Alignments for a candidate for patD in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for patD in Paraburkholderia bryophila 376MFSha3.1

Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate H281DRAFT_00213 H281DRAFT_00213 aldehyde dehydrogenase (NAD+)

Query= BRENDA::P23883
         (495 letters)



>FitnessBrowser__Burk376:H281DRAFT_00213
          Length = 479

 Score =  358 bits (920), Expect = e-103
 Identities = 209/481 (43%), Positives = 291/481 (60%), Gaps = 15/481 (3%)

Query: 19  ENRLFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLS 78
           E R FI GE++AA+  ET   +DP    P  ++ARG + DID A+ AAR  FE G W  +
Sbjct: 3   EARHFIGGEWSAASGGETIAVLDPSDGQPFTQLARGTAADIDAAVHAARRAFE-GAWGAA 61

Query: 79  SPAKRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKV 138
           S A+R  VL +L+ L+ A  EELA LE  DTGKP++ + R D     R   +YA A DK+
Sbjct: 62  SAAERGRVLYRLSMLVAARQEELAQLEARDTGKPLKQA-RADSAALVRYFEFYAGAADKL 120

Query: 139 YGEVATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPL 198
           +GE     +    M +REP GV   IVPWN+P+ +    +G ALA GN+ ++KP+E + L
Sbjct: 121 HGETLPYQAGYTVMTIREPHGVTGHIVPWNYPMQIFGRSVGAALAVGNACVVKPAEDACL 180

Query: 199 SAIRLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGD 258
           S +R+A LA EAGLP G LN+VTG+GHEAG AL+RH+ ID I+FTGS  TGK + + A +
Sbjct: 181 SVLRVAELAAEAGLPAGALNIVTGYGHEAGAALARHSGIDHISFTGSPETGKLVTQMAAE 240

Query: 259 SNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEF 318
           +++  V LE GGKS  +VFAD  DL  A     + I  N GQ C AG+R+L++ +I +  
Sbjct: 241 NHVP-VTLELGGKSPQLVFADA-DLDAALPVLVSAIVQNAGQTCSAGSRVLIDRAIYEPL 298

Query: 319 LALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGE-------SKGQLLLDGR 371
           L  L       + G P       G LI+      V  F+ + +       + G+++ +  
Sbjct: 299 LDRLSSAFNALRVG-PSHADLDCGPLINAKQQRRVWDFLSDAQHDGIAMAAHGEVIPEAP 357

Query: 372 NAGLAAAIGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWT 431
            +G   A  PT+  DV  +  L+R+E+FGPVL    F+ E++AL LAN +QYGL A +WT
Sbjct: 358 ESGFYQA--PTLLRDVPASHRLARDEVFGPVLAAMSFSDEDEALALANGTQYGLVAGIWT 415

Query: 432 RDLSRAHRMSRRLKAGSVFVNNYN-DGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIW 490
           RD +R  R++RRL++G VF+NNY   G + +PFGG K SG+GR+K   AL  FT LKTI 
Sbjct: 416 RDGARQMRLARRLRSGQVFINNYGAGGGVELPFGGVKHSGHGREKGFEALYGFTALKTIA 475

Query: 491 I 491
           I
Sbjct: 476 I 476


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: 607
Number of extensions: 34
Number of successful extensions: 7
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: 479
Length adjustment: 34
Effective length of query: 461
Effective length of database: 445
Effective search space:   205145
Effective search space used:   205145
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 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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 paper from 2022 on GapMind for carbon sources, or view the source code.

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