Aligments for a candidate for xad in Pseudomonas stutzeri RCH2

GapMind for catabolism of small carbon sources

Aligments for a candidate for xad in Pseudomonas stutzeri RCH2

Align xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate GFF233 Psest_0234 dihydroxy-acid dehydratase

Query= BRENDA::P39358
         (655 letters)



>lcl|FitnessBrowser__psRCH2:GFF233 Psest_0234 dihydroxy-acid
           dehydratase
          Length = 612

 Score =  206 bits (525), Expect = 2e-57
 Identities = 167/511 (32%), Positives = 248/511 (48%), Gaps = 67/511 (13%)

Query: 120 DGRTQGTTGMFDSLPYRNDASMVMRRLIRSLPDAKAVIGVASCDKGLPATMMALAAQHNI 179
           DG   G  GM  SLP R   +  +  ++ +   A A++ +++CDK  P  +MA A + NI
Sbjct: 81  DGIAMGHDGMLYSLPSREIIADSVEYMVNA-HCADAIVCISNCDKITPGMLMA-ALRLNI 138

Query: 180 ATVLVPGGA-----TLPAKDGEDNGKVQTIGARFANGELSLQDARRAGCKACASSGGGCQ 234
             V V GG      T  A  G D      I A  +  +  + +  R+ C  C    G C 
Sbjct: 139 PVVFVSGGPMEAGKTKLASHGLDLVDAMVIAADESASDEKVAEYERSACPTC----GSCS 194

Query: 235 FLGTAGTSQVVAEGLGLAIPHSALAPSGEPVWREIARASARAALNLSQK-------GITT 287
            + TA +   +AE LGLA+P +    +      ++   + R  + L ++        +  
Sbjct: 195 GMFTANSMNCLAEALGLALPGNGSTLATHSDREQLFLRAGRTVVELCKRYYGEGDESVLP 254

Query: 288 REILTDKAIENAMTVHAAFGGSTNLLLHIPAIAHQAGCHIPTVDDWIR----INKRVPRL 343
           R I + +A ENAMT+  A GGSTN +LH+ A A +A      VD  +R    ++++VP+L
Sbjct: 255 RNIASRRAFENAMTLDIAMGGSTNTILHLLAAAQEA-----EVDFDLRAIDALSRKVPQL 309

Query: 344 VSVLPNGPVYHPTVNAFMAGGVPEVMLHLRSLGLLHEDVMTVTGSTLKENLDWWEHSERR 403
             V PN   YH   +   AGG+  ++  L   GLLH DV TV   TL E +  W+ ++ +
Sbjct: 310 CKVAPNIQKYH-MEDVHRAGGIFSILGELARGGLLHTDVPTVHSRTLAEGIAQWDITQTQ 368

Query: 404 QR------------------FKQLL----LDQEQINADEVIMSPQQAKARGLTSTITFPV 441
                               F Q      LD ++ N    I S + A ++     + +  
Sbjct: 369 DEAVHTFFKAGPAGIPTQTAFSQSTRWDSLDDDRENG--CIRSVEHAYSQEGGLAVLY-- 424

Query: 442 GNIAPEGSVIKSTAIDPSMIDEQGIYYHKGVAKVYLSEKSAIYDIKHDKIKAGDILVIIG 501
           GNIA +G V+K+  +D S      I+  +G AK+Y S+ SA+  I  D++KAGDI++I  
Sbjct: 425 GNIALDGCVVKTAGVDES------IHVFEGTAKIYESQDSAVKGILADEVKAGDIVIIRY 478

Query: 502 VGP-SGTGMEETYQVTSALKHLSYGKHVSLITDARFSGVSTGACIGHVGPEALAGGPIGK 560
            GP  G GM+E    TS LK    GK  +L+TD RFSG ++G  IGH  PEA AGG IG 
Sbjct: 479 EGPKGGPGMQEMLYPTSYLKSKGLGKDCALLTDGRFSGGTSGLSIGHASPEAAAGGAIGL 538

Query: 561 LRTGDLIEIKIDCRELHGEVNFLGTRSDEQL 591
           +R GD + I I  R +  +V      SDE+L
Sbjct: 539 VRDGDKVLIDIPNRSIQLQV------SDEEL 563


Lambda     K      H
   0.317    0.135    0.400 

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: 909
Number of extensions: 52
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 655
Length of database: 612
Length adjustment: 38
Effective length of query: 617
Effective length of database: 574
Effective search space:   354158
Effective search space used:   354158
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: 54 (25.4 bits)

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

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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 preprint 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