Align succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized)
to candidate WP_052123206.1 Q763_RS03145 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::B1XMM6 (454 letters) >NCBI__GCF_000769915.1:WP_052123206.1 Length = 451 Score = 405 bits (1042), Expect = e-117 Identities = 205/449 (45%), Positives = 294/449 (65%), Gaps = 3/449 (0%) Query: 5 TINPTTGEICQRFKALTPAEIDAKLAKAQEAFQAYRRTSFSQRRQWLENAAAILERDTSK 64 T NP ++ T +++ L +Q++F+ + +T +R ++++N +L + Sbjct: 4 TTNPYDLSTLSEYQYYTDIQVNQMLEISQKSFRKWGKTPLKKRVKFIKNLIFVLTKKQHL 63 Query: 65 FAEIMTTEMGKTHQSAIAEAEKSALVCRYYAEHGEQFLANEYTETQATESYVCYQPLGIL 124 AE + EMGK + AIAE +K +L+C +Y EH E+FL +E + A ES+V ++PLG++ Sbjct: 64 LAEKCSQEMGKPLKQAIAEVKKCSLLCEFYLEHAEKFLQDEKISSDAGESFVTHEPLGVI 123 Query: 125 LAVMPWNFPFWQVFRFAAPALMAGNVAVLKHASNVPQCALAVEAILEAAGFPEGVFQTLL 184 L VMPWNFP+WQVFRFA PA++AGN V+KHASNV +CA +E + + A FPE ++Q L Sbjct: 124 LGVMPWNFPYWQVFRFAIPAIIAGNTVVVKHASNVAECAQLLEELFKEAEFPEMIYQNLQ 183 Query: 185 IGASQVEQVIKDPRVKAATLTGSEPAGASLASLAGQEIKPTLLELGGSDPFVVFPSADLD 244 I SQV+ VI++P +K +LTGSE AGA++AS A IK ++LELGGS+ F+V ADLD Sbjct: 184 ISGSQVKNVIENPIIKGVSLTGSEKAGATVASTAANLIKKSVLELGGSNAFIVLEDADLD 243 Query: 245 EAVEVGTVARTMNNGQSCIAAKRFILHEAIAAEFLEKLHLKFASLKIGDPMAPETDIGPL 304 +AV V AR N GQSCIAAKRF++H ++ EFL++ + LK G+PM +TDIGPL Sbjct: 244 KAVPVAVTARMQNTGQSCIAAKRFLVHSSLYDEFLKRFTTEVKKLKSGNPMDEDTDIGPL 303 Query: 305 ATEGILQDISRQVDQAVAAGAKILLGGRPLDRAGYFYPPTILTEIPPGAKILQEELFAPV 364 A + +DI +QV+++V GAK+++GGR R FY PTI+ + + EE+F PV Sbjct: 304 ARVDLAEDIEKQVNKSVDMGAKVIIGGR---RNNAFYEPTIVVNVTSDMPLFNEEVFGPV 360 Query: 365 AMVFTVKDLDQAIALANDIPFGLGASAWTNDPAEQQRFIQELDAGAVFINGMVKSDPRLP 424 A V ++A+ L+N FGLG + +T D + I + GAVFIN MVKSDP LP Sbjct: 361 APVIAFDSFEEAVKLSNYSDFGLGVNIFTEDIEGIKEKISLFEEGAVFINAMVKSDPALP 420 Query: 425 FGGTKRSGYGRELGLAGIRTFVNAKTVWL 453 FGG K+SG+GREL GI+ FVN KTV++ Sbjct: 421 FGGVKKSGFGRELAENGIKEFVNVKTVYI 449 Lambda K H 0.319 0.134 0.389 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: 485 Number of extensions: 15 Number of successful extensions: 2 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: 454 Length of database: 451 Length adjustment: 33 Effective length of query: 421 Effective length of database: 418 Effective search space: 175978 Effective search space used: 175978 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