Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_041098592.1 SUTH_RS08615 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::C6KEM4 (506 letters) >NCBI__GCF_000828635.1:WP_041098592.1 Length = 480 Score = 332 bits (850), Expect = 2e-95 Identities = 188/478 (39%), Positives = 271/478 (56%), Gaps = 12/478 (2%) Query: 9 RRGLFIGGAWREPCLGRRLPVVNPATEATIGDIPAGTAEDVEIAVAAARDAFSRDGGRQW 68 R I G W G L + NPAT +G +P A + A+ AA AF W Sbjct: 8 RNACLINGEWLA-ATGATLDIRNPATGEAVGSVPGFGAAETRRAIDAAHAAF-----HPW 61 Query: 69 SRAPGAVRANFLRAIAAKIKDRKSELALLETLDSGKPLDEASGDMDDVAACFEYYADLAE 128 A RA LR + + + +LA L T + GKPL EA G++ A+ E++A+ A Sbjct: 62 RAKTAAERAKILRRWFELMMENQEDLARLMTQEQGKPLAEARGEIAYAASFIEWFAEEAR 121 Query: 129 ALDGKQRSPISLPMENFKSYVLKEPIGVVGLITPWNYPLLMATWKVAPALAAGCTTILKP 188 + G I P+ + + VLK+P+GV ITPWN+P M T KVAPALAAGCT ++KP Sbjct: 122 RIYG---DVIPSPLADRRLIVLKQPVGVCAAITPWNFPAAMITRKVAPALAAGCTMVVKP 178 Query: 189 SELASVSCLELGAICMEIGLPPGVLNIITGLGPEAGAPLSSHSHVDKVAFTGSTETGKRI 248 +E +S L L + + GLPPGVLN++TG G L+S+ V K++FTGSTE G+ + Sbjct: 179 AEQTPLSALALAWLGQQAGLPPGVLNVVTGEPVAIGGELTSNPKVLKLSFTGSTEIGRLL 238 Query: 249 MTSAAQMVKPVSLELGGKSPLIVFDDIGDIDKAVEWTMFGIFANAGQVCSATSRLLLHEK 308 M A +K +SLELGG +P IVFDD D+D AV M + N GQ C T+R L+ E Sbjct: 239 MGQCAPTIKKMSLELGGNAPFIVFDD-ADLDAAVAGAMLSKYRNTGQTCVCTNRFLVQEG 297 Query: 309 IAKKFLDRLVAWAKNIKVSDPLEEGCRLGSVISEGQYEKIKKFISTARSEGATILYGGGR 368 + F RL A +KV LEEG G +I K+++ ++ A ++GA +L GG R Sbjct: 298 VHDAFAQRLAAAVAGLKVGYGLEEGVTQGPLIDGAGLAKVEELLADALAKGARVLCGGKR 357 Query: 369 PQHLRRGFFLEPTIITDVSTSMQIWQEEVFGPVICVKEFRTDSEAVELANDTHYGLAGAV 428 H + G F EPT++ + +M++ +EE+FGPV + F+ +++A+ +ANDT +GLA Sbjct: 358 --HAKGGTFFEPTVLAGATPAMRLAREEIFGPVAPIFSFKDEADAIRMANDTEFGLAAYF 415 Query: 429 ISNDQERCERISKALHSGIIWINCSQPCFVQAPWGGNKRSGFGRELGEWGLDNYLTVK 486 S D R R+ +AL G++ IN AP+GG K+SG GRE ++G++ YL +K Sbjct: 416 FSRDIARAWRVGEALDYGMVGINSGMISNEVAPFGGVKQSGLGREGSKYGIEEYLEIK 473 Lambda K H 0.318 0.136 0.418 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: 635 Number of extensions: 33 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: 506 Length of database: 480 Length adjustment: 34 Effective length of query: 472 Effective length of database: 446 Effective search space: 210512 Effective search space used: 210512 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