Align Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)
to candidate WP_076477023.1 BW971_RS04825 gamma-aminobutyraldehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_1974 (488 letters) >NCBI__GCF_900156495.1:WP_076477023.1 Length = 500 Score = 202 bits (513), Expect = 3e-56 Identities = 150/461 (32%), Positives = 226/461 (49%), Gaps = 8/461 (1%) Query: 5 YIAGEWLAGGGEAFESLNPVTQQVLWSGVGATAGQVESAVQAARQAFPDWARRTLEERIS 64 ++ G G G + P T +V+ + ATA V++AV AAR+A P W+ T +R + Sbjct: 15 WVEGAEFRGSGPLHRVIAPATDEVVATMSLATAADVDTAVAAARRALPAWSGATPAQRST 74 Query: 65 VLEAFAAALKNHADELAHTIGEETGKPLWEAAT-EVTSMVNKIAISVQSYRERTGEKSGP 123 VL FA L A LA TGK + A+ +V ++ + R+ G+ + Sbjct: 75 VLLDFARVLDREAHALAVQEVSHTGKTIRLASEFDVPGSIDNVTFFAGVARDLVGKATAE 134 Query: 124 LG-DATAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNSVLFKPSELTPKVAELTV 182 D T+ +R + GVV P+N+P + +PA+ AG +++ KP+E+TP Sbjct: 135 YSPDHTSSIRREAVGVVGSITPWNYPIQMAVWKALPAIAAGCTLVLKPAEITPLTTITLA 194 Query: 183 KCWIEAGLPAGVLNLLQG-ARETGIALAANPGIDGLFFTGSSRTGNHLHQQFAGRPDKIL 241 + EAGLP GV N+L G E G ALA +PG+D + FTGS+ G + Q A ++ Sbjct: 195 RLASEAGLPDGVFNVLTGTGAEVGAALAGHPGVDLVTFTGSTGVGRQVMAQAAVHGTRV- 253 Query: 242 ALEMGGNNPLVVDQVADLDAAVYTIIQSAFISAGQRCTCARRLLVPQGAWGDSLLARLVA 301 LE+GG P VV ADL+AAV+ + + I+AGQ CT A R +V + D ++ + Sbjct: 254 QLELGGKAPFVVFDDADLEAAVHGAVAGSLINAGQDCTAATRAIVAPALY-DDFVSGVAE 312 Query: 302 VSSTLSVGAFDQQPAPFMGSVVSLGAAKALMDAQEHLLANGAVALLEMTQPQAQSALLTP 361 + + + VG PA MGS+ S + + + G + P A P Sbjct: 313 LMAGVRVGD-PTDPATDMGSLSSRHHREKVAAMVDRARDTGIRVVTGGHVPDGPGAFYPP 371 Query: 362 GIL-DVSAVADRPDEELFGPLLQVIRYADFEAAIAEANDTAYGLAAGLLSDSEARYQQFW 420 +L DV A+ +E+FGP+L V + D + A+ A DT YGLAA + R Q+ Sbjct: 372 TLLADVGEGAEVYRDEIFGPVLTVSSFTDDDDALRRAGDTVYGLAASAWTRDVYRAQRAS 431 Query: 421 LESRAGIVNWNKQLTGAASSAPFGGVGASGNHRASAYYAAD 461 E RAG V W S P GG+ ASG + + Y+ D Sbjct: 432 REIRAGCV-WINDHIPIVSEMPHGGLRASGFGKDMSTYSMD 471 Lambda K H 0.316 0.132 0.388 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: 585 Number of extensions: 37 Number of successful extensions: 6 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: 488 Length of database: 500 Length adjustment: 34 Effective length of query: 454 Effective length of database: 466 Effective search space: 211564 Effective search space used: 211564 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 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