Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 326 bits (836), Expect = 1e-93 Identities = 189/486 (38%), Positives = 274/486 (56%), Gaps = 20/486 (4%) Query: 22 LFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPA 81 L+I+G + AA+ T + P + ++ G D A+ AAR F+ G W + Sbjct: 4 LYIDGTWRDAADGATRDIHCPADGHHVVTVSEGGEQDAVAAVVAARSAFDNGPWPHTPAP 63 Query: 82 KRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGE 141 +R A+L++LAD +EA +E+A LE+LDTGK S + D+ R +A G Sbjct: 64 ERAALLHRLADRLEADKDEVARLESLDTGKRFVES-QIDVDDIVSVFRHFASLAQGEAGR 122 Query: 142 VATTSSHEL-AMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSA 200 V + + +V EP+GV I PWN+PLL T WK+ P LAAGN+ ILKPSE +P +A Sbjct: 123 VVDAGMPGVVSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPSTA 182 Query: 201 IRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSN 260 I L G +AGLPDGV N+V G G G L+ ++D ++FTG TG++++ A + Sbjct: 183 IWLMGALSDAGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMVAAAPT- 241 Query: 261 MKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLA 320 +K+V LE GGK+ N++FAD DL A +F + GQVC AG RL++E+++ D+ + Sbjct: 242 VKKVALELGGKNPNVIFADA-DLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVD 300 Query: 321 LLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDG----RNAGLA 376 L ++A + G P D G LI AH D V +++ G ++G L G AG A Sbjct: 301 ELVRRAGRIRLGGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRPEGAGYA 360 Query: 377 AAIG------PTIFVDVDPNASLSREEIFGPVLVVTRFTS------EEQALQLANDSQYG 424 A + PTI D + S +EE FGPVL V RFT EE A+ +AND+ YG Sbjct: 361 AGLAEGFYYLPTILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYG 420 Query: 425 LGAAVWTRDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFT 484 L AVWT D RA R++ RL+ G++++N+Y+ +GGYKQSG GR+ + LE++ Sbjct: 421 LAGAVWTSDAGRAERVASRLRHGTIWINDYHPYVAQAEWGGYKQSGTGRELGIAGLEEYR 480 Query: 485 ELKTIW 490 E K IW Sbjct: 481 ETKHIW 486 Lambda K H 0.317 0.133 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: 626 Number of extensions: 29 Number of successful extensions: 6 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: 495 Length of database: 506 Length adjustment: 34 Effective length of query: 461 Effective length of database: 472 Effective search space: 217592 Effective search space used: 217592 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