Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012536595.1 AFE_RS07230 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000021485.1:WP_012536595.1 Length = 475 Score = 375 bits (964), Expect = e-108 Identities = 199/470 (42%), Positives = 298/470 (63%), Gaps = 6/470 (1%) Query: 51 SFVGGRWLPTPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISVKERSS 110 +F+ G W A F V P + L V+DCG EA AAV+AA AF++W++ +V +R+ Sbjct: 8 AFIDGCWTDLRARFVVQSPVNQQMLAEVSDCGPREADAAVQAATVAFAAWRQTTVYQRAL 67 Query: 111 LLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGDIIYTS 170 +L +W DL+ + ++LA++IT E GKP+++++ EI + W++EE +RV G+ I + Sbjct: 68 ILSRWADLIQVHAEDLARLITWEMGKPIRQSRAEIKTAVALARWYAEECKRVTGESIPSQ 127 Query: 171 AKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSALALAQ 230 DKR + K P+G ITPWN P +M+ RK+ ALAAGCTV++KP E TP SAL LA+ Sbjct: 128 FPDKRLQIWKVPIGPVFAITPWNSPVSMVVRKIAPALAAGCTVILKPDEQTPLSALKLAE 187 Query: 231 LANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAANSVKR 290 L A P G V+P + + E L D ++K+SFTGSTA G+ L + ++KR Sbjct: 188 LWAAAEGPAGTLQVLPSA--DPAPLAERLMADSRIAKLSFTGSTAVGQKLYAQGSPTIKR 245 Query: 291 VSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFVTKFAE 350 +S+ELGG AP ++F A++D AVA + +KFR AGQ+CV +NR V I F ++ E Sbjct: 246 LSLELGGHAPVLIFADADIDAAVAMTIHAKFRYAGQSCVAANRLYVDEAILPEFTARYLE 305 Query: 351 AMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGGNFFEP 410 AM L+VG+ F E T GPL++E AV+K + + DA+A+GA ++ GG + G + P Sbjct: 306 AM-GHLKVGDPFAEDTDIGPLVSEVAVQKFKAQLQDAMARGARLLCGG---DAQGLWCSP 361 Query: 411 TLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQIWRVA 470 TLL+++ EE+F P+ P+ F E EAVA AN GLA Y +++D + +R+A Sbjct: 362 TLLADLDPQSRIFHEESFSPLLPIQGFRSEAEAVARANDTPYGLAAYLWTRDLGRAYRIA 421 Query: 471 EQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCY 520 E L+ G+VGVN+G ++ + PFGG K SGLG EG K+G++EYL+++YV + Sbjct: 422 EALQCGIVGVNDGAPATPQAPFGGSKLSGLGAEGGKWGLEEYLQLRYVSF 471 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: 569 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: 523 Length of database: 475 Length adjustment: 34 Effective length of query: 489 Effective length of database: 441 Effective search space: 215649 Effective search space used: 215649 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 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