Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_041376699.1 PNAP_RS13165 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::Q88RC0 (480 letters) >NCBI__GCF_000015505.1:WP_041376699.1 Length = 490 Score = 593 bits (1529), Expect = e-174 Identities = 290/477 (60%), Positives = 361/477 (75%), Gaps = 3/477 (0%) Query: 3 LKDAQLFRQQAYINGEWLDADNGQTIKVTNPATGEVIGTVPKMGTAETRRAIEAADKALP 62 L D L + A ING+WL V++P+ G + V +G A+ AI AA+ A P Sbjct: 11 LNDPSLLKTDALINGQWLAG--ASRFDVSDPSNGNKLADVANLGPADAEAAIAAANAAWP 68 Query: 63 AWRALTAKERSAKLRRWFELMIENQDDLARLMTTEQGKPLAEAKGEIAYAASFIEWFAEE 122 AWR T KERS LR+WF+L++ NQ+DLAR+MT EQGKP AEAKGE+AY ASF+EWFAEE Sbjct: 69 AWRGKTGKERSIILRKWFDLLMANQEDLARIMTAEQGKPFAEAKGEVAYGASFVEWFAEE 128 Query: 123 AKRIYGDTIPGHQPDKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPA 182 AKR+ G+T+P ++RL+V+KQPIGV AITPWNFP AMITRK PALAAGCT+V+KPA Sbjct: 129 AKRVNGETLPQFDNNRRLMVLKQPIGVCVAITPWNFPLAMITRKVAPALAAGCTVVIKPA 188 Query: 183 SQTPYSALALVELAHRAGIPAGVLSVVT-GSAGEVGGELTGNSLVRKLSFTGSTEIGRQL 241 TP +ALA VELA RAG+P+GVL+++T + VG + +VR +SFTGSTE+GR L Sbjct: 189 ELTPLTALAAVELAVRAGVPSGVLNILTTDESAAVGKVFCASDVVRHISFTGSTEVGRIL 248 Query: 242 MEECAKDIKKVSLELGGNAPFIVFDDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDGV 301 M + A IKK+SLELGGNAPFIVFDDAD+D AVEGA+ SKYRN GQTCVCANRIYVQ+GV Sbjct: 249 MAQSAPSIKKLSLELGGNAPFIVFDDADIDSAVEGAMASKYRNAGQTCVCANRIYVQEGV 308 Query: 302 YDAFAEKLAAAVAKLKIGNGLEEGTTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSGGKLI 361 YD F K A V LK+GNG E+G GPLI+ AV KV+ H++DA++KG K+L+GG + Sbjct: 309 YDQFVHKFAEKVRLLKVGNGFEDGVGQGPLIEDAAVHKVERHVQDALAKGGKLLAGGHKL 368 Query: 362 EGNFFEPTILVDVPKTAAVAKEETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYARDM 421 EG FFEPT++ + A+EETFGP AP+FRF E E I +N+TEFGLASYFY+RD+ Sbjct: 369 EGQFFEPTVISEAHADMLCAREETFGPFAPVFRFTHEQEAIDAANNTEFGLASYFYSRDI 428 Query: 422 SRVFRVAEALEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCI 478 R++RVAEALEYGMVGIN G+I+ E PFGG+K SGLGREGS +G+E+YLEIKYLC+ Sbjct: 429 GRIYRVAEALEYGMVGINAGVIATEHVPFGGVKQSGLGREGSSHGMEEYLEIKYLCL 485 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: 694 Number of extensions: 13 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: 480 Length of database: 490 Length adjustment: 34 Effective length of query: 446 Effective length of database: 456 Effective search space: 203376 Effective search space used: 203376 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: 52 (24.6 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