Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_017549192.1 C792_RS0109240 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::Q88RC0 (480 letters) >NCBI__GCF_000330705.1:WP_017549192.1 Length = 459 Score = 447 bits (1151), Expect = e-130 Identities = 223/457 (48%), Positives = 303/457 (66%), Gaps = 2/457 (0%) Query: 26 QTIKVTNPATGEVIGTVPKMGTAETRRAIEAADKALPAWRALTAKERSAKLRRWFELMIE 85 + I V NPATGE I ++ K + IE A +A ++ A +RSA L W +L+ E Sbjct: 3 EEIAVMNPATGEEIRSIKKDSREDIEAKIETAHQAFKKYKKKNAHDRSALLSEWAKLIRE 62 Query: 86 NQDDLARLMTTEQGKPLAEAKGEIAYAASFIEWFAEEAKRIYGDTIPGHQPDKRLIVIKQ 145 N+D++A+L+T E GKPLAE+ GE+ YA S+I+++AEE KR+YG TIP H+ D RL+V KQ Sbjct: 63 NKDEIAQLITKENGKPLAESLGEVEYACSYIDYYAEEGKRVYGRTIPPHEDDVRLVVTKQ 122 Query: 146 PIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPYSALALVELAHRAGIPAGV 205 PIGV AAITPWNFP AM+ RKA PA+AAGCT ++KPA +TP SA+ ++LA AG AGV Sbjct: 123 PIGVVAAITPWNFPVAMMARKAAPAVAAGCTFLVKPARETPLSAMRFLDLAKDAGFEAGV 182 Query: 206 LSVVTGSAGEVGGELTGNSLVRKLSFTGSTEIGRQLMEECAKDIKKVSLELGGNAPFIVF 265 + V S + G + + V KL+FTGST +G++LME A +K +++ELGG+AP +V Sbjct: 183 IQYVNASGKDAGEVFSQSDKVMKLTFTGSTAVGKKLMEGAASTVKNITMELGGHAPLVVH 242 Query: 266 DDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDGVYDAFAEKLAAAVAKLKIGNGLEEG 325 DADL+ AV+ AI +K+RN+GQTCVCANR YV + + DAF+EK + V KLK+GNG++EG Sbjct: 243 KDADLETAVDHAIATKFRNSGQTCVCANRFYVHEDIADAFSEKFSEKVKKLKMGNGMDEG 302 Query: 326 TTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSG--GKLIEGNFFEPTILVDVPKTAAVAKE 383 GP+I+ KV EHI DA KG + +G G EG F EPT++ D + E Sbjct: 303 VQVGPMINKDGYDKVMEHINDARQKGGTITAGGNGNNSEGYFIEPTVITDATDEMIIMNE 362 Query: 384 ETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYARDMSRVFRVAEALEYGMVGINTGLI 443 ETFGP+AP+ F + E I +NDTE+GLA+YF+ R+ E L +G++G N G Sbjct: 363 ETFGPVAPIQTFSNLDEAIEKANDTEYGLAAYFFTESYRDGIRLQEGLNFGVLGWNNGKP 422 Query: 444 SNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCISV 480 S PFGG+K SG+GREG GIE YLE K + + Sbjct: 423 SAAHIPFGGLKESGIGREGGLEGIEPYLETKITSMKI 459 Lambda K H 0.317 0.134 0.384 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: 586 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: 480 Length of database: 459 Length adjustment: 33 Effective length of query: 447 Effective length of database: 426 Effective search space: 190422 Effective search space used: 190422 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 (21.6 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