Alignments for a candidate for dopDH in Collimonas pratensis Ter91

GapMind for catabolism of small carbon sources

Alignments for a candidate for dopDH in Collimonas pratensis Ter91

Align Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized)
to candidate WP_061936832.1 CPter91_RS03175 aldehyde dehydrogenase (NADP(+))

Query= SwissProt::Q08IC0
         (525 letters)



>NCBI__GCF_001584185.1:WP_061936832.1
          Length = 524

 Score =  607 bits (1565), Expect = e-178
 Identities = 322/525 (61%), Positives = 381/525 (72%), Gaps = 2/525 (0%)

Query: 1   MQLTGEMLIGAEAVAGSAGTLRAFDPSKGEPIDAPVFGVAAQADVERACELARDAFDAYR 60
           M ++G+ +IG+          +AFD  +G+ I+ P F  A   D+ERAC LA+ AFD YR
Sbjct: 1   MPISGQSIIGSSQAHSQGAVFQAFDTVQGKQIE-PDFHSAEPQDIERACALAQTAFDLYR 59

Query: 61  AQPLAARAAFLEAIADEIVALGDALIERAHAETGLPVARLQGERGRTVGQLRLFARVVRD 120
           A    ARA FLE IA +I+ +GD LI RA AE+GLP ARL+GERGRTVGQLRLFA V+R+
Sbjct: 60  ATGQEARAVFLETIAQQILDIGDELILRAMAESGLPRARLEGERGRTVGQLRLFAAVLRE 119

Query: 121 GRFLAASIDPAQPARTPLPRSDLRLQKVGLGPVVVFGASNFPLAFSVAGGDTASALAAGC 180
           G +  A IDP  P R PLPR DLRL+ + +GPV VFGASNFPLAFSVAGGDTA+ALAAGC
Sbjct: 120 GSWNDARIDPVLPERLPLPRVDLRLRNIAIGPVAVFGASNFPLAFSVAGGDTAAALAAGC 179

Query: 181 PVIVKAHEAHLGTSELVGRAIRAAVAKTGMPAGVFSLLVGPGRVIGGALVSHPAVQAVGF 240
           PV+VKAH AH GTSELVG A++ A+A   +P GVFSLL G G  +G ALV +P +QAVGF
Sbjct: 180 PVVVKAHPAHPGTSELVGHAVQKAIAACNLPEGVFSLLTGIGNALGTALVQNPRIQAVGF 239

Query: 241 TGSRQGGMALVQIANARPQPIPVYAEMSSINPVVLFPAALAARGDAIATGFVDSLTLGVG 300
           TGSRQGG+AL+Q+A ARPQPIPVYAEMSSINPV L PAALAAR +AIA GF DS+TLG G
Sbjct: 240 TGSRQGGLALMQVAAARPQPIPVYAEMSSINPVYLLPAALAARAEAIAKGFADSVTLGAG 299

Query: 301 QFCTNPGLVLAIDGPDLDRFETVAAQALAKKPAGVMLTQGIADAYRNGRGKLAELPGVRE 360
           QFCTNPGLVL + G D DRF  +A   L ++ A  MLT GI  AY+ G   LA    VR+
Sbjct: 300 QFCTNPGLVLGLAGADFDRFAQLAGAELMQRSAAAMLTTGIHAAYKQGVATLAAQDDVRQ 359

Query: 361 IGAGEAAQTDCQAGGALYEVGAQAFLAEPAFSHEVFGPASLIVRCRDLDEVARVLEALEG 420
           +  G AA    +A  AL+     AFLA P  S E+FGP SL+V C +  E+ +V E LEG
Sbjct: 360 LARGVAAD-GYRAVPALFVTSGAAFLANPLLSAEIFGPVSLLVACANEAELLQVSEQLEG 418

Query: 421 QLTATLQMDADDKPLARRLLPVLERKAGRLLVNGYPTGVEVCDAMVHGGPFPATSNPAVT 480
           QLT TLQMD DDK L R LLPVLERKAGR+L NG+PTGVEV  AMVHGGPFPATS+   T
Sbjct: 419 QLTVTLQMDDDDKALVRSLLPVLERKAGRILANGFPTGVEVSHAMVHGGPFPATSDSRST 478

Query: 481 SVGATAIERFLRPVCYQDFPDDLLPEGLQESNPLAIPRLRDGKAE 525
           SVG+ AI RFLRPV YQ+   DLLP  LQ++NPLAI + RDG+ E
Sbjct: 479 SVGSAAIYRFLRPVSYQNLAQDLLPAALQDANPLAIWQRRDGRLE 523


Lambda     K      H
   0.320    0.137    0.396 

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: 889
Number of extensions: 42
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: 525
Length of database: 524
Length adjustment: 35
Effective length of query: 490
Effective length of database: 489
Effective search space:   239610
Effective search space used:   239610
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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About GapMind

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources