Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_110748414.1 C7477_RS02030 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_003217235.1:WP_110748414.1 Length = 488 Score = 529 bits (1362), Expect = e-154 Identities = 267/475 (56%), Positives = 349/475 (73%), Gaps = 6/475 (1%) Query: 51 SFVGGRWLPTPA--TFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISVKER 108 + +GG W+ + T V +PA+G K GTV G E A+ AA AF SWK+ S ER Sbjct: 13 NLIGGEWVEADSGQTIDVINPATGLKFGTVPKSGKAETARAITAAAKAFESWKKTSAAER 72 Query: 109 SSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGDIIY 168 + L+RK +DL+I+N+D LA+++T E GKPL EA+GEI SA ++ W++EEARRVYGD + Sbjct: 73 ARLMRKLHDLIIENQDALAELLTLEQGKPLAEAKGEIGMSAAYILWYAEEARRVYGDTVP 132 Query: 169 TSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSALAL 228 + D+R LV K+PVGV + ITPWNFPS+M+ RK+G ALA+GCT VVKPA TPYS LA Sbjct: 133 SPWADRRILVTKEPVGVVAAITPWNFPSSMLARKIGPALASGCTAVVKPATQTPYSGLAW 192 Query: 229 AQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAANSV 288 L +AGIP GV N++ S A E+G L +PLV K++FTGST GKIL+ +A++V Sbjct: 193 GVLCEEAGIPDGVINILTGS---ASEIGGELTRNPLVRKLTFTGSTEVGKILIKQSADTV 249 Query: 289 KRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFVTKF 348 K+VSMELGG APFIVFD A++D+AV GA+A+KFRN+GQTCVC+NRF Q GI+D FV + Sbjct: 250 KKVSMELGGNAPFIVFDDADMDRAVEGAIAAKFRNSGQTCVCTNRFFAQAGIYDRFVERL 309 Query: 349 AEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGGNFF 408 A A +K L+VGNG E+GT QGPLI+E AVEKVE+ + DA AKG VVTGGKR G +F Sbjct: 310 AAAAEK-LKVGNGLEDGTQQGPLIDEGAVEKVEELITDAEAKGGKVVTGGKRSTLGLTYF 368 Query: 409 EPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQIWR 468 EPT++++ DM EE FGPVAPV KF E+EAV +AN+ + GLA YFY+QD + +R Sbjct: 369 EPTVITDAKPDMRFFKEEIFGPVAPVYKFGTEQEAVDLANSTEYGLACYFYTQDLGRTFR 428 Query: 469 VAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYGGL 523 V E L+ G++GVNEG+I++VE PFGG+K+SGLG+EG GI++YL+ KYVC GGL Sbjct: 429 VMEGLKYGLIGVNEGMITTVEAPFGGLKESGLGKEGGHQGIEDYLDTKYVCIGGL 483 Lambda K H 0.318 0.135 0.400 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: 697 Number of extensions: 24 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: 523 Length of database: 488 Length adjustment: 34 Effective length of query: 489 Effective length of database: 454 Effective search space: 222006 Effective search space used: 222006 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