Align Succinate-semialdehyde dehydrogenase, mitochondrial; At-SSADH1; Aldehyde dehydrogenase family 5 member F1; NAD(+)-dependent succinic semialdehyde dehydrogenase; Protein ENLARGED FIL EXPRESSING DOMAIN 1; EC 1.2.1.24 (characterized)
to candidate WP_017549143.1 C792_RS0108995 aldehyde dehydrogenase family protein
Query= SwissProt::Q9SAK4 (528 letters) >NCBI__GCF_000330705.1:WP_017549143.1 Length = 501 Score = 343 bits (881), Expect = 7e-99 Identities = 186/472 (39%), Positives = 286/472 (60%), Gaps = 11/472 (2%) Query: 57 IGGKWLDSYDNKTIKVNNPATGEIIADVACMGTKETNDAIASSYEAF--TSWSRLTAGER 114 I G+ ++S D T + NPATGE+IA VA ++ A+ ++ +AF + W A +R Sbjct: 19 INGEKVESSDGGTNDIINPATGEVIAKVAMATGEDAERAVMAARDAFENSKWKIYPASKR 78 Query: 115 SKVLRRWYDLLIAHKEELGQLITLEQGKPLKEAIGEVAYGASFIEYYAEEAKRVYGDI-- 172 +K+L R ++ +EL +L L GK + A G++ EYYA G Sbjct: 79 AKILNRIASIMRERFKELVELEVLNSGKSINAATGQINQAVEDFEYYAGAVCNHGGQTND 138 Query: 173 IPPNLSDRRLLVLKQPVGVVGAITPWNFPLAMITRKVGPALASGCTVVVKPSELTPLTAL 232 +P + K+PVGV I PWN+PL M KV PALA+GCTVV+KP+ LTPLTAL Sbjct: 139 VPGQFHN---YTEKEPVGVCAQIVPWNYPLMMAAWKVAPALAAGCTVVLKPASLTPLTAL 195 Query: 233 AAAELALQAGVPPGALNVVMGNAPEIGDALLTSPQVRKITFTGSTAVGKKLMAAAAPTVK 292 E+ +AGVP G +N++ G+ +GD L+ P+V K+ FTGST GK +M+ A+ T+K Sbjct: 196 ILGEICQEAGVPDGVINILPGSGSRVGDYLVEHPEVDKVAFTGSTDTGKDIMSKASRTLK 255 Query: 293 KVSLELGGNAPSIVFDDADLDVAVKGTLAAKFRNSGQTCVCANRVLVQDGIYDKFAEAFS 352 +++LELGG +P+++F DA+L+ AV ++ + N+GQ+C +R+ V+D IYDKF E F Sbjct: 256 RLTLELGGKSPALIFGDAELENAVASSVYGIYNNTGQSCDARSRIYVEDRIYDKFVEQFV 315 Query: 353 EAVQKLEVGDGFRDGTTQGPLINDAAVQKVETFVQDAVSKGAKIIIGGKRHSL----GMT 408 E +++++GD T G LI+ + ++ VE +++ A +GA I GG R S+ G Sbjct: 316 EKTKQMKMGDPMSKETHMGSLIDKSQLESVEAYIETARQEGATIAYGGNRLSIEGYEGGF 375 Query: 409 FYEPTVIRDVSDNMIMSKEEIFGPVAPLIRFKTEEDAIRIANDTIAGLAAYIFTNSVQRS 468 + EPT+I DV+++M + ++EIFGPV + RF E++A+ +AN+TI GLA+ I+T +++ Sbjct: 376 WLEPTIITDVTEDMTVVRDEIFGPVVVISRFSDEKEAVSLANNTIYGLASSIYTEDTRKA 435 Query: 469 WRVFEALEYGLVGVNEGLISTEVAPFGGVKQSGLGREGSKYGMDEYLEIKYV 520 RV + + G+V +N + PFGG KQSG GRE S +D Y E K + Sbjct: 436 KRVADKIRAGIVMINCPFSAFPGTPFGGYKQSGFGRELSAETLDLYSETKSI 487 Lambda K H 0.317 0.134 0.383 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: 604 Number of extensions: 25 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: 528 Length of database: 501 Length adjustment: 35 Effective length of query: 493 Effective length of database: 466 Effective search space: 229738 Effective search space used: 229738 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: 52 (24.6 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