G + A PWNFPV QV+R L G S+L+K S A + F AGVP Sbjct: 122 EYRPMGAILAIMPWNFPVWQVLRGAVPILLAGNSYLLKHAPNVLGSAAMIGEIFAAAGVP 181 Query: 201 AGVIGLVYGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHMKRATMELGGHAPV 260 GV G V +S +I P I VT TGS GK + + AG +K+ +ELGG P Sbjct: 182 EGVFGWVNATNDGVSQ-MINDPRIAAVTVTGSVRAGKAIGAQAGAALKKCVLELGGSDPF 240 Query: 261 IVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRALVKHAEGLKVGNGL 320 IV DAD+ AVKAA +++N GQVC + RF+V I + FT+ V LK+G+ Sbjct: 241 IVLNDADLDEAVKAAVIGRYQNTGQVCAAAKRFIVEAGIAEAFTQKFVAAVAALKMGDPR 300 Query: 321 EEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFAPTVIANVPLDADV 380 +E +G +A + + K GA++ G E+I GN++APTV+ NV + Sbjct: 301 DEQNYIGPMARFDLRDELHEQVRATLKEGATLLLGAEKIEGAGNYYAPTVLGNVTAEMTG 360 Query: 381 FNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLLTQRLEVGMLWINQ 440 F E FGPVA I + A+A AN FGL+ +T S LE G ++IN Sbjct: 361 FREELFGPVATITEARDADHALALANESEFGLSATVYTTSETQARRFADELECGGVFING 420 Query: 441 PATPWPEMPFGGVKDSGYGSE 461 + FGGVK SG+G E Sbjct: 421 YCASDARVAFGGVKKSGFGRE 441 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: 503 Number of extensions: 30 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: 461 Length adjustment: 33 Effective length of query: 448 Effective length of database: 428 Effective search space: 191744 Effective search space used: 191744 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 17 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