Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_211251871.1 Q366_RS07005 gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_000745975.1:WP_211251871.1 Length = 469 Score = 564 bits (1454), Expect = e-165 Identities = 273/469 (58%), Positives = 348/469 (74%), Gaps = 8/469 (1%) Query: 5 LLINGELVSGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVRA 64 LLING +V GE EK +++P + ++++ A+ QVD AV AA+AAF W + + RA Sbjct: 8 LLINGNIVDGEAEKTSLFSPENNEFIVDVPCATTAQVDLAVDAANAAFPAWKRKSFADRA 67 Query: 65 ECLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAG 124 L K AD I+E Q+ A+LES NCGKP DE+PAI D FRFFAGA RC++G AAG Sbjct: 68 TVLYKFADRIDEKAQLLAKLESLNCGKPFQRMLEDEMPAISDHFRFFAGACRCMSGSAAG 127 Query: 125 EYLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKL 184 EYLEG TSMIRRDP+GVV IAPWNYPLMMAAWK+APALAAGN VV KPSE TPLT L L Sbjct: 128 EYLEGFTSMIRRDPVGVVGQIAPWNYPLMMAAWKIAPALAAGNTVVFKPSECTPLTMLGL 187 Query: 185 AELAKDIFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKRTH 244 E K++FPAGV+NI+ G+G +G + GH K++MVS+TGS+ TG+ +++ S++KRTH Sbjct: 188 VEDIKELFPAGVLNIVTGKGSVIGKHIAGHEKIQMVSVTGSVNTGKQVLASATSNVKRTH 247 Query: 245 MELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLGAAV 304 +ELGGKAPVI FDD DI+ +VE + +GYYNAGQDCTAACR+Y Q IY +VEKL AAV Sbjct: 248 LELGGKAPVIAFDDCDIDDLVENMTLWGYYNAGQDCTAACRLYVQDKIYPEVVEKLTAAV 307 Query: 305 ATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKGNGYYYAPTL 364 ++ + ++GPL S E V VE AK H+K++ GG K GY+Y PTL Sbjct: 308 KSI-------DVNDIGPLISAEQREIVSSFVERAKKVPHLKIVAGGNK-IDRGYFYEPTL 359 Query: 365 LAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHRVSAR 424 + A QDD +VQ+E+FGPVVSVT F++ +Q + WAND +YGLASS+WT+D+ +AHRVS+ Sbjct: 360 IIDARQDDEVVQEEIFGPVVSVTRFNDADQAIEWANDCKYGLASSIWTRDIEKAHRVSSM 419 Query: 425 LQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVMVK 473 LQ+G TW+NT+FM SEMPHGG K+SGYGKD+S+YGLEDYTVVRH+MVK Sbjct: 420 LQFGVTWINTYFMYASEMPHGGFKMSGYGKDLSMYGLEDYTVVRHIMVK 468 Lambda K H 0.317 0.134 0.397 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: 595 Number of extensions: 18 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: 474 Length of database: 469 Length adjustment: 33 Effective length of query: 441 Effective length of database: 436 Effective search space: 192276 Effective search space used: 192276 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: 51 (24.3 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