Align succinate-semialdehyde dehydrogenase [NAD(P)+] (EC 1.2.1.16) (characterized)
to candidate WP_009779838.1 MED217_RS07225 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::Q8ZPI3 (462 letters) >NCBI__GCF_000152985.1:WP_009779838.1 Length = 476 Score = 377 bits (967), Expect = e-109 Identities = 198/465 (42%), Positives = 286/465 (61%), Gaps = 9/465 (1%) Query: 4 MTATQALS-------VNPATGQTLAAMPWANAQEIEHALSLAASGFKKWKMTSVAQRAQT 56 +TAT+ S +NP+TGQ L + QE A+ F WK S+ +RA+ Sbjct: 9 LTATEQASSSDTIQTINPSTGQPLNSYKMMTDQEASEAVKATHQAFLTWKTFSLEKRAEF 68 Query: 57 LRDIGQALRAHAEEMAQCITREMGKPIKQARAEVTKSAALCDWYAEHGPAMLNPEP-TLV 115 + IG++L H +++ + +T+EMGK Q EV +C++ A++GP +L E TL Sbjct: 69 INKIGESLSKHKDQLVKLMTQEMGKLTSQGEQEVDLCVGICEYTAKNGPEVLKDEERTLP 128 Query: 116 ENQQAVIEYRPLGVILAIMPWNFPLWQVLRGAVPILLAGNSYLLKHAPNVTGCAQMIARI 175 + + +I P+GVI I PWNFP +QV+R A+ L+AGN LLKHA NVTG A +I +I Sbjct: 129 DGGKGLITNAPIGVIYGIQPWNFPTYQVIRYAIANLMAGNGVLLKHAENVTGSALLIDKI 188 Query: 176 LAEAGTPAGVYGWVNANNEGVSQMINDPRIAAVTVTGSVRAGAAIGAQAGAALKKCVLEL 235 + EAG P ++ + ++E +I + + VT+TGS AG +G +AG ALKK VLEL Sbjct: 189 IREAGLPENIFTVLRISHEQSDAIIENDLVRGVTLTGSGAAGKVVGEKAGKALKKTVLEL 248 Query: 236 GGSDPFIVLNDADLELAVKAAVAGRYQNTGQVCAAAKRFIVEEGIAQAFTDRFVAAAAAL 295 G +D ++VL+DAD++ AV+ ++ GR N G+ C AAKRF+V E + F ++FVA + Sbjct: 249 GSNDAYLVLDDADVDTAVEWSIKGRIYNNGETCVAAKRFVVTEKVYDEFKEKFVAGMKEI 308 Query: 296 KMGDPLVEENDLGPMARFDLRDELHQQVQASVAEGARLLLGGEKIAGEGNYYAATVLADV 355 K GDP + D+GPMAR DLR++LH Q++ SVA GA +L GGE G+G +Y ATVL +V Sbjct: 309 KFGDPADDTVDIGPMARKDLREKLHNQLKESVANGAEILCGGELPEGDGYFYPATVLGNV 368 Query: 356 TPDMTAFRQELFGPVAAITVAKDAAHALALANDSEFGLSATIFTADDTLAAEMAA-RLEC 414 P A+ ELFGPVA++ AKD A+ +ANDS FGL IF+ D+ A E+A + Sbjct: 369 KPGQPAYDDELFGPVASLIKAKDNQDAMRIANDSRFGLGGGIFSKDEAAAFELAKNHFDT 428 Query: 415 GGVFINGYSASDARVAFGGVKKSGFGRELSHFGLHEFCNVQTVWK 459 G VFIN + + + FGGVK SG+GRE FG+ EF N + + + Sbjct: 429 GMVFINSFGVAQPNMPFGGVKASGYGREHGGFGVKEFVNEKAIMR 473 Lambda K H 0.319 0.131 0.386 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: 506 Number of extensions: 21 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: 462 Length of database: 476 Length adjustment: 33 Effective length of query: 429 Effective length of database: 443 Effective search space: 190047 Effective search space used: 190047 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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