Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_009763662.1 MICLODRAFT_RS20175 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::pseudo6_N2E2:Pf6N2E2_4383 (497 letters) >NCBI__GCF_000262405.1:WP_009763662.1 Length = 495 Score = 291 bits (746), Expect = 3e-83 Identities = 171/488 (35%), Positives = 274/488 (56%), Gaps = 14/488 (2%) Query: 10 EQRARDLK----IEGRAFINGEYTDAVSGETFDCLSPVDGRLLGKIASCDVADAQRAVEN 65 ++R DLK + G+A++ GE+ DA G+T P DG L+ ++ A+RA++ Sbjct: 9 DRRVVDLKDPSLLVGQAYVAGEWIDAPDGKTIPVTDPFDGALILEVPDLGPDAARRAIDK 68 Query: 66 ARATFSSGVWSRLAPSKRKATMIRFAGLLKQHAEELALLETLDMGKPISDSLNIDVPGAA 125 A A W++ +R A + R+ L+ +A++LAL+ T + GKP++++ + AA Sbjct: 69 AHAVQKD--WAKRTAKERSAILRRWYDLIVANADDLALILTTEQGKPLAEAKGEVISNAA 126 Query: 126 QALSWSGEAIDKLYDEV--AATPHDQLGLVTREPVGVVGAIVPWNFPLMMACWKLGPALS 183 + W E ++ +V ATP ++ +V ++PVGV AI PWNFP M K+GPAL+ Sbjct: 127 Y-IEWFAEEAKRIDGDVIPGATPSQRI-VVLKQPVGVCAAITPWNFPNGMITRKVGPALA 184 Query: 184 TGNSVVLKPSEKSPLTALRIAALAIEAGIPKGVLNVLPGYGHTVGKALALHMDVDTLVFT 243 G ++VLKP+ ++PL+AL +A LA AG+PKG +V+ G +G+ + V + FT Sbjct: 185 AGCTMVLKPAAQTPLSALALAVLAERAGVPKGAFSVVTGEAKPIGEEFCHNPKVAKITFT 244 Query: 244 GSTKIAKQLMIYSGESNMKRIWLEAGGKSPNIVFADAPDLQAAAESAASAIAFNQGEVCT 303 GST + + LM + + +KR+ LE GG +P IVF DA DL AA E A ++ N G+ C Sbjct: 245 GSTGVGRWLMKEAAD-GIKRLSLELGGNAPFIVFDDA-DLDAAVEGAMASKFRNAGQTCV 302 Query: 304 AGSRLLVERSIKDTFLPLVIEALKGWKPGNPLDPATNVGALVDTQQMNTVLSYIEAGHSD 363 +R+ V+ + + F + K G D +G L+D + + + ++ Sbjct: 303 CANRIYVQEGVAEAFAEKLAAKAGSLKLGRGTDAGVTMGPLIDDRAVAKMEEHVRDVLDK 362 Query: 364 GAKLVAGGKRILEETGGTYVEPTIFDGVSNAMKIAQEEIFGPVLSVIAFDTAEQAIEIAN 423 G KL+ GGKR + G T+ EPT+ GV+ AMK+ +EE F P+ +I F I +AN Sbjct: 363 GGKLLVGGKR--SDLGSTFFEPTVMTGVTQAMKVTKEETFAPLAPIITFKDEADVIAMAN 420 Query: 424 DTPYGLAAAVWTKDISKAHLTAKALRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHA 483 D+ +GLA+ + KD+++ A+AL +G V VN + APFGG KQSG GR+ S + Sbjct: 421 DSEFGLASYFYAKDMARVWRVAEALESGMVGVNTPALANEMAPFGGVKQSGLGREGSKYG 480 Query: 484 FDKYTELK 491 + + E+K Sbjct: 481 IEGFLEIK 488 Lambda K H 0.316 0.132 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: 630 Number of extensions: 33 Number of successful extensions: 5 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: 497 Length of database: 495 Length adjustment: 34 Effective length of query: 463 Effective length of database: 461 Effective search space: 213443 Effective search space used: 213443 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